Johnson-Arbor Kelly, Taha Sammy
Department of Plastic and Reconstructive Surgery, MedStar Georgetown University Hospital, 3800 Reservoir Road, NW, Washington, DC, 20007, USA.
The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
J Med Toxicol. 2025 Jul;21(3):355-359. doi: 10.1007/s13181-025-01081-w. Epub 2025 Jun 5.
Subcutaneous elemental mercury injection is typically not associated with systemic toxicity. This case report describes a man who developed persistent membranous nephropathy temporally associated with intentional subcutaneous elemental mercury injection.
A 21-year-old man injected elemental mercury into his left forearm after experiencing worsening depression during the COVID-19 pandemic. Several months later, he sought dermatology evaluation due to nodularity at the injection site. He underwent attempted excision of what was presumed to be a left forearm lipoma, but he did not report the history of mercury injection. He subsequently developed proteinuria and was diagnosed with membranous nephropathy. Treatment with rituximab did not improve his condition, and he eventually divulged the history of mercury injection three years after the initial exposure. He underwent surgical excision of the mercury deposits, left forearm flap reconstruction, and chelation with oral succimer. Despite these interventions, his proteinuria and urine protein to creatinine ratio remained persistently elevated, consistent with ongoing membranous nephropathy.
Renal pathology is associated with mercury toxicity after dermal or inhalational exposure but is rarely reported to occur after subcutaneous injection of elemental mercury. The pathophysiology of mercury-induced membranous nephropathy may involve formation of autoantibodies and cytokines after direct renal tubular injury. Surgical excision is the primary treatment for subcutaneous mercury exposure. Chelation may be considered for patients with evidence of systemic toxicity or ongoing mercury exposure, although the optimal timing of perioperative chelation has not been defined.
Significant systemic toxicity, including membranous nephropathy, may occur after subcutaneous mercury injection.
皮下注射单质汞通常不会引起全身毒性。本病例报告描述了一名男子,他在新冠疫情期间因抑郁症加重而故意皮下注射单质汞后,出现了持续性膜性肾病。
一名21岁男子在新冠疫情期间抑郁症加重后,将单质汞注射到左前臂。几个月后,他因注射部位出现结节而寻求皮肤科评估。他接受了左前臂脂肪瘤切除术,但未提及汞注射史。随后他出现蛋白尿,被诊断为膜性肾病。使用利妥昔单抗治疗未能改善其病情,最终在初次接触汞三年后,他透露了汞注射史。他接受了汞沉积物的手术切除、左前臂皮瓣重建,并口服二巯基丁二酸进行螯合治疗。尽管采取了这些干预措施,他的蛋白尿和尿蛋白肌酐比值仍持续升高,符合持续性膜性肾病的表现。
皮肤或吸入性接触汞后会出现肾脏病理改变与汞毒性相关,但皮下注射单质汞后很少有相关报道。汞诱导的膜性肾病的病理生理学可能涉及肾小管直接损伤后自身抗体和细胞因子的形成。手术切除是皮下汞接触的主要治疗方法。对于有全身毒性证据或持续汞接触的患者,可以考虑螯合治疗,尽管围手术期螯合的最佳时机尚未确定。
皮下注射汞后可能会出现包括膜性肾病在内的严重全身毒性。