Volume 44, Issue 11 p. 1281-1284
Original Article

Pyoderma gangrenosum and underlying diseases in Japanese patients: A regional long‐term study

Sae Inoue

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan

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Jun‐ichi Furuta

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan

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Yasuhiro Fujisawa

Corresponding Author

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan

Correspondence: Yasuhiro Fujisawa, M.D., Ph.D., Department of Dermatology, Faculty of Medicine, University of Tsukuba, 1‐1‐1 Tennodai, Tsukuba, Ibaraki 305‐8575, Japan. Email: fujisan@md.tsukuba.ac.jpSearch for more papers by this author
Saori Onizawa

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan

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Shusaku Ito

Hitachi General Hospital, Ibaraki, Japan

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Masayuki Sakiyama

National Defense Medical College Hospital, Saitama, Japan

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Keiko Kobayashi

Mito Red Cross Hospital, Ibaraki, Japan

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Toshiyuki Kanou

Ibaraki Prefectural Central Hospital, Ibaraki, Japan

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Tsunao Ohi

Tokyo Medical University Ibaraki Medical Center, Ibaraki, Japan

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Chimaki Okubo

Mito Medical Center, Ibaraki, Japan

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Yoshihiro Moriyama

Tsuchiura Kyodo General Hospital, Ibaraki, Japan

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Naoko Okiyama

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan

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Manabu Fujimoto

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan

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First published: 21 June 2017
Citations: 7

Abstract

Pyoderma gangrenosum (PG) is a chronic inflammatory disease of unknown cause that presents as an inflammatory and ulcerative disorder of the skin. PG is often associated with an underlying systemic disease. However, the frequencies of the underlying diseases are unclear in Japanese patients. In this retrospective, observational study, all patients diagnosed with PG who visited dermatology departments of nine regional hospitals in and around Ibaraki Prefecture were collected from 1982 to 2011 or 2014. The diagnoses of PG were based on the characteristic clinical and histological appearances and ruling out of infection. Sixty‐two PG patients, including 29 males and 33 females, were identified. The ages of onset were 16–89 years, and the mean age was 50.2 years. Fifty (80%) of the 62 patients presented with an ulcerative PG, and the lower leg was the most common site (74%). Forty‐six (74%) PG patients had underlying diseases. The most frequent was ulcerative colitis (32%), followed by myelodysplastic syndrome (11%), rheumatoid arthritis (6%) and aortitis syndrome (5%). For treatment, 54 cases (87%) received systemic corticosteroids and 10 received additional treatment with cyclosporin. There was no significant correlation between underlying diseases and response to the initial treatment. Multivariate analysis revealed that the number of affected sites negatively correlated with successful initial treatment. Fifteen (24%) of the 62 cases relapsed. In conclusion, ulcerative colitis and hematological disorders were frequently associated with PG while approximately a quarter of the cases were idiopathic.

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