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         Multiple Lymphomatous Polyposis 1

                                

 

A case of mucosa-associated lymphoid tissue lymphoma forming multiple lymphomatous polyposis in the small intestine.World J Gastro enterol. 2007 Mar 7;13(9):1453-7.

A 50-year old woman suffering from diabetes had a CT scan that revealed a diffuse thickening of small intestinal wall and swollen paraaortic lymph nodes. An esophagogastroduodenoscopy (EGD) confirmed multiple polypoid lesions in the duodenum and small intestine, and conventional histological testing revealed non-specific inflammatory changes. Further examinations including the immunohistochemical profiles of the biopsied specimens led us to diagnose the lesion as a marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue type, forming multiple lymphomatous polyposis sequentially spreading from duodenal bulb to terminal ileum. According to Lugano's classification, its staging was clinically diagnosed as stage II. Two courses of a standard CHOP (cyclophosphamide, doxorubicin hydrochloride, vincristine sulfate, and predonisolone) regimen with rituximab reduced the lesion and the patient had a almost complete response. A 5-year follow-up EGD and histological examinations detected no recurrence of the disease.

Gastrointestinal lymphomatous polyposis--clinical, endoscopical and evolution features. A case report.Rom J Gastroenterol. 2005 Sep;14(3): 273-8.

Primary gastrointestinal non-Hodgkin lymphoma accounts for 13-18% of all malignant tumours of small bowel and only 1 % of large bowel tumours (1). Multiple lymphomatous polyposis is a rare entity, characterized by the presence of multiple lymphomatous polyps along the gut (2). Majority of cases with gastrointestinal primary lymphoma are classified histologically as "mantle cell" lymphomas. A 59 year old patient was admitted to our clinic for fatigue and rectal bleeding. Endoscopic examination of the colon revealed an infiltrative-exulcerative lesion of the terminal ileon, a polypoid mass on ileocecal valve and multiple polyps over the entire colon and rectum. Gastroscopy revealed polyps into the duodenal bulb. Histopathological and immunohistochemical studies on biopsy specimens from colon and duodenum confirmed gastrointestinal non-Hodgkin lymphoma, probably "mantle cell" lymphoma. Because she was in an advanced stage she received only cytostatic treatment. A clinical, endoscopical and histopathological follow up at 3, 6 and 12 months was performed.

 Pathology of the Intestinal Polyp (Multiple Lymphomatous Polyposis)

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Multiple lymphomatous polyposis. J Surg Oncol. 1997 Apr;64(4):336-40.

Multiple lymphomatous polyposis (MLP) is a distinctive and particularly rare clinical type of malignant gastrointestinal lymphoma, which is classified as B-cell centrocytic non-Hodgkin's lymphoma. this rare entity has been recently reclassified as mantle cell lymphoma. We herein report three additional cases of MLP involving various segments of the gastrointestinal tract. MLP has an aggressive biologic behavior and a relatively poor prognosis and must be treated accordingly as a high-grade lymphoma with systemic chemotherapy.

Multiple lymphomatous polyposis of the gut. A case with unusually widespread distribution.J Clin Gastroenterol. 1994 Sep;19(2):139-42.

Multiple lymphomatous polyposis (MLP) is a term used to describe malignant lymphomas of the gastrointestinal tract that manifest as polyposis. The cell population of MLP is identical to that in "mantle cell lymphoma." In most instances, relatively small segments of small and large intestine are affected. We report a case of MLP in which involvement was unusually widespread. A 56-year-old man, with abdominal pain and weight loss, proved to have a large mass at the ileocecal valve as well as multiple polyps of the stomach and small and large intestine. MLP is distinctive both grossly and microscopically. Clinically, it may be confused with epithelial polyps, and histologically it must be distinguished from benign lymphoid proliferations as well as other types of lymphoma. The latter distinction is important because of the relatively poor prognosis (median survival of < 3 years).

 
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