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Journal articles on the topic 'Congenital Hepatic fibrosis COLL1'

Author: Grafiati

Published: 9 March 2023

Last updated: 10 March 2023

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1

Abdullah, Asaad M. A., and Hisham Nazer. "Congenital Hepatic Fibrosis." Annals of Saudi Medicine 15, no. 1 (January 1995): 82–83. http://dx.doi.org/10.5144/0256-4947.1995.82.

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2

Raskovic, Zorica, Biljana Vuletic, Zoran Igrutinovic, and Slavica Markovic. "Congenital hepatic fibrosis." Serbian Journal of Experimental and Clinical Research 14, no. 4 (2013): 175–79. http://dx.doi.org/10.5937/sjecr14-4339.

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3

De Vos, M., F. Barbier, and C. Cuvelier. "Congenital hepatic fibrosis." Journal of Hepatology 6, no. 2 (January 1988): 222–28. http://dx.doi.org/10.1016/s0168-8278(88)80036-9.

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4

Trizzino, Antonino, Piero Farruggia, Delia Russo, Paolo D??Angelo, Serena Tropia, Vincenzo Benigno, Giuseppe Tarantino, Vito Di Marco, and Maurizio Aric?? "Congenital Hepatic Fibrosis." Journal of Pediatric Hematology/Oncology 27, no. 10 (October 2005): 567–68. http://dx.doi.org/10.1097/01.mph.0000184577.46458.7e.

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5

Zlatković, Marija, Slaviša Ðuričić, and Pavle Plamenac. "Congenital hepatic fibrosis of heterotopic hepatic tissue." Pathology - Research and Practice 194, no. 7 (January 1998): 523–26. http://dx.doi.org/10.1016/s0344-0338(98)80123-4.

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6

DESMET, V. J. "What is congenital hepatic fibrosis?" Histopathology 20, no. 6 (April 3, 2007): 465–78. http://dx.doi.org/10.1111/j.1365-2559.1992.tb01031.x.

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7

Mankala, Vikas M., Jessica L. Davis, Chirag V. Patel, and Henry C. Lin. "Congenital Hepatic Fibrosis Presenting With Pancytopenia." JPGN Reports 2, no. 1 (January 13, 2021): e043. http://dx.doi.org/10.1097/pg9.0000000000000043.

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8

Yenice, Harun, Ziya Günal, and Sinan Erten. "A Case of Congenital Hepatic Fibrosis." Journal of Tepecik Education and Research Hospital 5, no. 1 (1995): 97–99. http://dx.doi.org/10.5222/terh.1995.08835.

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9

Zubair, Adeel S., Ali Metwaly, Justin M. Burns, and John A. Stauffer. "Intrahepatic cholangiocarcinoma with congenital hepatic fibrosis." International Journal of Hepatobiliary and Pancreatic Diseases 5 (2015): 103. http://dx.doi.org/10.5348/ijhpd-2015-43-cr-18.

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10

Wu, Wei Kelly, Ioannis A. Ziogas, Manhal Izzy, Anita K. Pai, Einar T. Hafberg, Lea K. Matsuoka, and Sophoclis P. Alexopoulos. "Liver transplantation for congenital hepatic fibrosis." Transplant International 34, no. 7 (May 30, 2021): 1281–92. http://dx.doi.org/10.1111/tri.13884.

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11

Popovych, O. O., L. V. Moroz, Yu V. Avdosiev, F. A. Chabanov, and O. O. Voinalovych. "Congenital hepatic fibrosis (a case report)." Zaporozhye Medical Journal 23, no. 6 (October 29, 2021): 882–88. http://dx.doi.org/10.14739/2310-1210.2021.6.229102.

