Madelung’s Disease with polyneuropathy in a non-alcoholic Mexican-American male

L. Salinas, Yanira Sanchez-De la Torre
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引用次数: 2

Abstract

Madelung’s disease, also known as benign symmetric lipomatosis or Launois-Bensaude syndrome was first described by Sir Benjamin Brodie in 1846 from a series of patients he had encountered characterizing adipose tumors deposited preferentially on the neck [1]. It is a disorder of fat metabolism with deposition of multiple, symmetrical and painless non-encapsulated lipomas. Depending on the type of Madelung’s Disease, the adipose tissue deposition can be seen in the neck, upper extremities, trunk and hip area. About 90% of the cases described in the literature have been associated with chronic alcoholism and tobacco use and in a population of European/ Mediterranean descent, reporting up to 1 in 25,000 cases in Italy to have the condition [2,3]. Rare cases have also been reported in Indians and one case in an African American male [4,5]. We present a case of a 48-year-old Hispanic male of Mexican ancestry with no significant history of alcoholism who presented to our emergency department with chief complaint of progressive proximal muscle weakness in upper and lower extremities resulting in an inability to walk or care for daily activities.
非酒精性墨西哥裔美国男性马德隆氏病伴多神经病变
马德隆病,也被称为良性对称脂肪瘤病或Launois-Bensaude综合征,最早由Benjamin Brodie爵士于1846年从他遇到的一系列患者中描述,这些患者的特征是脂肪肿瘤优先沉积在颈部[1]。它是一种脂肪代谢紊乱,伴有多发性、对称、无痛的非包膜性脂肪瘤沉积。根据马德隆病的类型,脂肪组织沉积可见于颈部、上肢、躯干和臀部区域。文献中描述的约90%的病例与慢性酒精中毒和烟草使用有关,在欧洲/地中海后裔人群中,据报道,在意大利,每25,000例病例中就有1例患有此病[2,3]。印度人也有罕见病例的报道,非洲裔美国男性也有一例[4,5]。我们报告一例48岁的墨西哥裔西班牙裔男性,无明显酗酒史,主诉上肢和下肢进行性近端肌无力,导致无法行走或照顾日常活动。
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