BIODERMA Congress Reports AAD 2023

Speakers: Boni Elewski, Matilde Iorizzo, Shari Lipner, Nilton Di Chiachhio, Brian Morrison, Adam Rubin, Antonella Tosti, Sergio Vañó-Galván, Maryanne Senna, Jerry Shapiro, Valerie Callender, Amy McMichael, Dr Rodrigo Pirmez, Daniel Asz Sigall and Bruna Duque Estrada

Report written by Dr. Ben Esdaile

Boni Elewski from Alabama started with tips for treating onychomycosis and suggested not treating until the fungus has been confirmed especially given rising resistance to antifungals. She discussed her use of prolonged courses of oral terbinafine, oral itraconazole (usually pulsed) and fluconazole. Her preference is to extend the course until cure is achieved with up to 6 months for terbinafine in toenail disease and 6 pulses of itraconazole (200mg bd for 1 week with 4 week break). She also described the use of fluconazole 200mg one to twice a week (‘’fungal Fridays’) again until clearance achieved. She also gave a useful tip for stopping statins 2 days before and starting 2 days after pulses of itraconazole to try and prevent rhabdomyolysis.

Matilde Iorizzo from Switzerland talked about new treatments for nail psoriasis. She discussed intralesional methotrexate injections (25mg/ml) into the nail matrix on a 6 weekly basis for 6 months with a slightly better outcomes compared to intralesional steroids in a small study. She discussed new topicals on the horizon including cyclosporine compounded as hydrogel and tofacitinib. She also discussed the potential benefits of ducravacitinib (TYK2i) in nail psoriasis. In nail lichen planus she discussed the challenges in treatment and good results with tofacitinib but with the caveat that ongoing treatment is required.

Shari Lipner from New York gave us tips for treating brittle nails. Most cases are idiopathic but can be secondary to dermatologic conditions, systemic diseases and occupation. It often presents with onychoschizia and onychorrhexis. She discussed treatment options and in particular lifestyle measure including avoiding water and irritants, avoid nail cosmetics and the importance of nail moisturisation. She discussed that vitamins and supplements have no vigorous trials to support their use. Biotin deficiency is rare and is obtained in a normal diet and the evidence for oral biotin supplementation is weak. She also bought to our attention that biotic can interfere with lab test including thyroid function and cardiac enzymes and should be stopped before blood test. In terms of treatments she discussed the importance of lifestyle measure but improvement can be achieved with lacquers but these can be expensive.

Nilton Di Chiachhio from Brazil discussed retronychia with proximal ingrowing of the nail. The underlying problem is that the nail does not grow forward. He discussed treatment options with anti-inflammatory and potent topical steroids in mild cases, intralesional steroid in moderate cases and nail avulsion in severe cases.

Brian Morrison from Miami talked about HPV-associated nail disease with a novel case report of local hyperthermia treating warts with a halogen tungsten lamp with good results in a child. He discussed reported success with the combination of fluorouracil and salicylic acid with 2-6 months of treatment. He also discussed the potential of intralesional cidovir and the MMR vaccine. Finally he showed a promising paper with the use of the nonavalent HPV vaccination clearing warts in some cases.

Adam Rubin from Philadelphia gave an update on his approach to managing melanonychia and the potential role of nail clippings to help in the diagnosis of nail unit melanoma as well as diagnosing other causes including blood and infection. He also highlighted the potential benefits of also being able to locate the origin in the nail matrix.

Antonella Tosti from Miami talked about when and how to prescribe oral minoxodil. She showed evidence of its use in numerous hair loss disorders. In AGA she recommended a dose of 0.25-2.5mg in women and 0.25 to 5mg in men. She discussed that side effects are dose dependent including hypertrichosis. She suggested avoiding in cardiovascular disorders, women with hirsutism and men with hypertrichosis. She discussed the possibility of ankle oedema and the extremely rare and unpredictable risk of pericardial effusion with just 3 cases in the literature. She discussed that the combination with low dose spironolactone (25mg) is to help with the potential of ankle oedema. She suggested continuing topical minoxodil as well and warned that effects can take 6 months. She suggested stopping treatment one month before pregnancy.

Sergio Vañó-Galván from Spain gave us an update on anti-androgens including the potential use of oral dutasteride at a dose of 0.5mg 2-3 x week with an improvement in its side effect profile. He also discussed the use of topical finasteride 0.25% being almost as effective as oral finasteride. He also discussed mesotherapy with dutasteride in some selected cases being beneficial. He went on to discuss more novel anti-androgen including mesotherapy with bicalutamide, oral bicalutamide 10-50mg daily as well as the potential use of topical clascoterone.

Maryanne Senna from Massachusetts updated us on her use of JAK inhibitors for Alopecia areata and discussed a tool to use to evaluate the severity. She discussed her experience and dosing with tofacitinib and baricitinib.

Jerry Shapiro from New York updated us on 5-alpha reductase inhibitors. He discussed the use of topical finasteride 0.25% via a spray and it benefits of no systemic sexual side effects. He also discussed the potential use of dutasteride in mesotherapy.

Valerie Callender from Maryland then gave useful tips on managing dry itchy scalps in women of colour. She discussed different grooming practices as well as the importance of the frequency of shampooing (weekly or alternate weeks) and daily hair moisturisers. She also gave a useful tip that scalp itching and hair breakage can be seen in early or occult CCCA.

Amy McMichael from North Carolina gave us tips for managing Central Centrifugal cicatricial alopecia (CCCA). She highlighted that a ¼ have genetic underpinning and this can be important to let patients know rather than assuming relation to hair practices. She suggested using dermoscopy to check and treat any inflammation and to biopsy if not sure. She also discussed that seborrhoeic dermatitis may be related and there may be potential with 10% topical metformin but there is currently not enough data.

