Tag: #SurgicalOncology
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Decoding Fibrothecal Tumors of the Ovary A Rare Yet Benign Ovarian Neoplasm
Introduction Fibrothecal tumors of the ovary represent a rare and diagnostically challenging entity in gynecological oncology. Affecting fewer than 4% of all ovarian tumors, these growths typically occur in post-menopausal women and often mimic malignant ovarian pathologies. In this insightful case report, researchers from the University Hospital Center Ibn Sina in Morocco present the clinical…
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Surgical Management of Extrahepatic Biliary Neuroendocrine Tumors A Rare Case Report
Introduction Extrahepatic biliary neuroendocrine tumors (EBNETs) are exceptionally rare neoplasms, with limited documented cases worldwide. These tumors often present diagnostic challenges due to their resemblance to more common biliary malignancies like cholangiocarcinoma. This article delves into a recently published case that highlights the surgical approach and clinical considerations for EBNETs. Visit https://www.clinmedcasereportsjournal.org/acr for more groundbreaking…
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Pediatric Dysgerminoma: Understanding a Rare Ovarian Tumor
Introduction Pediatric dysgerminoma is a rare malignant ovarian tumor, accounting for only 1%–2% of all ovarian cancers. Though most commonly seen in young women, its occurrence in pediatric patients is exceptionally rare. In this blog, we explore a unique case of pediatric dysgerminoma, shedding light on its clinical presentation, diagnosis, and treatment. For more groundbreaking…
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Malignant Transformation of an Urachal Cyst: A Rare Case Report
Introduction Malignant transformation of an urachal cyst is an exceptionally rare occurrence, representing less than 1% of all bladder cancers. This case study provides insights into the clinical presentation, diagnostic process, and surgical management of an affected patient. For more groundbreaking research in this field, visit ClinMed Case Reports Journal. Case Summary A 27-year-old male…
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