KAROLIJEVA BOLEST – BOLEST O KOJOJ SE MALO RAZMIŠLJA: PRIKAZ BOLESNIKA

  • Andrija Rančić Doktor medicine, lekar na specijalizaciji interne medicine Klinike za gastroenterologiju i hepatologiju UKCa Niš
Ključne reči: Karolijeva bolest, holangitis, fibroza jetre, ciroza jetre

Sažetak


Karolijeva bolest je retko oboljenje, koje karakteriše dilatacija velikih intrahepatičnih žučnih kanala. Javlja se u retkoj izolovanoj formi, koju odlikuju ponovljene epizode holangitisa i periportalna fibroza (tip I). Znatno češća varijanta povezana je sa kongenitalnom fibrozom jetre (tip II). Iako se bolest može javiti tokom čitavog života, najčešće se javlja pre tridesete godine. Incidencija i prevalencija ove bolesti nisu poznate, ali je procena da se javlja jednom u 10.000 do 20.000 slučajeva. Glavni simptomi su povišena telesna temperatura, bol ispod desnog rebarnog luka, napadi žutice, svrab po koži, mučnina i povraćanje. Dijagnostika se vrši kliničkim pregledom, ultrazvučnim pregledom, kompjuterizovanom tomografijom abdomena, a u cilju definitivne dijagnostike primenjuju se endoskopska retrogradna holangiopankreatografija i biopsija jetre. U slučaju razvoja ciroze jetre i portne hipertenzije radi se proksimalna endoskopija. Prikazujemo klinički slučaj čoveka starijeg životnog doba, koji nekoliko godina unazad boluje od Karolijeve bolesti. Prikazani su dijagnostički izazovi i primenjena terapija.

Reference

Abdalla EK, Forsmark CE, Lauwers GY, Vauthey JN. Monolobar Caroli’s Disease and cholangiocarcinoma. HPB Surg 1999; 11: 271–276. [CrossRef] [PubMed]

Alhaddad M, Elsabaawy M, Elshaarawy O, Ehsan NA, Maher D, Elazab D et al. Congenital hepatic fibrosis (CHF): a report of two cases and an overview. Ann Clin Lab Res 2017; 5: 1. [CrossRef]

Ananthakrishnan AN, Saeian K. Caroli’s disease: Identification and treatment strategy. Curr Gastroenterol Rep 2007; 9(2): 151-155. [CrossRef] [PubMed]

Bettini G, Mandrioli L, Morini M. Bile duct dysplasia and congenital hepatic fibrosis associated with polycystic kidney (Caroli syndrome) in a rat. Vet Pathol 2003; 40: 693–694. [CrossRef] [PubMed]

Biswas NK, Raju U, Sodhi K. Caroli’s disease. Med J Armed Forces India 2007; 63(4): 388–389. [CrossRef] [PubMed]

Blechacz B. Cholangiocarcinoma: Current knowledge and new developments. Gut Liver 2017; 11(1): 13-26. [CrossRef] [PubMed]

Correia PC, Morgado B. Caroli's disease as a cause of chronic epigastric abdominal pain: Two case reports and a brief review of the literature. Cureus 2017; 9(9): e1701. [CrossRef] [PubMed]

Dayton MT, Longmire WP Jr, Tompkins RK. Caroli’s disease: a premalignant condition? Am J Surg 1983, 145: 41–48. [CrossRef] [PubMed]

Desmet VJ. Pathogenesis of ductal plate abnormalities. Mayo Clin Proc 1998; 73: 80–89. [CrossRef] [PubMed]

Fahrner R, Dennler SGC, Dondorf F, Ardelt M, Rauchfuss F, Settmacher U. Liver resection and transplantation in Caroli disease and syndrome. J Visc Surg 2019; 156(2): 91-95. [CrossRef] [PubMed]

Ghadir MR, Bagheri M, Ghanooni AH. Congenital hepatic fibrosis leading to cirrhosis and hepatocellular carcinoma: a case report. J Med Case Reports 2011; 5: 160. [CrossRef] [PubMed]

Hadžić N, Strazzabosco M. Fibropolycystic liver diseases and congenital biliary abnormalities. Sherlock's diseases of the liver and biliary system 2018; 13: 313–317. [CrossRef]

Hao X, Liu S, Dong Q, Zhang H, Zhao J, Su L.  Whole exome sequencing identifies recessive PKHD1 mutations in a Chinese twin family with Caroli disease. PLoS One 2014; 9: 0. [CrossRef] [PubMed]

Ilić S. Tumori i ciste jetre. U: Interna medicina, Prosveta, Niš, 2004, 357.

