Karoli syndrome: a clinical case
https://doi.org/10.5922/2223-2427-2025-10-1-6
Abstract
Aim. Description of a clinical case of a rare genetic disease in a patient with Caroli C syndrome.
Methods. The paper presents data from the clinical history of the disease, data from laboratory and radiation research methods, and an analysis of the diagnostic path that led to the diagnosis of Carli syndrome in a patient who was treated at the Republican Clinical Hospital of the Ministry of Health of the Republic of Tatarstan.
Results. Consideration of this clinical case allows us to define a step-by-step diagnostic algorithm that led to the diagnosis of Caroli syndrome. When choosing treatment methods, the team of authors came to the conclusion that there is no single treatment concept and decided on symptomatic therapy for this nosology. The patient was discharged 10 days after the start of treatment in a satisfactory condition. The peculiarities of this clinical case include the late onset of the disease.
Conclusion. Due to the extremely narrow degree of prevalence, the diagnosis of Caroli syndrome is a complex clinical task in patients with symptoms of cholangitis, cholangiolithiasis, mechanical jaundice, cholestatic variant of viral hepatitis B. The diagnostic search consists of many stages and requires the joint participation of specialists of different profiles. To date, there are only symptomatic treatment methods for Caroli syndrome, the only etiologically significant method of treating these patients is orthotopic liver transplantation.
About the Authors
B. A. SakhabetdinovRussian Federation
Bulat A. Sakhabetdinov - Assistant of the Department of Topographic Anatomy and Operative Surgery
Butlerova, 49, Kazan, 420012
Yu. R. Safina
Russian Federation
Yulia R. Safina - Resident of the Department of Surgical Diseases
Butlerova, 49, Kazan, 420012
L. I. Ziganshin
Russian Federation
Lenar I. Ziganshin - Head of the Department of Surgery No. 2, first category physician, surgical oncologist, endoscopist
Orenburgsky tract, 138, Kazan, 420064
A. I. Kurbangaleev
Russian Federation
Arsen I. Kurbangaleev – PhD, Associate Professor, Department of Surgical Diseases
Butlerova, 49, Kazan, 420012
D. R. Sayapova
Russian Federation
Dinara I. Sayapova – PhD, Associate Professor, Department of Urology Academician E.N. Sitdykova
Butlerova, 49, Kazan, 420012
References
1. Ilchenko A.A. Diseases of the gallbladder and biliary tract: A guide for doctors. Moscow: Anakharsis, 2006. 448 p. ( in Russ.)
2. Krylov N. N. Surgical diseases Volume 1. Ed. Krylov N.N. Moscow: GEOTAR-Media, 2019. 816 p. ( in Russ.)
3. Wang ZX, Li YG, Wang RL, Li YW, Li ZY, Wang LF, Yang HY, Zhu Y, Wang Y, Bai YF, He TT, Zhang XF, Xiao XH. Clinical classification of Caroli’s disease: an analysis of 30 patients. HPB (Oxford). 2015 Mar;17(3):278-83. https://doi.org/10.1111/hpb.12330. Epub 2014 Oct 19.
4. Mumoli N, Cei M. Caroli disease. Mayo Clin Proc. 2007 Feb;82(2):208. https://doi.org/10.4065/82.2.208
5. S N. Styazhkina, DV Zaitsev, M N. Klimentov, V V. Larin, MA Gasanova, MI Chakmina Caroly›s disease with multiple cholangiogenic abscesses of the left lobe of the liver: a clinical case. Perm Medical Journal. 2023; 40(6):128-134. (in Russ.) https://doi.org/10.17816/pmj406128-134
6. Nikitin I.G., Karabinenko A.A., Nikitin A.E., Dedov E.I., Zhukova D.G., Presnova E.D., Korvyakov S.A., Azimov R.H., Reznik E.V. Karoli›s disease (clinical observation). Russian Journal of Gastroenterology, Hepatology, Coloproctology. 2018;28(6):77–83. (in Russ.)
7. Skvortsov V.V., Levitan B.N., Lunkov M.V., Morozov A.V. Karoli›s disease and syndrome: the current state of the problem. Experimental and Clinical Gastroenterology. 2018;150(2):115-120. (in Russ.)
