Treatment of mesenteric desmoid tumours with the antioestrogenic agent toremifene: case histories and an overview of the literature

被引:27
作者
Bus, PJ [1 ]
Verspaget, HW [1 ]
van Krieken, JHJM [1 ]
de Roos, A [1 ]
Keizer, HJ [1 ]
Bemelman, WA [1 ]
Vasen, HFA [1 ]
Lamers, CBHW [1 ]
Griffioen, G [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Gastroenterol Hepatol, NL-2300 RC Leiden, Netherlands
关键词
aggressive fibromatosis; anti-oestrogen; desmoid tumours; toremifene;
D O I
10.1097/00042737-199910000-00018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Desmoid tumours are histologically benign but due to their infiltration and compression of surrounding structures potentially life-threatening fibromatous lesions of unknown aetiology, The annual incidence rate is 2-4 per million people, The mesenteric variant constitutes about 10% of all desmoid tumours, although in familial adenomatous polyposis (FAP) patients this may be up to 70%, Due to the small number of patients with mesenteric desmoids the therapy is mainly empirical. This report describes the rationale as well as the value of the short- and long-term treatment (up to 6 years) with the anti-oestrogenic agent toremifene in combination with sulindac in two patients suffering from such a mesenteric desmoid tumour, These patients did not respond to sulindac alone and previous treatment with tamoxifen together with this non-steroidal anti-inflammatory drug had also failed, An overview of the literature on the management of these dismal tumours is presented, Eur J Gastroenterol Hepatol 11:1179 -1183 (C) 1999 Lippincott Williams & Wilkins.
引用
收藏
页码:1179 / 1183
页数:5
相关论文
共 75 条
[1]   MORTALITY IN PATIENTS WITH FAMILIAL ADENOMATOUS POLYPOSIS [J].
ARVANITIS, ML ;
JAGELMAN, DG ;
FAZIO, VW ;
LAVERY, IC ;
MCGANNON, E .
DISEASES OF THE COLON & RECTUM, 1990, 33 (08) :639-642
[2]   ROLE OF BRACHYTHERAPY IN THE MANAGEMENT OF DESMOID TUMORS [J].
ASSAD, WA ;
NORI, D ;
HILARIS, BS ;
SHIU, MH ;
HAJDU, SI .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1986, 12 (06) :901-906
[3]  
Bauernhofer T, 1996, CANCER, V77, P1061, DOI 10.1002/(SICI)1097-0142(19960315)77:6<1061::AID-CNCR9>3.3.CO
[4]  
2-E
[5]   MESENTERIC DESMOID TUMOR IN GARDNERS-SYNDROME TREATED BY SULINDAC [J].
BELLIVEAU, P ;
GRAHAM, AM .
DISEASES OF THE COLON & RECTUM, 1984, 27 (01) :53-54
[6]   BREAST-CANCER, DESMOID TUMORS, AND FAMILIAL ADENOMATOUS POLYPOSIS - A UNIFYING HYPOTHESIS [J].
BENSON, JR ;
BAUM, M .
LANCET, 1993, 342 (8875) :848-850
[7]   DESMOID TUMORS TREATED WITH TRIPHENYLETHYLENES [J].
BROOKS, MD ;
EBBS, SR ;
COLLETTA, AA ;
BAUM, M .
EUROPEAN JOURNAL OF CANCER, 1992, 28A (6-7) :1014-1018
[8]   INCIDENCE OF ASSOCIATED DISEASES IN FAMILIAL POLYPOSIS-COLI [J].
BULOW, S .
SEMINARS IN SURGICAL ONCOLOGY, 1987, 3 (02) :84-87
[9]   EXTRACOLONIC LESIONS ASSOCIATED WITH POLYPOSIS COLI [J].
BUSSEY, HJR .
PROCEEDINGS OF THE ROYAL SOCIETY OF MEDICINE-LONDON, 1972, 65 (03) :294-&
[10]   FAMILIAL ADENOMATOUS POLYPOSIS - DESMOID TUMORS AND LACK OF OPHTHALMIC LESIONS (CHRPE) ASSOCIATED WITH APC MUTATIONS BEYOND CODON-1444 [J].
CASPARI, R ;
OLSCHWANG, S ;
FRIEDL, W ;
MANDL, M ;
BOISSON, C ;
BOKER, T ;
AUGUSTIN, A ;
KADMON, M ;
MOSLEIN, G ;
THOMAS, G ;
PROPPING, P .
HUMAN MOLECULAR GENETICS, 1995, 4 (03) :337-340