Volume 41, Issue 11 pp. 1003-1005
Concise Communication

Refractory bullous pemphigoid leaving numerous milia during recovery

Shusuke Uchida

Corresponding Author

Shusuke Uchida

Department of Dermatology, Kinki University Faculty of Medicine, Osaka-Sayama, Japan

Correspondence: Shusuke Uchida, M.D., Department of Dermatology, Kinki University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka 589-8511, Japan. Email: [email protected]Search for more papers by this author
Naoki Oiso

Naoki Oiso

Department of Dermatology, Kinki University Faculty of Medicine, Osaka-Sayama, Japan

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Hiroshi Koga

Hiroshi Koga

Department of Dermatology, Kurume University School of Medicine, Kurume, Japan

Kurume University Institute of Cutaneous Cell Biology, Kurume, Japan

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Norito Ishii

Norito Ishii

Department of Dermatology, Kurume University School of Medicine, Kurume, Japan

Kurume University Institute of Cutaneous Cell Biology, Kurume, Japan

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Kazunori Okahashi

Kazunori Okahashi

Department of Dermatology, Kinki University Faculty of Medicine, Osaka-Sayama, Japan

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Hiromasa Matsuda

Hiromasa Matsuda

Department of Dermatology, Kinki University Faculty of Medicine, Osaka-Sayama, Japan

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Takashi Hashimoto

Takashi Hashimoto

Department of Dermatology, Kurume University School of Medicine, Kurume, Japan

Kurume University Institute of Cutaneous Cell Biology, Kurume, Japan

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Akira Kawada

Akira Kawada

Department of Dermatology, Kinki University Faculty of Medicine, Osaka-Sayama, Japan

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First published: 25 October 2014
Citations: 11

Abstract

Recovery with milia may occur in bullous pemphigoid (BP), mucous membrane pemphigoid (MMP) and epidermolysis bullosa acquisita (EBA). Scarring commonly occurs in MMP and EBA. Here, we report a 62-year-old man patient with BP, who was left with numerous milia during recovery. The patient had immunoglobulin (Ig)G autoantibodies to the recombinant protein of the BP180-NC16a domain and the soluble 120-kDa ectodomain of BP180 (linear IgA bullous dermatosis [LAD]-1). There are cases of BP with IgG autoantibodies to LAD-1 and/or the recombinant protein of BP180 C-terminal domain. Extensive milia formation during recovery may be associated with immunological predisposition and/or improper interaction between hemidesmosomes and the extracellular matrix components.

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