Dr Rodrigo Pirmez from Brazil discussed his technique in using mesotherapy. He highlighted the limited evidence but this is growing. He discussed the use of minoxodil, dutasteride and finasteride. He also discussed a novel technique of MMP with microinfusions into the skin using a tattoo machine.

Daniel Asz Sigall from Mexico discussed treatment of hair loss in trangender individuals. He discussed treatment of trans men with topical or oral minoxodil first line. He discussed that the effects of oestrogen on hair is controversial in trans women but again first line would be topical or oral minoxodil and then multiple anti-androgens.

Bruna Duque Estrada from Brazil gave a talk on a new method of injecting eyebrows using a cannula and ultrasound guidance to deliver steroids in a less painful technique with a diffuse pattern of hair regrowth.

Yolanda Lenzy from Massachusetts discussed ethnic hair care practices and numerous useful tips onhair cleansing weekly or biweekly and the importance of touching patient’s hair when examining scalps. She also warned against the term protective styling and the importance of giving advice (such as loose cornrows or flat twists) rather than just telling patients what they can’t do.

Marina Hordinksy from Minnesota gave an update on PRP and showed 2 FDA cleared devices but further studies are needed as well as further studies with hybrid products with hyaluronic acid to find optimal conditions.

Ronda Farah from Minnesota warned us about novel Exosomes product

From mesenchymal cells and platelets. She warned that these are expensive, they are not FDA approved and there are concerns about potential infection and malignancy. Good studies are lacking.

The session concluded with Martin Zaiac from Miami giving an overview of painful nails with numerous nail tumours (onychomatrixomas, digital fibromas, pyogenic granulomas, exostoses and digital mucous cysts), nail deformities, inflammatory and infectious diseases (paronychia) and external agents.

Speakers: Jerry Shapiro, Natasha Mesinkovska, Sergio Vano-Galvan, Lidia Rudnicka, Elise Olsen, Kristen Lo Sicco, Pearl Grimes, Leonard Sperling, Rodney Sinclair and Rodrigo Pirmez

Report written by Dr. Ben Esdaile

The session was started by Jerry Shapiro from New York who discussed updates in Alopecia Areata. He discussed that oral minoxodil is now standardly used in combination with JAK inhibitors (JAKi) for severe disease. He showed data from Ritlecitinib (JAK3/TEC inhibitor) that seems extremely efficacious with mild adverse effects. He gave advice on the use of Baracitinib at 4mg daily giving excellent reduction in SALT scores (less then 20 i.e 80% scalp coverage). He looked at data showing little difference in performance between the JAKi but advised that SALT scores increase on stopping but you can down titrate in some. In terms of good candidates for JAKi he used the VICTIM mnemonic so to use in caution with patients with a history of Viral (hepatitis), Infections (TB), Coronary artery disease, Thromboembolic history, Immunisations and Malignancy. He recommends checking a full blood count, liver function tests, Quantiferon, hepatitis screen and pregnancy test prior to starting and then annually. He also recommended a lipid test at 12 weeks.

Natasha Mesinkovska from California discussed how she manages hair loss in women. She gave a number of top tips including asking about allergies in alopecia areata as a possible aggravating factor. She suggested that we ask what products patients are using again to look for potential allergies. She also suggested asking about previous scalp surgeries as well as the use of Botulinum toxin as Botulinum-induced frontal alopecia (BIFA) has been reported.

Sergio Vano-Galvan from Spain gave an update on hair surgery. He discussed the importance of selecting the correct patient and the fact in some cases medical management can negate the need for transplantation. He also highlighted the importance of ongoing medical management after transplantation. He then showed how his team performs transplant with micrografts. He also showed that excisional surgery is an option in some cicatricial alopecias.

Lidia Rudnicka from Poland gave an un update on dermoscopy (trichoscopy) for hair loss. She advised the use of trichoscopy in every patient with hair loss and reminded us that every patient could have two diseases of the scalp. She carefully went through dermoscopic signs in the hair shaft and the follicular openings to help with common hair loss conditions. She reminded us that the exclamation mark hair in alopecia areata is suggestive of activity and is a poor prognostic sign.

Elise Olsen from North Carolina gave an update on 5-alpha reductase inhibitors in women with hair loss. She went through the evidence and side effect profiles of finasteride and dutasteride. She suggested the use of 1-2.5mg finasteride and showed that there is no reason not to use 5mg. Dutasteride 0.5mg is more effective but with a longer half-life. Both finasteride and dutasteride are effective for women with AGA. She advises against the use of dutasteride in women of child bearing age and to ensure using contraception if using finasteride. She showed some evidence for the use of topical finasteride as well as in combination with minoxodil.

Kristen Lo Sicco from New York talked about anti-androgens for Androgenetic Alopecia for both injectables and topicals. She showed benefits of topical finasteride 0.25% daily in combination with 5% topical minoxodil. She also showed some interesting potential benefits with 2% Ketoconazole shampoo (3-7 x week) use for AGA. She also showed encouraging data with Clascoterone 7.5% solution twice daily. She also confirmed potential benefits of mesotherapy (transdermal microinjections) of dutasteride every 3 months with minimal side effects.

Pearl Grimes from California gave an update on Central Centrifugal Cicatricial Alopecia (CCCA). She showed that this is a truly devastating disease to those affected in Quality of Life studies. She showed some studies showing a relationship with CCCA and seborrhoeic dermatitis. Pathogenesis involves genetics, possible grooming practices (chemicals, heat, dermatitis and trauma) and low vitamin D.

Leonard Sperling from Maryland talked about what’s new in pathology of hair disease in the last 2 years. He showed a paper that showed sebaceous gland atrophy as a dependable and distinctive sign in seborrhoeic dermatitis and possible psoriasis. He discussed the importance of biopsying the correct site (not bald spots in cicatricial alopecia) and the use of a dermatoscope to aid the correct site. He also advised the importance of good clinical information for the pathologist.

