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外周T细胞淋巴瘤:9例临床病理研究

Peripheral T-cell lymphoma: a clinicopathologic study of nine cases.

作者信息

Brisbane J U, Berman L D, Neiman R S

出版信息

Am J Clin Pathol. 1983 Mar;79(3):285-93. doi: 10.1093/ajcp/79.3.285.

Abstract

The clinicopathologic features of nine cases of peripheral T-cell lymphoma were analyzed. Although the youngest patient was 18 years old, the median age was 59.8 years. They usually presented with widespread disease and had an aggressive course. Seven have died with a median survival of 10.9 months. Five cases were of mixed cell type, sharing certain histopathologic features that we believe are characteristic of peripheral T-cell lymphomas. Three cases were of large cell type; one was a small cell (PDL) type. This latter patient lived symptom-free without treatment for over 3 years, despite stage III disease. Another patient, whose tumor had nodular sclerosis-like fibrosis, is in complete remission two years after chemotherapy for stage III B disease. Because peripheral T-cell lymphoma is morphologically heterogeneous, it may be clinically heterogeneous as well. We believe that classification according to a modified Rappaport system may clarify possible variations in biologic behavior.

摘要

分析了9例外周T细胞淋巴瘤的临床病理特征。虽然最年轻的患者为18岁,但中位年龄为59.8岁。他们通常表现为疾病广泛播散且病程侵袭性强。7例患者已死亡,中位生存期为10.9个月。5例为混合细胞型,具有某些我们认为是外周T细胞淋巴瘤特征性的组织病理学特征。3例为大细胞型;1例为小细胞(PDL)型。尽管处于Ⅲ期疾病,但后一例患者未经治疗无症状生存超过3年。另一例肿瘤有结节硬化样纤维化的患者,在接受ⅢB期疾病化疗两年后完全缓解。由于外周T细胞淋巴瘤在形态学上具有异质性,其在临床上可能也具有异质性。我们认为根据改良的Rappaport系统进行分类可能会阐明生物学行为的可能差异。

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