Primary intestinal lymphoma: clinical manifestations and possible effect of environmental factors.

作者: Bracha Ramot , Amira Many

DOI: 10.1007/978-3-642-80686-5_20

关键词: Developed countryDiseaseWestern worldDermatologyIntestinal lymphomaMedicineLymphomaMalabsorptionMedical literatureSmall intestine

摘要: Lymphoma of the small intestine can occur as a late secondary manifestation disseminated lymphoma, or far less commonly, primary lesion originating in mesenteric lymph nodes [1–6]. The latter disease be further subdivided into two categories: a) Solitary lymphoma that occurs most commonly terminal ileum and is encountered more frequently young children, b) Diffuse multifocal intestinal occurring proximal primarily older age groups. In entity malabsorption has been described [3–5]. syndrome by EDELMAN et al. (1966), only rarely developed countries Western world [7]. These authors, reviewing medical literature West, were able to find 48 cases, which they regarded 32 well established 16 probable. On other hand, not rare among certain populations whose common denominator appears are under-privileged terms nutrition, hygiene care [7–11]. Israel relatively prevalent Arabs first second generations Jewish immigrants from mid-eastern North Africa virtually non exsistent Jews European origin [7–10]. This was also Mediterranean as, Africa, Italy, Spain Iran, Mexico, South America African-Cape-Coloured people [11–13]. evidence thus would seem suggest predisposition environmentally determined. One could speculate about unique vulnerability due genetic factors combination environmental influences. this work we summarized present day knowledge on analysed possible effects its development. possibility abnormalities lymphoreticular system effect will discussed.

参考文章(16)
Paul A. Crabbé, Joseph F. Heremans, Selective IgA deficiency with steatorrhea. A new syndrome. The American Journal of Medicine. ,vol. 42, pp. 319- 326 ,(1967) , 10.1016/0002-9343(67)90031-9
Marvin H. Sleisenger, Thomas P. Almy, David P. Barr, The sprue syndrome secondary to lyrnphoma of the small bowel The American Journal of Medicine. ,vol. 15, pp. 666- 674 ,(1953) , 10.1016/0002-9343(53)90155-7
HAROLD H. SCUDAMORE, Observations on Secondary Malabsorption Syndromes of Intestinal Origin Annals of Internal Medicine. ,vol. 55, pp. 433- 447 ,(1961) , 10.7326/0003-4819-55-3-433
P.W. Brunt, W. Sircus, N. Maclean, NEOPLASIA AND THE CŒLIAC SYNDROME IN ADULTS The Lancet. ,vol. 293, pp. 180- 184 ,(1969) , 10.1016/S0140-6736(69)91192-1
D. Eakins, T. Fulton, D. R. Hadden, Reticulum cell sarcoma of the small bowel and steatorrhoea Gut. ,vol. 5, pp. 315- 323 ,(1964) , 10.1136/GUT.5.4.315
M. Seligmann, F. Danon, D. Hurez, E. Mihaesco, J.-L. Preud'homme, Alpha-chain disease: a new immunoglobulin abnormality. Science. ,vol. 162, pp. 1396- 1397 ,(1968) , 10.1126/SCIENCE.162.3860.1396
SAUL A. ROSENBERG, HENRY D. DIAMOND, BERNARD JASLOWITZ, LLOYD F. CRAVER, Lymphosarcoma: a review of 1269 cases. Medicine. ,vol. 40, pp. 31- 84 ,(1961) , 10.1097/00005792-196102000-00002
C F McCarthy, I D Fraser, K T Evans, A E Read, Lymphoreticular dysfunction in idiopathic steatorrhoea. Gut. ,vol. 7, pp. 140- 148 ,(1966) , 10.1136/GUT.7.2.140
O.D. Harris, W.T. Cooke, H. Thompson, J.A.H. Waterhouse, Malignancy in adult coeliac disease and idiopathic steatorrhoea. The American Journal of Medicine. ,vol. 42, pp. 899- 912 ,(1967) , 10.1016/0002-9343(67)90071-X