Literature DB >> 16426924

Multiple organ involvement in eosinophilic polymyositis: an autopsy report.

Keisuke Ishizawa1, Daisuke Adachi, Kouetsu Kuboi, Takashi Yamaguchi, Tomoko Mitsuhashi, Yoshihiko Shimizu, Toshihide Mimura, Shigetaka Nishimura, Michio Shimizu, Takanori Hirose.   

Abstract

This report describes autopsy findings of eosinophilic polymyositis in a 29-year-old woman. She complained of muscle pain and tenderness. A serum examination disclosed elevated creatine kinase, and echocardiography showed lowered cardiac function. Electromyography demonstrated myopathic potentials, and the skeletal muscle biopsy revealed degeneration of muscle fibers accompanying marked eosinophilic infiltration. Peripheral eosinophilia was not prominent. A systemic examination excluded possible etiologic factors, such as hypereosinophilic syndrome, collagen vascular diseases, or parasites. The patient died of heart failure after a 4-month clinical course. The autopsy disclosed a set of histological changes indicating tissue injuries, that is, loss of muscle fibers, interstitial fibrosis, and/or infiltrates of lymphocytes not only in the skeletal muscles and heart but also in various visceral organs. Eosinophils were sparsely scattered. These results indicate that the overrun of eosinophils underlying eosinophilic polymyositis, regardless of the presence of hypereosinophilic syndrome or other systemic disorders, could involve wide-ranging visceral organs.

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Year:  2005        PMID: 16426924     DOI: 10.1016/j.humpath.2005.10.006

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  1 in total

1.  Severe Rhabdomyolysis without Systemic Involvement: A Rare Case of Idiopathic Eosinophilic Polymyositis.

Authors:  Ayesha Farooq; Vivek Choksi; Andrew Chu; Dhruti Mankodi; Sameer Shaharyar; Keith O'Brien; Uday Shankar
Journal:  Case Rep Rheumatol       Date:  2015-07-01
  1 in total

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