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References Adler JT, Meyer-Rochow GY, Chen H, Benn DE, Robinson BG, Sippel RS, Sidhu SB. Pheochromocytoma: current approaches and future directions. Oncologist 13, 779–793, 2008. Ahlawat SK, Jain S, Kumari S, Varma S, Sharma BK. Pheochromocytoma associated with pregnancy: case report and review of the literature. Obstet Gynecol Surv 54, 728–737, 1999. Amar L, Baudin E, Burnichon N, Peyrard S, Silvera S, Bertherat J, Bertagna X, Schlumberger M, Jeunemaitre X, Gimenez-Roqueplo AP, Plouin PF. Succinate dehydrogenase B gene mutations predict

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Glucose Homeostasis in Patients with Pheochromocytoma

References 1. Diamanti-Kandarakis E, Zapanti E, Peridis MH, Ntavos P, Mastorakos G. Insulin resistance in pheochromocytoma improves more by surgical rather than by medical treatment. Hormones (Athens) 2: 61-66, 2003. 2. Turnbull DM, Johnston DG, Alberti KGMM, Hall R . Hormonal and metabolic studies in a patient with pheochromocytoma. J Clin Endocrinol Metab 51: 930-933, 1980. 3. Stenström G, Sjöström L, Smith U . Diabetes mellitus in pheochromocytoma: fasting blood glucose levels before and after

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Clipless laparoscopic adrenalectomy for pheochromocytoma

Pheochromocytoma (PCC) is an uncommon catecholamine-secreting neuroendocrine tumor originating from the adrenal medulla or from sympathetic ganglia chromaffin cells. Surgical removal is the only effective way to cure the disease, but this surgery carries a high risk of adverse cardiovascular events, visceral injuries, and intraoperative blood loss [ 1 , 2 ]. Currently, laparoscopic adrenalectomy is the criterion standard treatment of adrenal tumors, including PCC [ 3 ]. Compared with the open adrenalectomy, there is less pain, less blood loss, a shorter

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Pheochromocytoma, diagnosis and treatment: Review of the literature

References Adas M, Koc B, Adas G, Yalcin O, Celik S, Kemik O. Pitfalls in the diagnosis of pheochromocytoma: A case series and review of the literature. J Epidemiol Res 2, 49–55, 2016. Allolio B. Adrenal incidentalomas. In: Adrenal Disorders (Eds. Margioris AN, Chrousos GP), pp 249–261, Humana Press, Totowa, NJ, 2001. Amar L, Servais A, Gimenez-Roqueplo AP, Zinzindohoue F, Chatellier G, Plouin PF. Year of diagnosis, features at presentation, and risk of recurrence in patients with pheochromocytoma or secreting paraganglioma. J Clin Endocrinol

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Genetic and epigenetic differences of benign and malignant pheochromocytomas and paragangliomas (PPGLs)

, Giraud S, Murat A, Niccoli-Sire P, Richard S, Rohmer V, Sadoul JL, Strompf L, Schlumberger M, Bertagna X, Plouin PF, Jeunemaitre X, Gimenez-Roqueplo AP. Genetic testing in pheochromocytoma or functional paraganglioma. J Clin Oncol 23, 8812-8818, 2005. Amar L, Baudin E, Burnichon N, Peyrard S, Silvera S, Bertherat J, Bertagna X, Schlumberger M, Jeunemaitre X, Gimenez-Roqueplo AP, Plouin PF. Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas. J Clin Endocrinol Metab 92, 3822-3828, 2007

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Methods of Paraclinic Diagnosis of Catecholamine Secreting Tumours, Especially of Pheochromocytoma

Bibliography 1. Fliedner SMJ, Brabant G, Lehnert H. Pheochromocytoma and paraganglioma: genotype versus anatomic location as determinants of tumor phenotype. Cell Tissue Res. 2018 Jan 24. doi: 10.1007/s00441-017-2760-3. 2. Constantin Dumitrache. Endocrinologie clinica. Editura Naţional, 2012. pag 533-534. 3. Zuber SM, Kantorovich V, Pacak K. Hypertension in pheochromocytoma: characteristics and treatment. Endocrinol Metab Clin North Am. 2011;40(2):295-311. 4. Bausch B, Tischler AS, Schmid KW et al. Max Schottelius: Pioneer in

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Recommedition for Apllication and Determination Tumor Markers of Neuroendocrine System

-2011. Fischer-Cilbrie R, Hagn C, Kilpatric L, Winkler H. Chromogranin C: a third component of the acidic proteins in chromaffin granules. J Neurochem 1986; 47 : 318-324. Hagn C, Schmid KW, Fisher Colbrie R, Winkler H. Chromatogranin A, B and C in human adrenal medulla and endocrine tissues. Lab Invest 1986; 55 : 505-11. Schober M, Fischer-Cilbrie R, Schmid KW, Bussolati G, O'Connor DT Winkler H. Comparsion of chromogranins A, B and secretogranin II in human adrenal medulla and pheochromocytoma. Lab Invest 1987; 57

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Secondary Hypertension: Differential Diagnosis and Basic Principles of Treatment

. Primary aldosteronism: diagnostic and treatment strategies. Nat Clin Practice Nephrol 2006; 2(4):198-208. 28. Rossi GP. A comprehensive review of the clinical aspects of primary aldosteronism. Nat Rev Endocrinol 2011; 7(8):485-95. 29. Diederich S, Quinkler M, Morganti A, Bidlingmaier M. Endocirne Hypertension-Diagnosis and Treatment of Hormone-Induced Blood Pressure Disorders. Bremen: UNI-MED 2013: 12-87. 30. Pacak K, Eisenhofer G, Ahlman H, Bornstein SR, Gimenze- Roquelpo AP, Grossman AB, et al. Pheochromocytoma

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Transperitoneal laparoscopic adrenalectomy: a review and single-center experience

References 1. Gagner M, Lacroix A, Bolte E. Laparoscopic adrenalectomy in Cushing’s syndrome and pheochromocytoma. N Engl J Med. 1992; 327:1033. 2. Smith CD, Weber CJ, Amerson JR. Laparoscopic adrenalectomy: new gold standard. World J Surg. 1999; 23:389-96. 3. Terachi T, Matsuda T, Terai A, Ogawa O, Kakehi Y, Kawakita M, et al. Transperitoneal laparoscopic adrenalectomy: experience in 100 patients. J Endourol. 1997; 11:361-5. 4. Kulis T, Knezevic N, Pekez M, Kastelan D, Grkovic M, Kastelan Z

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Clinical Usefulness of 99mTc-HYNIC-TOC and 131I-MIBG Scintigraphy in the Evaluation of Adrenal Tumors

;171(1):201-4. 19. Rubello D, Bui C, Casara D, Gross MD, Fig LM, Shapiro B. Functional scintigraphy of the adrenal gland. Eur J Endocrin. 2002;147(1):13-28. 20. Avram AM, Fig LM, Gross MD. Adrenal gland scintigraphy. Semin Nucl Med. 2006 Jul;36(3):212-27. 21. Blanchet EM, Martucci V, Pacak K. Pheochromocytoma and paraganglioma: current functional and future molecular imaging. Front Oncol. 2012;1:58. 22. McDermott S, McCarthy CJ, Blake MA. Images of pheochromocytoma in adrenal glands. Gland surg. 2015;4(4):350. 23. Maurea S, Mainenti PP, Ponsiglione A

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