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恶性腹膜间皮瘤伴发类风湿性多肌痛样综合征。

Malignant Peritoneal Mesothelioma Presenting with Polymyalgia Rheumatica-like Syndrome.

机构信息

Department of Internal Medicine, Akiota Hospital, Japan.

Department of Surgery, Akiota Hospital, Japan.

出版信息

Intern Med. 2020 Oct 15;59(20):2629-2632. doi: 10.2169/internalmedicine.4809-20. Epub 2020 Jun 23.

Abstract

A 30-year-old man was admitted to our hospital because of pain in his proximal extremities. The pain mimicked polymyalgia rheumatica (PMR) and it temporarily improved by a low dose of glucocorticoids, but his symptoms relapsed many times. After six years of glucocorticoid treatment, he developed abdominal pain and ascites, for which he was diagnosed with malignant peritoneal mesothelioma (MPM). His PMR-like symptoms improved with cytoreductive surgery and chemotherapy for MPM. Finally, we diagnosed this PMR-like syndrome to be paraneoplastic syndrome with MPM. Although cases of MPM complicated by PMR-like syndrome are rare, MPM should be taken into account in the differential diagnosis.

摘要

一位 30 岁男性因四肢近端疼痛而入院。疼痛类似于巨细胞性多关节炎(PMR),小剂量糖皮质激素可暂时缓解,但症状多次复发。糖皮质激素治疗 6 年后,他出现腹痛和腹水,被诊断为恶性腹膜间皮瘤(MPM)。他的 PMR 样症状随着 MPM 的细胞减灭术和化疗而改善。最终,我们诊断该 PMR 样综合征为伴 MPM 的副肿瘤综合征。虽然 MPM 并发 PMR 样综合征的病例很少见,但在鉴别诊断中应考虑 MPM。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba3a/7662062/449cbff0d705/1349-7235-59-2629-g001.jpg

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