Abstract

RAMIREZ, Luis A et al. SECONDARY INTESTINAL LYMPHOMATOUS PO- LYPOSIS IMMUNE CELLS B: PRIMARY FOLLICULAR LYMPHOMA NON-HODGKIN LYMPHOMA. A CASE PRESENTATION . Gen [online]. 2015, vol.69, n.4, pp.137-140. ISSN 2477-975X.

Patient women 30 years of age, with 7 months of current disease, characterized by asthenia, adinamia, mucous skin pallor, loss of weight 12 kg in the last month, and episodes of evacuations liquid 10 days of evolution in #15 times a day in copious amounts, without mucus, or blood; also meant vomiting #01 time per day of food content. Personal history, family, and psychobiological habits: not contributorios. Functional exploration: denies symptoms B. positive physical examination: vital signs: normal BMI: 17.2 kg/m2 light pale mucosa and muscular hypotrophy. Positive paraclinical: anemia macrocytic e hyperchromic severe, without alteration of the Leukocyte count, LDH: 1578 u / and the rest of basic chemistry was normal. Abdominal ultrasound: normal. CT of abdomen with doublecontrast: splenomegaly mild retroperitoneal adenopathies and mesenteric nonspecific aspect, upper digestive endoscopy: duodenal polyposis. Enteroscopy: Intestinal polyposis. Colo- noscopy: normal. Biopsy and immunohistochemical: intestinal lymphomatous polyposis: Lymphoma non-Hodgkins immune b cells follicular lymphoma. An uncommon type of extranodal lymphoma cell line B, uncommon as a form of presentation of lymphomatous polyposis, that we have to make differential diagnosis with: 1. Mantle cell Lymphoma. 2. Reactive follicular Lymphoid Hyperplasia. 3. Epithelial polyp. 4. Nodal follicular Lymphoma secondary commitment.

Keywords : Lymphomatous polyposis; Non-Hodgkings; Intestinal.

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