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人类嗜 T 细胞病毒 1 型相关性淋巴瘤表现为巨大淋巴结病。

HTLV-1-Associated Lymphoma Presented as Massive Lymphadenopathy.

机构信息

Brookdale University Hospital Medical Center, Brooklyn, NY, USA.

出版信息

J Investig Med High Impact Case Rep. 2021 Jan-Dec;9:23247096211013235. doi: 10.1177/23247096211013235.

Abstract

Adult T-cell leukemia/lymphoma is an aggressive T-cell malignancy caused by the long-term infection of human T-cell lymphotropic virus type 1 (HTLV-1). Our understanding of clinical features still largely relies on the Shimoyama classification developed 30 years ago, which described the 4 clinical subtypes (the smoldering, chronic, lymphoma, and acute types) based on the manifestations of lymphocytosis, elevated lactate dehydrogenase, hypercalcemia, lymphadenopathy, and involvement of the skin, lung, liver, spleen, central nervous system, bone, ascites, pleural effusion, and gastrointestinal tract. HTLV-1-associated lymphoma has a variety of presentations but the presentation of massive lymphadenopathy and compression symptoms is rare and has not been emphasized in the literature. In this article, we describe 2 cases of adult T-cell leukemia/lymphomas that presented with massive cervical nodes or mediastinal nodes with compressing symptoms as the major presenting clinical features. Clinicians should remain aware of this type of presentation by HTLV-1-associated lymphoma, especially in patients who came from endemic areas, even if not all clinical features are present and particularly with hypercalcemia and lytic bone lesions.

摘要

成人 T 细胞白血病/淋巴瘤是一种由人类 T 细胞嗜淋巴细胞病毒 1(HTLV-1)长期感染引起的侵袭性 T 细胞恶性肿瘤。我们对临床特征的理解在很大程度上仍然依赖于 30 年前开发的 Shimoyama 分类,该分类根据淋巴细胞增多、乳酸脱氢酶升高、高钙血症、淋巴结病以及皮肤、肺、肝、脾、中枢神经系统、骨骼、腹水、胸腔积液和胃肠道受累的表现,描述了 4 种临床亚型(惰性、慢性、淋巴瘤和急性)。HTLV-1 相关淋巴瘤有多种表现,但大量淋巴结病和压迫症状的表现较为罕见,在文献中并未得到强调。本文描述了 2 例以大量颈淋巴结或纵隔淋巴结肿大伴有压迫症状为主要表现的成人 T 细胞白血病/淋巴瘤病例。临床医生应注意到这种 HTLV-1 相关淋巴瘤的表现类型,特别是对于来自流行地区的患者,即使并非所有临床特征都存在,特别是伴有高钙血症和溶骨性骨病变时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51af/8114285/65c1513a9c4e/10.1177_23247096211013235-fig1.jpg

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