Jarufe N, Figueroa E, Muñoz C, Moisan F, Varas J, Valbuena JR et al. Anatomic hepatectomy as a definitive treatment for hepatolithiasis: a cohort study. HPB (Oxford) 2012; 14: 604-610. [CrossRef] [PubMed]

Kassahun WT, Kahn T, Wittekind C, Mossner J, Caca K, Hauss J et al. Caroli's disease: liver resection and liver transplantation. Experience in 33 patients. Surgery 2005; 138: 888–898. [CrossRef] [PubMed]

Madjov R, Chervenkov P, Madjova V, Balev B. Caroli's disease. Report of 5 cases and review of literature. Hepatogastroent 2005; 52: 606–609.  [PubMed]

Mamone G, Cortis K, Sarah A, Caruso S, Miraglia R. Hepatic morphology abnormalities: beyond cirrhosis. Abdom Radiol 2018; 43(7): 1612-1626. [CrossRef] [PubMed]

Moslim A, Gunasekaran G, Vogt D, Cruise M, Morris-Stiff G. Surgical management of Caroli's disease: Single center experience and review of the literature. J Gastrointest Surg 2015; 19(11): 2019-27. [CrossRef] [PubMed]

Moslim MA, Gunasekaran G, Vogt D, Cruise M, Morris-Stiff G. Surgical Management of Caroli's Disease: Single Center Experience and Review of the Literature. J Gastrointest Surg 2015; 19: 2019-2027. [CrossRef] [PubMed]

Parada L, Hallen M, Hagerstrand I, Tranberg K, Johansson B. Clonal chromosomal abnormalities in congenital bile duct dilatation (Caroli’s disease). Gut 1999; 45: 780–782. [CrossRef] [PubMed]

Preston D, Flanigan DP. Biliary carcinoma associated with biliary cysts. Cancer 1977; 40: 880-883. [CrossRef] [PubMed]

Schiewe R, Baudisch E, Ehrhardt G. Congenital intrahepatic bile duct cysts with calcinosis and malignant degenerations. Bruns Beitr Klin Chir 1968; 216: 264-271. [PubMed]

Sgro M, Rossetti S, Barozzino T, Toi A, Langer J, Harris PC et al. Caroli’ s disease: prenatal diagnosis, postnatal outcome and genetic analysis. Ultrasound Obstet Gynecol 2004; 23: 73–76. [CrossRef] [PubMed]

Soares C, Goldstein SD, Ghaseb MA, Kamel I, Hackam DJ, Pawlik TM. Pediatric choledochal cysts: diagnosis and current management. Pediatr Surg Int 2017; 33(6): 637-650. [CrossRef] [PubMed]

Sweeney WE, Avner ED, Adam MP, Mirzaa GM, Pagon RA, Wallace SP et al. Polycystic Kidney Disease, Autosomal Recessive. In: GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. [PubMed]

Torra R, Badenas C, Darnell A, Brú C, Escorsell A, Estivill X. Autosomal dominant polycystic kidney disease with anticipation and Caroli's disease associated with a PKD1 mutation. Rapid communication. Kidney Int 1997; 52(1): 33-38. [CrossRef] [PubMed]

Yamaguchi T, Cristaudi A, Kokudo T, Uldry E, Demartines N, Halkic N. Surgical treatment for monolobular Caroli's disease ‒ Report of a 30-year single center case series. Biosci Trends 2018; 12(4): 426-431. [CrossRef] [PubMed]

Yang XY, Zhu LP, Liu XQ, Zhang CY, Yao Y, Wu Y. Genetic diagnosis of Caroli syndrome with autosomal recessive polycystic kidney disease: a case report and literature review. Beijing Da Xue Xue Bao Yi Xue Ban 2018; 50(2): 335-339. [PubMed]

Yonem O, Bayraktar Y. Clinical characteristics of Caroli’s disease. World J Gastroenterol 2007; 13(13): 1930-1933. [CrossRef] [PubMed]

Objavljeno
2023/06/16
Rubrika
Prikaz bolesnika