Kurt Habibe, Arnold Christina A, Payne Jason E, Miller Michael J, Skoracki Roman J, Iwenofu O Hans
Department of Pathology and Laboratory Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Department of Pathology and Laboratory Medicine, MD Anderson Cancer Center, Houston, TX, USA.
Mod Pathol. 2016 Jan;29(1):75-82. doi: 10.1038/modpathol.2015.135. Epub 2015 Nov 20.
Massive localized lymphedema is a monstrous tumefactive pseudosarcoma seen in middle-aged morbidly obese adults. Since its initial description in 1998, the etiology remains unknown, although associations with trauma, surgeries, and hypothyroidism have been reported. Herein, we report the largest study of massive localized lymphedema and expand upon its clinicopathologic features. Fifty-four cases from 46 patients were retrospectively identified from the institutional archives of The Ohio State University Wexner Medical Center between 2002 and 2015. Forty-six patients (21 males and 25 females, mean age 50 years) presented with large masses developing over a 5-60-month period. The majority of patients were Caucasian (n=39). All patients were obese with a mean weight of 384.7 lb and a mean body mass index of 59.6 kg/m(2). Thirty-six patients had a history of atherosclerotic cardiovascular disease and diabetes mellitus type 2 was present in 22 patients. Eight patients had multifocal massive localized lymphedema. The sites included thigh (n=33), abdomen (n=17), suprapubic region (n=1), mons pubis (n=6), scrotum (n=2), perianal region (n=1), and right flank (n=1). Mostly, the clinical impression was benign processes, including pannus or lymphedema pseudotumor. Grossly, the mean weight was 8237 g and the mean size was 53.2 cm. Histologically, eight cases showed a unique pattern of dystrophic calcifications mimicking hyperchromatic, atypical nuclei that might lead to misdiagnosis of liposarcoma, four cases showed focal metaplastic ossification, and three cases showed multinucleated cells in addition to prototypic features of massive localized lymphedema. We report that this is the largest series of massive localized lymphedema. This is a lesion mostly seen in morbidly obese patients and the thigh is the most common site of involvement. We note a marked racial predilection for Caucasians and a tendency towards multiplicity. We suggest that obesity itself and the related metabolic syndrome have an important role in its pathogenesis.
巨大局限性淋巴水肿是一种见于中年病态肥胖成年人的巨大肿瘤样假肉瘤。自1998年首次描述以来,其病因仍不清楚,尽管有报道称与创伤、手术及甲状腺功能减退有关。在此,我们报告了关于巨大局限性淋巴水肿的最大规模研究,并详述了其临床病理特征。2002年至2015年间,从俄亥俄州立大学韦克斯纳医学中心的机构档案中回顾性鉴定出46例患者的54例病例。46例患者(21例男性和25例女性,平均年龄50岁)在5至60个月的时间里出现了巨大肿块。大多数患者为白种人(n = 39)。所有患者均肥胖,平均体重为384.7磅,平均体重指数为59.6kg/m²。36例患者有动脉粥样硬化性心血管疾病史,22例患者患有2型糖尿病。8例患者有多灶性巨大局限性淋巴水肿。受累部位包括大腿(n = 33)、腹部(n = 17)、耻骨上区域(n = 1)、阴阜(n = 6)、阴囊(n = 2)、肛周区域(n = 1)和右胁腹(n = 1)。大多数情况下,临床印象为良性病变,包括血管翳或淋巴水肿假瘤。大体上,平均重量为8237克,平均大小为53.2厘米。组织学上,8例显示出一种独特的营养不良性钙化模式,类似于核深染、非典型核,可能导致脂肪肉瘤的误诊;4例显示局灶性化生骨化;3例除具有巨大局限性淋巴水肿的典型特征外,还显示有多核细胞。我们报告这是最大系列的巨大局限性淋巴水肿。这是一种主要见于病态肥胖患者的病变,大腿是最常见的受累部位。我们注意到白种人有明显的种族偏好以及多灶性倾向。我们认为肥胖本身及相关代谢综合征在其发病机制中起重要作用。