Rekik Mariem, Bahloul Emna, Ben Rejeb Mohamed, Sellami Khadija, Charfi Slim, Chouk Hamza, Boudaouara Tahya, Turki Hamida
Dermatology Department Hedi Chaker University Hospital, Sfax University Sfax Tunisia.
Dermatology Department Farhat Hached University Hospital Sousse Tunisia.
Clin Case Rep. 2022 Jul 18;10(7). doi: 10.1002/ccr3.6098. eCollection 2022 Jul.
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.
H综合征是一种罕见的遗传性皮肤病。它可能累及面部,表现为:面部毛细血管扩张、色素减退和色素沉着性皮损、多毛症、皮下浸润导致的脸颊肿胀以及湿疹样皮损。我们描述了一种在非朗格汉斯细胞组织细胞增生症范围内具有皮肤镜和组织学特征的新的面部表型。