Gologorsky Yakov, Gologorsky Daniel, Yarygina Anna S, Surti Urvashi, Zirwas Matthew J
University of Pittsburgh School of Medicine, Pennsylvania, USA.
Cutis. 2007 Mar;79(3):227-32.
Familial multiple lipomatosis (FML) is a rare entity. We report a family with this disease. Karyotypic analysis was performed on tissue isolated from excised lipomas and peripheral blood. No chromosomal abnormalities were found. This is the first report of karyotypic analysis of lipomas removed from a patient with FML. The finding of a normal karyotype is important because approximately 25% of spontaneous lipomas will have abnormal karyotypes; therefore, we felt there was a significant probability that familial lipomas in FML would have abnormal karyotypes.
家族性多发性脂肪瘤(FML)是一种罕见的病症。我们报告了一个患有这种疾病的家族。对从切除的脂肪瘤和外周血中分离出的组织进行了核型分析。未发现染色体异常。这是首次对FML患者切除的脂肪瘤进行核型分析的报告。核型正常这一发现很重要,因为大约25%的自发性脂肪瘤会有异常核型;因此,我们认为FML中的家族性脂肪瘤很有可能具有异常核型。