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再探巨大局部性淋巴水肿:肥胖流行迅速上升的一种并发症。

Massive localized lymphedema revisited: a quickly rising complication of the obesity epidemic.

作者信息

Chopra Karan, Tadisina Kashyap K, Brewer Michael, Holton Luther H, Banda Abhishake K, Singh Devinder P

机构信息

From the *Department of Plastic and Reconstructive Surgery, The Johns Hopkins Hospital, Johns Hopkins University School of Medicine; †Division of Plastic Surgery, University of Maryland Medical Center, Baltimore, MD; and ‡University of Illinois at Chicago College of Medicine, Chicago, IL.

出版信息

Ann Plast Surg. 2015 Jan;74(1):126-32. doi: 10.1097/SAP.0b013e31828bb332.

Abstract

Massive localized lymphedema (MLL) is a rising and potentially fatal complication of the obesity epidemic. Described as a benign lymphoproliferative overgrowth of obese patients, MLL is a form of secondary lymphedema, caused by the obstruction of lymphatic flow, with characteristic clinical and histological presentation. Patients have a large mass with classic skin changes often accompanied by lymphatic weeping that require complex reconstruction. Although oftentimes benign, if left untreated, MLL can progress to angiosarcoma, further supporting the need for more research into MLL and its sequelae. We present a unique case of MLL of the mons pubis in a 52-year-old man with a body mass index of 75.7 kg/m. The literature was comprehensively reviewed with a total of 65 cases of MLL being described, 9 of which resulted in angiosarcoma (10.3% of all cases), 6 of which resulted in death (9.2% of all cases). We found a female predominance of 1.24 to 1, an average weight of 183 kg, and a 48.5% majority of cases in the thigh.

摘要

巨大局限性淋巴水肿(MLL)是肥胖流行中一种日益增多且可能致命的并发症。MLL被描述为肥胖患者的一种良性淋巴组织增生性过度生长,是继发性淋巴水肿的一种形式,由淋巴液流动受阻引起,具有特征性的临床和组织学表现。患者有一个伴有典型皮肤改变的巨大肿块,常伴有淋巴液渗出,需要进行复杂的重建手术。尽管MLL通常为良性,但如果不治疗,可进展为血管肉瘤,这进一步支持了对MLL及其后遗症进行更多研究的必要性。我们报告了一例52岁男性耻骨联合处MLL的独特病例,其体重指数为75.7kg/m²。我们对文献进行了全面回顾,共描述了65例MLL病例,其中9例发展为血管肉瘤(占所有病例的10.3%),6例死亡(占所有病例的9.2%)。我们发现女性占比为1.24比1,平均体重为183kg,且48.5%的病例发生在大腿。

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