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Congenital hepatic fibrosis (CHF) is an autosomal recessive disorder of intrauterine morphogenesis of the portobiliary system, characterized by periportal fibrosis and defective remodeling of the bile ducts. The article describes the features of the clinical course, diagnosis and treatment of type I CHF in the different terms of a patient’s life: from birth to her pregnancy, during pregnancy and after childbirth. The aim of this work is to familiarize specialists with the problem of diagnosis and treatment of type I CHF in a patient with a provisional misdiagnosis of cryptogenic liver cirrhosis. Results. The features of type I CHF that determine a wider diagnostic testing in long-term unspecified liver pathology cases were identified. First-time decompensation of portal hypertension (PH) occurred at 35 weeks of gestation with the development of ascitic-edematous syndrome, hypersplenism, preeclampsia without signs of hepatic encephalopathy (HE). Cesarean section was performed at 37 weeks’ gestation and healthy baby was born. One year and 9 months after delivery, hypersplenism compensation was achieved by performing splenic artery embolization (SAE). There were no clinical manifestations of HE throughout the follow-up period. Conclusions. The diagnostic algorithm for a long-term compensated unspecified liver pathology with PH should confirm or rule out CHF. Type I CHF patients can give birth to a healthy child. SAE successfully compensates for hypersplenism and PH in type I CHF. Transient elastography is an effective method for the assessment of liver fibrosis progression in patients with type I CHF.

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12

Brown, D. L., T. Van Winkle, T. Cecere, S. Rushton, C. Brachelente, and J. M. Cullen. "Congenital Hepatic Fibrosis in 5 Dogs." Veterinary Pathology 47, no. 1 (January 2010): 102–7. http://dx.doi.org/10.1177/0300985809353313.

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13

El-Youssef, M., Y. Mu, L. Huang, and S. E. Crawford. "APOPTOSIS EXPRESSION IN CONGENITAL HEPATIC FIBROSIS." Journal of Pediatric Gastroenterology & Nutrition 29, no. 4 (October 1999): 512. http://dx.doi.org/10.1097/00005176-199910000-00119.

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14

Poddar, Ujjal, Babur R. Thapa, Rakesh K. Vashishta, Chakkodbail S. Girish, and Kartar Singh. "Congenital hepatic fibrosis in Indian children." Journal of Gastroenterology and Hepatology 14, no. 12 (December 1999): 1192–96. http://dx.doi.org/10.1046/j.1440-1746.1999.02028.x.

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15

Evans-Jones, G., and R. Cudmore. "Choledochal cyst and congenital hepatic fibrosis." Journal of Pediatric Surgery 25, no. 12 (December 1990): 1259–60. http://dx.doi.org/10.1016/0022-3468(90)90524-d.

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16

Akhan, Okan, Ali Devrim Karaosmanoğlu, and Bilge Ergen. "Imaging findings in congenital hepatic fibrosis." European Journal of Radiology 61, no. 1 (January 2007): 18–24. http://dx.doi.org/10.1016/j.ejrad.2006.11.007.

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17

Abdullah, A. M. A., H. Nazer, M. Atiyeh, and M. A. Ali. "Congenital Hepatic Fibrosis in Saudi Arabia." Journal of Tropical Pediatrics 37, no. 5 (October 1, 1991): 240–43. http://dx.doi.org/10.1093/tropej/37.5.240.

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18

Besnard, M., D. Pariente, M. Hadchouel, O. Bernard, and P. Chaumont. "Portal cavernoma in congenital hepatic fibrosis." Pediatric Radiology 24, no. 1 (March 1994): 61–65. http://dx.doi.org/10.1007/bf02017666.

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19

Ernst, O., F. Gottrand, M. Calvo, L. Michaud, G. Sergent, D. Mizrahi, and C. L'Herminé. "Congenital hepatic fibrosis: findings at MR cholangiopancreatography." American Journal of Roentgenology 170, no. 2 (February 1998): 409–12. http://dx.doi.org/10.2214/ajr.170.2.9456955.

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20

Zuppan, Craig W., Hong Dang Bui, and Bruce G. Grill. "Diffuse Hepatic Fibrosis in Congenital Cytomegalovirus Infection." Journal of Pediatric Gastroenterology and Nutrition 5, no. 3 (May 1986): 489–91. http://dx.doi.org/10.1097/00005176-198605000-00029.

