Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Vitaly Kantorovich"'
Autor:
Neelam Baral, MD, Rashika Bansal, MD, Binaya Basyal, MD, Wen Lee, MD, Kanchan Kulkarni, MD, Vitaly Kantorovich, MD, Meeta Sharma, MD
Publikováno v:
AACE Clinical Case Reports, Vol 7, Iss 1, Pp 43-46 (2021)
Objective: Many tumors can metastasize to the adrenal glands, making the diagnosis of adrenal masses challenging. Awareness that rare primary tumors can metastasize to the adrenals and consideration of biopsy for their diagnosis, sometimes at extra-a
Externí odkaz:
https://doaj.org/article/b9cc40758b2249e791749e1354dd4b97
Autor:
Vitaly Kantorovich, Karel Pacak
Publikováno v:
F1000Research, Vol 7 (2018)
Pheochromocytomas (PCCs) and paragangliomas (PGLs) are rare chromaffin cell tumors (PPGLs) that at times raise significant challenges in clinical recognition, diagnosis, and therapy and when undiagnosed could associate with severe morbidity. Recent d
Externí odkaz:
https://doaj.org/article/fbd76b853fbb4a36a49249b531fd0729
Publikováno v:
Journal of the Endocrine Society. 6:A564-A565
Background Arginine vasopressin (AVP) is a nonapeptide released from the neurohypophysis in response to increases in plasma osmolality, hypovolemia, hypotension, and angiotensin II. V2 receptors, expressed on the basolateral membrane of the renal col
Publikováno v:
Journal of the Endocrine Society. 6:A93-A94
Background Pheochromocytoma (PC) is a rare neuroendocrine tumor with an annual incidence of 2 to 8 cases per million that can secrete excess catecholamines precipitating hyper-adrenergic symptoms. In rarer instances, PCs can also secrete substances o
Publikováno v:
Journal of the Endocrine Society. 6:A573-A574
Background Ectopic Cushing's syndrome is associated with high morbidity and mortality rates and patients can rapidly decline if not intervened on earlier. We report a case of Ectopic Cushing's syndrome and highlight the challenges that were encounter
Publikováno v:
Journal of the Endocrine Society. 6:A520-A520
Pancreatic neuroendocrine tumors (PNETs) although rare, have recently increased in incidence . Clinically they can be classified as functional or nonfunctional depending on presence or absence of active hormone symptomatology and this has a bearing o
Autor:
Misbah Azmath, Vitaly Kantorovich
Publikováno v:
Journal of the Endocrine Society. 6:A899-A899
Introduction Insulinoma is a rare pancreatic neuroendocrine tumor (PNET) accounting for 1-2% of pancreatic neoplasms. Usually benign, even small tumors can cause significant morbidity due to hypoglycemia. Surgical resection is preferable choice of tr
Publikováno v:
Journal of the Endocrine Society. 6:A479-A479
ACTH-secreting pituitary adenomas account for about two-thirds of cases of endogenous Cushing's syndrome and are considered the most common cause of endogenous hypercortisolemia. Silent corticotroph adenomas (SCAs) are pituitary tumors that stain pos
Publikováno v:
Journal of the Endocrine Society. 6:A536-A536
Introduction Silent corticotroph adenomas (SCA) are an unusual and rare variant of non- functioning pituitary adenomas (NFA) that do not produce biochemical hypercortisolism or clinical Cushing's disease (CD), yet stain strongly for ACTH on immunohis
Autor:
Karel Pacak, Vitaly Kantorovich
Publikováno v:
Contemporary Endocrinology ISBN: 9783030674540
Endocrine Emergencies ISBN: 9781627036962
Endocrine Emergencies ISBN: 9781627036962
Hypertensive crisis caused by pheochromocytoma/paraganglioma-related hypercatecholaminemia represents true endocrine emergency and associates with significant morbidity. Although rare, it is associated with potentially devastating complications and s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e1fae723842a88f7e4e6dd55b6ef5ae
https://doi.org/10.1007/978-3-030-67455-7_14
https://doi.org/10.1007/978-3-030-67455-7_14