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Sustained weight reduction following 12 weeks of intermittent fasting intervention in people with insulin-treated type 2 diabetes-Two-year follow-up of the randomised controlled InterFast-2 trial.
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Interdisciplinary Metabolic Medicine Trials Unit, Division of Endocrinology and Diabetology, Medical University of Graz, Graz, Austria.
Primary Laryngeal Lymphoma: A Case Report of a Rare Entity.
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October 2024
Otorhinolaryngology, Saveetha institute of medical and technical sciences, Chennai, IND.
Article Synopsis
- * A case study of a 53-year-old male with symptoms like weight loss, hoarseness, and dysphagia led to the diagnosis of diffuse large B-cell lymphoma (DLBCL) through a biopsy, following imaging that revealed a significant lesion in the larynx.
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Early Diagnosis of Papillary Carcinoma in a Thyroglossal Duct Cyst: A Multidisciplinary Approach and the Crucial Role of Fine-Needle Aspiration Cytology.
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Maxillofacial Surgery Department, Unidade Local de Saúde de Coimbra, Coimbra, PRT.
Papillary carcinoma within a thyroglossal duct cyst is a rare and challenging presentation of thyroid malignancy, requiring a nuanced approach to diagnosis and treatment. This report details the case of a 40-year-old male who presented with a two-year history of submental swelling and intermittent respiratory difficulty. Initial imaging suggested a simple thyroglossal duct cyst.
View Article and Find Full Text PDFHemophagocytic lymphohistiocytosis secondary to visceral leishmaniasis: A case report of a rare complication of visceral leishmaniasis.
IDCases
August 2024
Department of Pediatrics and Child Health, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
Hemophagocytic lymphohistiocytosis (HLH) is a rare, potentially life-threatening clinical syndrome characterized by hyperactivation of inflammatory mediators and harmful end-organ damage Visceral leishmaniasis (VL)-induced HLH is a rare disease with significant diagnostic and management implications. Herein, we present a case of secondary HLH as a complication of visceral leishmaniasis in a two-year-old toddler. A 2-year-old male toddler was admitted for evaluation of a prolonged 4-week fever.
View Article and Find Full Text PDFPediatric dacryolith masquerading as congenital nasolacrimal duct obstruction.
Am J Ophthalmol Case Rep
December 2024
Govindram Seksaria Institute of Dacryology, L.V. Prasad Eye Institute, Hyderabad, 34, India.
Purpose: To report a rare case of a pediatric dacryolith masquerading as congenital nasolacrimal duct obstruction (CNLDO).
Observations: A two-year-old male child presented with history of intermittent epiphora and discharge since the age of six months. Clinical evaluation demonstrated raised tear meniscus height and delayed fluorescein dye disappearance test in the right eye.
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