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21

Jiang, Chang, Qiang Zhou, Meishan Jin, Junqi Niu, and Yanhang Gao. "Congenital hepatic fibrosis with polycystic kidney disease." Medicine 98, no. 20 (May 2019): e15600. http://dx.doi.org/10.1097/md.0000000000015600.

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22

Yoshikawa, H., T. Fukuda, T. Oyamada, and T. Yoshikawa. "Congenital Hepatic Fibrosis in a Newborn Calf." Veterinary Pathology 39, no. 1 (January 2002): 143–45. http://dx.doi.org/10.1354/vp.39-1-143.

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23

Minami, Koichi, Genkichi Izumi, Toshihiko Yanagawa, Yozo Shimoyamada, and Norishige Yoshikawa. "Septo-optic dysplasia with congenital hepatic fibrosis." Pediatric Neurology 29, no. 2 (August 2003): 157–59. http://dx.doi.org/10.1016/s0887-8994(03)00147-4.

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24

Alsomali, Mohammed I., Martha M. Yearsley, Douglas M. Levin, and Wei Chen. "Diagnosis of Congenital Hepatic Fibrosis in Adulthood." American Journal of Clinical Pathology 153, no. 1 (October 4, 2019): 119–25. http://dx.doi.org/10.1093/ajcp/aqz140.

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Abstract Objectives We studied clinicopathologic features of congenital hepatic fibrosis (CHF) that could aid the diagnosis of this relatively rare condition during adulthood. Methods Five consecutive adult CHF cases were identified in a single institution. Results Clinical manifestations of CHF varied from asymptomatic to requiring liver transplantation. Three of five cases had other disease associations, including Joubert syndrome, Caroli disease, polycystic kidney disease, and congenital anomaly of hepatic vasculature. No unique common radiologic findings were found. Histologically, all cases showed characteristic abnormal interlobular bile ducts embedded in fibrotic portal stroma, with varying degrees of liver fibrosis. Conclusions While other disease associations and characteristic liver histomorphology are helpful clues to suspect the diagnosis of CHF in adult patients, other differential diagnoses should be excluded clinically and radiologically. This study highlights the importance of a multidisciplinary diagnostic approach by pathologists, radiologists, and hepatologists for the accurate diagnosis of CHF during adulthood.

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25

Homsi, Maher, Sumair Ahmad, Neil Vyas, and Nnaemeka Anyadike. "A Unique Case of Congenital Hepatic Fibrosis." American Journal of Gastroenterology 112 (October 2017): S1227. http://dx.doi.org/10.14309/00000434-201710001-02232.

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26

Shrestha, Ananta, Mamun Al-Mahtab, Salimur Rahman, Jahangir Sarkar, and Thupten K. Lama. "Its Congenital Hepatic Fibrosis; Not Cirrhosis At All." Nepalese Medical Journal 1, no. 2 (December 2, 2018): 124–26. http://dx.doi.org/10.3126/nmj.v1i2.21624.

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Congenital hepatic fibrosis is a rare condition characterized by extensive fibrosis of liver but with preserved normal lobular architecture inherited as autosomal recessive trait. We report a 19 year-old-female admitted to Bangabandhu Sheikh Mujib Medical University with the complaints of lump in upper abdomen since last 13 years and episodes of fever and abdominal pain for same duration. She was diagnosed with hepatic TB on hepatic histology. Congenital hepatic fibrosis is a rare cause of portal hypertension that presents during childhood. Prognosis of congenital hepatic fibrosis is good. Life threatening events in these patients are related with variceal bleeding and episodes of cholangitis. Owing to relatively good liver function these patients tolerate portosystemic shunt surgeries quite well.Though rare, congenital hepatic fibrosis should be included in the differential diagnosis of portal hypertension in early life.

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27

TAKATORI, Masao, Shogo IWABUCHI, Takeshi HAYASHI, Yasuto TAKAHASHI, Michihiro SUZUKI, Shiro IINO, Shiro MAEYAMA, and Toshiyuki UCHIKOSHI. "Congenital Hepatic Fibrosis with Fatal Cholestatic Liver Damage." Internal Medicine 39, no. 11 (2000): 930–35. http://dx.doi.org/10.2169/internalmedicine.39.930.

