Suppr超能文献

T细胞大颗粒淋巴细胞白血病的不寻常表现

Unusual Presentation of T-cell Large Granular Lymphocytic Leukemia.

作者信息

Abu Rous Fawzi, Gutta Radhika, Chacko Rebecca, Kuriakose Philip, Dabak Vrushali

机构信息

Hematology and Oncology, Henry Ford Health System, Detroit, USA.

Internal Medicine, Henry Ford Health System, Detroit, USA.

出版信息

Cureus. 2022 Jul 11;14(7):e26742. doi: 10.7759/cureus.26742. eCollection 2022 Jul.

Abstract

Large granular lymphocytic (LGL) leukemia is a rare chronic lymphoproliferative disorder that can arise from T- or natural killer-cell lineages. It is an indolent disease that typically occurs in the sixth decade of life. Most cases of T-cell LGL leukemia (T-LGL) are associated with autoimmune disorders. Patients with T-LGL are generally asymptomatic; however, they can present with symptoms related to neutropenia, infections, and autoimmune disorders. Here, we report two cases of T-LGL in which the patients presented with liver dysfunction.

摘要

大颗粒淋巴细胞(LGL)白血病是一种罕见的慢性淋巴细胞增殖性疾病,可起源于T细胞或自然杀伤细胞谱系。它是一种惰性疾病,通常发生在人生的第六个十年。大多数T细胞LGL白血病(T-LGL)病例与自身免疫性疾病有关。T-LGL患者通常无症状;然而,他们可能会出现与中性粒细胞减少、感染和自身免疫性疾病相关的症状。在此,我们报告两例T-LGL患者出现肝功能障碍的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37a4/9364958/5c4fec8276f9/cureus-0014-00000026742-i01.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验