Results 1 to 10 of about 45,090 (245)

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   +2 more sources

Metoclopramide‐Induced Pheochromocytoma Crisis: A Case Report and Literature Review [PDF]

Clinical Case Reports
Pheochromocytoma is a catecholamine‐secreting neuroendocrine tumor originating in the adrenal medulla. In patients with pheochromocytoma, paroxysmal over‐secretion of catecholamines can be triggered by various medications, including the commonly used ...
Yuki Yamanishi, Kazuki Iio, Keiki Shimizu, Wataru Kasahara, Jun Hamaguchi   +4 more
doaj   +2 more sources

Composite pheochromocytoma associated with neurofibromatosis type 1

IJU Case Reports, 2023
Introduction Composite pheochromocytoma is a rare tumor, occurring in only 3% of pheochromocytomas. We report a case of composite pheochromocytoma with neurofibromatosis type 1.
Akira Tachibana, Kota Iida, Yoshitaka Itami, Masaya Hashimura, Yukinari Hosokawa, Kiyohide Fujimoto   +5 more
doaj   +2 more sources

From Childhood Migraine Headache to Pheochromocytoma [PDF]

Case Reports in Endocrinology, 2014
Pheochromocytoma may have multiple clinical manifestations including paroxysmal hypertension, tachycardia, sweating, nausea, and headache (Phillips et al., 2002). Migraine has some of the manifestations seen with pheochromocytoma.
Y. M. Hazimeh, M. Luidens, M. E. Ehlers, V. Sharma   +3 more
doaj   +2 more sources

Anesthesia and Outcome of 33 Surgeries in 24 Multiple Endocrine Neoplasia Type 2A (MEN2A) Patients: A National Rare Disease Center’s Experience

Frontiers in Endocrinology, 2022
BackgroundMultiple endocrine neoplasia type 2A (MEN2A) is a rare syndrome that presents as medullary thyroid carcinoma, pheochromocytoma, and hyperparathyroidism.
Yaohan Li, Di Jin, Le Shen, Le Shen, Yuguang Huang, Yuguang Huang   +5 more
doaj   +1 more source

Progressive metastatic pheochromocytoma induced by multiple endocrine neoplasia type 2A with a lethal outcome

IJU Case Reports, 2022
Introduction Patients with multiple endocrine neoplasia type 2A (MEN2A) harboring a pathological variant in the RET gene are characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, and hyperparathyroidism.
Koshiro Nishimoto, Noriaki Lukas Santo, Masato Yonamine, Kazuhiro Takekoshi, Go Kaneko, Suguru Shirotake, Hisayo Fukushima, Yoshitaka Okada, Masanori Yasuda, Akihiro Sakurai, Masafumi Oyama, Kento Kanao   +11 more
doaj   +1 more source

Targeting heat shock protein 90 for the treatment of malignant pheochromocytoma. [PDF]

PLoS ONE, 2013
Metastatic pheochromocytoma represents one of the major clinical challenges in the field of neuroendocrine oncology. Recent molecular characterization of pheochromocytoma suggests new treatment options with targeted therapies.
Alessio Giubellino, Carole Sourbier, Min-Jung Lee, Brad Scroggins, Petra Bullova, Michael Landau, Weiwen Ying, Len Neckers, Jane B Trepel, Karel Pacak   +9 more
doaj   +1 more source

Global trends and current status in pheochromocytoma: a bibliometric analysis of publications in the last 20 years

Frontiers in Endocrinology, 2023
ObjectivePheochromocytoma is a rare catecholamine-producing neuroendocrine tumour originating from the chromaffin cells of the adrenal medulla or extra-adrenal paraganglia. However, there are few bibliometric studies on Pheochromocytoma.
Bi-ling Huang, Bi-ling Huang, Qi Liu, Qi Liu, Yuan-yuan Teng, Yuan-yuan Teng, Shu-qin Peng, Shu-qin Peng, Ze Liu, Ze Liu, Ming-liu Li, Ming-liu Li, Jie-yu Liang, Jie-yu Liang, Yi Zhang, Yi Zhang, Min Wang, Min Wang   +17 more
doaj   +1 more source

Comparison of pheochromocytoma-specific morbidity and mortality among adults with bilateral pheochromocytomas undergoing total adrenalectomy vs cortical-sparing adrenalectomy [PDF]

, 2019
Importance Large studies investigating long-term outcomes of patients with bilateral pheochromocytomas treated with either total or cortical-sparing adrenalectomies are needed to inform clinical management.Objective To determine the association of ...
Eng, Charis, International Bilateral-Pheochromocytoma-Registry Group, [Study group], Neumann, Hartmut P. H.   +2 more
core   +2 more sources

Pheochromocytoma with Takotsubo Syndrome and acute heart failure: a case report

World Journal of Surgical Oncology, 2022
Background Pheochromocytoma is a neuroendocrine tumor that can overproduce catecholamines. Heart failure and Takotsubo Syndrome (TTS) caused by excessive catecholamines are uncommon pheochromocytoma complications.
Lin Yang, Yiying Zhang, Yanqun Hu, Zhi Yang   +3 more
doaj   +1 more source