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1.
J Cutan Med Surg ; 27(2): 184, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-36722004
3.
Pediatr Dermatol ; 39(5): 757-760, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-35657009

RESUMO

Inflammatory linear verrucous epidermal nevus (ILVEN) is a rare type of epidermal nevus, commonly arising in childhood. We present a case of a 13-year-old female with Blaschkoid psoriasiform plaques extending from her left foot to the scalp, sparing the right side of the body. While treatment options historically show variable success, we trialed an IL-17a receptor inhibitor as studies have shown increased levels of IL-17 receptor expression in ILVEN keratinocytes. At both 3 and 6 months after treatment initiation there was found to be significant improvement. We propose brodalumab as an effective treatment option for widespread ILVEN.


Assuntos
Nevo Sebáceo de Jadassohn , Nevo , Neoplasias Cutâneas , Adolescente , Anticorpos Monoclonais Humanizados , Feminino , Humanos , Interleucina-17 , Nevo Sebáceo de Jadassohn/tratamento farmacológico , Receptores de Interleucina-17
4.
JAAD Case Rep ; 24: 48-51, 2022 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-35600569
5.
J Cutan Med Surg ; 23(1): 20-28, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-29890839

RESUMO

BACKGROUND:: Mohs micrographic surgery (MMS) is a surgical modality that achieves high cure rates of nonmelanoma skin cancers but is dependent on accurate histologic examination of surgical margins. Therefore, quality assurance is essential to ongoing assessment of histological margins. OBJECTIVES:: To prospectively determine the concordance rate between a Mohs surgeon (MS) and dermatopathologist (DP) with respect to tumour status (ie, present or absent) and tumour type. Secondary end points were to determine the relationship between discordant interpretations and slide quality and to assess the feasibility of using an electronic webform for data collection. METHODS:: Ten percent (10%) of the planned MMS cases between January 2015 and March 2016 were randomly selected by a histotechnologist at the start of each month. The MS and DP were blinded to the chosen cases, and slides were reviewed independently at the beginning of the following month. Data were collected using an online webform. A blinded third party determined if there were discrepancies in interpretation, and any discordant slides were reviewed together and a consensus was reached. RESULTS:: A total of 270 slides from 54 total cases were reviewed. The overall tumour status concordance rate was 93.6%. Cohen's κ was 0.86. Tumour type concordance was 98.9%. No discrepancy required a change in patient care. All discrepant slides were from cases that required multiple stages. CONCLUSIONS:: This is the first study looking at MS-DP concordance in Canada, and our findings support the MS acting as his or her own pathologist.


Assuntos
Cirurgia de Mohs/normas , Neoplasias Cutâneas/classificação , Neoplasias Cutâneas/patologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Canadá , Feminino , Histocitoquímica , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Garantia da Qualidade dos Cuidados de Saúde , Neoplasias Cutâneas/diagnóstico , Neoplasias Cutâneas/cirurgia
6.
J Cutan Med Surg ; 22(1): 65-70, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-28673091

RESUMO

Lichen myxedematosus is an idiopathic, cutaneous mucinosis with 2 clinicopathologic subsets. There is the generalised papular and sclerodermoid form, more properly termed scleromyxedema, and the localised papular form. We report the first case, to our knowledge, of lichen myxedematosus in association with rheumatoid arthritis as well as a case in association with dermatomyositis. An up-to-date literature review on cutaneous mucinoses and connective tissue diseases, excluding the common association of primary and secondary mucinoses with systemic lupus erythematosus, was also performed.


Assuntos
Doenças do Tecido Conjuntivo , Mucinoses , Humanos , Masculino , Pessoa de Meia-Idade , Escleromixedema , Pele/patologia
7.
J Dermatolog Treat ; 28(4): 332-337, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-27759482

RESUMO

PURPOSE: Omalizumab is a recombinant humanized monoclonal antibody that inhibits the binding of immunoglobulin E (IgE) to the high-affinity IgE receptor (FceRI) on the surface of mast cells and basophils. Omalizumab has been approved for use in asthma, and new reports show promise in a variety of dermatologic diseases. Herein, we review the literature on omalizumab in dermatology and discuss the safety, efficacy and mechanisms of action for this emerging therapy. MATERIALS AND METHODS: PubMED, MEDLINE and Embase databases were searched for the period 1 January 1990 to 1 September 2016. Articles sourced were graded according to the Oxford Center for Evidence-Based Medicine Levels of Evidence Grades of Recommendation criteria. RESULTS: A total of 99 articles met our inclusion criteria. They included reports on the use of omalizumab in chronic spontaneous urticaria, atopic dermatitis, mastocytosis, hyper-IgE syndrome, bullous pemphigoid, Netherton syndrome, urticarial vasculitis, Churg-Strauss syndrome and toxic epidermal necrolysis. CONCLUSIONS: Omalizumab is effective in a variety of recalcitrant immune-mediated and autoimmune skin disorders. It is a safe and effective treatment for use in chronic idiopathic urticaria (Grade of recommendation: A). Randomized clinical trials with long-term follow-ups are warranted to firmly establish the role of omalizumab in the treatment of dermatologic disease.


Assuntos
Antialérgicos/uso terapêutico , Omalizumab/uso terapêutico , Dermatopatias/tratamento farmacológico , Antialérgicos/efeitos adversos , Anticorpos Monoclonais/efeitos adversos , Anticorpos Monoclonais/uso terapêutico , Doenças Autoimunes/tratamento farmacológico , Doenças Autoimunes/imunologia , Doença Crônica , Dermatite Atópica/tratamento farmacológico , Dermatite Atópica/imunologia , Guias como Assunto , Humanos , Imunoglobulina E/imunologia , Omalizumab/efeitos adversos , Omalizumab/imunologia , Penfigoide Bolhoso/tratamento farmacológico , Penfigoide Bolhoso/imunologia , Dermatopatias/imunologia , Urticária/tratamento farmacológico , Urticária/imunologia
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