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外周T细胞淋巴瘤的骨髓组织学和免疫组化研究:38例病例分析

Bone marrow histologic and immunohistochemical findings in peripheral. T-cell lymphoma: A study of 38 cases.

作者信息

Gaulard P, Kanavaros P, Farcet J P, Rocha F D, Haioun C, Divine M, Reyes F, Zafrani E S

机构信息

Département de Pathologie Tissulaire et Cellulaire, Hôpital Henri Mondor, Créteil, France.

出版信息

Hum Pathol. 1991 Apr;22(4):331-8. doi: 10.1016/0046-8177(91)90081-y.

DOI:10.1016/0046-8177(91)90081-y
PMID:2050367
Abstract

The histologic and immunohistochemical findings in bone marrow (BM) biopsies from 38 patients with peripheral T-cell lymphoma (PTCL) are reported. Routine light microscopy showed that BM involvement was unequivocal in 12 cases and questionable in 14 cases. There was no histologic evidence of lymphoma in the remaining 12 cases. Immunohistochemistry performed on BM frozen sections demonstrated the T-cell origin of the infiltrating lymphoid cells in 24 of the 26 patients with unequivocal or questionable involvement. The malignant nature of these cells was suggested by demonstration of an aberrant T-cell phenotype identical to that observed in the other sites of involvement. In addition, in four of the 12 cases with apparently normal BM at routine light microscopy, immunohistochemistry revealed a minimal but phenotypically abnormal T-cell population, suggesting mild infiltration by lymphoma. These combined histologic and immunohistochemical data documented a high incidence (73%) of BM involvement by PTCL. In addition, a very peculiar sinusal pattern of BM involvement was found in five patients who presented an unusual type of hepatosplenic T-cell lymphoma expressing the gamma delta T-cell receptor. The present study demonstrates the high incidence of BM involvement by PTCL and emphasizes the value of frozen section immunohistochemistry to establish this diagnosis, especially when routine light microscopy findings are questionable.

摘要

报告了38例外周T细胞淋巴瘤(PTCL)患者骨髓活检的组织学和免疫组化结果。常规光学显微镜检查显示,12例骨髓受累明确,14例可疑。其余12例无淋巴瘤组织学证据。对骨髓冰冻切片进行的免疫组化显示,在26例受累明确或可疑的患者中,有24例浸润性淋巴细胞起源于T细胞。这些细胞的恶性性质通过显示与在其他受累部位观察到的相同的异常T细胞表型得以提示。此外,在12例常规光学显微镜下骨髓明显正常的病例中,有4例免疫组化显示存在少量但表型异常的T细胞群体,提示有淋巴瘤轻度浸润。这些组织学和免疫组化数据综合表明,PTCL骨髓受累的发生率很高(73%)。此外,在5例表现为表达γδ T细胞受体的不寻常类型肝脾T细胞淋巴瘤的患者中,发现了一种非常特殊的骨髓受累窦状模式。本研究证明了PTCL骨髓受累的高发生率,并强调了冰冻切片免疫组化在确立该诊断中的价值,尤其是当常规光学显微镜检查结果可疑时。

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