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<ArticleSet><Article><Journal><PublisherName></PublisherName><JournalTitle>Journal of Research in Medical Sciences</JournalTitle><Issn>1735-1995</Issn><Volume>17</Volume><Issue>7</Issue><PubDate PubStatus="epublish"><Year>2012</Year><Month>05</Month><Day>15</Day></PubDate></Journal><ArticleTitle>Primary gastrointestinal lymphoma</ArticleTitle><FirstPage>8365</FirstPage><LastPage>8365</LastPage><Language>EN</Language><AuthorList><Author><FirstName>Amir</FirstName><LastName>Aledavood</LastName></Author><Author><FirstName>Mohammad Reza</FirstName><LastName>Ghavam Nasiri</LastName></Author><Author><FirstName>Bahram</FirstName><LastName>Memar</LastName></Author><Author><FirstName>Soodabeh</FirstName><LastName>Shahidsales</LastName><Affiliation>Cancer Research Center, Omid Hospital , School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. shahidsaless@mums.ac.ir</Affiliation></Author><Author><FirstName>Hamid Reza</FirstName><LastName>Raziee</LastName></Author><Author><FirstName>Kamran</FirstName><LastName>Ghafarzadegan</LastName></Author><Author><FirstName>Samira</FirstName><LastName>Mohtashami</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2012</Year><Month>05</Month><Day>15</Day></PubDate><PubDate PubStatus="accepted"><Year>2012</Year><Month>05</Month><Day>17</Day></PubDate></History><Abstract>BACKGROUND: Extranodal lymphoma may arise anywhere outside lymph nodes mostly in the gastrointestinal (GI) tract as non-Hodgkin's disease. We reviewed the clinicopathological features and treatment results of patients with primary GI lymphoma. METHODS: A total number of 30 cases with primary GI lymphoma were included in this study. Patients referred to the Radiation Oncology Department of Omid Hospital (Mashhad, Iran) during a 5-year period (2006-11). Clinical, paraclinical, and radiological data was collected from medical records of the patients.  RESULTS: Out of the 30 patients with primary GI lymphoma in the study, 12 were female (40%) and 18 were male (60%) (male to female ratio: 3/2). B symptoms were present in 27 patients (90%). Antidiuretic&amp;nbsp;hormone (LDH) levels were elevated in 9 patients (32.1%). The most common primary site was stomach in 14 cases (46.7%). Other common sites included small intestine and colon each in 8 patients (26.7%). All patients had histopathologically proven non-Hodgkin's lymphoma. The most common histologic subtype was diffuse large B-cell lymphoma (DLBL) in 16 patients (53.3%). In addition, 28 patients (93.3%) received chemotherapy with cyclophosphamide, vincristine, doxorubicin, prednisolone (CHOP regimen). The median course of chemotherapy was 6 cources. Moreover, 8 patients (26.7%) received radiotherapy with cobalt 60. The median follow-up time was 26 months. The overall 5-year survival rate was 53% and the median survival time was 60 months.  CONCLUSION: Primary GI lymphoma is commonly seen in stomach and small intestine and mostly is DLBCL or mucosa-associated lymphoid tissue (MALT) lymphoma. KEYWORDS: Primary Gastrointestinal Lymphoma, Diffuse Large B-Cell Lymphoma, Extranodal Lymphoma</Abstract></Article></ArticleSet>
