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良性头部组织细胞增多症:一例报告及文献复习

Benign cephalic histiocytosis: a case report and review.

作者信息

Jih Debra M, Salcedo Stephen L, Jaworsky Christine

机构信息

Department of Dermatology, Metrohealth Medical Center, Case Western Reserve School of Medicine, Cleveland, Ohio 44109-1998, USA.

出版信息

J Am Acad Dermatol. 2002 Dec;47(6):908-13. doi: 10.1067/mjd.2002.124602.

Abstract

Benign cephalic histiocytosis is a rare non-Langerhans histiocytosis characterized by a self-healing eruption of papules and macules on the head and neck that occurs during infancy or childhood. Histologic and ultrastructural evaluations show a dermal proliferation of histiocytes with intracytoplasmic comma-shaped bodies, coated vesicles, and desmosome-like structures with an absence of Birbeck granules. We report a case of benign cephalic histiocytosis in a 9-month-old boy who presented with tan papules on his face that spread to his lower extremity and subsequently began to regress at 30 months of age. We review the features of this rare entity through a literature review and discuss the differential diagnosis.

摘要

良性头部组织细胞增多症是一种罕见的非朗格汉斯组织细胞增多症,其特征为在婴儿期或儿童期头部和颈部出现自愈性丘疹和斑疹。组织学和超微结构评估显示,组织细胞在真皮层增殖,伴有胞浆内逗号形小体、包被小泡和类桥粒结构,且无伯贝克颗粒。我们报告一例9个月大男孩的良性头部组织细胞增多症,该患儿面部出现棕褐色丘疹,后蔓延至下肢,30个月大时丘疹开始消退。我们通过文献回顾对这一罕见疾病的特征进行了综述,并讨论了鉴别诊断。

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