Results 21 to 30 of about 74,512 (199)

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

A rare case report of hypertrophic cardiomyopathy induced by catecholamine-producing tumor [PDF]

, 2018
RATIONALE: Catecholamine-producing tumors are rare, occurring in less than 0.2% of patients with hypertension, but can have relevant cardiovascular morbidity and mortality. PATIENT CONCERNS: A 37-year-old woman presented with a history of dyspnea, chest
Bisogni, Valeria, Bonvicini, Maria, Ciardi, Antonio, Concistré, Antonio, De Toma, Giorgio, Frustaci, Andrea, Iannucci, Gino, Letizia, Claudio, Mezzadri, Martina, Oliviero, Gaia, Olmati, Federica, Petramala, Luigi, Saracino, Vincenza   +12 more
core   +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

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

α-Toxin permeabilized rat pheochromocytoma cells [PDF]

, 1985
The channel forming α-toxin of Staphylococcus aureus (about 50 μg/ml) markedly reduces the Ca2+ requirement for dopamine release by the rat pheochromocytoma cell line (PC 12).
Baker, Bhakdi, Brooks, Dunn, Flodgaard, Füssle, Gratzl, Greene, Greene, Knight, Knight, Sillen, Wilson   +12 more
core   +1 more source

Giant cystic pheochromocytoma with low risk of malignancy: A case report and literature teview [PDF]

, 2017
Giant pheochromocytomas are rare silent entities that do not present with the classical symptoms commonly seen in catecholamine-secreting tumors. In many cases they are accidentally discovered.
Baijoo, Shanta, Greaves, Wesley, Harnanan, Dave, Maharaj, Ravi, Parbhu, Sangeeta, Ramcharan, Wesley, Warner, Wayne A   +6 more
core   +4 more sources

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

Millimolar concentrations of free magnesium enhance exocytosis from permeabilized rat pheochromocytoma (PC 12) cells [PDF]

, 1989
The role of Mg2+ during the final steps of exocytosis was investigated using rat pheochromocytoma cells (PC12) permeabilized with bacterial pore forming toxins.
Ahnert-Hilger, Ahnert-Hilger, Ahnert-Hilger, Ahnert-Hilger, Ahnert-Hilger, Ammann, Bader, Bhakdi, Bhakdi, Ekerdt, Flodgaard, Föhr, Gilman, Greene, Knight, Lind, Sillen, Simon   +17 more
core   +1 more source

A rare long-term undetected pheochromocytoma leading to Takotsubo syndrome in an older male patient: a case report

BMC Endocrine Disorders, 2020
Background Takotsubo syndrome is an uncommon, acute, and reversible cardiomyopathy that occurs primarily in postmenopausal females. The clinical presentation of the syndrome resembles acute coronary syndrome, but coronary angiography reveals no ...
Min Chen, Tong Zhao, Guoping Chen, Shenjiang Hu   +3 more
doaj   +1 more source