Conroy Peter B, Davel Sue, Malherbe Jacques A J, Carrivick Simon J, Briggs Edward N
Department of Intensive Care, Joondalup Health Campus, Joondalup, Western Australia, Australia.
Department of General Medicine, Joondalup Health Campus, Joondalup, Western Australia, Australia.
Am J Case Rep. 2025 Apr 26;26:e946969. doi: 10.12659/AJCR.946969.
BACKGROUND Acute porphyrias arise from genetic defects in heme synthesis. Significant increases in urine porphobilinogen (PBG) levels are diagnostic, enabling further testing and the commencement of targeted therapies. We report a rare case of an elderly woman with a delayed diagnosis of acute variegate porphyria (VP) neurovisceral crisis, anuria, and multiorgan failure precipitated by methicillin-sensitive Staphylococcus aureus (MSSA) sepsis. Diagnostic and therapeutic difficulties confirming an acute VP crisis in the anuric patient are explored. CASE REPORT A 77-year-old South African woman presented with undifferentiated MSSA sepsis. Despite escalation to intensive care and treatment of her infection, she developed encephalopathy, tetraparesis, autonomic dysfunction, and anuric renal failure, requiring renal replacement therapy. Given her anuric state, novel assays of the dialysate effluent were performed and revealed elevated PBG levels. Xanthochromic cerebrospinal fluid was also obtained. Taken together with confirmatory plasma porphyrin spectrography, an acute VP neurovisceral crisis with multiorgan failure was established. Intravenous heme-arginate combined with extracorporeal filtration via continuous renal replacement therapy and therapeutic plasma exchange were initiated. Inappropriate blood leak detector clamping occurred during extracorporeal filtration due to the presence of porphyrins in the effluent. Despite these aggressive measures, the patient died due to her illness. CONCLUSIONS Progressive neurological compromise, coupled with undifferentiated multiorgan failure, should prompt consideration of an underlying acute porphyric crisis. In anuric porphyria patients, PBG assays of extracorporeal circuit effluents may be of diagnostic value. Effluent PBGs can interfere with the extracorporeal circuit blood leak detector, thereby offering further clinical suspicion of an underlying acute porphyric crisis.
急性卟啉病源于血红素合成的基因缺陷。尿卟胆原(PBG)水平显著升高具有诊断意义,可据此进行进一步检查并启动靶向治疗。我们报告了一例罕见病例,一名老年女性因耐甲氧西林金黄色葡萄球菌(MSSA)败血症引发急性混合型卟啉病(VP)神经内脏危象、无尿和多器官功能衰竭,诊断延迟。探讨了在无尿患者中确诊急性VP危象的诊断和治疗困难。
一名77岁的南非女性因未分化的MSSA败血症就诊。尽管病情升级至重症监护并对其感染进行了治疗,但她仍出现了脑病、四肢轻瘫、自主神经功能障碍和无尿性肾衰竭,需要进行肾脏替代治疗。鉴于她的无尿状态,对透析液流出物进行了新型检测,结果显示PBG水平升高。还获取了黄变脑脊液。结合血浆卟啉光谱分析结果,确诊为伴有多器官功能衰竭的急性VP神经内脏危象。开始静脉注射血红素精氨酸,同时通过连续性肾脏替代疗法进行体外血液滤过以及治疗性血浆置换。由于流出物中存在卟啉,在体外血液滤过过程中发生了不当的血液泄漏探测器夹闭。尽管采取了这些积极措施,患者仍因病死亡。
进行性神经功能损害,再加上未分化的多器官功能衰竭,应促使考虑潜在的急性卟啉危象。对于无尿性卟啉病患者,体外循环流出物的PBG检测可能具有诊断价值。流出物中的PBG可能会干扰体外循环血液泄漏探测器,从而进一步提示存在潜在的急性卟啉危象。