Petrides Petro E, Andrassy Joachim, Guba Markus, Stangl Manfred, Bronisch Olivia, Beykirch Maria K
IPNET Center Munich, Hematology Oncology Center, Munich, Germany.
LMU University of Munich Medical School, Munich, Germany.
Case Rep Transplant. 2025 Jun 19;2025:5522456. doi: 10.1155/crit/5522456. eCollection 2025.
Acute intermittent porphyria is a rare inborn disease of porphyrin metabolism which can cause severe abdominal pain attacks and neurological symptoms. Here, we report a patient with a 20-year history of severe chronic manifestations of acute intermittent porphyria that led to end-stage renal disease and liver function impairment. Since only transplants can cure both disease manifestations, a combined liver and renal transplantation was performed. The patient recovered so well that she delivered a very low birth extreme premature baby 16 months later which developed normally over the next 5 years. Our case represents the third case in the literature with a successful combined liver/renal transplantation of a patient with acute porphyria. Thus, transplantation seems to be a viable backup option, should novel therapies such as siRNA treatment with givosiran fail.
急性间歇性卟啉病是一种罕见的卟啉代谢先天性疾病,可引发严重的腹痛发作和神经症状。在此,我们报告一名患有急性间歇性卟啉病严重慢性表现长达20年的患者,该疾病导致了终末期肾病和肝功能损害。由于只有移植才能治愈这两种疾病表现,因此进行了肝肾联合移植。患者恢复良好,16个月后产下一名极低出生体重的极早产儿,该婴儿在接下来的5年中发育正常。我们的病例是文献中第三例急性卟啉病患者成功进行肝肾联合移植的病例。因此,如果诸如用吉沃赛安进行小干扰RNA治疗等新疗法失败,移植似乎是一种可行的备用选择。