Amicrobial pustulosis associated with IgA nephropathy and Sjögren’s syndrome - 19/08/11
Doi : 10.1016/j.jaad.2007.05.023
Ken Natsuga, MD a, ⁎ 
, Daisuke Sawamura, MD, PhD a, Erina Homma, MD a, Toshifumi Nomura, MD a, Masataka Abe, MD, PhD a, Ryuichi Muramatsu, MD c, Toshio Mochizuki, MD, PhD b, Takao Koike, MD, PhD b, Hiroshi Shimizu, MD, PhD a
, Daisuke Sawamura, MD, PhD a, Erina Homma, MD a, Toshifumi Nomura, MD a, Masataka Abe, MD, PhD a, Ryuichi Muramatsu, MD c, Toshio Mochizuki, MD, PhD b, Takao Koike, MD, PhD b, Hiroshi Shimizu, MD, PhD a a From the Departments of Dermatology
b Medicine II, Hokkaido University Graduate School of Medicine, Sapporo
c Division of Dermatology, Iwamizawa Municipal General Hospital
Reprint requests: Ken Natsuga, MD, Department of Dermatology, Hokkaido University Graduate School of Medicine, N15, W7, Sapporo 060-8638, Japan.Sapporo and Iwamizawa, Japan
Abstract |
Amicrobial pustulosis is a rare clinical entity characterized by a relapsing pustular eruption, primarily involving the skin folds. We describe a case of amicrobial pustulosis associated with autoimmune diseases (APAD). The patient suffered from IgA nephropathy and Sjögren’s syndrome. Skin symptoms were alleviated dramatically after corticosteroid pulse therapy and tonsillectomy.
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| Funding sources: None. Conflicts of interest: None declared. |
© 2007
American Academy of Dermatology, Inc.. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 57 - N° 3
P. 523-526 - septembre 2007 Retour au numéro
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