Case Report

1. Abstract Conventional ERCP is difficult for the treatment of refractory choledocholithiasis. This paper reports a case of giant stones in the common bile duct and left hepatic duct treated by ESWL combined with SpyGlass-guided laser lithotripsy.

1. Abstract Synchronous pancreatic neuroendocrine tumor (pNET) and pancreatic cyst are very rare. Herein, we report a case of pNET combined with a pancreatic cyst in a 49-year-old female. The patient first presented with a complaint of persistent pain in the right upper abdomen. As a follow-up, CT scan was performed that showed a solid …

Synchronous Pancreatic Neuroendocrine Tumor and Pancreatic Cyst: A Case Report Read More »

1. Abstract Echinococcosis is the chronic parasitic disease arising due to contamination of an organism by larval form of Echinococcus granulosus helminth. This disease represents a serious diagnostic and medical problem. This article describes clinical observation of echinococcosis with damage of liver, lung and brain. Dynamics of clinical data, morphological and histological changes of organs …

Echinococcosis of the Liver, Lungs and Brain. Clinical Observation Read More »

1. Abstract 1.1. Background: Hepatoid Adenocarcinoma of the Stomach (HAS) is a unique and rare subtype of gastric cancer with poor prognosis and hepatocellular carcinoma-like features. However, the standard therapies are still in the development stage.

1. Abstract 1.1. Background: Abdominal cocoon syndrome is a rare condition that refers to total or partial encapsulation of the small intestines leading to recurrent bowel obstruction. It usually affects young ladies from tropical and subtropical area. DOI:http://dx.doi.org/10.47829/JJGH.2022.8301

1. Abstract 1.1. Background. This study describes a case series that addresses the complex anesthetic management of adrenalectomy for patients with pheochromocytoma. It is a rare tumor, originating in the chromaffin cells of the adrenal medulla and a catecholamine-secreting agent, whose most common triad of symptoms is headache, sweating and tachycardia. DOI:http://dx.doi.org/10.47829/JJGH.2021.8201

1. Abstract Primary Biliary Cholangitis (PBC) isa cholestatic disease of autoimmune origin characterized by the destruction of small to medium size intrahepatic bile ducts due to lymphocytic infiltration. The diagnosis is made by the presence of Anti-Mitochondrial Antibodies (AMAs) specific for the disease. PBC typically affects middle-aged women and is often associated with other autoimmune …

Primary Biliary Cholangitis and Type 1 Diabetes in A Male Patient: A Case Report Read More »

1. Abstract The isolated location of tuberculosis is very rare constituting less than 1% of all locations. We report through this observation the case of a 23-year-old patient, who complains of chronic pain in the right hypochondrium in a context of deterioration of the general condition. The biological assessment showed a biological inflammatory syndrome. A …

Pseudotumoral Form of Primary Hepatic Tuberculosis: A Rare Case Report with Review of the Literature Read More »