Rodney Sinclair from Australia talked about the use of low dose oral minoxodil. He explained that minoxodil is poorly soluble and the maximum topical concentration is 5% (It has stability issues above this). Percutaneous absorption is also low 1.5-4% and therefore oral minoxodil has benefits.

Rodrigo Pirmez from Brazil discussed his approach to managing Frontal Fibrosing Alopecia. He discussed the complexity in managing the condition and each patient is unique depending on the features present. As it is a scarring condition he treats early and aggressively. His first line systemic agent is hydroxychloroquine with doxycycline being an alternative. He tends to add in dutasteride or finasteride as well. He uses tacrolimus topically due to concerns of atrophy with potent topical steroids and uses 2.5mg/ml of triamcinolone for ongoing inflammation on a 4-6 weekly basis. He uses oral minoxodil 1.25mg in all cases to help with hair density. His second and third line treatments tend to be methotrexate and ciclosporin. He treats eyebrow alopecia with triamcinolone and sometimes bimatoprost. For facial papules he uses isotretinoin with a loading dose of 40mg daily for 2 weeks and then maintaining on 10-20mg 2-3x week before trying to taper in 3-6 months. He advises all his patients to avoid sunscreen on the hairline.

Leopoldo Santos from Brazil talked about procedures beyond PRP and transplantation and specifically about mesotherapy and a tattoo machine (MMP) to deliver drugs including dutasteride and minoxodil. He showed us how to do a scalp ring block to make the procedure more comfortable.

Finally, Azael Freties-Martinez from Spain discussed alopecia in cancer patients and survivors. He discussed chemotherapy-induced alopecia (CIA) and the potential of scalp cooling systems helping in 50%. There is 15-30% chance of persistent chemotherapy induced alopecia (pCIA). He used to manage this with 5% topical minoxodil but now uses oral minoxodil 0.5-5mg daily. He does not use finasteride but an option is spironolactone 200mg daily. He also discussed endocrine therapy induce alopecia (from tamofixen or aromatase inhibitors) with management being similar to pCIA.

Speakers: Morgan Wilson, Mark Lebwohl, Rebecca Larson, Aimilios Lallas and Stephen Stone

Report written by Dr. Ben Esdaile

The session was started by Morgan Wilson from Illinois who gave us some clinicopathological pearls. He showed us that fungus and hypertrophic lichen planus can mimic Squamous Cell Carcinomas especially when numerous SCCs are diagnosed on the lower legs. He then discussed the use of the PRAME (PRefentially expressed Antigen in Melanoma) immunohistochemistry stain in helping to diagnose melanoma. He showed that when diffusely positive (with 76-100% cells stain) this is more common in melanoma than naevus.

Mark Lebwohl from New York gave us some further pearls. He discussed the use of an Il-36 blocker (Spesolimab) in sick patients with acute generalised pustular psoriasis with one infusion causing clearance within 24 hours. He also showed a dramatic case of extensive ulcerative pyoderma gangrenosum not responding to a TNF blocker, high dose prednisolone and ciclosporin but with a dramatic response to Spesolimab infusions. He then showed a case of extensive Darier’s disease previously not responding to topicals and oral acitretin but responding to bexarotene 150-300mg daily (pre-treat with statin, monitor thyroid function and start low dose levothyroxine to reduce side effects). He finished his talk with showing case reports of the potential of JAK inhibitors for numerous resistant inflammatory dermatoses.

Rebecca Larson from Illinois gave some surgical procedural pearls. She showed us the use of micropore tape on a simple tape dispenser to assist nursing staff applying dressings. She showed some useful dressing for the scalp (pony-tail dressing), using a shower cap to protect ear dressings and a novel nasal pack made from the tip of a surgical glove, a cotton ball and Vaseline to keep in the nose for 24-hours post-surgery. In terms of procedural tips she gave an excellent tip of using steri-strips placed horizontally along the wound in extremely fragile skin before suturing.

Aimilios Lallas from Greece gave his dermoscopy pearls and recommended that dermoscopy should be used in the evaluation of all skin lesions. He discussed the importance of symmetry and asymmetry in trying to detect malignancy. He showed the use of pigmented structures (blue globules) in diagnosing BCCs. He showed how dermoscopy can help determine subtypes of BCC for example blue globules can help in detecting nodular components in mixed superficial and nodular basal cell carcinomas. He showed the use of detecting white peri-follicular circles as a diagnostic clue for squamous cell carcinoma. He highlighted useful tips for detecting naevus-associated melanoma with polygonal (grey polygons) lines and an inverse network. He then gave some tips for using dermoscopy in inflammatory skin conditions including white crossing lines in lichen planus and yellow scale in eczema and white scale and dotted parallel lines of blood vessels in psoriasis.

Stephen Stone from Illinois finished the session and gave some more practical pearls. He started with localised neuropathic pruritus (notalagia paraesthetic, brachoradial pruritus) and suggested the use of naltrexone 50mg daily with side effects including nausea and fatigue. He also recommended a product called Dermeleve with strontium bought over the counter as well as reports of benefits of butorphanol nasal spray. He discussed the use of N-acetylcysteine for trichotillomania, nail biting and skin picking at a dose of 2000mg per day for a 6-month course. In Hailey-Hailey disease he advised acitretin between 10-25mg day and another option of naltrexone for associated itch. He finished with a few mini pearls including: red scrotum syndrome he suggested doxycycline 100mg twice daily sometimes being helpful. He suggested biopsying unilateral inguinal fold rashes. Silver nitrate cautery in aphthous stomatis to speed up healing. In generalised Granuloma annulare he suggested methotrexate 15mg per week. He discussed the use of apremilast as a mouth wash for treating lichen planus (2 x 30mg tablets in water bottle 2 x week) leading to 80% improvement. He discussed getting patients to remove their apple-type watches prior to skin surgery due to their potential damage when using a hyfrecator. His gave advice for smelly feet with the use of clindamycin gel, BPO wash in shower and topical metronidazole (also useful for smelly venous ulcers as well). He also discussed the use of ultrasound gel to a viral wart before cryotherapy as it can increase the freezing time, improve the rate of treatment efficacy, and reduce the adverse events associated with cryotherapy.

