Results 51 to 60 of about 5,504 (210)

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Intrahepatic Cholangiocarcinoma: Epidemiological Trends, Risk Factors, Diagnostic Challenges, and Advances in Personalized Therapy—A Comprehensive Review

Journal of Gastroenterology and Hepatology, Volume 41, Issue 6, Page 1701-1721, June 2026.
ABSTRACT Intrahepatic cholangiocarcinoma (iCCA) ranks as the second most common primary liver cancer, compared to about 20% of cases. Its global incidence has climbed over the past four decades, yet early detection remains indefinable due to its asymptomatic nature. Five‐year survival rate of approximately is under 10%.
Yaqoob Muhammad, YuZhu Jin, Kai Luo, He Bai, Xudong Zhang, Xu Sun, Zahoor Maheen, Ali Tanveer, Saeed Muddasar Muhammad, Jialin Qu, Guixin Zhang   +10 more
wiley   +1 more source

Multicohort Validation of Gut Microbiome Signatures for Cholangiocarcinoma Diagnosis and Functional Characterization of Bifidobacterium Pseudocatenulatum

Advanced Science, Volume 13, Issue 27, 13 May 2026.
This study analyzes gut bacteria in cholangiocarcinoma patients, revealing distinct microbial signatures that enable accurate disease detection. Species‐based diagnostic models achieved over 98% accuracy in identifying cholangiocarcinoma and distinguished it from other liver diseases. The research demonstrates that specific beneficial bacteria suppress
Benchen Rao, Jianwen Jiang, Ruiqing Zhang, Dongya Zhang, Chenchen Zhang, Ang Li, Haifeng Lu, Hua Zhang, Lin Zhou, Wenzhi Guo, Peihao Wen, Jianfeng Xue, Jie Pan, Tuerganaili Aji, Zhou Lan, Xianzhi Jiang, Shusen Zheng, Zujiang Yu, Zhigang Ren   +18 more
wiley   +1 more source

Non-cirrhotic portal hypertension secondary to cholangiointestinal anastomotic stricture after choledochal cyst excision: a case report

Frontiers in Medicine, 2023
BackgroundCystectomy accompanied by biliary system reconstruction is an important treatment option for choledochal cysts, but the risk of post-operative complications is high.
Xu Zhang, Xu Zhang, Xu Zhang, Xu Zhang, Jun Qing Yan, Jun Qing Yan, Jun Qing Yan, Jun Qing Yan, Yan Ying Gao, Yan Ying Gao, Yan Ying Gao, Yan Ying Gao, De Zhao Song, De Zhao Song, De Zhao Song, De Zhao Song, Cheng Lou, Cheng Lou, Cheng Lou, Cheng Lou   +19 more
doaj   +1 more source

Diagnostic dilemma of cystic biliary atresia: A series of two cases and brief review of the diagnostic modalities

JPGN Reports, Volume 7, Issue 2, Page 355-361, May 2026.
Abstract Cystic biliary atresia (CBA) is a rare variant of biliary atresia that closely resembles choledochal cyst (CC), complicating diagnosis and potentially delaying critical surgical intervention. We report two cases of CBA that were difficult to diagnose.
Hamza Hassan Khan, Leslie Hirsig Spence, Nagraj Kasi   +2 more
wiley   +1 more source

Cystic biliary atresia: A distinct clinical entity that may mimic choledochal cyst

Radiology Case Reports, 2018
Cystic biliary atresia (CBA) is a relatively uncommon but clinically significant variant of biliary atresia. The presence of a cyst in the hepatic hilum on imaging in an infant with cholestasis supports the diagnosis of CBA, but can also be seen in ...
Gary R. Schooler, MD, Alisha Mavis, MD
doaj   +1 more source

Suspected Acute Pancreatitis With Peripancreatic Fluid Collection in an Adolescent: A Possible Association With Energy Drink Overconsumption

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Acute pancreatitis is uncommon in adolescents without underlying risk factors. Excessive consumption of energy drink–type beverages has been rarely reported as a possible contributing factor, although causality remains uncertain. We report a 14‐year‐old male who presented with severe epigastric pain radiating to the back and recurrent vomiting.
Hafiza Tooba Siddiqui, Muhammad Umar, Mirza Mohammad Ali Baig, Hasnain Wajeeh Saqib, Mohammed Hammad Jaber Amin   +4 more
wiley   +1 more source

Choledochal cyst Todani IA case report

, 2016
BackgroundCholedochal cyst is a congenital dilatation of the biliary tree. It may affect only the extrahepatic bile duct (type I, II and III), intrahepatic (type V) or both (type IVa). Vater first described choledochal cyst in 1723. Open excision was the
Medina Lira, Ana Karen, Frigerio, Pamela, Mayorga Soto, Argenis Jose   +2 more
core   +1 more source

Prenatal Detection of Fetal Abdominal Cysts: Can We Reassure Future Parents?

Prenatal Diagnosis, Volume 46, Issue 4, Page 483-491, April 2026.
ABSTRACT Objective This study aimed to evaluate the perinatal outcome of fetal abdominal cysts based on the timing of prenatal diagnosis and identify prenatal characteristics associated with postnatal surgical intervention. Methods Fetuses with prenatally detected isolated abdominal cysts referred between January 2007 and December 2022 were included ...
H. Heinrich, E. W. M. Grijseels, R. Bakx, R. R. Gorter, E. van den Boogaard, E. van Leeuwen, A. Elvan‐Taşpınar, I. H. Linskens, E. Pajkrt   +8 more
wiley   +1 more source

Type IVA choledochal cyst: a rare cause of cirrhosis in adults

The Egyptian Journal of Internal Medicine, 2022
Background Choledochal cysts (CDCs) are characterized by congenital cystic dilations of the intrahepatic or extrahepatic bile ducts or both. CDCs are very rarely reported in sub-Saharan Africa.
Chantelli Iamblaudiot Razafindrazoto, Andry Lalaina Rinà Rakotozafindrabe, Sakaiza Malala Randrianambininjanahary, Nitah Harivony Randriamifidy, Domoina Harivonjy Hasina Laingonirina, Sonny Maherison, Lova Hasina Ny Ony Narindra Rajaonarison, Tovo Harimanana Rabenjanahary, Soloniaina Hélio Razafimahefa, Rado Manitrala Ramanampamonjy   +9 more
doaj   +1 more source