8. Dumitrascu T, Lupescu I, Ionescu M. The Todani classification for bile duct cysts: an overview. Acta Chir Belg. 2012 Sep-Oct;112(5):340-5. https://doi.org/10.1080/00015458.2012.11680849
9. Li J, Liu LW, Luo J, Liu JX, Liu XJ, Zhu ZJ, Sun LY, Zhao XY. Clinicopathological features of Caroli disease/ Caroli syndrome: an analysis of 21 cases. Zhonghua Yi Xue Za Zhi. 2020 Oct 20;100(38):3005-3009. Chinese. https://doi.org/10.3760/cma.j.cn112137-20200630-01995
10. Galyan T.N., Tarba N.S., Khovrin V.V., Polishchuk L.O., Bagmet N.N., Fisenko E.P. Monolobar form of Karoli›s disease with intrahepatic concretion (clinical observation). Medical imaging. 2017;21(2): 85–89. (in Russ.). https://doi.org/10.24835/1607-0763-2017-2-85-89
11. Kuttykuzhanova G.G., Tanirbergenova A.Zh., Abdirazakova S.Zh., Urikbaeva Z.Zh. Caroli disease (clinical observation). Journal of Infectology. 2021;13(3):150-152. (in Russ.) https://doi.org/10.22625/2072-6732-2021-13-3-150-152
12. Kyalwazi B, Kudaravalli P, John S. Caroli Disease. 2024 Aug 16. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 30020679.
13. Baumgartner K, Kübler J, Bitzer M, Bösmüller H, Horger M. Caroli-Syndrom [Caroli’s syndrome]. Rofo. 2020 Feb;192(2):119-122. German. https://doi.org/10.1055/a-1024-4526
14. European Association for the Study of the Liver. EASL Clinical Practice Guidelines on the management of cystic liver diseases. J Hepatol. 2022 Oct;77(4):1083-1108. https://doi.org/10.1016/j.jhep.2022.06.002. Epub 2022 Jun 18. Erratum in: J Hepatol. 2023 Nov;79(5):1338. https://doi.org/10.1016/j.jhep.2023.09.003
15. Jiang L, Shu J, Yu Z. Repeated epigastric pain caused by Caroli’s disease. Asian J Surg. 2022 Jul;45(7):1432-1433. https://doi.org/10.1016/j.asjsur.2022.02.035
16. K.R. Ruziboyzoda, M.K. Gulzoda, B.I. Safarov. Diagnostics and surgical tactics for hepatolithiasis. Bulletin of the National Medical and Surgical Center named after N. I. Pirogov. - 2021;(4):46-50. (in Russ.). https://doi.org/10.25881/20728255_2021_16_4_46
17. Varganov VM, Larin VV, Zaitsev DV. Caroli disease: optimizing the choice of surgical strategy using 3D modeling, 3D printing and therapy. Pirogov Russian Journal of Surgery. 2023;(7):88 93. (In Russ.) https://doi.org/10.17116/hirurgia202307188
18. Yao X, Ao W, Fang J, Mao G, Chen C, Yu L, Cai H, Xu C. Imaging manifestations of Caroli disease with autosomal recessive polycystic kidney disease: a case report and literature review. BMC Pregnancy Childbirth. 2021 Apr 12;21(1):294. https://doi.org/10.1186/s12884-021-03768-8
19. Bonilla Larrama LF, Alas-Pineda CU, Pacheco AG, Díaz-Cerrato VS, Molinero Leiva KP. Caroli disease incidentally discovered in a 23-years old male: A case report. Radiol Case Rep. 2024 Oct 4;20(1):1-5. https://doi.org/10.1016/j.radcr.2024.09.080
20. Lefere M, Thijs M, De Hertogh G, Verslype C, Laleman W, Vanbeckevoort D, Van Steenbergen W, Claus F. Caroli disease: review of eight cases with emphasis on magnetic resonance imaging features. Eur J Gastroenterol Hepatol. 2011 Jul;23(7):578-85. https://doi.org/10.1097/MEG.0b013e3283470fcd
Review
For citations:
Sakhabetdinov B.A., Safina Yu.R., Ziganshin L.I., Kurbangaleev A.I., Sayapova D.R. Karoli syndrome: a clinical case. Surgical practice (Russia). 2025;(1):76-85. (In Russ.) https://doi.org/10.5922/2223-2427-2025-10-1-6