Annals of Clinical Gastroenterology and Hepatology ISSN: 2640-2750

Luis Arturo Gutiérrez-Gonzalez*, Eillen Macias, Freddy Herrera-Vivas, Franz Otaiza, Juan Carlos Gonzalez Duran and Guillermo Veitia

Abstract

Inflammatory Bowel Disease (IBD)-associated arthritis is called Enteropathic Arthritis (EA) which is classified among the group of Spondyloarthritis (SpA), because its presentation is variable. The current trend is to classify them as autoinflammatory rather than autoimmune d...

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Abstract Read Full Article HTML DOI: 10.29328/journal.acgh.1001021 Cite this Article

Yu Zhong Wen, Shi Jie Dai, Su Fen Cheng, Jun Shi and Jun Hua Ai*

Abstract

Hepatocellular carcinoma (HCC) is characterized by high morbidity, high recurrence, and high mortality rates. In China, the morbidity of HCC is fifth among all malignant tumors and HCC is the third most common cause of cancer-related deaths. Most HCC patients also have liver ...

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Abstract Read Full Article HTML DOI: 10.29328/journal.acgh.1001020 Cite this Article

Zubin Sharma*, Ravindra Pradeep Sharma and Divya Sharma

Abstract

Acute pancreatitis is inflammation of the pancreas that may be accompanied by a systemic inflammatory response which results in impairment of the functioning of various organs, systems. Pancreatitis associated vascular complications very often cause morbidity and mortality. T...

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Abstract Read Full Article HTML DOI: 10.29328/journal.acgh.1001019 Cite this Article

Steve M D’Souza, Lindsey B Cundra, Byung Soo Yoo, Parth J Parekh and David A Johnson*

Abstract

There is growing evidence that gastroesophageal disease is influenced by the esophageal microbiome, and that commensal bacteria of the oropharynx, stomach, and colon are thought to have a role in modulatiing pathogenesis. These emerging hypotheses are based on observed change...

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Abstract Read Full Article HTML DOI: 10.29328/journal.acgh.1001018 Cite this Article

Anubha Bajaj*

Familial adenomatous polyposis is an autosomal dominant syndrome of variable penetration and constitutes the second frequent inherited syndrome enunciating the emergence of a colorectal carcinoma.

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Abstract Read Full Article HTML DOI: 10.29328/journal.acgh.1001017 Cite this Article

Makki H Fayadh*, Salim Awadh, Loai El Kiwisney, Abdul Hadi Quadri, Prasad K Shetty and Mervat Naguib

Abstract

Celiac disease affects 1% of the world population; however it is under diagnosed in UAE. The disease has many clinical manifestations, ranging from severe malabsorption to minimally symptomatic or non-symptomatic presentation. Hypocalcaemia is a common finding in celiac disea...

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Abstract Read Full Article HTML DOI: 10.29328/journal.acgh.1001016 Cite this Article

Fahri Yetisir* and Kerim Güzel

Abstract

Introduction: Pancreatic pseudocysts (PPs) are mostly delayed complications of acute or chronic pancreatitis and trauma. Pancreatic pseudocysts are usually managed by supportive medical treatment without surgical procedure. All the surgical interventions (per...

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Abstract Read Full Article HTML DOI: 10.29328/journal.acgh.1001015 Cite this Article

Sarhani Asmae*, Paupard Thierry, Ghani Sara, Salihoun Mouna and Kabbaj Nawal

Abstract

Heterotopic gastric mucosa (HGM) is an islet of gastric mucosa within the esophageal mucosa. These lesions can sit throughout the digestive tract and rarely in the upper third of the esophagus. The pathophysiology of HGM remains poorly understood.

Our study aims to ...

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Abstract Read Full Article HTML DOI: 10.29328/journal.acgh.1001014 Cite this Article

Abu Omar Y*, Wang Y, Agrawal R, Randhawa T, Majeed M, Attar BM, Demetria MV and Simons-Linares CR

Abstract

Introduction: Fluid management is the cornerstone of treatment for acute pancreatitis (AP), but the proper rate and volume is still controversial. We aim to evaluate the role of aggressive hydration in AP patients.

Methods: We retro...

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Abstract Read Full Article HTML DOI: 10.29328/journal.acgh.1001013 Cite this Article

Vitantonio Guglielmi*, Mario Correale and Gioacchino Leandro

Abstract

Background: This article reviews current knowledge of Gaucher’s disease (GD) and liver involvement and reports our experience: how many patients with chronic liver disease of unknown origin could be affected by Gaucher’s disease.

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Abstract Read Full Article HTML DOI: 10.29328/journal.acgh.1001012 Cite this Article