Results 61 to 70 of about 40,494 (191)

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, Vahideh Abarzadeh-Bairami, Seyyed-Reza Sadat-Ebrahimi   +2 more
doaj   +1 more source

Clinical Experiences of Pheochromocytoma in Korea [PDF]

, 2010
∙ The authors have no financial conflicts of interest. Purpose: We report herein 119 patients with pheochromocytoma at our institute over the last 23 years.
Adler, Amar, Brouwers, Cheol Kyu Oh, Chrisoulidou, Favia, Gimenez-Roqueplo, Goldstein, Ho Song Yu, Jae Seung Chung, Kasperlik-Zaluska, Kopetschke, Kwang Hyun Kim, La Batide-Alanore, Lee, Lenders, Lenders, Lo, Lucon, Mannelli, McNeil, Modlin, Neumann, Neumann, Pacak, Park, Pigny, Pruszczyk, Sawka, Sawka, Sidhu, Won Sik Ham, Won Tae Kim, Young Deuk Choi, Yun Byung Chae   +34 more
core   +3 more sources

Nerve growth factor nonresponsive pheochromocytoma cells: altered internalization results in signaling dysfunction. [PDF]

, 1992
Variant rat pheochromocytoma (PC12) cells which fail to respond to nerve growth factor (NGF) (PC12nnr5) (Green, S. H., R. E. Rydel, J. L. Connoly, and L. A. Greene. 1986. J. Cell Biol. 102:830-843) bind NGF at both high and low affinity sites.
Bradshaw, RA, Eveleth, DD
core  

Pheochromocytoma Crisis [PDF]

, 2017
Pheochromocytomas are rare tumours of the adrenal gland that secrete catecholamines. The classical presentation of these tumours consists of a clinical triad of headaches, palpitations and diaphoresis.
Castelino, Tanya, Mitmaker, Elliot
core   +2 more sources

Ocular muscle metastasis as the initial presentation of a malignant pheochromocytoma: A unique case

Clinical Case Reports, 2020
In this paper, we discuss a unique manifestation of malignant pheochromocytoma, which presented with ocular pain. The histopathological study pointed to a possible pheochromocytoma origin.
Gholamreza Khataminia, Abdolhasan Talaiezadeh, Ali Bagheri, Pedram Nazari, Amir Mohammad Papan, Nematollah Jazayeri, Roya Baghlani   +6 more
doaj   +1 more source

Effective treatment with mitotane for a canine case of presumed ectopic Cushing’s syndrome-related pheochromocytoma [PDF]

, 2022
Background: In humans, ectopic Cushing’s syndrome (ECS) is characterized by hypercortisolemia, which is caused by small lung carcinoma, bronchial carcinoids, and pheochromocytoma.
Hasegawa, Moe, Isshiki, Saneyuki, Miura, Konatsu, Oda, Mayumi, Sakai, Yusuke, Sunahara, Hiroshi   +5 more
core   +1 more source

Metabolic Regulation of Epithelial to Mesenchymal Transition: Implications for Endocrine Cancer [PDF]

, 2019
York University ...
Bhattacharya, Debasmita, Scimè, Anthony
core   +1 more source

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  

A comparative analysis of surgically excised hereditary and sporadic pheochromocytomas: Insights from a single‐center experience

Kaohsiung Journal of Medical Sciences
Pheochromocytoma 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, Muzaffer Serdar Deniz, Belma Ozlem Tural Balsak, Yilmaz Aslan, Altug Tuncel, Dilek Berker   +5 more
doaj   +1 more source

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