Results 21 to 30 of about 78,822 (240)

Preoperative Management of Pheochromocytoma and Paraganglioma

Frontiers in Endocrinology, 2020
Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine tumors, characterized by excessive release of catecholamines (CAs), and manifested as the classic triad of headaches, palpitations, profuse sweating, and a variety of other signs and ...
Fang Fang, Li Ding, Qing He, Ming Liu
semanticscholar   +1 more source

Pheochromocytomas and paragangliomas [PDF]

Current Opinion in Pediatrics, 2021
Purpose of review Great progress has been made in understanding the genetic and molecular basis of pheochromocytoma and paragangliomas (PPGLs). This review highlights the new standards in the diagnosis and management of pediatric PPGLs. Recent findings The vast majority of pediatric
Yen, Kevin, Lodish, Maya
openaire   +4 more sources

A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?

International Journal of Endocrinology, 2018
Pheochromocytoma is very rare at a pediatric age, and when it is present, the probability of a causative genetic mutation is high. Due to high costs of genetic surveys and an increasing number of genes associated with pheochromocytoma, a sequential ...
Bernardo Dias Pereira, Tiago Nunes da Silva, Ana Teresa Bernardo, Rui César, Henrique Vara Luiz, Karel Pacak, Luísa Mota-Vieira   +6 more
doaj   +1 more source

The importance of pheochromocytoma case detection in patients with neurofibromatosis type 1: A case report and review of literature

SAGE Open Medical Case Reports, 2017
Neurofibromatosis type 1 is a complex, multi-system genetic disorder that is associated with an increased prevalence of pheochromocytoma and paraganglioma compared to the general population, 1.0%–5.7% versus 0.2%–0.6%, respectively.
Joshua M Tate, Janelle B Gyorffy, Jeffrey A Colburn   +2 more
doaj   +1 more source

Early-Onset Isolated Bilateral Pheochromocytoma As a Major Clinical Manifestation of von-Hippel Lindau Syndrome Type 2C

Journal of Pediatric Research, 2018
Pheochromocytoma is a rare disease that is characterized by the increased production and secretion of catecholamines from the adrenal medulla. The disease is autosomal dominant, and frequently sporadic and unilateral. Pheochromocytoma, which is diagnosed
Sezer Acar, Hale Tuhan, Korcan Demir, Ayça Aykut, Asude Durmaz, Ünal Utku Karaarslan, Gözde İnci, Oğuz Ateş, Ece Böber, Ayhan Abacı   +9 more
doaj   +1 more source

Hereditary pheochromocytoma/paraganglioma syndrome with a novel mutation in the succinate dehydrogenase subunit B gene in a Japanese family: two case reports

Journal of Medical Case Reports, 2021
Background Pheochromocytoma and paraganglioma caused by succinate dehydrogenase gene mutations is called hereditary pheochromocytoma/paraganglioma syndrome.
Rei Hirose, Yuya Tsurutani, Chiho Sugisawa, Kosuke Inoue, Sachiko Suematsu, Maki Nagata, Naoki Hasegawa, Yukio Kakuta, Masato Yonamine, Kazuhiro Takekoshi, Noriko Kimura, Jun Saito, Tetsuo Nishikawa   +12 more
doaj   +1 more source

Silent Hypertensive Crisis in an Adolescent: First Case Report of Pediatric Pheochromocytoma from Indonesia

Global Pediatric Health, 2021
Secondary hypertension in children, to the rare extent, can be caused by endocrine factors such as pheochromocytoma, an adrenal tumor that secretes catecholamine. Only a few cases have been reported in the past 3 decades.
Cahyani Gita Ambarsari, Eka Laksmi Hidayati, Bambang Tridjaja, Chaidir Arif Mochtar, Haryanti Fauzia Wulandari, Agnes Stephanie Harahap, Angela Grace   +6 more
doaj   +1 more source

Effective treatment with mitotane for a canine case of Ectopic Cushing's syndrome-related pheochromocytoma.

Open Veterinary Journal, 2022
In humans, ectopic Cushing's syndrome (ECS) is characterized by hypercortisolemia, which is caused by small lung carcinoma, bronchial carcinoids, and pheochromocytoma.
Konatsu Miura, Hiroshi Sunahara, Yusuke Sakai   +2 more
doaj   +1 more source

Extra-adrenal pheochromocytoma with initial symptom of haemoptysis: a case report and review of literature

BMC Surgery, 2021
Background Pheochromocytoma is a catecholamine-secreting tumour that leads to various symptoms. Haemoptysis is rarely caused by a pheochromocytoma occurring outside the bronchus or thoracic cavity.
Yutaka Endo, Minoru Kitago, Masahiro Shinoda, Hiroshi Yagi, Yuta Abe, Shutaro Hori, Masanori Odaira, Takahiro Yokose, Kaori Kameyama, Yuko Kitagawa   +9 more
doaj   +1 more source

Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy

JAMA Network Open, 2019
Key Points Question Is cortical-sparing adrenalectomy associated with increased pheochromocytoma-specific morbidity and mortality for patients with bilateral pheochromocytomas compared with total adrenalectomy?
H. Neumann, U. Tsoy, I. Bancos, V. Amodru, M. Walz, Amit Tirosh, R. Kaur, T. Mckenzie, X. Qi, T. Bandgar, R. Petrov, M. Yukina, A. Roslyakova, A. V. D. van der Horst-Schrivers, Annika M. A. Berends, A. Hoff, L. A. Castroneves, A. M. Ferrara, S. Rizzati, C. Mian, S. Dvorakova, K. Hasse-Lazar, A. Kvachenyuk, M. Peczkowska, P. Loli, F. Erenler, T. Krauss, M. Almeida, Longfei Liu, Feizhou Zhu, M. Recasens, N. Wohllk, E. Corssmit, Zulfiya R. Shafigullina, J. Calissendorff, S. Grozinsky-Glasberg, T. Kunavisarut, C. Schalin-Jäntti, F. Castinetti, P. Vlček, D. Beltsevich, V. Egorov, F. Schiavi, T. Links, R. Lechan, B. Bausch, W. Young, C. Eng   +47 more
semanticscholar   +1 more source