نتایج جستجو برای: cholestatic jaundice

تعداد نتایج: 11202  

Journal: :Journal of Medical Case Reports 2008
Aliye Soylu Mustafa Gurkan Taskale Aydin Ciltas Mustafa Kalayci A Baki Kumbasar

INTRODUCTION Non-specific abnormalities in liver function tests might accompany the clinical course of hyperthyroidism. Hyperthyroidism can cause the elevation of hepatic enzymes and bilirubin. Jaundice is rare in overt hyperthyroidism, especially in subclinical hyperthyroidism. On the other hand, the use of anti-thyroid drugs has rarely been associated with toxic hepatitis and cholestatic jaun...

2013
Aamer Aleem Mohammad Al-Katari Khalid Alsaleh Khalid AlSwat Abdulmalik Al-Sheikh

Vanishing bile duct syndrome (VBDS) is a condition resulting from severe bile duct injury, progressive destruction, and disappearance of intrahepatic bile ducts (ductopenia) leading to cholestasis, biliary cirrhosis, and liver failure. VBDS can be associated with a variety of disorders, including Hodgkin's lymphoma (HL). We describe a 33-year-old male patient who presented with lymphadenopathy ...

Journal: :Pediatric gastroenterology, hepatology & nutrition 2016
Jong Sub Choi Hyeoh Won Yoo Kyung Jae Lee Jung Min Ko Jin Soo Moon Jae Sung Ko

Carnitine palmitoyltransferase 1A (CPT1A) is an enzyme functioning in mitochondrial fatty acid oxidation (FAO) of the liver. Patients with CPT1A deficiency have impaired mitochondrial FAO and display hypoketotic hypoglycemia and hepatic encephalopathy as typical manifestations. In this report, we present a case of CPT1A deficiency presenting jaundice as the first manifestation. A 1.9 years old ...

Journal: :American family physician 2017
Matthew V Fargo Scott P Grogan Aaron Saguil

Jaundice in adults can be an indicator of significant underlying disease. It is caused by elevated serum bilirubin levels in the unconjugated or conjugated form. The evaluation of jaundice relies on the history and physical examination. The initial laboratory evaluation should include fractionated bilirubin, a complete blood count, alanine transaminase, aspartate transaminase, alkaline phosphat...

Journal: :Journal of Gastriontestinal and Abdominal Radiology ISGAR 2023

Abstract Choledochal cyst (CDC) is a rare surgical cause of cholestatic jaundice in infants. Spontaneous rupture an unusual presentation previously undiagnosed CDC and also biliary peritonitis children. Here, we report case 1-year-old boy who was evaluated for progressive abdominal distension. Ultrasonogram showed gross ascites with echogenic particles, dilated common bile duct (CBD), hepatic (...

Journal: :Canadian liver journal 2022

BACKGROUND: Widespread administration of COVID-19 vaccinations have led to reports rare but potentially serious side effects. METHODS: We present two cases acute hepatitis following mRNA BNT162b2 (Comirnaty, Pfizer-BioNTech) vaccination. RESULTS: A 25-year-old male presented hospital with progressive jaundice 5 days his second dose Comirnaty. Initial bloodwork revealed severe hepatocellular enzy...

2011
Francis Aba Uba Mohammed A.Latif Ayad Alaa F. Hamza

Introduction Neonatal cholestasis is defined as prolonged elevation of serum levels of conjugated bilirubin beyond the first 14 days of life. Neonatal hyperbilirubinaemia is usually physiologic, unconjugated, and self-limited. Only 2–15% of neonates remain jaundiced past 2 weeks of life, and just 0.2–0.4% have cholestatic jaundice from either intrahepatic cholestasis or structural abnormalities...

Journal: :Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi 2004
Ko Chang Jing-Jou Yan Hsin-Chun Lee Kung Hung Liu Nan Yao Lee Wen-Chien Ko

Acute Q fever was previously regarded as an uncommon infectious disease in Taiwan but has been increasingly recognized recently. Acute febrile illness, hepatitis, and pneumonia are the 3 most common manifestations of this condition, whereas jaundice is rarely reported among patients with acute Q fever. We report 2 cases of acute Q fever with jaundice and multi-organ involvement. The first patie...

Journal: :acta medica iranica 0
kavehmanesh z kosari f

this report presents an 11 year-old girl with benign recurrent cholestasis (bric) who developed episodes of severe jaundice and pruritus at the ages of 2.5 and 10 years. each episode lasted for 3-4 months. the peak level of serum bilirubin reached 33-37 mg/dl.liver function tests were all normal during the attack except for increased alkaline phosphatase and prolonged prothrombin time responsiv...

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