García-Fraile Lucio J, García-Buey Luisa, Alonso Cerezo Concepción, Sanz Sanz Jesús, de Los Santos Gil Ignacio
Service of Infectious Diseases and Internal Medicine, Hospital Universitario de la Princesa, IIP, Universidad Autónoma de Madrid, Madrid, Spain.
Gastroenterology and Hepatology Service, Hospital Universitario de la Princesa, IIP, Universidad Autónoma de Madrid, Spain.
Gastroenterol Hepatol. 2022 Apr;45(4):249-255. doi: 10.1016/j.gastrohep.2021.09.001. Epub 2021 Sep 22.
Porphyria cutanea tarda (PCT) is common and usually associated with HCV chronic infection and HFE polymorphisms. Since DAA IFN-free regimens availability, SVR for HCV is nearly a constant and we wonder whether HCV SVR determine PCT evolution.
Retrospective observational study including patients with HCV associated PCT from the Gastroenterology and Infectious Diseases Departments at our Hospital, treated with DAA (Apr/2015-Apr/2017). Clinical variables of PCT were collected at PCT diagnosis, after PCT treatment, before DAA use and after SVR achievement. UROD activity and C282Y/H63D polymorphisms were registered. SPSS 22.0.
13 HCV-PCT patients included: median age 52.5 years; 4 females; 8 HCV/HIV co-infected (all on undetectable viral load). Classical PCT factors: 12 smoked, 9 alcohol abuse, 6 former IDU. 10 type I PCT and 1 type II PCT. HFE polymorphism: 2 cases with C282Y/H63D; H63D polymorphism in 8. PCT manifestations resolved with PCT treatment in 4 patients, almost completely in 7 patients, 1 patient referred stabilization and one worsened. After DAA treatment all the residual lesions resolved, what always led to specific treatment interruption.
Our series of cases of HCV-associated PCT shows that SVR after DAA treatment leads to PCT resolution. Porphyrin levels are not needed after ending PCT specific treatment interruption when there are no residual skin lesions in HCV-associated PCT.
迟发性皮肤卟啉病(PCT)较为常见,通常与丙型肝炎病毒(HCV)慢性感染及HFE基因多态性相关。自从无干扰素直接抗病毒药物(DAA)方案问世以来,HCV的持续病毒学应答(SVR)几乎是一个常量,我们想知道HCV的SVR是否会决定PCT的病情发展。
回顾性观察研究,纳入我院胃肠病科和传染病科接受DAA治疗(2015年4月至2017年4月)的HCV相关PCT患者。在PCT诊断时、PCT治疗后、使用DAA前及实现SVR后收集PCT的临床变量。记录尿卟啉原脱羧酶(UROD)活性及C282Y/H63D基因多态性。使用SPSS 22.0软件。
纳入13例HCV-PCT患者:中位年龄52.5岁;4例女性;其中8例HCV/HIV合并感染(所有患者病毒载量均不可检测)。典型的PCT相关因素:1例吸烟,9例酗酒,6例有静脉注射毒品史。10例为I型PCT,1例为II型PCT。HFE基因多态性:2例存在C282Y/H63D;8例存在H63D基因多态性。4例患者的PCT表现经PCT治疗后得到缓解,7例患者几乎完全缓解,1例患者病情稳定,1例患者病情恶化。DAA治疗后所有残留病变均消失,这总是导致特定治疗中断。
我们的HCV相关PCT病例系列表明,DAA治疗后的SVR可使PCT得到缓解。在HCV相关PCT中,若不存在残留皮肤病变,在结束PCT特异性治疗中断后无需检测卟啉水平。