Curras-Martin Diana, Patel Swapnil, Qaisar Huzaif, Mehandru Sushil K, Masud Avais, Hossain Mohammad A, Lamba Gurpreet S, Dounis Harry, Levitt Michael, Asif Arif
Department of Medicine, Internal Medicine Residency Program, Jersey Shore University Medical Center, Hackensack Meridian Health, Neptune, NJ, 07753, USA.
J Med Case Rep. 2019 Sep 5;13(1):281. doi: 10.1186/s13256-019-2187-4.
Renal involvement in idiopathic hypereosinophilic syndrome is uncommon. The mechanism of kidney damage can be explained as occurring via two distinct pathways: (1) thromboembolic ischemic changes secondary to endocardial disruption mediated by eosinophilic cytotoxicity to the myocardium and (2) direct eosinophilic cytotoxic effect to the kidney.
We present a case of a 63-year-old Caucasian man who presented to our hospital with 2 weeks of progressively generalized weakness. He was diagnosed with idiopathic hypereosinophilic syndrome with multiorgan involvement and acute kidney injury with biopsy-proven thrombotic microangiopathy. Full remission was achieved after 8 weeks of corticosteroid therapy.
Further studies are needed to investigate if age and absence of frank thrombocytopenia can serve as a prognostic feature of idiopathic hypereosinophilic syndrome, as seen in this case.
特发性高嗜酸性粒细胞综合征累及肾脏的情况并不常见。肾脏损伤的机制可通过两种不同途径来解释:(1)嗜酸性粒细胞对心肌的细胞毒性介导的心内膜破坏继发的血栓栓塞性缺血改变,以及(2)嗜酸性粒细胞对肾脏的直接细胞毒性作用。
我们报告一例63岁的白种男性患者,因进行性全身乏力2周前来我院就诊。他被诊断为特发性高嗜酸性粒细胞综合征,伴有多器官受累及急性肾损伤,活检证实为血栓性微血管病。皮质类固醇治疗8周后实现完全缓解。
如本病例所示,是否年龄及无明显血小板减少可作为特发性高嗜酸性粒细胞综合征的预后特征,仍需进一步研究。