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原发性脾淋巴瘤

Primary splenic lymphoma.

作者信息

Isaacson P G

机构信息

Department of Histopathology, University College London Medical School.

出版信息

Cancer Surv. 1997;30:193-212.

PMID:9547993
Abstract

Although a number of lymphomas and leukaemias can involve the spleen and may present clinically with splenomegaly, only the B cell disorders SMZL and hepatosplenic gamma/delta T cell lymphoma can be considered true primary splenic lymphomas. The former is not uncommon and has histological features which may be to a certain extent recapitulated by other B cell lymphomas when they involve the spleen. In view of the characteristic clinically indolent behaviour of SMZL and its favourable response to splenectomy, rather than chemotherapy, the differential diagnosis from other B cell lymphomas is important. Hepatosplenic gamma/delta T cell lymphoma is rare; for the purpose of precise classification, it needs to be distinguished from other NK like T cell lymphomas and NK cells lymphomas that sometimes involve the spleen.

摘要

尽管许多淋巴瘤和白血病可累及脾脏,并可能在临床上表现为脾肿大,但只有B细胞疾病脾边缘区淋巴瘤(SMZL)和肝脾γ/δT细胞淋巴瘤可被视为真正的原发性脾脏淋巴瘤。前者并不罕见,具有组织学特征,当其他B细胞淋巴瘤累及脾脏时,在一定程度上可能会重现这些特征。鉴于SMZL具有临床上惰性的特征以及对脾切除术而非化疗的良好反应,与其他B细胞淋巴瘤进行鉴别诊断很重要。肝脾γ/δT细胞淋巴瘤很罕见;为了进行精确分类,需要将其与其他有时累及脾脏的NK样T细胞淋巴瘤和NK细胞淋巴瘤区分开来。

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