Malignant complications of coeliac disease

被引:57
作者
Brousse, N
Meijer, JWR
机构
[1] Hop Necker Enfants Malad, Dept Pathol, Serv Anat & Cytol Pathol, F-75743 Paris, France
[2] Rijnstate Hosp, Dept Pathol, Arnhem, Netherlands
关键词
coeliac disease; malignant tumors; epithelial tumors; lymphoma; enteropathy associated T-cell lymphoma; ulcerative jejunitis; refractory coeliac disease;
D O I
10.1016/j.bpg.2005.02.002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Patients with coeliac disease (CD), particularly those who are undiagnosed or do not adhere to a strict gluten free diet (GFD), are prone to develop complications. Malignant complications are the most serious and should be suspected when expected responses to GFD are not achieved or sustained. Lymphomas, mostly T-cell type, and other malignant tumours, particularly carcinoma of the small bowel, less frequently of stomach and oesophagus, are associated with CD. Loss of response to a gluten free diet (refractory coeliac disease) and ulcerative jejunitis are two recently described complications of CD that may progress to an Enteropathy-Associated T-cell Lymphoma (EATL). Coeliac disease-related lymphoma most often appears at extra-nodal sites, essentially the small bowel, although one have to realise that T-cell lymphomas arising in sites outside the small bowel could be related to coeliac disease. Workup of an EATL must include immunehistology and if necessary T-cell flow cytometry and T-cell rearrangement. Adequate imaging with CT and PET-scanning is mandatory.
引用
收藏
页码:401 / 412
页数:12
相关论文
共 47 条
[11]   From hyperplasia to T cell lymphoma [J].
Cerf-Bensussan, N ;
Brousse, N ;
Cellier, C .
GUT, 2002, 51 (03) :304-305
[12]   Natural killer cell lymphoma of small intestine with features of enteropathy but lack of association with celiac disease [J].
Chuang, SS ;
Jung, YC .
HUMAN PATHOLOGY, 2004, 35 (05) :639-642
[13]   Mortality in patients with coeliac disease and their relatives:: a cohort study [J].
Corrao, G ;
Corazza, GR ;
Bagnardi, V ;
Brusco, G ;
Ciacci, C ;
Cottone, M ;
Guidetti, CS ;
Usai, P ;
Cesari, P ;
Pelli, MA ;
Loperfido, S ;
Volta, U ;
Calabró, A ;
Certo, M .
LANCET, 2001, 358 (9279) :356-361
[14]   Frequency of clonal intraepithelial T lymphocyte proliferations in enteropathy-type intestinal T cell lymphoma, coeliac disease, and refractory sprue [J].
Daum, S ;
Weiss, D ;
Hummel, M ;
Ullrich, R ;
Heise, W ;
Stein, H ;
Riecken, EO ;
Foss, HD .
GUT, 2001, 49 (06) :804-812
[15]   Distinction between coeliac disease and refractory sprue:: a simple immunohistochemical method [J].
de Serre, NPM ;
Cellier, C ;
Jabri, B ;
Delabesse, E ;
Verkarre, V ;
Roche, B ;
Lavergne, A ;
Brière, J ;
Mauvieux, L ;
Leborgne, M ;
Barbier, JP ;
Modigliani, R ;
Matuchansky, C ;
Macintyre, E ;
Cerf-Bensussan, N ;
Brousse, N .
HISTOPATHOLOGY, 2000, 37 (01) :70-77
[16]   Enteropathy-associated T-cell lymphomas have a cytotoxic T-cell phenotype [J].
deBruin, PC ;
Connolly, CE ;
Oudejans, JJ ;
Kummer, JA ;
Jansen, W ;
McCarthy, CF ;
Meijer, CJLM .
HISTOPATHOLOGY, 1997, 31 (04) :313-317
[17]   First steps in unraveling the genotype of enteropathy-type T-cell lymphoma [J].
Du, MQ ;
Isaacson, PG .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (05) :1527-1529
[18]   Expression of killer cell inhibitory receptors is restricted to true NK cell lymphomas and a subset of intestinal enteropathy-type T cell lymphomas with a cytotoxic phenotype [J].
Dukers, DF ;
Vermeer, MH ;
Jaspars, LH ;
Sander, CA ;
Flaig, MJ ;
Vos, W ;
Willemze, R ;
Meijer, CJLM .
JOURNAL OF CLINICAL PATHOLOGY, 2001, 54 (03) :224-228
[19]   Heterogeneity of intraepithelial lymphocytes in refractory sprue: potential implications of CD30 expression [J].
Farstad, IN ;
Johansen, FE ;
Vlatkovic, L ;
Jahnsen, J ;
Scott, H ;
Fausa, O ;
Bjorneklett, A ;
Brandtzaeg, P ;
Halstensen, TS .
GUT, 2002, 51 (03) :372-378
[20]   Enteropathy-type intestinal T-cell lymphoma: Clinical features and treatment of 31 patients in a single center [J].
Gale, J ;
Simmonds, PD ;
Mead, GM ;
Sweetenham, JW ;
Wright, DH .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (04) :795-803