Successful antiviral treatment of chronic hepatitis C in patients with rare comorbidities. Two case-reports

被引:2
作者
Guardigni, Viola [1 ]
Fabbri, Gabriele [1 ]
Grilli, Anastasio [1 ]
Contini, Carlo [1 ]
机构
[1] Univ Ferrara, Dept Clin & Expt Med, Sect Infect Dis, I-44100 Ferrara, Italy
关键词
Charcot Marie Tooth Disease; Ehlers-Danlos Syndrome; Peg-Interferon; HCV; EHLERS-DANLOS-SYNDROME; MARIE-TOOTH-DISEASE; PERIPHERAL NEUROPATHY; VIRUS-INFECTION;
D O I
10.1016/S1665-2681(19)30939-1
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Antiviral therapy in patients suffering from chronic hepatitis C virus (HCV) infection and rare comorbidities cannot be easily started, as it can reduce the likelihood of a good therapeutic response with an increased frequency of side effects. We report two patients presenting unusual comorbidities associated with chronic C hepatitis: one with the Ehlers-Danlos Syndrome (EDS), a rare genetic disease caused by a defect in collagen synthesis, the other one with the Charcot Marie Tooth (CMT) disease, an uncommon but severe form of demyelinating peripheral neuropathy. Both patients were successfully treated with pegylated Interferon (Peg-IFN) and ribavirin (RBV) combined therapy, with the achievement of a sustained viral response (SVR) and a low occurrence of adverse effects. Up to now there are no reports of patients suffering from chronic C hepatitis associated with these uncommon but severe comorbidities treated with antiviral therapy. In conclusion, in such clinical situations, anti-HCV therapy may be started and tailored, especially if the patient is highly motivated and if optimal predictors of response (i.e. young age, favourable genotype and low baseline viraemia) do exist.
引用
收藏
页码:404 / 408
页数:5
相关论文
共 21 条
[2]  
Bacon BR, 2005, AM J MANAG CARE, V11, pS296
[3]  
Beighton P, 1998, AM J MED GENET, V77, P31, DOI 10.1002/(SICI)1096-8628(19980428)77:1<31::AID-AJMG8>3.0.CO
[4]  
2-O
[5]   Chronic hepatitis C virus infection: genotyping and its clinical role [J].
Bowden, D. Scott ;
Berzsenyi, Mark D. .
FUTURE MICROBIOLOGY, 2006, 1 (01) :103-112
[6]   CURRENT TREATMENTS OF CHRONIC IMMUNE-MEDIATED DEMYELINATING POLYNEUROPATHIES [J].
Brannagan, Thomas H., III .
MUSCLE & NERVE, 2009, 39 (05) :563-578
[7]  
Craxì A, 2011, J HEPATOL, V55, P245, DOI 10.1016/j.jhep.2011.02.023
[8]   Clinical and genetic features of vascular Ehlers-Danlos syndrome [J].
Germain, DP .
ANNALS OF VASCULAR SURGERY, 2002, 16 (03) :391-397
[9]   Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy [J].
Irobi, J ;
Van Impe, K ;
Seeman, P ;
Jordanova, A ;
Dierick, I ;
Verpoorten, N ;
Michalik, A ;
De Vriendt, E ;
Jacobs, A ;
Van Gerwen, V ;
Vennekens, K ;
Mazanec, R ;
Tournev, I ;
Hilton-Jones, D ;
Talbot, K ;
Kremensky, N ;
Van Den Bosch, L ;
Robberecht, W ;
Vandekerckhove, J ;
Van Broeckhoven, C ;
Gettemans, J ;
De Jonghe, P ;
Timmerman, V .
NATURE GENETICS, 2004, 36 (06) :597-601
[10]  
Iurassich S, 2004, Med Lav, V95, P223