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鼻窦淋巴瘤:来自麻省总医院的58例临床病理分析

Sinonasal lymphoma: a clinicopathologic analysis of 58 cases from the Massachusetts General Hospital.

作者信息

Cuadra-Garcia I, Proulx G M, Wu C L, Wang C C, Pilch B Z, Harris N L, Ferry J A

机构信息

Departamento de Patologia, Hospital de Oncologia, Centro Medico Nacional Siglo XXI, Instituto Mexicano del Segura Social, Mexico City.

出版信息

Am J Surg Pathol. 1999 Nov;23(11):1356-69. doi: 10.1097/00000478-199911000-00006.

Abstract

Few large series compare lymphomas of the nasal cavity with those of the paranasal sinuses. We studied the cases of 58 patients, 34 males and 24 females, aged 7 to 92 years (mean, 57 years), who had lymphoma involving the nasal cavity or paranasal sinuses. Thirty-three patients had diffuse large B-cell lymphoma (DLBCL). Twenty-three were male and 10 were female, with an age range of 7 to 91 years (mean, 63 years); two were HIV-positive. Only 2 of 11 cases tested (one in an HIV-positive patient and one of lymphomatoid granulomatosis type) were Epstein-Barr virus (EBV)-positive. Thirty (91%) involved paranasal sinuses, 10 with nasal involvement, whereas three cases had nasal, but not sinus, involvement. At last follow-up, 16 (67%) were free of disease 7 to 169 months later (mean, 65 months), and 8 (33%) had died of disease 2 to 166 months later (mean, 45 months). Seventeen patients had nasal-type natural killer (NK)/T-cell lymphoma. There were 10 women and 7 men, aged 27 to 78 years (mean, 48 years). Thirteen of 14 were EBV-positive. Sixteen patients had nasal involvement, eight with sinus involvement. Eleven (73%) of 15 were alive and well 6 to 321 months later (mean, 139 months), three (20%) died of lymphoma 1, 11, and 12 months later, and one (7%) is alive with disease. There was one case each of marginal zone B-cell lymphoma, Burkitt's lymphoma, Burkitt-like lymphoma, peripheral T-cell lymphoma of unspecified type, and adult T-cell lymphoma/leukemia. In an additional three cases, the lymphomas were composed predominantly of large cells, but no immunophenotyping could be performed for subclassification. In 19 cases (17 DLBCLs, 1 Burkitt-like lymphoma, and 1 lymphoma of uncertain lineage), presenting symptoms included complaints related to the eyes. In 16 cases (13 DLBCLs, 1 Burkitt-like lymphoma, 1 nasal NK/T-cell lymphoma, and 1 lymphoma of uncertain lineage), the orbit was invaded by lymphoma. In our series, the most common lymphoma to arise in the sinonasal area is DLBCL, followed by nasal NK/T-cell lymphoma. Comparison of these two types of lymphoma showed that lymphomas involving sinuses without nasal involvement were predominantly DLBCLs (20 of 21), whereas nasal cavity lymphomas without sinus involvement were usually NK/T-cell type (8 of 11) (p = 0.000125). Compared with patients with DLBCL, patients with nasal NK/T-cell lymphoma were overall younger, with a lower male-to-female ratio. Lymphomas of B-cell lineage were more likely to be associated with symptoms related to the eyes (p < 0.0005) and to have extension to the orbit (p < 0.01) than were lymphomas of T- or NK-cell lineage. In contrast to results of Asian studies in which nasal NK/T-cell lymphoma has a very poor prognosis, our nasal NK/T-cell lymphomas had an outcome similar to that of DLBCL.

摘要

很少有大型系列研究比较鼻腔淋巴瘤和鼻窦淋巴瘤。我们研究了58例患者的病例,其中男性34例,女性24例,年龄7至92岁(平均57岁),这些患者患有累及鼻腔或鼻窦的淋巴瘤。33例患者患有弥漫性大B细胞淋巴瘤(DLBCL)。其中男性23例,女性10例,年龄范围7至91岁(平均63岁);2例为HIV阳性。在检测的11例病例中,仅2例(1例HIV阳性患者和1例淋巴瘤样肉芽肿型)为EB病毒(EBV)阳性。30例(91%)累及鼻窦,10例累及鼻腔,而3例仅累及鼻腔,未累及鼻窦。在最后一次随访时,16例(67%)在7至169个月后(平均65个月)无疾病,8例(33%)在2至166个月后(平均45个月)死于疾病。17例患者患有鼻型自然杀伤(NK)/T细胞淋巴瘤。其中女性10例,男性7例,年龄27至78岁(平均48岁)。14例中有13例为EBV阳性。16例累及鼻腔,8例累及鼻窦。15例中的11例(73%)在6至321个月后(平均139个月)存活且状况良好,3例(20%)在1、11和12个月后死于淋巴瘤,1例(7%)带瘤存活。有1例边缘区B细胞淋巴瘤、1例伯基特淋巴瘤、1例伯基特样淋巴瘤、1例未特定类型的外周T细胞淋巴瘤和1例成人T细胞淋巴瘤/白血病。另外3例中,淋巴瘤主要由大细胞组成,但无法进行免疫表型分析以进行亚分类。19例(17例DLBCL、1例伯基特样淋巴瘤和1例来源不确定的淋巴瘤)的主要症状包括与眼睛相关的主诉。16例(13例DLBCL、1例伯基特样淋巴瘤、1例鼻NK/T细胞淋巴瘤和1例来源不确定的淋巴瘤)眼眶被淋巴瘤侵犯。在我们的系列研究中,鼻窦区域最常见的淋巴瘤是DLBCL,其次是鼻NK/T细胞淋巴瘤。这两种淋巴瘤的比较显示,不累及鼻腔的鼻窦淋巴瘤主要是DLBCL(21例中的20例),而不累及鼻窦的鼻腔淋巴瘤通常是NK/T细胞型(11例中的8例)(p = 0.000125)。与DLBCL患者相比,鼻NK/T细胞淋巴瘤患者总体更年轻,男女比例更低。B细胞谱系淋巴瘤比T或NK细胞谱系淋巴瘤更可能与眼睛相关症状有关(p < 0.0005)且更易侵犯眼眶(p < 0.01)。与亚洲研究结果不同,亚洲研究中鼻NK/T细胞淋巴瘤预后很差,而我们研究中的鼻NK/T细胞淋巴瘤预后与DLBCL相似。

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