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Journal of the American Academy of Dermatology
Volume 74, n° 6
page 1234 (juin 2016)
Doi : 10.1016/j.jaad.2015.12.006
accepted : 5 December 2015
Reviews

Evaluation and management of the patient with multiple syringomas: A systematic review of the literature
 

Kiyanna Williams, BS a, Kanade Shinkai, MD, PhD b,
a University of California San Francisco School of Medicine, San Francisco, California 
b Department of Dermatology, University of California San Francisco, San Francisco, California 

Correspondence to: Kanade Shinkai, MD, PhD, Department of Dermatology, University of California San Francisco, 1701 Divisadero St, 3rd fl, San Francisco, CA 94115.Department of DermatologyUniversity of California San Francisco1701 Divisadero St3rd flSan FranciscoCA94115
Abstract

Syringomas are benign adnexal tumors with distinct histopathologic features, including the characteristic comma (“tadpole”) shaped tail comprised of dilated, cystic eccrine ducts. Clinically, syringomas typically present in adolescent females predominantly in the periorbital region. They may present as solitary or multiple lesions, and more rare sites of involvement include the genitals, palms, scalp, and the chest. Over the past 50 years, there have been >800 reported cases of syringoma either alone or in conjunction with a systemic syndrome, most commonly Down syndrome. The primary aim of this systematic review is to discuss the clinical features and associations of syringomas with a focus on the patient with multiple syringomas. Its secondary aims are to explore pathophysiology with a focus on multiple syringomas and provide comprehensive data on both traditional and novel treatments. Importantly, multiple syringomas present across a broad clinical spectrum. Though noted in many textbooks to be related to tumor syndromes, the association of syringomas with inherited tumor syndromes is only rarely reported in the literature. Despite multiple reported cases of syringoma, the pathophysiology remains poorly understood and treatment continues to pose a significant challenge.

The full text of this article is available in PDF format.

Key words : eruptive syringoma, familial syringoma, multiple syringomas, syringoma, syringoma syndromes, syringoma treatment

Abbreviations used : DM, DS, TCA



 Funding sources: None.
 Conflicts of interest: None declared.



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