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. 1984 Jul;116(1):1–8.

Lymphoma-associated ulcerative bowel disease in the hamster (Mesocricetus auratus) induced by an unusual agent.

E A Manci, L S Heath, S S Leinbach, J H Coggin Jr
PMCID: PMC1900378  PMID: 6377905

Abstract

In a hamster model of non-Hodgkin's lymphoma which closely parallels the disease in man, and which is induced by an unusual agent(s), a diarrheal bowel disease was a major cause of mortality. This study was initiated to characterize this bowel disease and its relation to lymphoma induction and to natural diseases seen in the hamster. The studies showed that the bowel disease was an ulcerative process and was distinct from natural diseases. The incidence of the bowel disease correlated directly with that of the lymphoma in repeated epizootics, in titration studies, and in agent inactivation tests. The ulcerative bowel lesions were seen at the same stage of the disease as acute and chronic inflammatory infiltrates with necrosis in the thymus and mesenteric lymph nodes. Since necrosis in the gut-associated lymphoid tissue can lead to perforation and sepsis, these bowel lesions were lethal, whereas similar necrosis in other lymphoid tissues (thymus and lymph nodes) could be clinically undetectable. Similar lesions have been reported in man. The ulcerative bowel disease was a reliable early clinical marker for exposure of hamsters to this lymphomagenic agent(s).

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Selected References

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  1. Ambrose K. R., Coggin J. H., Jr An epizootic in hamsters of lymphomas of undetermined origin and mode of transmission. J Natl Cancer Inst. 1975 Apr;54(4):877–880. [PubMed] [Google Scholar]
  2. Amend N. K., Loeffler D. G., Ward B. C., Van Hoosier G. L., Jr Transmission of enteritis in the Syrian hamster. Lab Anim Sci. 1976 Aug;26(4):566–572. [PubMed] [Google Scholar]
  3. Boothe A. D., Cheville N. F. The pathology of proliferative ileitis of the golden syrian hamster. Pathol Vet. 1967;4(1):31–44. doi: 10.1177/030098586700400104. [DOI] [PubMed] [Google Scholar]
  4. Boydstun J. S., Jr, Gaffey T. A., Bartholomew L. G. Clinicopathologic study of nonspecific ulcers of the small intestine. Dig Dis Sci. 1981 Oct;26(10):911–916. doi: 10.1007/BF01309496. [DOI] [PubMed] [Google Scholar]
  5. Cleary K. R., Osborne B. M., Butler J. J. Lymph node infarction foreshadowing malignant lymphoma. Am J Surg Pathol. 1982 Jul;6(5):435–442. doi: 10.1097/00000478-198207000-00005. [DOI] [PubMed] [Google Scholar]
  6. Coggin J. H., Jr, Bellomy B. B., Thomas K. V., Pollock W. J. B-cell and T-cell lymphomas and other associated diseases induced by an infectious DNA viroid-like agent in hamsters (Mesocricetus auratus). Am J Pathol. 1983 Mar;110(3):254–266. [PMC free article] [PubMed] [Google Scholar]
  7. Coggin J. H., Jr Embryonic antigens in malignancy and pregnancy: common denominators in immune regulation. Ciba Found Symp. 1983;96:28–54. doi: 10.1002/9780470720776.ch3. [DOI] [PubMed] [Google Scholar]
  8. Coggin J. H., Jr, Oakes J. E., Huebner R. J., Gilden R. Unusual filterable oncogenic agent isolated from horizontally transmitted Syrian hamster lymphomas. Nature. 1981 Mar 26;290(5804):336–338. doi: 10.1038/290336a0. [DOI] [PubMed] [Google Scholar]
  9. Coggin J. H., Jr, Thomas K. V., Huebner R. Horizontally transmitted lymphomas of Syrian hamsters. Fed Proc. 1978 May 15;37(7):2086–2088. [PubMed] [Google Scholar]
  10. Diamandopoulos G. T. Induction of lymphocytic leukemia, lymphosarcoma, reticulum cell sarcoma, and osteogenic sarcoma in the Syrian golden hamster by oncogenic DNA simian virus 40. J Natl Cancer Inst. 1973 May;50(5):1347–1365. doi: 10.1093/jnci/50.5.1347. [DOI] [PubMed] [Google Scholar]
  11. Frisk C. S., Wagner J. E. Experimental hamster enteritis: an electron microscopic study. Am J Vet Res. 1977 Nov;38(11):1861–1868. [PubMed] [Google Scholar]
  12. Frisk C. S., Wagner J. E., Owens D. R. Hamster (Mesocricetus auratus) enteritis caused by epithelial cell-invasive Escherichia coli. Infect Immun. 1981 Mar;31(3):1232–1238. doi: 10.1128/iai.31.3.1232-1238.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Fu Y. S., Perzin K. H. Lymphosarcoma of the small intestine. A clinicopathologic study. Cancer. 1972 Mar;29(3):645–659. doi: 10.1002/1097-0142(197203)29:3<645::aid-cncr2820290318>3.0.co;2-4. [DOI] [PubMed] [Google Scholar]
  14. GREENDYKE R. M., BRIERTY R. E., SWISHER S. N. IN VITRO STUDIES ON ERYTHROPHAGOCYTOSIS. Blood. 1963 Sep;22:295–312. [PubMed] [Google Scholar]
  15. Gorelkin L., Majmudar B. Spontaneous primary lymph node infarction in a patient with lymphoma. South Med J. 1978 Nov;71(11):1451–1452. doi: 10.1097/00007611-197811000-00047. [DOI] [PubMed] [Google Scholar]
  16. Graffi A., Bender E., Schramm T., Kuhn W., Schneiders F. Induction of transmissible lymphomas in Syrian hamsters by application of DNA from viral hamster papovavirus-induced tumors and by cell-free filtrates from human tumors. Proc Natl Acad Sci U S A. 1969 Dec;64(4):1172–1175. doi: 10.1073/pnas.64.4.1172. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. IRVINE W. T., JOHNSTONE J. M. Lymphosarcoma of the small intestine with special reference to perforating tumours. Br J Surg. 1955 May;42(176):611–618. doi: 10.1002/bjs.18004217608. [DOI] [PubMed] [Google Scholar]
  18. Isaacson P., Wright D. H. Malignant histiocytosis of the intestine. Its relationship to malabsorption and ulcerative jejunitis. Hum Pathol. 1978 Nov;9(6):661–677. doi: 10.1016/s0046-8177(78)80049-5. [DOI] [PubMed] [Google Scholar]
  19. Jacoby R. O. Transmissible ileal hyperplasia of hamsters. I. Histogenesis and immunocytochemistry. Am J Pathol. 1978 Jun;91(3):433–450. [PMC free article] [PubMed] [Google Scholar]
  20. Jonas A. M., Tomita Y., Wyand D. S. Enzootic intestinal adenocarcinoma in hamsters. J Am Vet Med Assoc. 1965 Nov 15;147(10):1102–1108. [PubMed] [Google Scholar]
  21. Pour P., Kmoch N., Greiser E., Mohr U., Althoff J., Cardesa A. Spontaneous tumors and common diseases in two colonies of Syrian hamsters. I. Incidence and sites. J Natl Cancer Inst. 1976 May;56(5):931–935. doi: 10.1093/jnci/56.5.931. [DOI] [PubMed] [Google Scholar]
  22. Wood B. A., Dutz W., Cross S. S. Neonatal infection with mouse thymic virus: spleen and lymph node necrosis. J Gen Virol. 1981 Nov;57(Pt 1):139–147. doi: 10.1099/0022-1317-57-1-139. [DOI] [PubMed] [Google Scholar]

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