Xanthoma Disseminatum In a Pair of Blind, Deaf Male Twins

Author:

Natanzi Naveed1,Peng David2,Ahdoot Eli1,Ghatan Sandra3,Reinstandler Amy2,Ram Ramin2

Affiliation:

1. Western University of Health Sciences, 309 East Second Street, Pomona, CA 91766, USA

2. Department of Dermatology, University of Southern California, Los Angeles, CA 90033, USA

3. University of California, Los Angeles, CA 90095, USA

Abstract

Xanthoma disseminatum (XD) is a rare normolipemic histiocytic disorder of non-Langerhans cell origin characterized by erythematous to tan/brown papules in flexor surfaces. Considered a generally benign, chronic disease of unknown etiology, XD typically affects the skin, mucous membranes, and less commonly, other organs. To date, there has been no typical or consistent inheritance pattern described, nor has it ever been considered as a component of any known syndrome. We describe, for the first time, two cases of XD in a pair of blind and deaf twin brothers.

Publisher

Hindawi Limited

Subject

General Medicine

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Infiltrative chiasmatopathy in xanthoma disseminatum: a rare entity;BMJ Case Reports;2018-12

2. A Case of Xanthoma Disseminatum with Laryngeal Involvement;Journal of The Korean Society of Laryngology, Phoniatrics and Logopedics;2015-06-30

3. Histiocytosis;Pediatric Skin of Color;2015

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