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HOME > Endocrinol Metab > Volume 25(3); 2010 > Article
Case Report A Case of Pheochromocytoma Presented with Cardiogenic Shock and Followed by Spontaneous Remission.
Jae Wook Kwak, Jong Sang Kim, Yun Jong Seo, Jae Hui Jang, Sun Hui Park, Hyo Heon Kim
Endocrinology and Metabolism 2010;25(3):236-239
DOI: https://doi.org/10.3803/EnM.2010.25.3.236
Published online: September 1, 2010
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1Department of Internal Medicine, Sahmyook-Seoul Hospital, Seoul, Korea. 1022p@hanmail.net
2Department of Radiology, Sahmyook-Seoul Hospital, Seoul, Korea.
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Abstract

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 extremely rare, but it can be lethal because of the dramatic change in the circulation such as an acute abdominal emergency or shock. Spontaneous remission of the clinical symptoms due to necrosis of the pheochromocytoma is rare. We describe such a case that presented with cardiogenic shock due to extensive necrosis of the pheochromocytoma and this was followed by spontaneous remission of the clinical symptoms without removal of the pheochromocytoma.

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