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28

OKAJIMA, Tugio, Shigeo SUGANO, Kouji ISHII, Wataru YAMAMURO, Yasukiyo SUMINO, Kazuo HURUKAWA, Takahito ITO, and Tohru ABEI. "Congenital hepatic fibrosis associated with Cruveilhier-Baumgarten syndrome." Kanzo 27, no. 12 (1986): 1744–50. http://dx.doi.org/10.2957/kanzo.27.1744.

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29

Yönem, Özlem, Nihal Özkayar, Ferhun Balkancı, Özgür Harmancı, Cenk Sökmensüer, Osman Ersoy, and Yusuf Bayraktar. "Is Congenital Hepatic Fibrosis a Pure Liver Disease?" American Journal of Gastroenterology 101, no. 6 (June 2006): 1253–59. http://dx.doi.org/10.1111/j.1572-0241.2006.00642.x.

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30

Freeze, Hudson H. "New Diagnosis and Treatment of Congenital Hepatic Fibrosis." Journal of Pediatric Gastroenterology & Nutrition 29, no. 1 (July 1999): 104–6. http://dx.doi.org/10.1097/00005176-199907000-00027.

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31

Zeitoun, Delphine, Giuseppe Brancatelli, Magali Colombat, Michael P. Federle, Dominique Valla, Tong Wu, Claude Degott, and Valérie Vilgrain. "Congenital Hepatic Fibrosis: CT Findings in 18 Adults." Radiology 231, no. 1 (April 2004): 109–16. http://dx.doi.org/10.1148/radiol.2311030108.

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32

Li, Dezhao, Junjie Qin, Shijuan Sun, and Xu Li. "Congenital hepatic fibrosis and coexistent retinal macular degeneration." Medicine 98, no. 35 (August 2019): e16909. http://dx.doi.org/10.1097/md.0000000000016909.

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33

Bayraktar, Yusuf. "Novel variant syndrome associated with congenital hepatic fibrosis." World Journal of Clinical Cases 3, no. 10 (2015): 904. http://dx.doi.org/10.12998/wjcc.v3.i10.904.

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34

Rossi, Gloria, Teresa Di Chio, Silvia Nastasio, and Giuseppe Maggiore. "Spontaneous Extrahepatic Portosystemic Shunt in Congenital Hepatic Fibrosis." Journal of Pediatric Gastroenterology and Nutrition 66, no. 4 (April 2018): e108. http://dx.doi.org/10.1097/mpg.0000000000001143.

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35

Paradis, Valérie, Paulette Bioulac-Sage, and Charles Balabaud. "Congenital hepatic fibrosis with multiple HNF1α hepatocellular adenomas." Clinics and Research in Hepatology and Gastroenterology 38, no. 6 (December 2014): e115-e116. http://dx.doi.org/10.1016/j.clinre.2014.03.011.

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36

Byrd, L. M., and P. Bullen. "Congenital hepatic fibrosis and portal hypertension in pregnancy." International Journal of Gynecology & Obstetrics 88, no. 2 (December 8, 2004): 142–43. http://dx.doi.org/10.1016/j.ijgo.2004.11.005.

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37

Acharyya, B. C., M. K. Goenka, S. Chatterjee, and U. Goenka. "Dealing with congenital hepatic fibrosis? Remember COACH syndrome." Clinical Journal of Gastroenterology 7, no. 1 (December 11, 2013): 48–51. http://dx.doi.org/10.1007/s12328-013-0418-6.

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38

Stillman, Alfred E. "Hepatobiliary Scintigraphy for Cholestasis in Congenital Hepatic Fibrosis." American Journal of Diseases of Children 139, no. 1 (January 1, 1985): 41. http://dx.doi.org/10.1001/archpedi.1985.02140030043025.

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39

Gocmen, Rahsan, Okan Akhan, and Beril Talim. "Congenital absence of the portal vein associated with congenital hepatic fibrosis." Pediatric Radiology 37, no. 9 (July 14, 2007): 920–24. http://dx.doi.org/10.1007/s00247-007-0533-y.

