Mantle cell lymphoma, blastoid (centroblastic) variantが疑われた一例

石井 源一郎, 眞 柏村, 淳男 三方
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Abstract

A 64-year-old man with chronic hepatitis (type C) presented with left abdominal to back pain and cervical lymph nodes swelling in Nov. 1995. Biopsy specimen from cervical lymph nodes was diagnosed as malignant lymphoma. Physical examination revealed systemic lymph nodes swelling, splenomegaly and bone marrow involvement. He received two courses of CHOP and MEVP therapy without much effect and died after five months later. Tissue specimen showed diffuse atypical lymphocytes infiltration and no residual atrophic germinal centers are found. Most of the tumor cells showed medium to large sized and round (without cleaving) nuclei and a predominant nucleolus. Starry sky appearance and frequent mitoses are observed, suggesting rapidly proliferating nature.Immunohistchemical study on paraffin section and flow cytometrical analysis demonstrated that CD5, CD20, CD21, sIgM and sIgD were positive on neoplastic cells but CD3 and CD10 were negative. These morphological and immunohistchemical findings lead us to diagnose this lymphoma as blastoid (centroblastic) variant of mantle cell lymphoma.
Mantle cell lymphoma, blastoid (centroblastic) variant被怀疑的一个例子
一名64岁男性慢性丙型肝炎患者于1995年11月出现左腹部至背部疼痛和颈部淋巴结肿胀。颈部淋巴结活检诊断为恶性淋巴瘤。体格检查发现全身淋巴结肿大、脾肿大及骨髓受累。患者接受CHOP和MEVP两疗程治疗,效果不明显,5个月后死亡。组织标本显示弥漫性非典型淋巴细胞浸润,未见萎缩性生发中心残留。大多数肿瘤细胞显示中至大、圆(无裂)核,以核仁为主。观察到星空的出现和频繁的有丝分裂,表明自然界正在迅速增殖。免疫组织化学石蜡切片和流式细胞术分析显示,肿瘤细胞CD5、CD20、CD21、sIgM和sIgD阳性,CD3和CD10阴性。这些形态学和免疫组织化学的发现使我们诊断该淋巴瘤为胚状细胞(中母细胞)变异体套细胞淋巴瘤。
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