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.
Giant Uterine Leiomyoma Associated with Erythrocytosis: First Reported Case in Peru
1. Abstract 1.1. Introduction Myomatous-erythrocytic syndrome is an exceptionally rare clinical entity characterized by the coexistence of giant uterine leiomyomas defined as fibroids measuring ≥20 cm and erythrocytosis, marked by an abnormal elevation in red blood cell mass, hemoglobin, and hematocrit.
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Proof of Efficacy and Safety of Activated NK Cell Immunotherapy (ANK Therapy) for Various Types of Cancer, and Investigation into The Possibility That PD-L1 Is Useful as A Biomarker for Predicting Efficacy
1. Introduction Activated natural killer cell immunotherapy (ANK therapy) is a treatment in which NK cells are extracted from the patient’s own blood, expanded, activated, and then returned to the body.
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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