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血管内 NK/T 细胞淋巴瘤,EB 病毒阳性伴多器官累及:临床难题。

Intravascular NK/T-cell lymphoma, Epstein-Barr virus positive with multiorgan involvement: a clinical dilemma.

机构信息

Pathology Unit, Azienda Unità Sanitaria Locale/IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Department of Experimental Medicine, Medical School, Section of Pathological Anatomy and Histology, University of Perugia, Perugia, Italy.

出版信息

BMC Cancer. 2018 Nov 15;18(1):1115. doi: 10.1186/s12885-018-5001-6.

Abstract

BACKGROUND

Intravascular lymphoma is a rare type of non-Hodgkin lymphoma mostly of B-cell lineage. A few cases of intravascular lymphoma have been found to be of NK/T-cell origin, mainly affecting the skin and central nervous system.

CASE PRESENTATION

A 54-year-old Caucasian man sought care because of a 2 weeks history of jaundice and intermittent fever, not responsive to antibiotics and antipyretics. Laboratory tests showed low blood oxygen concentration and pancytopenia. Serum microbiological tests were negative. Computerized tomography (CT) scan revealed hepatosplenomegaly and diffuse ground-glass opacities in both lungs without interlobular septal thickening. Despite oxygen therapy, the clinical conditions rapidly deteriorated leading to death 3 days after admission. Autopsy revealed a multiorgan involvement by an Epstein-Barr virus positive NK/T-cell lymphoma, strikingly growing within the blood vessel lumina, in absence of skin lesions.

CONCLUSIONS

The current case highlights the pathological features of this rare entity, the protean clinical presentation of which is often misleading, resulting in delayed diagnosis and treatment.

摘要

背景

血管内淋巴瘤是一种罕见的非霍奇金淋巴瘤,主要来源于 B 细胞系。少数血管内淋巴瘤来源于 NK/T 细胞,主要影响皮肤和中枢神经系统。

病例介绍

一名 54 岁白人男性因黄疸和间歇性发热 2 周,抗生素和退热药物治疗无效而就诊。实验室检查显示低血氧浓度和全血细胞减少。血清微生物学检查为阴性。计算机断层扫描(CT)显示肝脾肿大,双肺弥漫性磨玻璃影,无小叶间隔增厚。尽管给予氧疗,临床状况迅速恶化,入院后 3 天死亡。尸检显示多器官受累,存在 EBV 阳性 NK/T 细胞淋巴瘤,在血管腔内明显生长,无皮肤病变。

结论

本病例强调了这种罕见实体的病理特征,其多变的临床表现常具有误导性,导致诊断和治疗延迟。

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