Unusual facial lesions in H syndrome.

Autor: Rekik M; Dermatology Department Hedi Chaker University Hospital, Sfax University Sfax Tunisia., Bahloul E; Dermatology Department Hedi Chaker University Hospital, Sfax University Sfax Tunisia., Ben Rejeb M; Dermatology Department Farhat Hached University Hospital Sousse Tunisia., Sellami K; Dermatology Department Hedi Chaker University Hospital, Sfax University Sfax Tunisia., Charfi S; Pathological Anatomy Department Habib Bourguiba University Hospital, Sfax University Sfax Tunisia., Chouk H; Genetics Department Farhat Hached University Hospital Sousse Tunisia., Boudaouara T; Pathological Anatomy Department Habib Bourguiba University Hospital, Sfax University Sfax Tunisia., Turki H; Dermatology Department Hedi Chaker University Hospital, Sfax University Sfax Tunisia.
Jazyk: angličtina
Zdroj: Clinical case reports [Clin Case Rep] 2022 Jul 18; Vol. 10 (7). Date of Electronic Publication: 2022 Jul 18 (Print Publication: 2022).
DOI: 10.1002/ccr3.6098
Abstrakt: H Syndrome is a rare genodermatosis. It may include facial involvement such as: facial telangiectasia, both hypo- and hyperpigmented lesions, hirsutism, swollen cheeks due to subcutaneous infiltration and eczematous lesions. We describe a new facial phenotype with dermoscopic and histological features in the spectrum of non-Langerhans cell histiocytosis.
Competing Interests: None.
(© 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.)
Databáze: MEDLINE
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