Gotowe bibliografie tematyczne / Catecholamine-secreting tumor

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Gotowa bibliografia na temat „Catecholamine-secreting tumor”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Catecholamine-secreting tumor"

Ueda, Teruyuki, Kazuaki Shimizu, Hiroshi Takakuwa, et al. "A catecholamine-secreting glomus jugular tumor." Nihon Naika Gakkai Zasshi 91, no. 2 (2002): 731–33. http://dx.doi.org/10.2169/naika.91.731.

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Rastogi,, Amit, Vansh Priya,, Paurush Ambesh,, and Vertika Sachan. "Glomus Jugulare Tumor: Selective Catecholamine Screening – A Golden Miss?" World Journal of Endocrine Surgery 9, no. 2 (2017): 65–67. http://dx.doi.org/10.5005/jp-journals-10002-1213.

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Streszczenie:

ABSTRACT Glomus jugulare tumor is a type of paraganglioma which has an association with catecholamine secretion but only in < 5% of cases. Any such occult or undetected catecholamine-secreting tumor poses anesthetic challenges in the perioperative period. A routine catecholamine assay and rigorous hemodynamic monitoring in such cases minimize perioperative anesthetic complications. How to cite this article Rastogi A, Priya V, Ambesh P, Sachan V. Glomus Jugulare Tumor: Selective Catecholamine Screening – A Golden Miss? World J Endoc Surg 2017;9(2):65-67.

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Simpson, Lauren N., Betsy D. Hughes, Isaac O. Karikari, et al. "Catecholamine-Secreting Paraganglioma of the Thoracic Spinal Column." Neurosurgery 70, no. 4 (2011): E1049—E1052. http://dx.doi.org/10.1227/neu.0b013e31822e5aae.

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Abstract BACKGROUND AND IMPORTANCE: Paragangliomas are rare tumors of neuroendocrine origin that arise from paraganglionic tissue of the extrachromaffin cell system. These lesions may be seen at various sites along the neuraxis. Primary thoracic paragangliomas have rarely been reported in the literature, with secretory thoracic lesions being exceedingly rare as only 3 previous cases have been cited. CLINICAL PRESENTATION: A 49-year-old woman presented with episodes of hypertension, palpitations, and diaphoresis. Workup revealed positive urine catecholamines and a thoracic spine mass extending

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Matishak, Mark Z., Lindsay Symon, Anthony Cheeseman, and Roger Pamphlett. "Catecholamine-secreting paragangliomas of the base of the skull." Journal of Neurosurgery 66, no. 4 (1987): 604–8. http://dx.doi.org/10.3171/jns.1987.66.4.0604.

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✓ Two cases of catecholamine-secreting paragangliomas of the base of the skull are described. The patients presented with uncontrollable hypertension and, after investigation, tumors were discovered in the regions of the glomus jugulare and pterygopalatine ganglion, respectively. After cardiovascular stabilization and tumor embolization, the tumors were surgically removed, with subsequent resolution of hypertension. The incidence of these tumors is discussed.

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Schwaber, Mitchell K., Gerald S. Gussack, and Wanda Kirkpatrick. "The Role of Radiation Therapy in the Management of Catecholamine-Secreting Glomus Tumors." Otolaryngology–Head and Neck Surgery 98, no. 2 (1988): 150–54. http://dx.doi.org/10.1177/019459988809800209.

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The major source of controversy that surrounds the use of radiation for glomus tumors is the finding of persistent chief cells years after completion of the treatment. Questions have been raised as to the viability of the irradiated chief cell and its capacity to proliferate. The radiotherapists consider a stable glomus tumor a radiation “cure,” whereas skull base surgeons are fearful that these lesions will continue to slowly grow and cause problems 20 to 30 years later. We have recently managed a patient who was not a candidate for surgery, with a catecholamine-secreting glomus jugulare tumo

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NAKAMIZO, MUNENAGA, SHIN-ETSU KAMATA, MASAOKI UCHIDA, MIYUKI YOKOTA, YUKITOSHI SATOH, and HAJIME ARAMAKI. "Case report of a catecholamine-secreting carotid body tumor." Nippon Jibiinkoka Gakkai Kaiho 92, no. 2 (1989): 246–52. http://dx.doi.org/10.3950/jibiinkoka.92.246.

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Inci, Servet, and Vural Bertan. "Catecholamine-secreting carotid body tumor and intracranial aneurysm: coincidence?" Surgical Neurology 53, no. 5 (2000): 488–92. http://dx.doi.org/10.1016/s0090-3019(00)00226-3.

