Results 81 to 90 of about 45,090 (245)

A Descriptive Evaluation of Evidence‐Based Rounds in Critical Care Using Mixed Data Types

Journal of Advanced Nursing, EarlyView.
ABSTRACT Objectives To pilot and evaluate the implementation of a structured Evidence‐Based Rounds (EBR) education model in critical care. Design A mixed data type design was used to evaluate Evidence‐Based Rounds in a critical care setting. Structured observational data were captured and open‐ended survey responses were submitted by attendees. Content
P. Yerbury, S. Sutherland, T. Venes, A. Nair, J. Ede   +4 more
wiley   +1 more source

PHEOCHROMOCYTOMA

Survey of Anesthesiology, 1976
In the 25-year period 1950-1975 forty-four patients with pheochromocytoma were observed at Vanderbilt University Affiliated Hospitals. Bilateral adrenal tumors occurred in 3 patients (6.8%) and extra-adrenal tumors occurred in 7 others (16%), 33 patients (75%) had single tumors arising in one of the adrenal glands; in one of these 5 years after ...
H W, Scott, J A, Oates, A S, Nies, H, Burko, D L, Page, R K, Rhamy   +5 more
openaire   +3 more sources

Pheochromocytoma

, 2023
Feokromocitom je rijedak neuroendokrini tumor koji nastaje iz kromafinih stanica srži nadbubrežne žlijezde. Feokromocitomi proizvode prekomjerne količine hormona, kateholamina, koji su inače bitni u regulaciji tjelesnih funkcija te uzrokuju sekundarnu ...
Španić, Matej
core   +2 more sources

A rare case of Ganglioneuroblastoma Encapsulated in Pheochromocytoma

Acta Medica, 2016
Pheochromocytoma and Ganglioneuroblastoma are separate diseases and a rare combination in which the diagnosis can only be confirmed by pathological examination after tumor excision.
Nathália Vieira Sousa, Luísa Coelho Marques de Oliveira, Paulo José Oliveira Cortez, Vitor Engrácia Valenti, David Mathew Garner, Dalmo Antônio Ribeiro Moreira   +5 more
doaj   +1 more source

Unexpected metastatic pheochromocytoma - an unusual presentation

, 2008
The classic triad of pheochromocytoma consists of episodic headache, sweating, and tachycardia. General clinicians should be aware, however, that this rare entity might present with a wide spectrum of clinical symptoms.
Stucki, Armin, Stanga, Zeno, Birrenbach, Tanja, Cottagnoud, Philippe   +3 more
core   +1 more source

BSAVA Petsavers Article: Validation of an ELISA assay for measurement of the metabolite of serotonin, 5‐hydroxyindole acetic acid (5‐HIAA), in canine urine

Journal of Small Animal Practice, EarlyView.
Objectives Serotonin (5‐hydroxytryptophan), implicated in a number of canine diseases, has a very short half‐life in the serum. Urine concentration of its breakdown product 5‐hydroxyindole acetic acid after an 8 hour fast is a more reliable measure of circulating serotonin in humans.
D. Castillo, A. Swallow, T. Williams, P. Watson   +3 more
wiley   +1 more source

Undiagnosed pheochromocytoma presenting as a pancreatic tumor: A case report

Open Medicine, 2020
Pheochromocytoma is a rare catecholamine-producing tumor of the adrenal gland. Patients with known pheochromocytoma undergoing surgery require preoperative treatment with alpha-blockers to reduce the risk of intraoperative complications related to ...
Legocka Malgorzata Emilia, Toutounchi Sadegh, Pogorzelski Ryszard, Krajewska Ewa, Celejewski Krzysztof, Galazka Zbigniew   +5 more
doaj   +1 more source

Feocromocitoma recidivante em gestação: relato de caso e revisão da literatura. [PDF]

, 1998
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Tocoginecologia, Curso de Medicina, Florianópolis ...
Alves, Daniela Salvador
core  

Pathologic Fracture as Primary Presentation of Malignant Pheochromocytoma: A Case Report

Acta Medica Iranica, 2019
Pheochromocytoma is a relatively rare tumor with no age preference. This tumor is usually diagnosed accidentally.  Pathologic fracture as the primary presentation of malignant pheochromocytoma is an uncommon presentation.
Azar Fanipakdel, Yasamin Davoudi, Seyed Alireza Javadinia, Mahdi Silanian Toosi   +3 more
doaj  

Bilateral pheochromocytoma with ganglioneuroma component associated with multiple neuroendocrine neoplasia type 2A: a case report

Journal of Medical Case Reports, 2017
Background Composite pheochromocytoma/paragangliomas are very rare tumors composed of ordinary pheochromocytoma paragangliomas associated with neurogenic tumors. Several hereditary susceptibility disorders are known to be associated with pheochromocytoma/
Boubacar Efared, Gabrielle Atsame-Ebang, Soufiane Tahirou, Khalid Mazaz, Nawal Hammas, Hinde El Fatemi, Laila Chbani   +6 more
doaj   +1 more source