Familial multiple lipomatosis: Report of a new family

被引：0
|
作者：
Gologorsky, Yakov [1 ]
Gologorsky, Daniel
Yarygina, Anna S.
Surti, Urvashi
Zirwas, Matthew J.
机构：
[1] Univ Pittsburgh, Sch Med, Pittsburgh, PA 15261 USA
[2] Cornell Univ, Ithaca, NY USA
来源：
CUTIS | 2007年 / 79卷 / 03期
关键词：
D O I：
暂无
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
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.
引用
收藏
页码：227 / 232
页数：6
相关论文
共 50 条
  • [21] Encephalocraniocutaneous Lipomatosis (ECCL) in a Patient With History of Familial Multiple Lipomatosis (FML)
    Prontera, Paolo
    Stangoni, Gabriela
    Manes, Iris
    Mencarelli, Amedea
    Donti, Emilio
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2009, 149A (03) : 543 - 545
  • [22] Minimally invasive approach to familial multiple lipomatosis
    Ronan, SJ
    Broderick, T
    PLASTIC AND RECONSTRUCTIVE SURGERY, 2000, 106 (04) : 878 - 880
  • [23] FAMILIAL MULTIPLE SYMMETRICAL LIPOMATOSIS WITH PERIPHERAL NEUROPATHY
    CHALK, CH
    MILLS, KR
    JACOBS, JM
    DONAGHY, M
    NEUROLOGY, 1990, 40 (08) : 1246 - 1250
  • [24] INTESTINAL LIPOMA AND FAMILIAL MULTIPLE LIPOMATOSIS - A CASUAL ASSOCIATION
    BLANC, JF
    ZERBIB, F
    HAMDI, D
    BERNARD, PH
    LAMOULIATTE, H
    QUINTON, A
    GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE, 1995, 19 (04): : 456 - 457
  • [25] Multiple lipomatosis in a patient with familial atypical mole syndrome
    Tsao, H
    Sober, AJ
    BRITISH JOURNAL OF DERMATOLOGY, 1998, 139 (06) : 1118 - 1119
  • [26] Colonic lipoma and familial multiple lipomatosis: A chance association?
    Sockeel, P.
    Massoure, M. -P.
    GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE, 2008, 32 (10): : 872 - 873
  • [27] FAMILIAL HYPOCALCIURIC HYPERCALCEMIA - REPORT OF A NEW FAMILY
    GOMEZ, JM
    JORGE, S
    SOLER, J
    LUCAS, T
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1982, 5 (02) : 125 - 127
  • [28] Multiple symmetric lipomatosis: a case report
    Banitahmaseb, A.
    Karaman, E.
    Ozdogan, A.
    Banitahmaseb, E. K.
    Dervisoglu, S.
    TURKISH ARCHIVES OF OTORHINOLARYNGOLOGY, 2005, 43 (01) : 48 - 54
  • [29] Familial generalized multiple glomangiomyoma:: Report of a new family, with immunohistochemical and ultrastructural studies and review of the literature
    Calduch, L
    Monteagudo, C
    Martínez-Ruiz, E
    Ramón, D
    Pinazo, I
    Cardá, C
    Jordá, E
    PEDIATRIC DERMATOLOGY, 2002, 19 (05) : 402 - 408
  • [30] Multiple familial lipomatosis with polyneuropathy, an inherited dominant condition.
    Stoll, C
    Alembik, Y
    Truttmann, M
    ANNALES DE GENETIQUE, 1996, 39 (04): : 193 - 196
12345