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Dusitkasem, Sasima, Blair H. Herndon, Dalton Paluzzi, Joseph Kuhn, Robert H. Small, and John C. Coffman. "From Bad to Worse: Paraganglioma Diagnosis during Induction of Labor for Coexisting Preeclampsia." Case Reports in Anesthesiology 2017 (2017): 1–5. http://dx.doi.org/10.1155/2017/5495808.

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Pheochromocytomas and extra-adrenal paragangliomas are catecholamine-secreting tumors that rarely occur in pregnancy. The diagnosis of these tumors in pregnancy can be challenging given that many of the signs and symptoms are commonly attributed to preeclampsia or other more common diagnoses. Early diagnosis and appropriate management are essential in optimizing maternal and fetal outcomes. We report a rare case of a catecholamine-secreting tumor in which diagnosis occurring at the time labor was being induced for concomitant preeclampsia with severe features. Her initial presentation in hyper

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Patil, Nanda, Shubhang Monpara, and Pranjal Shah. "Adrenal Pheochromocytoma - A Case Presentation with Review of Literature." International Journal of Health Sciences and Research 12, no. 8 (2022): 118–21. http://dx.doi.org/10.52403/ijhsr.20220817.

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Pheochromocytoma is a rare catecholamine secreting tumor which arises from adrenal medulla and extra-adrenal sites. Its clinical presentation is sustained or intermittent hypertension often with paroxysmal symptoms. Imaging studies and estimation of catecholamines and metanephrine in a 24 hours urine sample helps to arrive at definite diagnosis. Correct diagnosis is very important because resection of tumor dramatically reverses clinical symptoms. We present a case of adrenal pheochromocytoma in a 34-year-old female patient to highlight its rarity, clinical presentation and histopathological f

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TAKAOKA, Seiji, Sumio AMAGASA, Hideo HORIKAWA, Yoshihide MIURA, and Katsuya YAMAGUCHI. "Anesthetic Management for a Patient with Undiagnosed Catecholamine-secreting Tumor." JOURNAL OF JAPAN SOCIETY FOR CLINICAL ANESTHESIA 14, no. 1 (1994): 54–58. http://dx.doi.org/10.2199/jjsca.14.54.

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Książki na temat "Catecholamine-secreting tumor"

Liu, Yang. Perioperative Management of Pheochromocytoma. Edited by Erin S. Williams, Olutoyin A. Olutoye, Catherine P. Seipel, and Titilopemi A. O. Aina. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190678333.003.0044.

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Pheochromocytomas are rare neuroendocrine tumors that arise from catecholamine producing cells in the adrenal glands. In the pediatric population, catecholamine-secreting tumors typically present around ages 11 and 12 and occur in 0.8% to 1.7% of hypertensive children. Pheochromocytomas represent significant management challenges to the anesthesiologist, particularly when undiagnosed. Many different anesthetic techniques and various antihypertensive agents have been successfully used to attenuate the intraoperative variations in blood pressure. After resection, periodic follow-up is highly rec

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Części książek na temat "Catecholamine-secreting tumor"

Mehta, Mansi, Alice Kit-wah Lee, and Kenneth Howell Hupart. "Catecholamine Secreting Tumor Presenting With Stroke." In The Endocrine Society's 95th Annual Meeting and Expo, June 15–18, 2013 - San Francisco. The Endocrine Society, 2013. http://dx.doi.org/10.1210/endo-meetings.2013.ahpaa.11.mon-81.

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Trikha, Anjan, and Manpreet Kaur. "Anaesthesia for Catecholamine-Secreting Glomus Jugulare Tumor Resection." In Anaesthesia for Uncommon and Emerging Procedures. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-64739-1_32.

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"Pheochromocytoma (Catecholamine-Secreting Tumor)." In Metabolic and Endocrine Physiology. Teton NewMedia, 2012. http://dx.doi.org/10.1201/b16175-38.

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Young, William, and Irina Bancos. "Huge Catecholamine-Secreting Tumor." In Adrenal Disorders. Elsevier, 2023. http://dx.doi.org/10.1016/b978-0-323-79285-1.00037-6.

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Hasani-Ranjbar, Shirin, Azadeh Ebrahim-Habibi, and Bagher Larijani. "Familial Catecholamine-Secreting Tumors - Three Distinct Families with Hereditary Pheochromocytoma." In Pheochromocytoma - A New View of the Old Problem. InTech, 2011. http://dx.doi.org/10.5772/27305.

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