Angioimmunoblastic T-Cell Lymphoma

医学 高丙种球蛋白血症 内科学 胃肠病学 淋巴瘤 T细胞淋巴瘤 贫血 淋巴增殖性病變 病理 皮肤病科 疾病
作者
Florence Lachenal,Françoise Berger,Hervé Ghesquières,Pierre Biron,A. Hot,Evelyne Callet‐Bauchu,Catherine Chassagne,Bertrand Coiffier,I. Durieu,H Rousset,Gilles Salles
出处
期刊:Medicine [Wolters Kluwer]
卷期号:86 (5): 282-292 被引量:134
标识
DOI:10.1097/md.0b013e3181573059
摘要

We retrospectively analyzed 77 patients with pathologically diagnosed angioimmunoblastic T-cell lymphoma from a single city. There were 43 men and 34 women; the median age was 64.5 years (range, 30-91 yr). Average time between first symptoms of the disease and diagnosis was 3.6 months. At diagnosis, peripheral nodes were present in all but 1 patient, and were generalized in 90% of cases. Constitutional symptoms were reported in 77% of cases and spleen enlargement in 51%. A cutaneous eruption-morbilliform, urticarial, or more polymorphic-was present in 45% of patients; in one-third of them, the eruption occurred after drug administration. Other clinical manifestations included pleuritis (22%); arthralgia or arthritis (17%); ear, nose, and throat involvement (14%); central or peripheral neurologic manifestations (10%); and ascites (5%). Most patients presented with advanced disease at diagnosis (bone marrow involvement in 60% of cases). The main laboratory abnormalities were elevated lactate dehydrogenase levels (71%), inflammatory syndrome (67%), hypergammaglobulinemia (50%), anemia (51%), and lymphopenia (52%). Auto- or disimmune manifestations were reported in one-third of patients: autoimmune hemolytic anemia was present at diagnosis in 19% of patients and thrombocytopenic purpura in 7%. Documented vasculitis was described in 12% of cases. Clonality was analyzed in lymph nodes in 47 patients: T-cell and B-cell clones were found in 45 (96%) and 20 (45%) patients, respectively. Chromosomal abnormalities were identified in 62% of cases: trisomies 3, 5, 18, 19, additional X chromosome, and deletion of chromosome 7 were the most common abnormalities. The current study underlines the diversity of presenting manifestations of angioimmunoblastic T-cell lymphoma. Abbreviations: AITL = angioimmunoblastic T-cell lymphoma, AILD = angioimmunoblastic lymphadenopathy with dysproteinemia, CSF = cerebrospinal fluid, EBERs = Epstein-Barr virus-encoded small RNAs, ENT = ear, nose, and throat, HIV = human immunodeficiency virus, Ig = immunoglobulin, IL = interleukin, IPI = International Prognostic Index, LDH = lactate dehydrogenase, PCR = polymerase chain reaction, TCR = T-cell receptor.
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