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Pneumomediastinum and subcutaneous emphysema secondary to amyopathic dermatomyositis with cryptogenic organizing pneumonia in invasive breast cancer: a case report and review of literature

Identifieur interne : 001975 ( Main/Exploration ); précédent : 001974; suivant : 001976

Pneumomediastinum and subcutaneous emphysema secondary to amyopathic dermatomyositis with cryptogenic organizing pneumonia in invasive breast cancer: a case report and review of literature

Auteurs : Sung Hwan Park [Corée du Sud] ; Yoon-Seup Kum [Corée du Sud] ; Kyung-Chan Kim [Corée du Sud] ; Jung-Yoon Choe [Corée du Sud] ; Sung-Hoon Park [Corée du Sud] ; Seong-Kyu Kim [Corée du Sud]

Source :

RBID : ISTEX:2042FA4DC1896AF1AE6A677EA2034CEC946AA53E

English descriptors

Abstract

Abstract: Amyopathic dermatomyositis (ADM) is recognized as a variant phenotype of dermatomyositis and characterized by typical skin manifestations without evidence of muscular inflammation. While interstitial lung disease (ILD) is occasionally found as one of the lung manifestations in ADM patients, the development of a pneumomediastinum and/or subcutaneous emphysema in this disease entity is one of the extremely rare pulmonary complications. These latter complicated pulmonary manifestations have been usually reported in idiopathic ADM with ILD without any other associated medical conditions. We report a case presented with the spontaneous pneumomediastinum and subcutaneous emphysema in both ADM and cryptogenic organizing pneumonia during adjuvant chemotherapy based on cyclophosphamide for breast cancer.

Url:
DOI: 10.1007/s00296-008-0808-0


Affiliations:


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Le document en format XML

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