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[Familial pheochromocytoma: four cases in one kindred (author's transl)].
, 1977 Yoshinori Mori +4 more
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Current Treatment Options in Oncology, 2001
The only definitive therapy for patients with pheochromocytoma is surgical resection [1,2**]. Advances in preoperative medical management of hypertension/hypovolemia and improved intraoperative anesthetic care have reduced the operative mortality rate for pheochromocytoma to less than 5% in most series.
Quan-Yang Duh, Monica S. Eigelberger
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The only definitive therapy for patients with pheochromocytoma is surgical resection [1,2**]. Advances in preoperative medical management of hypertension/hypovolemia and improved intraoperative anesthetic care have reduced the operative mortality rate for pheochromocytoma to less than 5% in most series.
Quan-Yang Duh, Monica S. Eigelberger
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Current Treatment Options in Oncology, 2003
Pheochromocytoma is a rare tumor, but it represents a potentially curable form of hypertension. In patients with inherited pheochromocytoma, benign and bilateral tumors are more common. The diagnosis of pheochromocytoma rests in biochemical confirmation of catecholamine excess.
Lee C. Pederson, Jeffrey E. Lee
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Pheochromocytoma is a rare tumor, but it represents a potentially curable form of hypertension. In patients with inherited pheochromocytoma, benign and bilateral tumors are more common. The diagnosis of pheochromocytoma rests in biochemical confirmation of catecholamine excess.
Lee C. Pederson, Jeffrey E. Lee
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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
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Ultrastructural Pathology, 1991
The cytoplasmic granules in an adrenal pheochromocytoma were predominantly ovoid with loose-fitting limiting membranes and eccentrically positioned dense cores. The occurrence of similar granules in a recurrent tumor involving the organ of Zuckerkandl in a second patient suggests that the latter tumor should be designated an extraadrenal ...
R R, Gómez +3 more
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The cytoplasmic granules in an adrenal pheochromocytoma were predominantly ovoid with loose-fitting limiting membranes and eccentrically positioned dense cores. The occurrence of similar granules in a recurrent tumor involving the organ of Zuckerkandl in a second patient suggests that the latter tumor should be designated an extraadrenal ...
R R, Gómez +3 more
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Endocrinology and Metabolism Clinics of North America, 1994
None of the endocrine causes for hypertension is more fascinating and challenging for the clinician than pheochromocytoma. Its protean manifestations can make diagnosis difficult, yet its sinister prognostic implications demand prompt recognition and expert management.
R W, Gifford, W M, Manger, E L, Bravo
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None of the endocrine causes for hypertension is more fascinating and challenging for the clinician than pheochromocytoma. Its protean manifestations can make diagnosis difficult, yet its sinister prognostic implications demand prompt recognition and expert management.
R W, Gifford, W M, Manger, E L, Bravo
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Endocrine Practice, 1997
To characterize the symptoms associated with pheochromocytoma and discuss the diagnosis and management of this tumor.We review the clinical manifestations in patients with pheochromocytoma, the biochemical and imaging studies recommended for diagnosis and localization of the tumor, and the available strategies for treatment.Pheochromocytoma is a tumor ...
A, Mena, M, Lawson, U M, Kabadi
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To characterize the symptoms associated with pheochromocytoma and discuss the diagnosis and management of this tumor.We review the clinical manifestations in patients with pheochromocytoma, the biochemical and imaging studies recommended for diagnosis and localization of the tumor, and the available strategies for treatment.Pheochromocytoma is a tumor ...
A, Mena, M, Lawson, U M, Kabadi
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The American Journal of Surgery, 1980
Twenty surgical and two autopsy cases of pheochromocytoma are reviewed. Preoperative diagnoses were reliably determined by urinary catecholamine excretion studies in most cases. Arteriography and computed axial tomography were the most consistently useful studies in localization of tumor.
J F, Teply, G H, Lawrence
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Twenty surgical and two autopsy cases of pheochromocytoma are reviewed. Preoperative diagnoses were reliably determined by urinary catecholamine excretion studies in most cases. Arteriography and computed axial tomography were the most consistently useful studies in localization of tumor.
J F, Teply, G H, Lawrence
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Radiologic Clinics of North America, 1996
Pheochromocytomas are rare tumors that can pose problems in diagnosis and detection. Although they usually present with classic symptoms, they can at times present with symptoms that mimic other clinical conditions. This article discusses the various imaging tests that are used in pheochromocytoma detection and also outlines an imaging algorithm used ...
I R, Francis, M, Korobkin
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Pheochromocytomas are rare tumors that can pose problems in diagnosis and detection. Although they usually present with classic symptoms, they can at times present with symptoms that mimic other clinical conditions. This article discusses the various imaging tests that are used in pheochromocytoma detection and also outlines an imaging algorithm used ...
I R, Francis, M, Korobkin
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