Choukri Mohammed, Taheri Hafsa, Seddik Rachid, Benkirane Souad, Hamama Afaf, Masrar Azzelarab, Agoumi Najia Benkirane, Chabraoui Layachi
Laboratoire central, Hôpital Al Farabi-Oujda, Rabat, Maroc.
Ann Biol Clin (Paris). 2013 Jan-Feb;71(1):107-12. doi: 10.1684/abc.2012.0782.
Recent classifications of non-Hodgkin's lymphomas based on combination of morphologic, immunophenotypic, and cytogenetic criteria have individualized mantle cell lymphoma (MCL). This clinico-biological entity which accounts for 3 to 10% of all non-Hodgkin's lymphomas, now appears to be a biological and therapeutic model for the understanding and treatment of hematologic malignancies. The present study consisting of two cases of MCL collated at laboratory of hematology of Rabat Ibn Sina hospital. The morphological appearance of MCL is characterized by diffuse or nodular lymph infiltration in the mantle zone, the osteo-medullary biopsy shows an interstitial infringement characterized by the presence of lymphocytes resembling centrocytes with cleaved and angular nuclei, dispersed chromatin, inconspicuous nucleoli and scanty cytoplasm. The flow cytometry showed immunophenotype positive for surface Ig, CD19, CD20, CD22, CD79b, CD5 and cyclin D1, and negative for CD10, CD23 and CD25. In conclusion, the methods of diagnosis and prognosis evaluation of mantle cell lymphoma are based on the nodular, medullary and blood morphology, the immunophenotypic, cytogenetic and molecular study of neoplastic cells.
近期基于形态学、免疫表型和细胞遗传学标准相结合的非霍奇金淋巴瘤分类已使套细胞淋巴瘤(MCL)个体化。这种临床生物学实体占所有非霍奇金淋巴瘤的3%至10%,现在似乎是理解和治疗血液系统恶性肿瘤的生物学和治疗模型。本研究由拉巴特伊本·西那医院血液学实验室整理的两例MCL病例组成。MCL的形态学表现特征为套区弥漫性或结节性淋巴细胞浸润,骨髓活检显示间质侵犯,其特征为存在类似中心细胞的淋巴细胞,核有切迹且呈角形,染色质分散,核仁不明显,细胞质稀少。流式细胞术显示免疫表型为表面Ig、CD19、CD20、CD22、CD79b、CD5和细胞周期蛋白D1阳性,CD10、CD23和CD25阴性。总之,套细胞淋巴瘤的诊断和预后评估方法基于结节、骨髓和血液形态学、肿瘤细胞的免疫表型、细胞遗传学和分子研究。