Speakers: Joel Claveau and Aimilios Lallas

Report written by Dr. Ben Esdaile

My final session of the AAD was hosted by Joel Claveau from Canada and Aimilios Lallas from Greece with numerous interactive dermoscopy cases.

Joel Claveau showed a difficult seborrhoeic keratosis and highlighted the importance of both modalities of dermoscopy when using hybrid devices as the non-polarised mode will show the milia-like cysts to aid the diagnosis. He showed the importance of symmetry in benign melanocytic lesions and examples of melanoma specific structures including atypical streaks and a blue-white veil. He showed a challenging case of Bowenoid papulosis in the groin with multiple grey dots aligned in a linear fashion. His next case highlighted the importance of age with an atypical rim of globules around a naevus in a melanoma in-situ. He showed a negative pigment network as a marker of melanoma as well as a nodular spitz naevus with shiny white streaks and dotted vessels in a child.

Aimilios Lallas then showed a few facial cases and reminded us of his inverse approach in helping detect early lentigo maligna. He showed pigmented actinic keratoses with scale, rosettes and erythema as well as white and wide follicular openings (WWF). He showed the sharp demarcation with an abrupt stop at edge in solar lentigo and milia-like cysts and comedo-like openings in classical seborrhoeic keratoses. He showed us that a pigment network on the face is most likely to be a solar lentigo. He described that in the inverse approach if none of the six non-melanoma features are present as the predominant feature then lentigo maligna should be suspected (the 6 non-melanoma features being scale, white and wide follicles, erythema and reticulate vessels, Fingerprinting, sharp demarcation and classic SK criteria). He then discussed ways of picking up early SCC with the presence of white structureless areas, dotted vessels and ulceration. His last case was that of erosive pustular dermatosis with dermoscopy showing multiple vessels and some pustules. He discussed the potential of systemic retinoids in recalcitrant cases.

Joel Claveau then completed his cases with a challenging case of an atypical fibroxanthoma with red and white structureless areas. He then showed a case of stasis dermatitis on the leg with dotted vessels and yellow crust mimicking squamous cell carcinoma in-situ. He highlighted the challenge of a recurrent naevus on the back mimicking melanoma (pseudomelanoma) with a rim of pale scar tissue as well as a difficult case of amelanotic melanoma on the scalp mimicking basal cell carcinoma. He had two further extremely challenging cases that reminded us of the importance of examining all skin lesion with dermoscopy with a verrucous seborrhoeic keratosis-like melanoma as well as metastatic melanoma mimicking squamous cell carcinoma.

Report written by Dr. Hélène Veillette

Systemic treatment of psoriasis reduces mortality. This was established based on robust data from the PSOLAR registry.

In Denmark, it has been shown that in patients with systemic lupus, major cardiac events are reduced by taking hydroxychloroquine.

Oral minoxidil is a new option for AGA and has an excellent safety profile (1.7% of patients have side effects). The side effects are as follows:

1. Tachycardia (first 24 hours)
2. Light-headedness (one to seven days)
3. Headache (15 to 20 days)
4. Hypertrichosis (one to three months)
5. Oedema (one to three months)

Report written by Dr. Hélène Veillette

Ensure that the lesion to be operated on is not too inflammatory. If necessary, treat with an intra-lesional corticosteroid (suggested dose: 20 to 40 mg/ml) and postpone surgery for one to two weeks.

Curettage of the bottom of the fistula is important, to thoroughly remove the biofilm.

The complications of deroofing are as follows:

1. Bleeding: ensure proper cauterisation, apply a compression bandage, and limit vigorous physical activity for 24 to 72 hours
2. Hypergranulation: treatment with a potent corticosteroid can be attempted. The alternative is to remove the hypergranulation surgically and make sure there is no residual fistula that could explain the phenomenon
3. Infection (uncommon)

It is safe to continue biotherapy in the post-operative period.

The following factors do not influence the time to recovery: body mass index, smoking, diabetes, number of surgical sites

Report written by Dr. Hélène Veillette

Infantile myofibroma: single lesion or multiple lesions: a chest X-ray, an echocardiogram and a whole-body MRI scan with and without contrast are recommended. Consider close follow-up every three to six months. 

In a patient who has taken cyclosporine, if there are multiple papules, consider the diagnosis of cyclosporine-induced sebaceous hyperplasia (can appear several years after discontinuation). The usual treatments for sebaceous hyperplasia can be attempted, including isotretinoin.

In a patient with moderate to severe psoriasis and melanoma, consider IL-17 and IL-23 inhibitors, or apremilast. Avoid JAK inhibitors and anti-TNF agents.

Report written by Dr. Hélène Veillette

Fixed pigmented erythema: Consider the following medications: Bactrim, doxycycline, tetracycline, NSAIDs, acetaminophen, vaccines and some more recent medications such as biotherapies.

Vemurafenib can induce panniculitis. This usually occurs around two weeks after the start of treatment. Treatment is optional as the lesions may resolve spontaneously. NSAIDs and systemic corticosteroids may be attempted depending on the clinical picture. 

Voriconazole can induce phototoxic reactions.

Dupilumab, probably through suppression of the Th2 pathway and the relative reactive increase in Th17 that may occur, can induce arthritis, enthesitis and psoriasis. The median time to onset of these symptoms is 16 weeks. The symptoms may resolve on discontinuation of the medication, but sometimes this takes several months.

