Cadet Bair, Leonard Kathryn, Singh Jaswinder P, Alam Ishmam
Department of Internal Medicine, Nassau University Medical Center, East Meadow, USA.
Department of Internal Medicine, American University of the Caribbean, Cupecoy, SXM.
Cureus. 2023 Aug 18;15(8):e43705. doi: 10.7759/cureus.43705. eCollection 2023 Aug.
Primary membranous glomerulopathy is the most common cause of idiopathic nephrotic syndrome, with increasing recognition as an autoimmune-mediated disease. We present the case of a 31-year-old Hispanic male with no prior medical or family history, presenting with one month of dyspnea on exertion, lower extremity, and periorbital edema with a recent diagnosis of pulmonary embolism. Upon further imaging, renal vein thrombosis was discovered with significant lab dysfunction concerning nephrotic syndrome. Further, a workup of kidney biopsy and serum antibody levels revealed the cause to be anti-phospholipase A2 receptor (PLA2R)-mediated.
原发性膜性肾小球病是特发性肾病综合征最常见的病因,越来越被认为是一种自身免疫介导的疾病。我们报告一例31岁的西班牙裔男性病例,该患者既往无病史及家族史,因劳力性呼吸困难、下肢及眶周水肿1个月就诊,近期诊断为肺栓塞。进一步影像学检查发现肾静脉血栓形成,伴有与肾病综合征相关的明显实验室功能障碍。此外,肾脏活检和血清抗体水平检查显示病因是抗磷脂酶A2受体(PLA2R)介导的。