- A Case of Malignant Pheochromocytoma
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Cho SR, Cheong SK, Chang SK
- KMID: 1677767
- Korean J Urol.
- 1977 Feb;18(1):53-57.
Pheochromocytoma is relatively uncommon disease that is mostly originated from adrenal medulla. Most of pheochromocytoma are benign, and malignant pheochromocytoma are very rate. A case of malignant pheochromocytoma from the... -
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- Two Cases of Pheochromocytoma
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Kwon HY, Yoon JB, Kim YG
- KMID: 1912467
- Korean J Urol.
- 1987 Jun;28(3):428-432.
Pheochromocytoma is one of surgically curable hypertensive syndromes. The tumor is bilateral or extra-adrenal in 5% of cases in adults and in an even greater percentage in children and is... -
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- Pheochromocytoma
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Lee KS, Goo GS
- KMID: 1940087
- J Korean Surg Soc.
- 1997 Nov;53(5):735-740.
No abstract availalbe. -
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- A Case of a Large Pheochromocytoma
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Kim BJ, Park YI, Min BK
- KMID: 1680696
- Korean J Urol.
- 1987 Dec;28(6):907-910.
Pheochromocytoma is one of the surgically curable hypertensive syndrome and may arise wherever chromaffin cells are located. A case of a left large adrenal pheochromocytoma developed in a 49 year... -
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- A Case of Nonfunctioning Cystic Pheochromocytoma
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Lee JM, Kim DH, Jeon YS, Kim MR, Park YH
- KMID: 2289274
- Korean J Urol.
- 1995 Dec;36(12):1399-1402.
Pheochromocytoma, derived from the neural crest, is one of the surgically curable hypertensive syndromes The clinical manifestations in patients with pheochromocytoma are highly variable. The vast majority are functioning tumors... -
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- Nonfunctioning Pheochromocytoma in an Elderly Patient: A Case Report
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Kwon HY, Yoon JB
- KMID: 2010617
- Korean J Urol.
- 1986 Aug;27(4):565-568.
This is a case report of a pheochromocytoma which developed in a 62-year-old woman. The diagnosis of a pheochromocytoma originating from the right adrenal gland was incidentally established rentgenologically. Transthoracic... -
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- A Case of Pheochromocytoma
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Youn CH, Rhee CK, Ahn MS, Cho SR
- KMID: 1912026
- Korean J Urol.
- 1984 Dec;25(6):795-798.
We report a case of left adrenal pheochromocytoma in 17-year-old girl, we observed all of vital sign were returned to normal in 19-th postoperative day -
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- A Case of Cystic Pheochromocytoma
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Oh MM, Jung CS, Myoung SC, Moon WC
- KMID: 2289684
- Korean J Urol.
- 1990 Oct;31(5):772-776.
Pheochromocytoma is a rare, but an important cause of surgically curable hypertension. Pheochromocytoma is a highly vascular tumor and not infrequently undergoes hemorrhagic necrosis and pseudocyst formation. Such cystic pheochromocytoma... -
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- A Case of Extra-adrenal Pheochromocytoma
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Jung CS, Park JT, Yoon YH, Kim SC, Nam SK
- KMID: 2060714
- Korean J Urol.
- 1997 Mar;38(3):315-318.
Pheochromocytoma is one of the surgically curable hypertensive diseases and can arise wherever chromaffin cells are located. Herein, a case of extra-adrenal pheochromocytoma developed in a 51 year-old male is... -
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- Pheochromocytoma and Renal Artery Stenosis
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Park JH, Chung JU, Kim SJ, Lee JS, Cho CK, Kim IW, Lim TH
- KMID: 1668799
- Korean Circ J.
- 1986 Sep;16(3):395-400.
- doi: 10.4070/kcj.1986.16.3.395
In hypertensive patients it is very important to detect renal artery stenosis or pheochromocytoma, since both diseases are curable causes of hypertension. However, renal artery stenosis can be induced by... -
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- Clinical evaluation of 12 cases of pheochromocytoma
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Lee YS, Oh KH
- KMID: 2289362
- Korean J Urol.
- 1993 Aug;34(4):619-625.
