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一项关于鼻腔、鼻窦及硬腭恶性淋巴瘤的临床病理研究,包括致死性中线肉芽肿病例。

A clinicopathologic study of malignant lymphomas of the nose, paranasal sinuses, and hard palate, including cases of lethal midline granuloma.

作者信息

Ratech H, Burke J S, Blayney D W, Sheibani K, Rappaport H

机构信息

James Irvine Center for the Study of Leukemia and Lymphoma, Division of Pathology, Duarte, California.

出版信息

Cancer. 1989 Dec 15;64(12):2525-31. doi: 10.1002/1097-0142(19891215)64:12<2525::aid-cncr2820641220>3.0.co;2-3.

Abstract

Malignant lymphomas of the nose, paranasal sinuses, and hard palate show marked clinicopathologic, immunologic, and prognostic diversity. The clinical features and pathologic spectrum of these lesions were studied in 20 cases (11 female and 9 male cases) with a mean age of 51 years at initial presentation. Malignant lymphomas of the large cell type were most frequently encountered (11/20). The next largest category was malignant lymphoma, diffuse, mixed small and large cell type (six of 20). Two thirds, 13 of 20 cases, had morphologic features suggestive of peripheral T-cell lymphomas. Necrosis, an angiocentric growth pattern, and epitheliotropism were found in nine, eight, and three cases, respectively. Of ten cases immunophenotyped on fresh-frozen or fixed, paraffin-embedded tissue sections, eight had a T-cell phenotype and two had a B-cell phenotype. Of 17 patients with sufficient follow-up data, ten are alive (median follow-up 33 months) and seven are dead (median survival 12 months). Patients with clinical Stages IE and IIE did not have a superior 5-year survival to those with more advanced disease. Histologic type also did not correlate with survival but this may be due to the aggressive histologic grade of the majority of cases and the retrospective nature of this study. The authors conclude that, despite the overall high-grade histologic type, the pathologic spectrum of malignant lymphomas involving this anatomic region is broad. Furthermore, some cases do not fit well into the National Cancer Institute (NCI) Working Formulation but more closely resemble the histologic features of peripheral T-cell lymphomas described in Japan.

摘要

鼻腔、鼻窦和硬腭的恶性淋巴瘤在临床病理、免疫及预后方面存在显著差异。对20例患者(11例女性,9例男性)进行了研究,这些患者初次就诊时的平均年龄为51岁,分析了这些病变的临床特征和病理谱。大细胞型恶性淋巴瘤最为常见(11/20)。其次是弥漫性混合小细胞和大细胞型恶性淋巴瘤(20例中的6例)。20例中有13例(三分之二)具有提示外周T细胞淋巴瘤的形态学特征。分别在9例、8例和3例中发现坏死、血管中心性生长模式和嗜上皮性。在对新鲜冷冻或固定石蜡包埋组织切片进行免疫表型分析的10例病例中,8例具有T细胞表型,2例具有B细胞表型。在17例有足够随访数据的患者中,10例存活(中位随访33个月),7例死亡(中位生存期12个月)。临床I E期和II E期患者的5年生存率并不优于病情更严重的患者。组织学类型也与生存率无关,但这可能是由于大多数病例的组织学分级侵袭性强以及本研究的回顾性性质所致。作者得出结论,尽管总体组织学类型为高级别,但累及该解剖区域的恶性淋巴瘤的病理谱很广。此外,一些病例不太符合美国国立癌症研究所(NCI)工作分类,但更类似于日本描述的外周T细胞淋巴瘤的组织学特征。

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