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2.
Skin Health Dis ; 3(3): e196, 2023 Jun.
Article in English | MEDLINE | ID: mdl-37275417

ABSTRACT

We present two cases of alopecic and aseptic nodules of the scalp (AANS) that were previously misdiagnosed. AANS is characterized by solitary or multiple dome-shaped alopecic nodules and predominantly affects young men. Dermatologists should be aware of this under recognized entity.

3.
J Dermatolog Treat ; 33(4): 2182-2191, 2022 Jun.
Article in English | MEDLINE | ID: mdl-34057875

ABSTRACT

BACKGROUND: Endocrine mucin-producing sweat gland carcinoma is a rare, under-reported cutaneous adnexal tumor that is often misdiagnosed and has an unknown incidence of metastasis. OBJECTIVE: To determine the incidence of metastasis and tumor recurrence, as well as diagnostic accuracy and current trends in treatment modality. METHODS: A search was performed following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Tumor pathology and clinical data concerning demographics, presentation, diagnosis, treatment and follow-up were assessed. RESULTS: A total of 36 publications with 110 cases were identified. Initial pathological diagnosis was incorrect in 45.5% of cases. One case of metastatic disease was reported. The incidence of locoregional recurrence was 10.6% over a mean follow-up period of 21.3 months. Of cases with known methods of resection, 34.6% were resected by excisional biopsy, 42.8% were resected by wide surgical excision, and 31.3% were cleared by Mohs micrographic surgery. LIMITATIONS: The low reported incidence and level of evidence was suboptimal with only case reports and retrospective case studies being reported. CONCLUSION: Reported cases of this pathology demonstrate poor diagnostic accuracy. High rates of misdiagnosis and inadequate definitive treatment suggest the need for more comprehensive work-up and management of lesions suspicious for this pathology.


Subject(s)
Adenocarcinoma, Mucinous , Eyelid Neoplasms , Sweat Gland Neoplasms , Adenocarcinoma, Mucinous/diagnosis , Adenocarcinoma, Mucinous/pathology , Adenocarcinoma, Mucinous/surgery , Eyelid Neoplasms/diagnosis , Eyelid Neoplasms/pathology , Eyelid Neoplasms/surgery , Humans , Mucins , Neoplasm Recurrence, Local , Retrospective Studies , Sweat Gland Neoplasms/diagnosis , Sweat Gland Neoplasms/pathology , Sweat Gland Neoplasms/surgery , Sweat Glands/pathology
5.
Dermatitis ; 32(4): 267-272, 2021.
Article in English | MEDLINE | ID: mdl-32209867

ABSTRACT

BACKGROUND: Allergic contact dermatitis (ACD) may occur secondary to topical antifungals containing potential allergens in their vehicles. Variation of allergenic ingredients among commonly used antifungal creams (AFCs) has not been well characterized. OBJECTIVE: The study goal was to assess the frequency of allergenic ingredients in 4 commonly used topical AFCs. METHODS: Topical AFCs (clotrimazole, ketoconazole, miconazole, and terbinafine) were selected, and the ingredient lists for these products were obtained from the US Food and Drug Administration's Online Label Repository via a proprietary name search. A systematic literature review was performed using the ingredient name on MEDLINE (PubMed) database to identify reports of ACD confirmed by patch testing. RESULTS: Of the 20 ingredients analyzed, 6 had frequent allergenic potential. Propylene glycol was the most common cause of ACD identified in the literature and is an ingredient in ketoconazole 2% and miconazole nitrate 2%. Ketoconazole 2% and miconazole nitrate 2% creams contained the highest number of potential allergens (n = 3) among the 4 creams analyzed. CONCLUSIONS: Of the 4 creams, terbinafine hydrochloride 1% and clotrimazole 1% contained the least number of potential allergenic ingredients. Awareness of the allergenic potential of commonly used AFCs may help health care providers when evaluating patients with ACD.


Subject(s)
Allergens/adverse effects , Allergens/analysis , Antifungal Agents/adverse effects , Antifungal Agents/chemistry , Dermatitis, Allergic Contact/etiology , Administration, Topical , Antifungal Agents/administration & dosage , Skin Cream/chemistry
6.
Dermatol Surg ; 47(1): 38-41, 2021 01 01.
Article in English | MEDLINE | ID: mdl-32826598

ABSTRACT

BACKGROUND: Dermatologic surgery services are largely absent in Africa and in Afro-Caribbean counties. In the USA, studies of people of African ancestry have demonstrated health care gaps, but there are no data for Africa nor a Afro-Caribbean country. Dermatology surgery has been largely absent from global health because there are few data to demonstrate the need. We sought to determine skin cancer tumor types, and local knowledge and perception in an Afro-Caribbean country. OBJECTIVE: We sought to determine whether there exist knowledge gaps and whether a dermatology surgery medical missions program would improve the health of Afro-Caribbean people. METHODS: First, we conducted a survey of knowledge and behaviors related to skin cancer. Second, we analyzed the number and types of tumors treated during a multi-year surgical dermatology project. RESULTS: In the survey, 62% did not know what melanoma was. Eighty-one percent did not think skin cancer is preventable. Of 163 surgical specimens, 64 were malignancies with 91% related to UV exposure. CONCLUSION: There is a need for a skin cancer treatment and education program in a country of mostly African-ancestry people.


Subject(s)
Dermatologic Surgical Procedures , Health Services Needs and Demand , Medical Missions , Skin Neoplasms/surgery , Adult , Female , Global Health , Grenada , Health Knowledge, Attitudes, Practice , Humans , Male , Retrospective Studies , Surveys and Questionnaires
7.
JAAD Case Rep ; 6(6): 500-502, 2020 Jun.
Article in English | MEDLINE | ID: mdl-32490108
8.
J Clin Mov Disord ; 6: 7, 2019.
Article in English | MEDLINE | ID: mdl-31890235

ABSTRACT

BACKGROUND: Gerstmann-Straussler-Scheinker disease (GSS), an autosomal dominant prion disorder, usually presents as a slowly progressive cerebellar ataxia followed by later cognitive decline. We present a member of the GSS Indiana Kindred with supranuclear palsy, a less common feature in GSS. CASE PRESENTATION: A 42-year-old man presented with 12 months of progressive gait and balance difficulty. Exam was notable for ataxia and cerebellar eye movement abnormalities. Genetic testing revealed a F198S variant in the prion protein (PRNP) gene, the pathological variant of GSS associated with his family, the Indiana kindred. Eighteen months after initial presentation supranuclear palsy developed. CONCLUSIONS: GSS is a neurodegenerative prion disease with diverse clinical presentations, and exhibits greater variability in disease phenotype compared to other inherited spongiform encephalopathies. GSS should be on the differential for patients with ataxia and supranuclear palsy, and it is important to assess both horizontal and vertical saccades and optokinetic nystagmus in patients with ataxia.

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