Results 41 to 50 of about 7,071 (219)

Rare Association Between Neurofibromatosis Type 1 and Adrenocortical Carcinoma. [PDF]

Clin Case Rep
Axial slice CT abdomen pelvis with portal venous contrast, revealing a well circumscribed 22 × 20 × 22 mm left adrenocortical adenocarcinoma (ACC) in a patient with neurofibromatosis type 1 (NF1). ABSTRACT Although rare, adrenocortical carcinoma (ACC) should be considered in individuals with neurofibromatosis type 1 (NF1) presenting with adrenal ...
Pluim Z, Choi JDW, Kakala B, Wong J, Clifton-Bligh R, Sywak M, Howle J.   +6 more
europepmc   +2 more sources

An unusual and interesting case of phaeochromocytoma

Journal of Clinical and Scientific Research, 2020
Phaeochromocytomas are catecholamine-secreting tumours that arise from chromaffin cells of the adrenal medulla. The common age of onset is between the third and fifth decades of life.
Sravanthi Guduru, Harsha Mutthineni, Goveen Manda, Modugu Nageswara Rao   +3 more
doaj   +1 more source

Unilateral and Bilateral Adrenalectomy for Pheochromocytoma Requires Adjustment of Urinary and Plasma Metanephrine Reference Ranges [PDF]

, 2013
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., Dullaart, Robin P. F., Kema, Ido P., Kerstens, Michiel N., Links, Thera P., Osinga, Thamara E., Sluiter, Wim J., van den Eijnden, Maartje H. A., van der Horst-Schrivers, Anouk N. A.   +8 more
core   +2 more sources

Microchip electrophoresis bioanalytical applications [PDF]

, 2008
Microchip electrophoresis (MCE) is a novel analytical technique resulting from miniaturization of capillary electrophoresis (CE) to a planar microfabricated separation device.
Vlcková, Markéta
core   +1 more source

A retrospective study on the association between urine metanephrines and cardiometabolic risk in patients with nonfunctioning adrenal incidentaloma

Scientific Reports, 2022
Several studies argued that cardiovascular evaluation of patients with nonfunctioning adrenal incidentaloma is of particular importance. Therefore, we aimed to evaluate the possibility of stratifying the cardiometabolic risk using metanephrine levels in ...
Mirko Parasiliti-Caprino, Chiara Lopez, Martina Bollati, Fabio Bioletto, Chiara Sola, Maria Chiara Di Carlo, Federico Ponzetto, Iacopo Gesmundo, Fabio Settanni, Ezio Ghigo, Giulio Mengozzi, Mauro Maccario, Roberta Giordano   +12 more
doaj   +1 more source

Transient hypercortisolism and symptomatic hyperthyroidism associated to primary hyperparathyroidism in an elderly patient: case report and literature review. [PDF]

, 2015
Background: Primary hyperparathyroidism (PHPT) is often found on routine blood tests, at a relatively asymptomatic stage. However many studies suggest different systemic effects related to PHPT, which could be enhanced by an abnormal cortisol release due
Armanini, Decio, Bordin, Luciana, Camozzi, V, Don\ue0, G, Iacobone, Maurizio, Mian, Caterina, Sabbadin, Chiara   +6 more
core   +2 more sources

Contemporary capabilities of CT texture analysis in the diagnosis of pheochromocytoma: associations with clinical, laboratory, and pathomorphological findings

Терапевтический архив
Aim. To investigate the presence of statistically significant correlations between clinical and laboratory characteristics and features of contrast-enhanced computed tomography (CT) images, as well as to assess the possibility of predicting group ...
Natalia V. Tarbaeva, Almaz V. Manaev, Anastassia Chevais, Dmitry G. Beltsevich, Liliya S. Urusova, Aminat K. Ebzeeva, Anna A. Roslyakova, Galina A. Mel'nichenko, Natalia G. Mokrysheva   +8 more
doaj   +1 more source

Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report [PDF]

, 2017
BackgroundRecent advance of genetic testing has contributed to the diagnosis of hereditary pheochromocytoma and paraganglioma (PPGL). The clinical characteristics of hereditary PPGL are varying among the types of mutational genes.
Adachi Yayoi, Aita Yuichi, Inaishi Takahiro, Kikumori Toyone, Kodera Yasuhiro, Miyajima Noriyuki, Nakanishi Kenichi, Noda Sumiyo, Shibata Masahiro, Takano Yuko, Takekoshi Kazuhiro, Takeuchi Dai, 會田 雄一, 竹越 一博   +13 more
core   +2 more sources

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

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, Eisha Sattar, Javeria Khan   +2 more
wiley   +1 more source

Concurrent primary hyperparathyroidism and pheochromocytoma in a Chinese lady with neurofibromatosis type 1

Endocrinology, Diabetes & Metabolism Case Reports, 2018
We report a case of elderly Chinese lady with neurofibromatosis type-1 presenting with longstanding palpitation, paroxysmal hypertension and osteoporosis.
Cheuk-Lik Wong, Chun-Kit Fok, Vicki Ho-Kee Tam   +2 more
doaj   +1 more source