Volume 39, Issue 12 pp. 1010-1015
Case Report

Bullous pyoderma gangrenosum: A case report and review of the published work

Masayuki Sakiyama

Corresponding Author

Masayuki Sakiyama

Department of Dermatology, National Defense Medical College, Tokorozawa, Japan

Correspondence: Masayuki Sakiyama, M.D., Department of Dermatology, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama 359-8513, Japan. Email: [email protected]Search for more papers by this author
Takashi Kobayashi

Takashi Kobayashi

Department of Dermatology, National Defense Medical College, Tokorozawa, Japan

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Yuiko Nagata

Yuiko Nagata

Department of Dermatology, National Defense Medical College, Tokorozawa, Japan

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Norihiro Fujimoto

Norihiro Fujimoto

Department of Dermatology, National Defense Medical College, Tokorozawa, Japan

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Takahiro Satoh

Takahiro Satoh

Department of Dermatology, National Defense Medical College, Tokorozawa, Japan

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Shingo Tajima

Shingo Tajima

Department of Dermatology, National Defense Medical College, Tokorozawa, Japan

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First published: 14 September 2012
Citations: 27

ABSTRACT

Pyoderma gangrenosum (PG) is an ulcerative skin disorder characterized by neutrophilic infiltrations. PG is generally classified into four types: (i) ulcerative; (ii) pustular; (iii) bullous; and (iv) vegetative. Among them, bullous PG is known as a rare type. Herein, we report a case of bullous PG together with a summary of the 12 PG cases treated in our department over the previous 15 years, and we review 38 well-documented bullous PG cases (65.8% female; aged 18–80 years [mean ± standard deviation, 51.6 ± 16.8]) in the published work, including the present case, from 1972–2011. Although the disease most frequently associated with PG is inflammatory bowel disease, bullous PG is most commonly associated with hematological disorders (25/38, 65.8%), which indicates the characteristic pathophysiology specific to bullous PG.

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