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鼻腔、鼻窦和鼻咽部非上皮性肿瘤:临床病理研究。X. 恶性淋巴瘤

Nonepithelial tumors of the nasal cavity, paranasal sinuses and nasopharynx: a clinicopathologic study. X. Malignant lymphomas.

作者信息

Fu Y S, Perzin K H

出版信息

Cancer. 1979 Feb;43(2):611-21. doi: 10.1002/1097-0142(197902)43:2<611::aid-cncr2820430231>3.0.co;2-x.

Abstract

In our series of 256 nonepithelial tumors involving the nasal cavity, paranasal sinuses and nasopharynx, 21 were apparently primary malignant lymphomas, including 17 ordinary lymphomas and 4 cases of "midline malignant reticulosis." Of the 15 patients who had ordinary lymphomas and had adequate follow-up, 8 died of lymphoma, 4 were living with disseminated disease, 1 died of other causes with persistent lymphoma and only 2 (13%) had no evidence of recurrence at 8 and 9 years after diagnosis. The tumor was controlled in its primary site by radiotherapy in 13 of 14 patients; however, all but 2 of these patients eventually developed disseminated disease. Of the 3 patients who had midline malignant reticulosis (MMR) and had adequate follow-up, all died of disease. MMR represents an unusual variant of malignant lymphoma and often produces the clinical picture of lethal midline granuloma.

摘要

在我们收治的256例累及鼻腔、鼻窦和鼻咽部的非上皮性肿瘤系列病例中,有21例显然是原发性恶性淋巴瘤,其中包括17例普通淋巴瘤和4例“中线恶性网状细胞增多症”。在15例患有普通淋巴瘤且有充分随访资料的患者中,8例死于淋巴瘤,4例有播散性疾病存活,1例因其他原因死亡但淋巴瘤持续存在,只有2例(13%)在诊断后8年和9年无复发迹象。14例患者中有13例通过放疗使肿瘤在原发部位得到控制;然而,除2例患者外,所有这些患者最终都出现了播散性疾病。在3例患有中线恶性网状细胞增多症(MMR)且有充分随访资料的患者中,全部死于该病。MMR是恶性淋巴瘤的一种不寻常变异型,常表现为致死性中线肉芽肿的临床症状。

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