Speaker: Dr. Maria K. Hordinsky

Report written by Dr. Hélène Veillette

1. Physiopathology

According to the speaker (Dr Maria K. Hordinsky), this article summarises the topic well: Senna, Maryanne Makredes et al. “Frontiers in Lichen Planopilaris and Frontal Fibrosing Alopecia Research: Pathobiology Progress and Translational Horizons”. JID Innovations: Skin Science from Molecules to Population Health vol. 2,3 100113. 1 Mar. 2022, doi:10.1016/j.xjidi.2022.100113

Here is a diagram taken from this article she presented that shows the physiopathological differences between FFA and LPP:

In addition, here is a table that summarises the clinical and histopathological differences between the two diseases (taken from the same article):

60% of FFA patients and 80% of LPP patients have inflammation in normal-appearing areas of the scalp.

2. Diagnosing FFA

Three clinical patterns: linear (48.8%), diffuse (45%, worst prognosis), double lines (6.2%, best prognosis)

Alopecia of the eyebrows (non-scarring): 73 to 95%

Loss of facial hair and occipital hair is possible

Loss of other body hair (non-scarring alopecia): pubic area and underarms, up to 50% of patients

Small facial papules with changes in skin texture: mostly on the temples, up to 22% of patients (low-dose isotretinoin (e.g. 5 to 10 mg/day) may be effective)

Rosacea-like eruption (erythema of the cheeks in particular)

Depression of facial veins, especially on the forehead

Hyperpigmentation (lichen planus pigmentosus): especially in dark-skinned people; face, neck, skin folds

Hypopigmentation: upper forehead, eyebrows, sometimes associated with vitiligo

3. Treating FFA

Here is the summary presented by Dr Sergio Vañó-Galván

Speakers: Dr. Hye Jin Chung, Dr. Woraphong Manuskiatti, Dr. Jihee Kim, and Dr. Davinder Parsad

Report written by Prof. Jihee Kim

Since the Asian population is increasing and almost 60% of the world is Asian, the demand for experienced dermatologic care for Asian skin will increase. This session was directed to suggests dermatologists learn to diagnose and treat common medical and cosmetic issues.

Dr. Hye Jin Chung presented an updated review on the approach to scars in Asian patients. When intralesional steroid injections fail to treat keloids or hypertrophic scars, Dr. Chung suggests fluorouracil/steroid injections, fractional ablative laser assisted drug delivery, or pulsed dye laser. She also discussed a detailed technique of keloid removal with a fillet flap in Asian patients.

Dr. Woraphong Manuskiatti presented clinical features and treatment options for common benign facial pigmented lesions in Asians. Solar lentigines, melasma, seborrheic keratosis, ABNOM, and PIH are common in Asians because melanocytes in Asian skin respond differently to visible light than in white skin. Visible light induces pigmentation that is darker and more persistent. He suggests treatment with a low fluence picosecond laser for melasma and use of concomitant oral tranexamic acid.

Dr. Jihee Kim presented special cosmetic considerations in neurotoxin, fillers, other 'skin boosters', and laser therapy in Asian patients. She stated that superficial dermal injections of neuromodulator (with or without intradermal injections of hyaluronic acid) and injections of poly-D,L-lactic acid or polynucleotide are common and successful anti-aging techniques.

Dr. Davinder Parsad discussed current developments in the treatment of pigmentary disorders, such as autologous non-cultured epidermal cell suspension for vitiligo and medicinal and laser treatment for acquired dermal macular hyperpigmentation.

Speakers: Drs. Kara M. Braudis, Nicholas Logemann, Palak Kishorkumar Parekh, Melissa Piliang, Michi Shinohara, Campbell Stewart, and Wendi E Wohltmann

Report written by Prof. Jihee Kim

In this interactive session, selection of education al and instructive dermatopathology cases were discussed along with clinicopathologic correlation and recent updates in dermatopathology.

Drs. Kara M. Braudis, Nicholas Logemann, Palak Kishorkumar Parekh, Melissa Piliang, Michi Shinohara, Campbell Stewart, and Wendi E Wohltmann from ‘Dermatopathology slide club’ shared interesting and educative cases, including various inflammatory (ischemic alopecia with therapeutic embolization, phytophotodermatitis etc.) and infectious disease (rat bite fever, blastomycosis, etc. as well as cutaneous malignancies (cutaneous endometriosis, cutaneous acral angiomatous harmatoma, spiradenoma with sebaceous and squamous differentiation, metastatic breast cancer etc.)

Speakers: Dr. Iwei Yeh and Dr. Kiran Motaparthi

Report written by Prof. Jihee Kim

This session provided an up to date coverage of cutaneous neoplasia, inflammatory skin disease, dermoscopy, molecular methods, translational research, and cutaneous infections.

Dr. Iwei Yeh presented “Updates in melanocytic neoplasia” in regards to pathology reporting and 8th AJCC staging. In 8th AJCC staging of primary cutaneous melanoma, T-category is determined by Breslow thickness and ulceration with cutoff point of 0.8 mm for tumor thickness. When measuring Breslow thickness, either excision or biopsy specimen, whichever the greatest is indicated and measurement around adnexal structures should be avoided. N-category is determined by number and extent of nodal disease and satellites, where most lymph node metastasis are detected by examination of the sentinel lymph node. M-category includes site of metastasis as well as LDH level. Recently PRAME immunohistochemistry (IHC) is suggested as a helpful adjunctive IHC modality yet its sensitivity and specificity may appear in different subtypes of melanoma. There are PRAME-negative melanomas and PRAME-positive melanocytic nevi; hence, connection with histopathologic and clinical characteristics is required.

Dr. Kiran Motaparthi presented “Inpatient dermatopathology” encompassing commonly encountered diagnostic mimickers within inpatient dermatology consultations. Toxic epidermal necrolysis (TEN) is a life-threatening condition commonly elicited by drugs. In this talk, simulators of TEN including, Toxic erythema of chemotherapy, drug-induced linear IgA disease and Acute generalized exanthematous pustulosis were described with case presentations. Additionally, cases of calciphylaxis, nutritional deficiency, acute graft-versus-host-disease and neutrophilic dermatosis due to cryptococcus infection were presented.

