Familial multiple gastrointestinal stromal tumours with associated abnormalities of the myenteric plexus layer and skeinoid fibres

被引:18
作者
Handra-Luca, A
Fléjou, JF
Molas, G
Sauvanet, A
Belghiti, J
Degott, C
Terris, B
机构
[1] Beaujon Hosp, Dept Pathol, Clichy, France
[2] Hop St Antoine, Dept Pathol, F-75571 Paris, France
[3] Beaujon Hosp, Dept Surg, Clichy, France
关键词
gastrointestinal stromal tumour; immunohistochemistry; CD117;
D O I
10.1046/j.1365-2559.2001.01214.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: Multiple familial gastrointestinal stromal tumours are rare. We report the third family with two cases of multiple gastrointestinal stromal tumours showing skeinoid fibres. Associated abnormalities of the myenteric plexus layer are described and new hypotheses for the histogenesis of gastrointestinal stromal tumours are formulated. Methods and results: Multiple gastrointestinal stromal tumours developed in the duodenum and proximal jejunum were removed from mother and son. No history of a specific syndrome or of mastocytosis was known. Light microscopy revealed typical gastrointestinal stromal tumours with skeinoid fibres. An unusual abnormality of the myenteric plexus layer, showing a diffuse spindle cell hyperplasia. was noted in the macroscopically normal digestive wall. No abnormalities of the ganglion cells were associated. Tumours and the spindle cell hyperplasia showed similar morphological and immunohistochemical features with expression of CD34 and CD117 antigens. Follow-up revealed recurrences in the mother. Conclusion: The morphological characteristics of these two cases of familial gastrointestinal stromal tumours and of the associated abnormalities of the myenteric plexus layer, help to better explain the histogenesis of multiple familial gastrointestinal stromal tumours. The hyperplasia of the myenteric plexus could be considered a risk factor for recurrent tumours.
引用
收藏
页码:359 / 363
页数:5
相关论文
共 17 条
[1]   Cause of familial and multiple gastrointestinal autonomic nerve tumors with hyperplasia of interstitial cells of cajal is germline mutation of the c-kit gene [J].
Hirota, S ;
Okazaki, T ;
Kitamura, Y ;
O'Brien, P ;
Kapusta, L ;
Dardick, I .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2000, 24 (02) :326-327
[2]   GASTROINTESTINAL STROMAL TUMORS - AN IMMUNOHISTOCHEMICAL STUDY OF 165 CASES [J].
HURLIMANN, J ;
GARDIOL, D .
HISTOPATHOLOGY, 1991, 19 (04) :311-320
[3]   Multiple small intestinal stromal tumors with skeinoid fibers in association with neurofibromatosis 1 (von Recklinghausen's disease) [J].
Ishida, T ;
Wada, I ;
Horiuchi, H ;
Oka, T ;
Machinami, R .
PATHOLOGY INTERNATIONAL, 1996, 46 (09) :689-695
[4]   Germline-activating mutation in the kinase domain of KIT gene in familial gastrointestinal stromal tumors [J].
Isozaki, K ;
Terris, B ;
Belghiti, J ;
Schiffmann, S ;
Hirota, S ;
Vanderwinden, JM .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (05) :1581-1585
[5]  
Kerr JZ, 1999, CANCER, V85, P220, DOI 10.1002/(SICI)1097-0142(19990101)85:1<220::AID-CNCR30>3.0.CO
[6]  
2-A
[7]  
Kindblom L. G., 1999, Modern Pathology, V12, p77A
[8]  
Langel D. J., 1999, Modern Pathology, V12, p78A
[9]   Gastrointestinal stromal tumors: Recent advances in understanding of their biology [J].
Miettinen, M ;
Sarlomo-Rikala, M ;
Lasota, J .
HUMAN PATHOLOGY, 1999, 30 (10) :1213-1220
[10]   SMALL-INTESTINAL STROMAL TUMORS WITH SKEINOID FIBERS IN NEUROFIBROMATOSIS - REPORT OF 4 CASES WITH ULTRASTRUCTURAL-STUDY OF SKEINOID FIBERS FROM PARAFFIN BLOCKS [J].
MIN, KW ;
BALATON, AJ .
ULTRASTRUCTURAL PATHOLOGY, 1993, 17 (3-4) :307-314