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一名肌无力女性患者的淀粉样变性非典型表现。

Atypical Presentation of Amyloidosis in a Female Patient with Muscle Weakness.

作者信息

Lashkari Raziyeh, Loghman Maryam, Aghaghazvini Leila, Saffar Hiva, Ziaadini Bentolhoda, Shahriarirad Reza, Nekooeian Mohammad, Nejadhosseinian Mohammad, Alikhani Majid

机构信息

Semnan University of Medical Sciences, Semnan, Iran.

Department of Internal Medicine, School of Medicine, Rheumatology Research Center, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Case Rep Med. 2023 Apr 13;2023:1553163. doi: 10.1155/2023/1553163. eCollection 2023.

Abstract

Muscle involvement represents a well-recognized but rare manifestation of amyloidosis. Here, we report a 40-year-old female who presented with muscle weakness, musculoskeletal pain, and proteinuria, which was eventually diagnosed as myopathic amyloidosis based on muscle biopsy results. A multidisciplinary approach appears to be the cornerstone of the diagnostic work up for recognizing the unusual amyloid myopathy.

摘要

肌肉受累是淀粉样变性一种公认但罕见的表现形式。在此,我们报告一名40岁女性,她出现肌肉无力、肌肉骨骼疼痛和蛋白尿,最终根据肌肉活检结果被诊断为肌病性淀粉样变性。多学科方法似乎是识别这种不寻常的淀粉样肌病诊断检查的基石。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/274e/10118899/6c122e30eb48/CRIM2023-1553163.001.jpg

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