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Benign recurrent intrahepatic cholestasis: late initial diagnosis in adulthood   
Yazarlar (9)
Fatih Ermis
Kemal Oncu
Melih Ozel
Dr. Öğr. Üyesi Yener YAZĞAN Dr. Öğr. Üyesi Yener YAZĞAN
Kastamonu Üniversitesi, Türkiye
Ahmet Kemal Gurbuz
Levent Demirturk
Hakan Demirci
Taner Akyol
Aptullah Hahoglu
Devamını Göster
Özet
Benign recurrent intrahepatic cholestasis (BRIC) is a rare autosomal recessive or sporadic disorder, characterized by recurrent episodes of intense pruritus and jaundice that resolve spontaneously without leaving considerable liver damage. The attacks can start at any age, but the first attack is usually seen before the second decade of life. We report the case of a young adult male patient with BRIC who presented with recurrent cholestatic jaundice and pruritus with negative work up for all possible etiologies and a liver biopsy consistent with intrahepatic cholestasis. He improved on treatment with rifampicin and has not suffered another attack on follow up. Although in adulthood, BRIC diagnosis should be kept in mind in patients with recurrent cholestatic attacks with symptom free intervals after main bile duct obstruction and other congenital or acquired causes of intrahepatic cholestasis excluded.
Anahtar Kelimeler
Benign recurrent intrahepatic cholestasis | Adulthood | Rifampicin
Makale Türü Özgün Makale
Makale Alt Türü ESCI dergilerinde yayımlanan tam makale
Dergi Adı ANNALS OF HEPATOLOGY
Dergi ISSN 1665-2681 Wos Dergi Scopus Dergi
Makale Dili İngilizce
Basım Tarihi 04-2010
Cilt No 9
Sayı 2
Sayfalar 207 / 210
Doi Numarası 10.1016/S1665-2681(19)31665-5
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
WoS 10
Benign recurrent intrahepatic cholestasis: late initial diagnosis in adulthood

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