Atypical Esophageal Perforation: Clinical Vigilance and Nutritional Management – Case Report
1. Abstract Boerhaave syndrome is a rare, life-threatening condition. Symptoms are often atypical, so early diagnosis is crucial for prompt treatment.
Case Report
Non-Purulent Empyema Salmonellosis in an Elderly Patient with Heart Failure: A Case Report and Literature Review
1. Abstract 1.1. Background Salmonella is a genus of bacteria that is primarily recognized for causing foodborne illnesses and gastrointestinal infections. However, cases involving empyema attributed to Salmonella remain quite rare, with only a handful of cases reported in the medical literature.
A Case of Familial Partial Lipodystrophy Type 3 with A Novel Pparg Variant of Unknown Significance
1. Abstract Familial partial lipodystrophy (FPLD) is a heterogeneous group of rare genetic disorders (estimated prevalence <1/100,000) characterized by a lipodystrophy phenotype combined with metabolic abnormalities such as insulin resistance and hypertriglyceridemia. Several subtypes have been described
A Rare Case of Mid-Ventricular and Apical Hypertrophic Cardiomyopathy with Hourglass Appearance on Echocardiogram
1. Abstract Hypertrophic obstructive cardiomyopathy (HOCM) is a genetically driven cardiac condition most often involving asymmetric septal hypertrophy. Mid-ventricular and apical variants are rare, accounting for less than 5% of cases in Western populations, and present unique diagnostic and prognostic challenges.
A New Method for Removing Active Oxygen by Generating Hydrogen Gas Using HPI
1. Abstract It is said that lifestyle-related diseases and deterioration of beauty caused by aging are caused by active oxygen. In particular, aging was coded in ICD-11, so it was positioned as a disease. In light of this, it can be seen that aging is reversible.
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An Alternative Approach to Current Guidelines: The Use of Top-Up Long-Acting Buprenorphine Injection for A Patient Presenting with Withdrawal Symptoms
1. Abstract A 34-year-old male patient with opioid use disorder (OUD), who was transitioned from daily oral buprenorphine/naloxone therapy.
Spontaneous Renal Rupture Revealing Tuberous Sclerosis Complex: A Case Report
1. Abstract Tuberous sclerosis complex (TSC) is a rare genetic disorder characterized by the development of benign tumours in various organs, primarily the kidneys. Renal involvement, often in the form of angiomyolipoma’s (AML).
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A Typical Presentation of Myasthenia Gravis: A Clinical Sequelae of Thymoma
https://doi.org/10.47829/ACMCR.2025.141109 Myasthenia gravis (MG) is an autoimmune disorder in which antibodies block the acetylcholine receptors in the post synaptic membrane causing skeletal muscle weakness.
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Enhancing Surgical Precision with Intraoperative Tumour Localisation Using Fluorescence Angiography in Partial Adrenalectomy Surgery
1. Abstract Partial adrenalectomy poses unique challenges due to the need to preserve adrenal function while ensuring complete tumour resection. In this case report.
Bronchoscopic Resection of Endotracheal Castleman Disease: A Rare Case Report
1. Abstract Castleman’s disease (CD) is an uncommon benign lymphoid hyperplasia, which was first reported by Benjamin Castleman in 1954. Pulmonary CD has been documented in the literature as a rare extranidal manifestation. We report a case of a 53-year-old woman with respiratory insufficiency presenting as an endotracheal lesion.
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