Between 1980 and 1991, we managed 12 cases of pheochromocytoma which consisted of 1 case of vesical pheochromocytoma, 1 case of malignant adrenal pheochromocytoma and 10 cases of benign adrenal... -
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- Pheochromocytoma of the urinary bladder
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Sung KT, Lee SK, Yoon JB
- KMID: 2060316
- Korean J Urol.
- 1991 Oct;32(5):829-835.
No abstract available. -
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- A Case of Pheochromocytoma of the Bladder
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Ahn TY, Chung SK, Han YT, Lee MC
- KMID: 1912314
- Korean J Urol.
- 1988 Oct;29(5):856-860.
Pheochromocytoma of the bladder is a rare tumor that often occurs with the symptoms complexes of micturitional attacks such as headache, palpitation and hypertension due to increased catecholamine secretion. Hereine... -
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- Primary Meningeal Pheochromocytoma: A Case Report
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Yoon IJ, Suh HS, Kim SN
- KMID: 2103852
- J Korean Radiol Soc.
- 2007 Apr;56(4):311-313.
- doi: 10.3348/jkrs.2007.56.4.311
Pheochromocytoma is a rare endocrine tumor arising from the chromaffin tissue, and it is able to produce and secrete catecholamines. Lymph nodes, liver, lung and bone are the most frequent... -
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- A Case of Pheochromocytoma Misdiagnosed as Activation of Behcet's Disease
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Kim YJ, Lee SY
- KMID: 1722648
- Korean J Med.
- 2013 Sep;85(3):334-337.
- doi: 10.3904/kjm.2013.85.3.334
A 30 year-old woman with a history of Behcet's disease was admitted to our clinic because of a paroxysmal attack of palpitations, headache, and ocular pain. Initially, we did not... -
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- Pheochromocytoma associated with cyanotic congenital heart disease
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Chung SJ, Lee YA, Shin CH, Yang SW, Bae EJ, Noh JI
- KMID: 1487166
- Korean J Pediatr.
- 2008 Jan;51(1):93-97.
- doi: 10.3345/kjp.2008.51.1.93
Pheochromocytoma is a rare tumor of childhood, arising from adrenal medullary and chromaffin tissue. Because chronic hypoxia may induce pheochromocytoma, there have been several reports of pheochromocytoma development in cyanotic... -
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- A Case of Pheochromocytoma
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Kim CM, Shim HY, Lee TY, Lee JG
- KMID: 1912213
- Korean J Urol.
- 1986 Apr;27(2):273-276.
Pheochromocytoma, derived from the neural crest, accounts for less than one percent of all patients with hypertension, but is most important because of its potentially lethal nature. It may occur... -
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- A Case of Pheochromocytoma Presented with Cardiogenic Shock and Followed by Spontaneous Remission
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Kwak JW, Kim JS, Seo YJ, Jang JH, Park SH, Kim HH
- KMID: 2169069
- Endocrinol Metab.
- 2010 Sep;25(3):236-239.
- doi: 10.3803/EnM.2010.25.3.236
Pheochromocytoma is derived from the chromaffin cells and patients with pheochromocytoma present with several signs and symptoms by producing, storing and secreting catecholamine. Spontaneous rupture or necrosis of pheochromocytoma is... -
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- A Case of Pheochromocytoma
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Cho HG, Rho YB, Ryu SB, Min BK
- KMID: 2114760
- Korean J Urol.
- 1984 Apr;25(2):215-218.
Pheochromcytomas are comparatively rare and arise wherever chromaffin cells are located Approximately 10-15% have been found outside the adrenal gland. A case of extra-adrenal pheochromocytoma which occurred in a 38-year-old... -
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- Early Detection and Successful Laparoscopic Adrenalectomy for Pheochromocytoma in Pregnancy; A Case Report
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Kim J
- KMID: 2316289
- Korean J Perinatol.
- 2016 Jun;27(2):118-121.
- doi: 10.14734/kjp.2016.27.2.118
Pheochromocytoma is an extremely rare tumor in pregnant women with potentially fatal consequences. We report a case of pregnant woman at 22 weeks of gestation with pheochromocytoma. A correct diagnosis... -
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