Suppr超能文献

病例报告:一例 TAFRO 综合征伴严重和持久血小板减少:诊断陷阱。

Case Report: A case of TAFRO syndrome with severe and prolonged thrombocytopenia: diagnostic pitfalls.

机构信息

Division of Geriatric and Community Medicine, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.

Division of Nephrology and Endocrinology, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.

出版信息

Front Immunol. 2023 Oct 13;14:1266187. doi: 10.3389/fimmu.2023.1266187. eCollection 2023.

Abstract

Thrombocytopenia, anasarca, myelofibrosis, renal dysfunction, and organomegaly (TAFRO) syndrome is a rare condition with diverse clinical and pathological characteristics related to multi-organ damage. We report a case of TAFRO syndrome complicated by immune thrombocytopenia with prolonged fever and thrombocytopenia for several weeks. A 61-year-old man was transferred with sepsis caused by Enterococcus faecalis, and developed disseminated intravascular coagulation. Antibiotics treatment was initiated: however, low-grade fever and thrombocytopenia persisted despite the adequate antimicrobial treatment. Systemic edema, pleural effusion, and ascites had developed before hospitalization, and renal and liver function had deteriorated, resulting in progressive multi-organ damage. Prednisolone 40 mg/day was initiated based on the assumption of a condition in which excessive production of inflammatory cytokines would lead to systemic deterioration and fatal organ damage. Subsequently, the fever resolved, and renal function began to normalize. However, thrombocytopenia did not show much recovery trend after Helicobacter pylori eradication therapy and initiation of thrombopoietin receptor agonists. Bone marrow biopsy results showed normal bone marrow with no malignant findings. Alternatively, significant clinical signs met the diagnostic criteria for TAFRO syndrome, and a renal biopsy revealed thrombotic microangiopathy, which is also reasonable for renal involvement in TAFRO syndrome. The use of cyclosporine remarkably corrected the thrombocytopenia. We considered this a case of TAFRO syndrome that developed after sepsis with disseminated intravascular coagulation and performed the differential diagnosis of prolonged thrombocytopenia and excluded it. Although TAFRO syndrome is a unique disease concept, diagnostic criteria may consist of nonspecific elements such as generalized edema, thrombocytopenia, persistent fever, and elevated inflammatory response, and there are many differential conditions to exclude, requiring caution in diagnosing TAFRO syndrome.

摘要

血小板减少症、全身水肿、骨髓纤维化、肾功能不全和器官肿大(TAFRO)综合征是一种罕见的疾病,具有与多器官损伤相关的多样化临床和病理特征。我们报告了一例 TAFRO 综合征合并免疫性血小板减少症的病例,该患者发热和血小板减少持续数周。一名 61 岁男性因粪肠球菌引起的败血症转入我院,并发弥漫性血管内凝血。给予抗生素治疗;然而,尽管抗菌治疗充分,仍持续低热和血小板减少。在住院前已出现全身水肿、胸腔积液和腹水,且肾功能和肝功能恶化,导致进行性多器官损伤。考虑到大量炎症细胞因子的产生会导致全身恶化和致命的器官损伤,给予患者泼尼松龙 40mg/天。随后,发热消退,肾功能开始恢复正常。然而,在根除幽门螺杆菌和开始使用血小板生成素受体激动剂后,血小板减少并未显示出明显的恢复趋势。骨髓活检结果显示骨髓正常,无恶性发现。此外,显著的临床症状符合 TAFRO 综合征的诊断标准,肾脏活检显示血栓性微血管病,这也符合 TAFRO 综合征的肾脏受累。环孢素的使用显著纠正了血小板减少症。我们认为这是一例在弥散性血管内凝血败血症后发生的 TAFRO 综合征,并对持续血小板减少症进行了鉴别诊断,排除了其他疾病。虽然 TAFRO 综合征是一种独特的疾病概念,但诊断标准可能包括全身性水肿、血小板减少症、持续发热和炎症反应升高等非特异性因素,需要排除许多鉴别条件,因此在诊断 TAFRO 综合征时需谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b4e/10611515/bb8844f73117/fimmu-14-1266187-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验