Volume 41, Issue 5 pp. 421-423
Concise Communication

Systemic sclerosis with sarcoidosis: Case report and review of the published work

Satoko Senda

Satoko Senda

Department of Dermatology, Graduate School of Medicine, Osaka University, Osaka, Japan

These authors are equally contributed to this work.Search for more papers by this author
Ken Igawa

Corresponding Author

Ken Igawa

Department of Dermatology, Graduate School of Medicine, Osaka University, Osaka, Japan

These authors are equally contributed to this work.Correspondence: Ken Igawa, M.D., Ph.D., Department of Dermatology, Graduate School of Medicine, Osaka University, 2-2 Yamada-oka, Suita City, Osaka 565-0871, Japan. Email: [email protected]Search for more papers by this author
Megumi Nishioka

Megumi Nishioka

Department of Dermatology, Graduate School of Medicine, Osaka University, Osaka, Japan

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Hiroyuki Murota

Hiroyuki Murota

Department of Dermatology, Graduate School of Medicine, Osaka University, Osaka, Japan

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Ichiro Katayama

Ichiro Katayama

Department of Dermatology, Graduate School of Medicine, Osaka University, Osaka, Japan

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First published: 12 March 2014
Citations: 19

Abstract

Sarcoidosis and systemic sclerosis (SSc) rarely coexist. Here, we report a Japanese female SSc patient who developed systemic sarcoidosis. Her SSc was a limited type negative for anti-Scl-70 antibody and positive for anticentromere antibody (ACA). Moreover, we performed a review of the English-language published work that described cases of concurrent SSc and sarcoidosis. Then, we found that most SSc and sarcoidosis concurrent patients positive for anti-Scl-70 antibody were male (77.8%). On the other hand, most patients positive for ACA were female (87.5%). These results suggest some relationships between autoantibody profiles and sex in SSc and sarcoidosis concurrence.

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