Speaker: Dr. Scott Elman

Report written by Prof. Jihee Kim

This session reviewed rheumatology disease with skin manifestations such as systemic lupus erythematous and dermatomyositis to provide insights for dermatologists to approach systemic rheumatologic disease. Due to overlapping agenda within session S017, I focused on the session on dermatomyositis.

Dr. Scott Elman presented “Dermatomyositis: Systemic Considerations for the Dermatologist”. Dermatomyositis is an uncommon inflammatory disease marked by muscle weakness and a distinctive skin rash presenting with two distinctive phenotypes; juvenile dermatomyositis (JDM) and adult dermatomyositis (DM), which can be further classified as a clinically amyopathic dermatomyositis (CADM) or hypomyopathic dermatomyositis. When evaluating a patient suspected for DM, systemic evaluation including skin, muscle, lung involvement as well as screening for potential malignancy. Treatment recommendations for patients with DM are based on disease severity, the presence of systemic symptoms, and myositis-specific antibody (MSA) profiles. The difficulty in interpreting MSA profiles exists due to serologic gap within patients with DM who test negative and clinically available tests vary in sensitivity and specificity. Thus, real-world MSA positivity with confirmed DM patients are reported between 20~50%. Recent studies have provide data on certain MSA is linked with more prominent DM phenotype.

• Anti-TIF1-gamma: Widespread disease, psoriasiform lesions, “Red/white” patches , and hyperkeratotic papules on hand
• SAE2: Diffuse erythema with ‘angel wings’ sign
• Anti-Jo-1: Mechanic’s Hands

In the presence of DM-specific skin lesion, proximal muscle weakness and/or elevated muscle enzymes, less invasive procedures compared to muscle biopsy, such as skin biopsy, EMG or MRI can be done. Malignancy work up in all DM patients is controversial yet, recent studies have specified predictors of malignancy associated DM. Therefore, thorough medical history, physical examination, and laboratory testing is necessary along with age=appropriate cancer screening.

Treatment approach to DM depends on the presence and severity of underlying muscle disease, presence of malignancy, and presence of interstitial lung disease. As a general measure, strict sun protection with topical corticosteroids and calcineurin inhibitors are used. Systemic immunosuppressants such as methotrexate, mycophenolate mofetil and IVIG have shown efficacy to date. Additionally, the use of JAK inhibitor (Tofacitinib) is reported in refractory DM patients.

Speakers: Dr. Drucker, Dr. Beck, and Dr. Guttman-Yassky

Report written by Prof. Jihee Kim

This session provided an up-to-date overview of atopic dermatitis (AD), new findings, and new therapeutics. It also emphasizes the high burden and comorbidities of AD, and identifies barrier and immunological alterations in AD that serve as the basis for new treatments.

Dr Drucker and Dr Beck presented an overview of the AD epidemiology and comorbidities and the role of the epidermal barrier, respectively. Dr Guttman-Yassky presented the immune system shifts in AD based on the comprehensive review on the translational studies.

AD is well known as a Th2-polarized disease, while In the chronic lesion of AD, Th1 cells are considered to induce chronic eczema with thick epidermis. Within past decade there have been a paradigm shift in pathogenesis of AD; Different phenotypes of AD, defined according to the patient age at onset, race, and ethnic background; disease duration; and other disease characteristics, have been recently described, underlying the need for a personalized treatment approach. Recent advancements in understanding AD pathogenesis resulted in a real translational revolution and led to the exponential expansion of the therapeutic pipeline. The study of biomarkers in clinical studies of emerging treatments is helping clarify the role of each cytokine and immune pathway in AD and will enable the identification of the distinct immunological fingerprints of each AD subtype.

Translational approach in AD can be done by;

1. Defining AD-specific biomarkers in skin and blood can help to Identify pathogenic pathways and develop precision medicine approaches
2. Skin profiling is considered the gold standard, linking cytokine activation, barrier defects and disease severity
3. Blood profiling may still be useful for patient stratification and therapeutic selection
4. Development of minimally-invasive skin biomarkers is important in both adults and particularly in children, where obtaining skin biopsies may be impossible
5. Tape-strips may provide useful means to investigate biomarkers in pediatric settings and in large clinical trials or longitudinal studies where biopsies are not practical

Speakers: Dr. Diane M Thiboutot, Dr. Del Rosso and Dr. Julie Claire Harper

Report written by Prof. Jihee Kim

This session provided an update on the treatment options for acne and rosacea including the uses of systemic medications.

Dr. Diane M Thiboutot presented novel insights in acne pathogenesis. Drivers of inflammation in the acne microenvironment includes c. acnes, antimicrobial Th17 cell clones and TREM- expressing macrophages. Firstly, among various phylotypes of c.acnes, acne subjects have greater proportions of c. acnes ribotypes 4 and 5. C. acnes phylotypes may have an increased propensity to induce acne due to induction of both Th1 and Th17 responses compared to healthy phylotypes. Meanwhile, the C. acnes strains associated with health induce Th17 clones that secret molecules sufficient to kill C. acnes by differentially modulate the CD4+ T cell responses, leading to the generation of Th17 cells. Therefore, C. acnes induces antimicrobial TH17 clones that trap and kill bacteria by T cell extracellular traps (TETs). TREM2 macrophages present in proximity to hair follicle epithelial cells and acne lesions are enriched with foamy macrophages expressing TREM2. Additionally, squalene, which is overproduced in acne lesions, induces TREM2 macrophages with enhanced phagocytic capacity for lipids and C. acnes, but squalene scavenges oxygen radicals, thus blocking the macrophage antimicrobial response. An increased understanding of the inflammatory drivers in acne, including strain differences of C. acnes may provide opportunities for therapeutic intervention.

