Results 91 to 100 of about 6,532 (206)
Extra-adrenal pheochromocytoma (paraganglioma).
The authors describe the case of a 19-year-old female patient with an abdominal paraaortic extra-adrenal pheochromocytoma (paraganglioma), presenting arterial hypertension. The predominant catecholamine produced by the tumor was norepinephrine (4110 pg/ml; normal < 450 pg/ml).
M J, Correia +5 more
openaire +1 more source
Unilateral and Bilateral Adrenalectomy for Pheochromocytoma Requires Adjustment of Urinary and Plasma Metanephrine Reference Ranges [PDF]
Context: Follow-up after adrenalectomy for pheochromocytoma is recommended because of a recurrence risk. During follow-up, plasma and/or urinary metanephrine (MN) and normetanephrine (NMN) are interpreted using reference ranges obtained in healthy ...
de Jong, Wilhelmina H. A. +8 more
core +2 more sources
Paraganglioma of the thyroid gland: A case report [PDF]
Introduction. Thyroid paraganglioma is a very rare malignant neuroendocrine tumor. Immunohistochemical features of thyroid paraganglioma are helpful for the diagnosis. Case report.
Filipović Aleksandar +2 more
core +1 more source
Extra adrenal retroperitoneal paraganglioma.
We herein report a case of a 45-year-old Saudi lady not diabetic nor hypertensive who presented to the emergency room with a one day history of severe central and lower abdominal pain. On examination, she was hemodynamically stable and abdominal examination showed tenderness in the lower abdomen.
Hayan A, Bismar, Khalid R, Murshid
openaire +1 more source
Retroperitoneal extra-adrenal paraganglioma: case report
Paraganglioma (PG), also known as extra-adrenal pheochromocytoma, is a rare neuroectodermal tumor. The incidence of extra-adrenal paraganglioma is between 00.1-0.1%. Paragangliomas originating from the retroperitoneum are generally functional. 40-50% of them are malignant and they generally have a slow progression.
Gundes, Ebubekir +3 more
openaire +2 more sources
Neuroendocrine Tumors (NETs) : A population-based study of incidence and survival in Girona province, 1994-2004 [PDF]
Els tumors neuroendocrins (TNEs) són un grup de neoplàsies poc freqüents i heterogènies i amb un ampli espectre d'agressivitat. Hi ha molt poca informació epidemiològica a nivell mundial, l'objectiu d'aquest estudi ha estat el de reportar-ne les dades a ...
Alsina Maqueda, Maria +3 more
core
Cytomorphologic spectrum in aspirates of extra-adrenal paraganglioma
Paraganglioma is a rare tumor arising from clusters of neuroendocrine cells in association with sympathetic and parasympathetic nervous system. It poses a diagnostic challenge because of its widespread anatomic distribution, subtle clinical manifestations, and a variety of morphologic patterns.The aim of this study is to have an insight into the ...
Uma Handa, Reetu Kundu, Harsh Mohan
openaire +3 more sources
Delayed Paraganglioma Diagnosis: A Case Report and Literature Update
Paragangliomas are rare catecholamine secreting neuroendocrine tumors arising from extra-adrenal autonomic ganglia. Almost all sympathetic paragangliomas secrete norepinephrine and present with hypertension, headache, sweating, and tachycardia episodes ...
Şamil Ecirli +5 more
doaj +1 more source
Ultrasonography of the Adrenal Gland [PDF]
With appropriate techniques and using liver, spleen or kidney as an acoustic window, normal adrenal gland and adrenal lesions can be delineated by ultrasonography. The right adrenal gland is usually evaluated by transverse oblique scans and coronal scans,
Brandsma, Rick +5 more
core +1 more source
Gastric paraganglioma: a case report and review of literature
Paragangliomas (PGLs) are rare neuroendocrine tumors which overproduce catecholamines (CAs). They are extra-adrenal, catecholamine-secreting tumors occurring outside the adrenal glands.
Chengyu Hu +8 more
doaj +1 more source

