Case Report

Degenerated Peutz-Jeghers Syndrome with Peritoneal Carcinomatosis: A Case Report and Overview of a Rare Disease

1. Abstract Peutz-Jeghers syndrome (PJS) is a genetic disease with dominant au- tosomic transmission, characterized by the development of hamar- tomatous polyps in the digestive tract, associated with muco-cutane- ous pigmentation. PJS is a serious condition that can be life threaten- ing due to the significant increase of cancer risk.

Corrosive Stricture in Oral Cavity- A Rare Presentation

1. Abstract 1.1. Introduction: Corrosive injury of the upper gastrointestinal tract has been commonly reported in medical literature. It can be due to ingestion of acid or alkali and may be accidental or suicidal. The extent of injury varies from involving the esophagus, stomach, and duodenum either individually or together but oral cavity is rarely …

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Severe Hereditary Hemochromatosis Due to Heterozygous H63D Mutation: Unusual Presentation

1. Abstract 1.1. Introduction Diagnosis of hereditary hemochromatosis is based on molecular sequencing of the HFE gene in search for one of the three most frequent mutations: p.Cys282Tyr (C282Y); p.His63Asp (H63D) and pSer65Cys (S65C). Iron overload linked to the H63D mutation especially in the heterozygous state is not conventionally considered significant enough to cause the …

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An Adolescent with Vomiting and Weight Loss

1. Abstract Pediatric Achalasia is a rare condition in children, often presents with common symptoms of vomiting and weight loss. We present a case of a 15-year-old female with persistent vomiting and weight loss who was initially diagnosed with eosinophilic esophagitis (EoE) due to endoscopic findings and elevated eosinophils on esophageal histology

A Case of New-onset Inflammatory Bowel Disease (IBD) Following Secukinumab (SEK) Treatment of Psoriasis: A Case Report with Clinicopathological Analysis

1. Abstract We present a case of new-onset IBD in a patient following SEK treatment for psoriasis. The Patient’s IBD symptoms were successfully treated with glucocorticoids and adalimumab. The published literature contains a small number of case reports of the new onset of IBD following the treatment of SEK. This report can provide a new …

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