Dr. Del Rosso presented the use of oral antibiotics therapy in acne vulgaris and rosacea. Broad-spectrum antibiotics such as tetracycline, doxycycline and minocycline have been used for over 1000 years with favourable safety profiles for chronic use. Commonly stated perspectives on oral antibiotic therapy for acne includes the component of recognized guidelines for moderate to severe acne especially for inflammatory lesions. Combination with topical therapy (especially benzoyl peroxide) can augment efficacy and reduce adverse sequelae. Anticipate a 3-6 months course of therapy with a discussed exit plan to limit exposure.

Sarecycline is defined as a narrow-spectrum tetracycline approved by FDA on 2018. Antibiotic activity of sarecycline antibiotic activity versus C. acnes Is comparable with doxycycline and minocycline with low propensity for C. acnes resistance. Additionally, narrow spectrum of antibiotic activity of sarecycline may correlate with a decreased tendency to disrupt normal flora including the GI tract microbiome.

Dr. Julie Claire Harper presented novel therapeutic insights in rosacea. First, classic subtypes of rosacea are no longer emphasized since different lesions/signs of rosacea will require multiple modes of treatment, and a combination treatment approach is necessary for most patients. The importance of mast cell stabilizers has been raised based on studies on rosacea triggers where inflammation through innate immunity and neurogenic dysregulations are suggested. Increased number of mast cells in the dermis of lesional rosacea skin vs uninvolved skin and mast cells are the key mediators of LL-37-induced rosacea inflammation. Among various mast cell stabilizers, hydroxychloroquine (HCQ) showed comparable efficacy with doxycycline and is generally deemed safe during pregnancy and may be an alternative treatment for women with rosacea. Additionally, 5% microencapsulated benzoyl peroxide cream gained FDA-approval for inflammatory lesions of rosacea. Oral sarecycline and low-dose minocycline which showed efficacy for acne have demonstrated in several clinical studies and can be an emerging treatment option for rosacea.

Speakers: Steven T. Chen (Harvard Medical School, Boston), Jennifer N. Choi (Northwestern University, Chicago) and Bernice Kwong (Stanford University, Palo Alto)

Report written by Dr. Joël Claveau

The cutaneous side effects of cancer immunotherapy were presented during this symposium. The number of indications for these treatments is constantly increasing (melanoma, various cutaneous and mucosal carcinomas, lung cancer, kidney cancer, urogenital and gynaecological neoplasms, some forms of lymphoma and leukaemia, neurological cancers, etc.). The main drugs used include PD-1 inhibitors (pembrolizumab, nivolumab and cemiplimab), PD-L1 inhibitors (atezolizumab, durvalumab and avelumab), CTLA-4 inhibitors (ipilimumab), and LAG inhibitors (relatlimab). Cutaneous side effects occur in 40% of patients and considerably affect their quality of life. The rash usually starts within the first three months but can occur at a late stage, even after stoppage of treatment. Interestingly, the development of an immune cutaneous side effect is associated with improved patient survival. Some common side effects include isolated pruritus, a maculopapular rash, eczematous dermatitis, a lichenoid rash, psoriasis, and vitiligo. Most of the time, immunotherapy does not need to be stopped and the rash can be controlled by using the right amount of topical steroids. For rarer or more severe rashes, dermatological intervention is important and the use of systemic steroids or other systemic agents is recommended. The wide variety of conditions reported have included bullous pemphigoid, cutaneous sarcoidosis, Sweet syndrome, panniculitis, and a severe rash characteristic of Stevens-Johnson syndrome, also called toxic epidermal necrolysis. Management of these severe cases will require a multidisciplinary approach and often a transfer to a specialised care unit (intensive care, burn unit, etc.).

Speaker: Kelly L Harms (MD, PhD, FAAD, Michigan Medicine, Ann Arbor, USA)

Report written by Dr. Joël Claveau

The management of patients with Merkel cell carcinoma (MCC) requires a multidisciplinary approach at all stages. MCC is a rare neuroendocrine carcinoma; it is estimated that there are around 2,800 cases/year in the United States compared with 5,400,000 cases of basal and squamous cell carcinomas. This tumour has a high risk of lymph node involvement and metastasis. The average age of patients is around 70 years. The main risk factors are being over 60, sun exposure, and immune suppression. Merkel cell polyomavirus was discovered and associated with this carcinoma in 2008. This carcinoma often has a non-specific presentation and the acronym AEIOU can help in the diagnosis (A: asymptomatic, E: expanding rapidly, I: immune suppression, O: older than 50 years, U: UV exposure). The tumour is usually reddish or purplish and grows rapidly for two to three months; it usually occurs in a photo-exposed area. For the histological diagnosis, it is a small-round-blue-cell tumour resembling small-cell lung cancer or lymphoma. The diagnosis is confirmed by immunohistochemistry with perinuclear staining with CK20 and other neuroendocrine markers as well as negative TTF-1 staining. The presence of polyomavirus is associated with a better prognosis and may be useful in the follow-up of patients.

In terms of management, if the clinical examination and radiological tests (usually a PET-CT scan) do not reveal enlarged lymph nodes, the sentinel node technique should be performed in all cases as the positivity rate is above 15-20%. In the rare cases where a resection margin of at least 1 cm is difficult to achieve (e.g. eyelid, nostril), Mohs surgery can be offered to the patient. Otherwise, a 1-2 cm margin should be offered and should be followed by additional radiotherapy at the local excision site for tumours > 1 cm. Usually, for clinical (palpable or radiological) lymph node involvement, the patient is offered complete lymph node dissection and sometimes even additional postoperative radiotherapy. For patients with sentinel node involvement, the approach will be more conservative, usually with radiotherapy to the affected nodal basin. Lastly, there is still no accepted adjuvant treatment for high-risk stage III patients, but immunotherapy (PD-L1 inhibitor/avelumab or PD-1 inhibitor/pembrolizumab) is increasingly standing out as a first alternative for inoperable stage III patients or stage IV patients, with a longer response time than with conventional chemotherapy (carboplatin or cisplatin + etoposide).

