Linear scleroderma with prominent multiple lymphadenopathy followed by the development of polymyositis: A case report and review of published work-Reference-Cited by-同舟云学术

Linear scleroderma with prominent multiple lymphadenopathy followed by the development of polymyositis: A case report and review of published work

Published:2016-10 Issue:10 Volume:43 Page:1224-1227
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Takahashi Takehiro¹,Asano Yoshihide¹,Hirakawa Maiko¹,Nakamura Kouki¹,Saigusa Ryosuke¹,Aozasa Naohiko¹,Sumida Hayakazu¹,Fujita Hideki¹,Sugaya Makoto¹,Ohmori Aki²,Shimizu Jun²,Sato Shinichi¹

Affiliation:

1. Department of Dermatology; University of Tokyo Graduate School of Medicine; Tokyo Japan

2. Department of Neurology; University of Tokyo Graduate School of Medicine; Tokyo Japan

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/1346-8138.13424/fullpdf

Reference12 articles.

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2. Clinical characteristics associated with antihistone antibodies in patients with localized scleroderma;Sato;J Am Acad Dermatol,1994

3. Antiphospholipid antibody in localised scleroderma;Sato;Ann Rheum Dis,2003

4. Distinct autoimmune syndromes in morphea: a review of 245 adult and pediatric cases;Leitenberger;Arch Dermatol,2009

5. Pansclerotic morphea with features of eosinophilic fasciitis: distinct entities or part of a continuum?;Odhav;Pediatr Dermatol,2014

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