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一例皮肌炎合并源于阑尾黏液腺癌的腹膜假黏液瘤。

A case of dermatomyositis associated with pseudomyxoma peritonei originating from mucinous adenocarcinoma of the appendix.

作者信息

Maekawa Y, Nakamura K, Nogami R

机构信息

Department of Dermatology, Kumamoto National Hospital, Japan.

出版信息

J Dermatol. 1992 Jul;19(7):420-3. doi: 10.1111/j.1346-8138.1992.tb03252.x.

Abstract

A 69-year-old Japanese woman with erythema, severe edema on the face, Gottron's papules and poikiloderma was diagnosed as having dermatomyositis. She also noticed muscle weakness in her extremities, although her electromyogram showed neurogenic patterns. Her levels of CA19-9 and CEA were elevated and a CT of her abdomen revealed a giant, multilobular, cystic lesion in the pelvis. This tumor was diagnosed as pseudomyxoma peritonei originating from a mucinous adenocarcinoma of the appendix.

摘要

一名69岁的日本女性,面部出现红斑、严重水肿、Gottron丘疹和皮肤异色症,被诊断为皮肌炎。她还注意到四肢肌肉无力,尽管其肌电图显示为神经源性模式。她的CA19-9和CEA水平升高,腹部CT显示盆腔有一个巨大的、多叶的囊性病变。该肿瘤被诊断为源于阑尾黏液腺癌的腹膜假黏液瘤。

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