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40

KOJIMA, Hideyuki, Yoshinobu MATSUMURA, Tatsuichi AN, Motoyuki YOSHIDA, Hitoshi YOSHIJI, Tatsuhiro TSUJIMOTO, Keisuke MATSUMURA, et al. "A case of congenital hepatic fibrosis without portal hypertension." Kanzo 36, no. 2 (1995): 101–6. http://dx.doi.org/10.2957/kanzo.36.101.

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41

Kakkar, Nandita, R. K. Vasishta, Amit Lamba, Anil Narang, and A. K. Banerjee. "Perinatal Recessive Polycystic Kidney Disease with Congenital Hepatic Fibrosis." Fetal and Pediatric Pathology 20, no. 3 (May 1, 2001): 227–34. http://dx.doi.org/10.3109/15513810109168616.

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42

Kaczorowski, Jeffrey, Jill Halterman, Patrice Spitalnik, Elizabeth Mannick, Chin-To Fong, and John Seaman. "Congenital Hepatic Fibrosis and Autosomal Dominant Polycystic Kidney Disease." Fetal and Pediatric Pathology 20, no. 3 (May 1, 2001): 245–48. http://dx.doi.org/10.3109/15513810109168619.

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43

Srinath, Arvind, and Benjamin L. Shneider. "Congenital Hepatic Fibrosis and Autosomal Recessive Polycystic Kidney Disease." Journal of Pediatric Gastroenterology and Nutrition 54, no. 5 (May 2012): 580–87. http://dx.doi.org/10.1097/mpg.0b013e31824711b7.

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44

Shin, Dong Soo, and Si Hong Lim. "A Case of Congenital Hepatic Fibrosis with Variceal Bleeding." Korean Journal of Pediatric Gastroenterology and Nutrition 7, no. 1 (2004): 98. http://dx.doi.org/10.5223/kjpgn.2004.7.1.98.

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45

Park, Jae Hyun, Myung Hwa Chung, Hee Jung Lee, Jee Hyun Lee, Yon Ho Choe, Sang Yong Song, Yeon Lim Suh, and Jin Bok Hwang. "A Case of Congenital Hepatic Fibrosis in Kabuki Syndrome." Korean Journal of Pediatric Gastroenterology and Nutrition 11, no. 1 (2008): 60. http://dx.doi.org/10.5223/kjpgn.2008.11.1.60.

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46

Cobben, Jan M., Martijn H. Breuning, Coen Schoots, Leo P. ten Kate, and Klaus Zerres. "Congenital hepatic fibrosis in autosomal-dominant polycystic kidney disease." Kidney International 38, no. 5 (November 1990): 880–85. http://dx.doi.org/10.1038/ki.1990.286.

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47

SÁNCHEZ, CARLOS, ENRIQUE GONZÁLEZ, and JAVIER GARAU. "Trimethoprim-sulfamethoxazole treatment of cholangitis complicating congenital hepatic fibrosis." Pediatric Infectious Disease Journal 5, no. 3 (May 1986): 360–62. http://dx.doi.org/10.1097/00006454-198605000-00016.

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48

NAKAMURA, FUKASHI, HIROSHI SASAKI, HIROKI KAJIHARA, and MICHIO YAMANOUE. "Laurence-Moon-Biedl syndrome accompanied by congenital hepatic fibrosis." Journal of Gastroenterology and Hepatology 5, no. 2 (March 1990): 206–10. http://dx.doi.org/10.1111/j.1440-1746.1990.tb01826.x.

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49

Perisic, VN. "Long-term studies on congenital hepatic fibrosis in children." Acta Paediatrica 84, no. 6 (June 1995): 695–96. http://dx.doi.org/10.1111/j.1651-2227.1995.tb13732.x.

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50

Movasseghi, A. R., and Z. Naseri. "Immunohistochemical Study of Congenital Hepatic Fibrosis in Aborted Calves." Journal of Comparative Pathology 143, no. 4 (November 2010): 342. http://dx.doi.org/10.1016/j.jcpa.2010.09.141.

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