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骨质疏松症、体重增加和非典型脂肪堆积——这不仅是库欣病的典型特征,也是马德隆病的典型特征:一例报告。

Osteoporosis, weight gain and atypical fat accumulations - a typical feature not only for Cushing's, but also Madelung's disease: A case report.

机构信息

Division of Nephrology and Hemodialysis, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

出版信息

Wien Klin Wochenschr. 2012 Mar;124(5-6):188-92. doi: 10.1007/s00508-011-0045-5. Epub 2011 Sep 15.

Abstract

Madelung's disease, or multiple symmetric lipomatosis, is an extremely rare disease and very likely to be under-diagnosed. It is characterized by multiple symmetrical non-encapsulated fat accumulations mainly located around the neck, shoulders, upper extremities and upper parts of the trunk. The disorder predominantly affects middle-aged men of Mediterranean origin with a history of ethanol intake. Reports of this uncommon disorder in women are very rare. The aim of this article is to report the endocrine and metabolic workup leading to the diagnosis of this uncommon disorder. A 55-year-old woman with osteoporosis was referred to our outpatient clinic with a suspected diagnosis of Cushing's disease. The patient complained of undesired weight gain with atypical fat accumulations predominantly in the upper trunk region during the previous 10 weeks. She presented with the characteristic physical features of Madelung's disease and underwent a thorough examination with endocrine and metabolic evaluation of this rare condition and was finally diagnosed with Madelung's disease. This report demonstrates how a diagnosis of this rare disorder can be reached efficiently. A history of osteoporosis in combination with weight gain and atypical fat accumulations ultimately led to the diagnosis of Madelung's diseases, a rather unknown disorder likely to be under-diagnosed. Although treatment options are limited, a diagnosis is still important for the affected individual.

摘要

马德隆氏病,又称多发性对称性脂肪瘤病,是一种极其罕见的疾病,很可能被漏诊。其特征是多个非包膜性脂肪堆积,主要位于颈部、肩部、上肢和躯干上部。这种疾病主要影响有饮酒史的中年地中海血统男性。女性中这种罕见疾病的报道非常罕见。本文旨在报告导致这一罕见疾病诊断的内分泌和代谢检查。一位 55 岁的骨质疏松症女性因疑似库欣病被转至我们的门诊。患者在过去 10 周内抱怨体重意外增加,且脂肪堆积非典型,主要集中在上半身区域。她表现出马德隆氏病的典型特征,并接受了全面检查,对这一罕见疾病进行了内分泌和代谢评估,最终被诊断为马德隆氏病。本报告展示了如何有效地诊断这种罕见疾病。骨质疏松症病史、体重增加和非典型脂肪堆积最终导致了马德隆氏病的诊断,这是一种相当未知的疾病,很可能被漏诊。尽管治疗选择有限,但对患者来说,诊断仍然很重要。

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