Literature DB >> 18311043

Three cases of polymyositis/dermatomyositis complicated by pneumomediastinum.

Keiko Shimamoto1, Yoshio Ozaki, Hideki Amuro, Yonsu Son, Maiko Ota-Imamura, Tsutomu Tanijiri, Takashi Yokoi, Yasuhiro Yagi, Tomoki Ito, Seibun Yonezu, Shirou Fukuhara.   

Abstract

Pneumomediastinum is a rare complication of dermatomyositis (DM) and Polymiositis (PM). We report here three cases of PM/DM who developed pneumomediastinum. First case was 61 years old woman with amyopathic dermatomyositis (aDM). Her aDM was complicated with skin ulceration due to vasculopathy, but complicated interstitial pneumonia was not severe. She developed subcutaneous emphysema and pneumomediastinum. Second case was 57 years old woman with DM, who had intractable skin phenomena and mild interstitial pneumonia. The patient became subcutaneous emphysema and pneumomediastinum following severe vasculopathy of skin. The last case was 63 years old man with PM. His PM was complicated with interstitial pneumonia. He had intractable respiratory symptom. Ten years later, he became subcutaneous emphysema and pneumomediastinum following pneumothorax. First and second cases suggest that their pneumomediastinum were due to vasculopathy. On the other hand, pneumomediastinum of the last patient seemed to be associated with interstitial pneumonia and steroid.

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Year:  2008        PMID: 18311043     DOI: 10.2177/jsci.31.56

Source DB:  PubMed          Journal:  Nihon Rinsho Meneki Gakkai Kaishi        ISSN: 0911-4300


  1 in total

Review 1.  Pneumomediastinum, pneumatosis intestinalis and pneumoperitoneum in a patient with polymyositis: case-based review.

Authors:  Melis Dilbil; Funda Erbasan; Bengisu Aslan; Tahir Saygın Öğüt; Mine Nokay; Veli Yazısız; Mustafa Ender Terzioğlu
Journal:  Rheumatol Int       Date:  2022-10-03       Impact factor: 3.580

  1 in total

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