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A Case of Cystic Pheochromocytoma / 대한비뇨기과학회지
Korean Journal of Urology ; : 772-776, 1990.
Article in Korean | WPRIM (Western Pacific) | ID: wpr-44914
Responsible library: WPRO
ABSTRACT
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 may be accompanied by shock and sepsis and commonly invade adjacent organs, in which cases its diagnosis and management may be difficult. Herein we present a case of adrenal cystic pheochromocytoma which was accompanied by sepsis and hypertension and mimicked pararenal abscess with a review of literatures.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Pheochromocytoma / Shock / Sepsis / Diagnosis / Abscess / Hypertension / Necrosis Type of study: Diagnostic study Language: Korean Journal: Korean Journal of Urology Year: 1990 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Pheochromocytoma / Shock / Sepsis / Diagnosis / Abscess / Hypertension / Necrosis Type of study: Diagnostic study Language: Korean Journal: Korean Journal of Urology Year: 1990 Document type: Article
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