原发性脾淋巴瘤。

Cancer surveys Pub Date : 1997-01-01
P G Isaacson
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引用次数: 0

摘要

虽然许多淋巴瘤和白血病可累及脾脏,临床上可能表现为脾肿大,但只有B细胞疾病SMZL和肝脾γ / δ T细胞淋巴瘤可被认为是真正的原发性脾淋巴瘤。前者并不罕见,其组织学特征在累及脾脏时可在一定程度上再现于其他B细胞淋巴瘤。鉴于SMZL在临床上表现为惰性,且其对脾切除术而非化疗的反应良好,因此与其他B细胞淋巴瘤的鉴别诊断很重要。肝脾γ / δ T细胞淋巴瘤是罕见的;为了准确分类,需要将其与其他NK如T细胞淋巴瘤和有时累及脾脏的NK细胞淋巴瘤区分开来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary splenic lymphoma.

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.

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