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Non‐Hodgkin's lymphomas in the Middle East. A study of 417 patients with emphasis on special features
Author(s) -
Salem Philip,
Anaissie Elias,
Allam Charles,
Geha Sima,
Hashimi Labib,
Ibrahim Nuhad,
Jabbour Joseph,
Habboubi Nassir,
Khalyl Maryse
Publication year - 1986
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/1097-0142(19860901)58:5<1162::aid-cncr2820580531>3.0.co;2-8
Subject(s) - medicine , emphasis (telecommunications) , middle east , history , archaeology , electrical engineering , engineering
A total of 417 evaluable patients with non‐Hodgkin's lymphomas were diagnosed between January 1974 and December 1983 at the American University of Beirut Medical Center in Beirut Lebanon. Of these, 179 (43%) patients had nodal lymphomas, and 183 (44%) had extranodal lymphomas. The commonest lymphoma was diffuse large cell (27%), followed by large cell immunoblastic (21%). The histopathologic pattern was follicular in 18% of the nodal lymphomas and in 5.3% of the extranodal forms. The most common site of extranodal lymphoma was the gastrointestinal tract (46.5%), followed by Waldeyer's ring (19%). Small intestinal lymphomas were three times more common than gastric lymphomas. Immuno‐proliferative small intestinal disease (IPSID) was diagnosed in 20 of 59 patients who had primary small intestinal lymphoma. Of the 34 patients who had Waldeyer's ring lymphoma, 7 had gastrointestinal involvement at some time during the course of the disease. Nodal lymphomas were associated with poor prognostic factors: (1) 82% were diffuse; (2) 77% had advanced disease at presentation; (3) 77% had intermediate‐or high‐grade malignancy lymphoma; (4) 40% had marrow involvement; and (5) 46% had B symptoms. In children, the most common lymphoma was Burkitt's, and 80% of pediatric lymphomas were high‐grade malignancy. In conclusion, this study delineates the special features of non‐Hodgkin's lymphomas in the Middle East: (1) The presence of IPSID; (2) the high incidence of extranodal forms, in particular the intestinal ones; and (3) the rarity of follicular lymphomas. Cancer 58:1162‐1166, 1986.