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[马扎布劳德综合征的临床病理特征]

[Clinical pathological aspects of Mazabraud's syndrome].

作者信息

Pollandt K, Lohmann C H, Werner M, Delling G

机构信息

Abteilung Osteopathologie, Pathologisches Institut, Universitätsklinikum Hamburg-Eppendorf, Germany.

出版信息

Pathologe. 2002 Sep;23(5):357-60. doi: 10.1007/s00292-002-0554-0. Epub 2002 Aug 21.

Abstract

Mazabraud's syndrome is a rare, sporadic disorder characterised by the association of mainly polyostotic fibrous dysplasia and intramuscular myxoma. Fibrous dysplasia is mostly diagnosed at a younger age, while myxomas only occur during adulthood. We report a case of a 42-year-old female with Mazabraud's syndrome where a polyostotic fibrous dysplasia was already diagnosed and at presentation two newly formed intramuscular myxomas were found in the gluteal muscle.

摘要

马扎布劳德综合征是一种罕见的散发性疾病,其特征主要是多骨型纤维发育不良与肌肉内黏液瘤并存。纤维发育不良大多在较年轻时被诊断出来,而黏液瘤仅在成年期出现。我们报告一例42岁患有马扎布劳德综合征的女性病例,该患者已被诊断为多骨型纤维发育不良,就诊时在臀肌中发现了两个新形成的肌肉内黏液瘤。

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