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Pheochromocytoma Complicated With Cardiomyopathy After Delivery: – A Case Report and Literature Review –

Pheochromocytoma in pregnancy is very rare but it is associated with very high maternal and fetal mortality. Therefore, it is important to include pheochromocytoma in the differential diagnosis of hypertension associated with pregnancy. It is difficult to make a diagnosis of pheochromocytoma in preg...

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Detalles Bibliográficos
Autores principales: Kim, Hyun-Joong, Kim, Duk-Kyung, Lee, Sang-Chul, Yang, Soon-Ha, Yang, Jung-Hyun, Lee, Won-Ro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531952/
https://www.ncbi.nlm.nih.gov/pubmed/9735667
http://dx.doi.org/10.3904/kjim.1998.13.2.117
Descripción
Sumario:Pheochromocytoma in pregnancy is very rare but it is associated with very high maternal and fetal mortality. Therefore, it is important to include pheochromocytoma in the differential diagnosis of hypertension associated with pregnancy. It is difficult to make a diagnosis of pheochromocytoma in pregnancy before delivery. The characteristic symptoms of pheochromocytoma could be initiated during delivery because the process of delivery, general anesthesia, fetal movement, induce acute surge of catecholamine release, which could also induce cardiomyopathy. Early diagnosis and intensive care can affect the prognosis of cardiomyopathy induced by pheochromocytoma. Proper management with alpha-blockade, beta-blockade and angiotensin converting enzyme inhibitor could acutely reverse the course of cardiomyopathy.