Results 61 to 70 of about 45,090 (245)
Recurrent malignant pheochromocytoma with lymph nodal metastasis in a child: A rare case
Journal 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
Pheochromocytoma – An ECG diagnosis?
, 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
Effects of Tributyltin Chloride on Human Neuronal Differentiation and Mice Brain Development
Environmental Toxicology, EarlyView.ABSTRACT According to the developmental origins of health and disease hypothesis, perinatal exposure to an environmental toxicant during the development of the nervous system could cause a permanent cellular modification that may promote the appearance of neurodegenerative diseases at an older age.
Ester López‐Gallardo +10 more
wiley +1 more source
Malignant pheochromocytoma invading the ureteral wall muscle layer: A case report
Urology Case ReportsPheochromocytoma 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
Urology 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
UroPrecision, 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
Bidirectional Ventricular Tachycardia due to Pheochromocytoma: A Case Report
Annals of Noninvasive ElectrocardiologyPheochromocytoma, 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
A case of pheochromocytoma presenting with cardiac manifestation: case report
BMC Pediatrics, 2020 Background Pheochromocytomas are rare tumors originating in chromaffin cells which predominantly are located in adrenal glands. Sustained or paroxysmal hypertension (HT) is the most frequent sign of pheochromocytoma.
Akbar Molaei +2 more
doaj +1 more source
Kaohsiung Journal of Medical SciencesPheochromocytoma is a tumor that usually originating from adrenal medullary chromaffin cells and producing one or more catecholamines, can manifest as hereditary or sporadic.
Narin Nasiroglu Imga +5 more
doaj +1 more source
Management of bladder pheochromocytoma by transurethral resection
Asian Journal of Urology, 2019 Bladder pheochromocytoma is the most common extra-adrenal genitourinary tumor. Endoscopic management is feared due to the risk of intra-operative hypertensive crisis.
Aditya P. Sharma +5 more
doaj +1 more source