Lahbabi Mounia, Ghissassi Meryem, Belahcen Faouzi, Ibrahimi Sidi Adil, Aqodad Nouredine
Gastroenterology Unit, Hospital University Hassan II, Fez, Morocco.
J Med Case Rep. 2012 Sep 4;6:278. doi: 10.1186/1752-1947-6-278.
The combination of polyethylene glycol (PEG)ylated interferon (pegylated interferon) and ribavirin has been shown to be an effective treatment for chronic hepatitis C virus. In general, common side effects related to this combination therapy are mild and are well tolerated. However, peripheral neuropathy including demyelinating polyneuropathy related to PEG-interferon α2a (pegylated interferon alfa-2a) is extremely rare. In the literature, only one case of acute inflammatory demyelinating polyneuropathy related to PEG-interferon α2a has been published previously.
To the best of our knowledge we present only the second case of acute inflammatory demyelinating polyneuropathy related to PEG-interferon α2a, occurring in a 63-year-old Caucasian man. He developed tingling, numbness, and weakness of his upper and lower extremities with acute neurological deficits after five weeks of a combination therapy with PEG-interferon α2a and ribavirin for chronic hepatitis C virus infection. His clinical course, neurological findings, and his electromyogram results were all consistent with acute inflammatory demyelinating polyneuropathy. Our patient recovered completely after interferon was stopped and symptomatic treatment and a further electromyogram showed a disappearance of neuropathy. Four weeks later, PEG-interferon α2a was reintroduced with a gradually increasing dose without any reappearance of neurological symptoms allowing hepatitis C seroconversion.
Recognition of this rare yet possible presentation is important for early and accurate diagnosis and treatment. This case report also suggests that the reintroduction of PEGylated interferon in patients who had presented with acute inflammatory demyelinating polyneuropathy related to interferon α may be safe, but this must be confirmed by further studies.
聚乙二醇(PEG)化干扰素(聚乙二醇化干扰素)与利巴韦林联合使用已被证明是治疗慢性丙型肝炎病毒的有效方法。一般来说,这种联合治疗的常见副作用较轻,耐受性良好。然而,与聚乙二醇干扰素α2a(聚乙二醇化干扰素α-2a)相关的周围神经病变,包括脱髓鞘性多发性神经病极为罕见。在文献中,此前仅发表过一例与聚乙二醇干扰素α2a相关的急性炎症性脱髓鞘性多发性神经病病例。
据我们所知,我们报告的是第二例与聚乙二醇干扰素α2a相关的急性炎症性脱髓鞘性多发性神经病,患者为一名63岁的白种男性。在接受聚乙二醇干扰素α2a和利巴韦林联合治疗慢性丙型肝炎病毒感染五周后,他出现了四肢刺痛、麻木和无力,并伴有急性神经功能缺损。他的临床病程、神经学检查结果以及肌电图结果均与急性炎症性脱髓鞘性多发性神经病相符。停用干扰素并进行对症治疗后,我们的患者完全康复,进一步的肌电图显示神经病变消失。四周后,重新逐渐增加剂量引入聚乙二醇干扰素α2a,未再出现任何神经症状,实现了丙型肝炎血清学转换。
认识到这种罕见但可能出现的情况对于早期准确诊断和治疗很重要。本病例报告还表明,对于曾出现与干扰素α相关的急性炎症性脱髓鞘性多发性神经病的患者,重新引入聚乙二醇化干扰素可能是安全的,但这必须通过进一步研究来证实。