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伴有纵隔受累及无症状慢性期的成人T细胞白血病-淋巴瘤

Adult T-cell leukemia-lymphoma with mediastinal involvement and an asymptomatic chronic phase.

作者信息

Amato D, Fernandes B J, Klein M

出版信息

Can Med Assoc J. 1984 Sep 15;131(6):595-600.

Abstract

A black, West Indian woman with adult T-cell leukemia-lymphoma (ATLL), hypercalcemia, peripheral and retroperitoneal lymphadenopathy, and serum antibodies to human T-lymphotropic virus (HTLV) was found to have massive mediastinal adenopathy, a feature not previously reported in patients with ATLL. In addition, she had had asymptomatic leukocytosis with marked lymphocytosis for at least 6 years before presenting with full-blown ATLL. These findings broaden the clinical picture of ATLL. Cell surface-marker studies and close follow-up are recommended for patients with apparent chronic lymphocytic leukemia, especially if they have pleomorphic lymphocytosis, are younger than usual or are from the Caribbean or Japan.

摘要

一名患有成人T细胞白血病淋巴瘤(ATLL)、高钙血症、外周和腹膜后淋巴结病且血清中有人T细胞嗜淋巴细胞病毒(HTLV)抗体的西印度黑人女性,被发现有巨大纵隔淋巴结病,这是ATLL患者此前未曾报道过的特征。此外,在出现典型的ATLL之前,她至少有6年的无症状白细胞增多伴明显淋巴细胞增多。这些发现拓宽了ATLL的临床症状。对于明显患有慢性淋巴细胞白血病的患者,尤其是那些有多形性淋巴细胞增多、年龄比一般患者小或者来自加勒比地区或日本的患者,建议进行细胞表面标志物研究并密切随访。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b50/1483631/4cf418c98711/canmedaj00368-0066-a.jpg

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