皮肌炎并发乳腺癌：一例报告

Dermatomyositis revealing breast cancer: report of a case.

作者信息

Lamquami Safae, Errarhay Sanae, Mamouni Nisrine, Bouchikhi Chahrazad, Banani Abdelaziz

机构信息

Obstetrics Gynecology Department I University, Hospital Hassan II, Fez, Morocco.

出版信息

Pan Afr Med J. 2015 Jun 5;21:89. doi: 10.11604/pamj.2015.21.89.6971. eCollection 2015.

DOI:10.11604/pamj.2015.21.89.6971

PMID:26491532

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4594990/

Abstract

Dermatomyositis (DM) is a rare connective corresponding to an inflammatory disease of skeletal muscles. Paraneoplastic origin must always be sought, primarily gynecological tumor in women, but the investigations are often made difficult by the fact that a primary tumor is often not detectable at the time of the cutaneous manifestations. This approach includes in addition to the monitoring report at regular intervals of 6 to 12 months for two years after diagnosis. We report a case of Dermatomyositis revealing breast cancer.

摘要

皮肌炎（DM）是一种罕见的结缔组织病，对应于骨骼肌的炎性疾病。必须始终寻找副肿瘤性病因，女性主要为妇科肿瘤，但由于在皮肤表现出现时原发性肿瘤往往无法检测到，这常常使检查变得困难。这种方法除了在诊断后两年内每隔6至12个月定期进行监测报告外，还包括其他内容。我们报告一例皮肌炎并发乳腺癌的病例。