Results 61 to 70 of about 48,572 (243)

Pheochromocytoma – An ECG diagnosis?

open access: yes, 2020
Pheochromocytoma is a rare catecholamine-secreting tumor in the adrenal medulla. In some cases, the first symptoms are cardiovascular. We report on two patients with pheochromocytoma, who both presented with bidirectional ventricular tachycardia (BDVT ...
Ljungström, Erik   +2 more
core   +1 more source

Research Trends and Mechanistic Insights Into Natural Medicines for Alzheimer's Disease: A Bibliometric Analysis and Narrative Review

open access: yesPhytotherapy Research, EarlyView.
Research landscape and mechanistic insights into natural medicines for Alzheimer's disease. ABSTRACT Natural medicines have been widely investigated for Alzheimer's disease (AD), but the development of this field and the relationship between bibliometric themes and experimental evidence remain insufficiently characterized.
Maoning Wang   +8 more
wiley   +1 more source

Bidirectional Ventricular Tachycardia due to Pheochromocytoma: A Case Report

open access: yesAnnals of Noninvasive Electrocardiology
Pheochromocytoma, a type of neuroendocrine tumor, can cause numerous symptoms and signs similar to those of other clinical conditions, with the classic triad being palpitations, headache, and diaphoresis.
Gui‐yang Li   +3 more
doaj   +1 more source

Epidemiologic Profile and Clinical Outcomes of Patients with Pheochromocytoma at the University of the Philippines - Philippine General Hospital (UP-PGH)

open access: yesJournal of the ASEAN Federation of Endocrine Societies
Objective. This study aims to describe the epidemiologic profile and determine the clinical outcomes of patients with pheochromocytoma at the University of the Philippines Philippine General Hospital (UP-PGH). Methodology.
Edrome Hernandez   +2 more
doaj   +1 more source

Recurrent malignant pheochromocytoma with lymph nodal metastasis in a child: A rare case

open access: yesJournal of Indian Association of Pediatric Surgeons, 2017
Malignant pheochromocytoma in children manifesting as local recurrence with multiple lymph nodal metastasis is a rare entity. We report a case of a 14-year-old child with recurrent sporadic malignant pheochromocytoma presenting 8 years after primary ...
Jayesh Mittal   +3 more
doaj   +1 more source

Functional urinary bladder paraganglioma in a child presenting with obstructive uropathy: A rare case report

open access: yesUroPrecision, EarlyView.
Abstract Background Pediatric urinary bladder paraganglioma is an exceptionally rare neuroendocrine tumor arising from chromaffin cells within the detrusor muscle. Due to its rarity and variable presentation, early diagnosis can be challenging, often requiring a high index of clinical suspicion and multimodal evaluation.
Shameer Tahir   +2 more
wiley   +1 more source

Pheochromocytoma [PDF]

open access: yesCancer, 1972
S, Warren, R N, Chute
openaire   +4 more sources

Malignant pheochromocytoma invading the ureteral wall muscle layer: A case report

open access: yesUrology Case Reports
Pheochromocytoma is a neuroendocrine tumor for which surgical resection is the main treatment.Malignant pheochromocytoma is very rare. Here,we present a case of adrenal pheochromocytoma invading the ureteral wall muscle layer, which resulted in left ...
Guang-Jie Li   +5 more
doaj   +1 more source

Giant cystic pheochromocytoma: A silent entity

open access: yesUrology Annals, 2016
Pheochromocytoma is a catecholamine secreting tumor that originate from chromaffin cells. Usually, it is solid neoplasm of the adrenal medulla, however cystic pheochromocytoma is a rare neuro-endocrine tumour that is frequently asymptomatic and often ...
Amit Gupta   +3 more
doaj   +1 more source

Feocromocitoma em crianças: relato de três casos [PDF]

open access: yes, 2011
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Amorim, Hugo Jefter Mendes de
core  

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