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Fumarate Hydratase-Deficient Renal Cell Carcinoma With Paraganglioma Detected on 18F-FDG PET/CT.
Clin Nucl Med
December 2024
Nuclear Medicine, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China.
We report FDG PET/CT findings of fumarate hydratase-deficient renal cell carcinoma coincidence with para-aortic paraganglioma in a 27-year-old man. He presented with painless gross hematuria for 3 days. CT identified an enhancing lesion in the left kidney, suggestive of a tumor.
View Article and Find Full Text PDFObstructive Jaundice Caused by Metastatic Neuroendocrine Tumor of the Ampulla of Vater in a Young Adult: A Case Report.
Case Rep Gastroenterol
April 2024
Department of Internal Medicine, Division of Gastroenterology, King Fahd Hospital of the University, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
Introduction: Ampullary neuroendocrine tumors (NETs) are usually diagnosed in the 5th-6th decades of life, and no cases were reported in <20 years of age. We report a rare case, presenting at a very young age, of well-differentiated NET involving the ampulla of Vater with lymph node metastasis.
Case Presentation: An 18-year-old man presented with a 3-month history of upper abdominal pain and jaundice.
An Atypical Presentation of Childhood Paraganglioma with Seizures: A Case Report and Review of the Literature.
Case Rep Endocrinol
November 2023
Neurology Unit, Department of Paediatrics, College of Medicine, University of Lagos, Lagos University Teaching Hospital, Lagos, Nigeria.
Introduction: A paraganglioma (PGL) is a tumour derived from extra-adrenal chromaffin cells of the sympathetic paravertebral ganglia of the thorax, abdomen, and pelvis. Cardiovascular manifestations predominate but neurological symptoms like seizures can occur requiring a high index of suspicion for prompt diagnosis and treatment. .
View Article and Find Full Text PDFPheochromocytoma and paraganglioma at a children's hospital in Argentina. A case series.
Arch Argent Pediatr
April 2024
Department of Endocrinology, Hospital General de Niños Ricardo Gutiérrez, City of Buenos Aires, Argentina.
Pheochromocytomas and paragangliomas are neuroendocrine tumors producing catecholamines. Pheochromocytomas occur in the adrenal medulla, while paragangliomas are those that occur outside the adrenal gland. Here we describe a case series of children with a pathological diagnosis of pheochromocytoma or paraganglioma who consulted at a tertiary care children's hospital in Argentina.
View Article and Find Full Text PDFFunctional retroperitoneal paraganglioma invading the inferior vena cava in the elderly, a case report and literature review.
Int J Surg Case Rep
August 2023
Department of Endocrinology-Diabetology and Nutrition, Mohammed VI University Hospital Center, Faculty of Medicine and Pharmacy, University of Mohammed 1st, Oujda, Morocco; Laboratory of Epidemiology, Clinical Research and Public Health, Faculty of Medicine and Pharmacy, University of Mohammed first, Oujda, Morocco. Electronic address:
Introduction And Importance: Phaeochromocytomas and paragangliomas are rare neuroendocrine neoplasms that grow outside the adrenal gland and arise from the primitive neural crest cells. The retroperitoneal location is extremely rare with an incidence of 2-8 per million.
Case Presentation: Here we report a case of an 80 years old man presenting with abdominal pain and vomiting associated with hypertensive peaks and weight loss.
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