Report written by Dr. Joël Claveau

Staging, work-up and management of high-risk cutaneous squamous cell carcinoma

Mariam Totoncy, Emily S Ruiz, Ashlez Wysong, USA

Respect the dormant beast: optimize your management of high-risk cutaneous SCCS

Emily S Ruiz, Yaohui Gloria Xu, Addison Michael Demer, Vishal Patel, MD, USA

With population ageing and sun exposure habits in the last 20 years, the incidence of cutaneous squamous cell carcinoma has been strongly increasing. In order to facilitate the management of high-risk squamous cell carcinoma, adequate, easy-to-use and reproducible staging is highly desirable. Over the past few years, various organisations and institutions (NCCN, AJCC, BWH, others) have proposed staging systems. Although there is currently no consensus, the presenters primarily focused on the Brigham and Women’s Hospital (BWH) system.

In the BWH classification, the risk factors are tumour diameter = or > 2 cm, invasion beyond fat, poor histological differentiation, and perineural invasion (PNI = or > 0.1 mm). Patients are classified as follows: T1: 0 criteria, T2a: 1 criterion, T2b: 2 or 3 criteria, T3: 4 criteria or bone invasion. Some working groups are trying to refine this staging, mainly in the T2a category. Lastly, other factors to consider that can lead to a poor prognosis are satellitosis, in-transit metastases, and immunosuppression (e.g. solid organ transplant recipient or patient with chronic lymphocytic leukaemia). When Mohs surgery is used as a surgical approach for these carcinomas, the central part (“debulking”) should be carefully analysed from a histological standpoint to allow for this staging.

One session reviewed the importance of a radiological investigation in these high-risk patients (BWH Stages T2b and T3), especially for recurrent tumours and immunocompromised patients. Radiological tests allow for a better preoperative evaluation. They are recommended to look for bone invasion and possible orbital involvement and assess soft tissues and lymph nodes. Ultrasound is often the best test to evaluate lymph nodes, computed tomography is very good for revealing underlying bone involvement, and magnetic resonance can help us demonstrate significant nerve involvement and evaluate underlying soft tissues. Lastly, a PET-CT scan is usually recommended to investigate systemic metastatic involvement.

A multidisciplinary approach should be encouraged for the management of high-risk carcinomas. Patients with more aggressive or complex tumours are often presented at consensus meetings to obtain the opinions of the various specialists involved. In America, the surgical approach to high-risk carcinomas is often based on the NCCN guidelines. Indeed, Mohs surgery or any other surgical technique allowing for an “en-face” pathological assessment of the peripheral and deep margins (e.g. Tübingen technique) is recommended. Mohs surgery has a success rate of 96 to 97%. If standard excision is favoured, it is advisable to take larger margins (e.g. 1 cm), assess the pathological margins postoperatively, and wait before performing complex reconstruction techniques. “Secondary intention” healing, primary closure or skin grafting should be favoured. If the margins are positive, it is advisable to operate again using Mohs surgery or a similar technique. The use of radiotherapy as primary treatment is reserved exclusively for poor surgical candidates.

The role of the sentinel node technique is not as well defined for high-risk cutaneous squamous cell carcinoma as it is for melanoma. It is currently being studied in many centres and is usually offered to very high-risk patients without any clinical lymph node involvement. It is primarily offered for tumours with multiple risk factors, recurring tumours, and immunocompromised patients. Recent publications have shown an SLN positivity rate of 5 to 6% in high-risk patients (BWH T2b or higher).

According to NCCN, radiotherapy mainly plays an adjuvant role for aggressive tumours with extensive PNI, nerve involvement = or > 0.1 mm, or clinically or radiologically evident nerve involvement. It is sometimes offered after positive surgical margins if a new operation is not possible, if there is inoperable local recurrence, or after lymph node dissection showing >3 affected lymph nodes or extracapsular spread.

Lastly, a major development in the management of inoperable cutaneous squamous cell carcinoma and cutaneous SCC that cannot be controlled by radiotherapy is anti-PD-1 immunotherapy with cemiplimab or pembrolizumab. In cases of locally advanced or metastatic carcinoma, cemiplimab has demonstrated an objective response rate of 47% with a highly favourable safety profile, even in the elderly. Its use in organ transplant recipients is problematic, with a 50% risk of graft rejection during treatment. Lastly, according to some recent publications including one in NEJM, the role of neo-adjuvant cemiplimab (one dose every three weeks with a maximum of four doses before surgery) appears to be a very promising approach with pathological complete response in 50% of patients at the time of tumour excision (“off-label” use for the moment).

Report written by Prof. Brigitte Dréno

1. Androgenic alopecia is more common in transgender people and is often associated with acne
2. Three common associations should be investigated in cases of acne in adult women: seborrhoeic dermatitis, anxiety syndrome, and polycystic ovary syndrome
3. A novel treatment for SD in addition to antifungal agents and topical lithium: roflumilast, a selective phosphodiesterase 4 inhibitor with an interesting effect on pruritus
4. A meta-analysis reviewed all available topical treatments for rosacea: azelaic acid 20% was the most effective against inflammatory lesions and azelaic acid 15% the best tolerated
5. A possible new development in topical acne treatments: metformin, which acts by blocking the androgen receptors of the sebaceous glands: it acts rapidly, primarily on inflammatory lesions at 4 weeks
6. Another potential new topical therapy: an NLRP3 inhibitor, which has successfully passed phase I safety testing; this will be followed by a phase 2 study 
7. Truncal acne: requires specific management and has a sometimes major and often underestimated impact on quality of life
8. Ivermectin in rosacea: two targets of interest identified in addition to papulo-pustules, erythema and pruritus
9. Trifarotene at a low concentration of 0.0005%: a meta-analysis of three studies confirmed its efficacy in truncal acne and its very good safety profile 
10. The fourth generation of retinoids with trifarotene, specific to RAR-gamma, acts both on keratinocyte proliferation/differentiation genes and on the genes involved in innate immunity and inflammation.