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Pheochromocytoma Presenting as Partial HELLP Syndrome

Diagnosis of pheochromocytoma in partial HELLP syndrome is extremely rare. We report a case of a 25-year-old multigravida woman at 30 weeks of gestation who presented with clinical features consistent with partial HELLP syndrome. Her symptoms were not controlled by pharmacologic therapy, and the pat...

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Detalles Bibliográficos
Autores principales: Daaboul, Yazan, Korjian, Serge, Khalil, Lamis, Nemr, Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4553187/
https://www.ncbi.nlm.nih.gov/pubmed/26351602
http://dx.doi.org/10.1155/2015/294326
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author Daaboul, Yazan
Korjian, Serge
Khalil, Lamis
Nemr, Rita
author_facet Daaboul, Yazan
Korjian, Serge
Khalil, Lamis
Nemr, Rita
author_sort Daaboul, Yazan
collection PubMed
description Diagnosis of pheochromocytoma in partial HELLP syndrome is extremely rare. We report a case of a 25-year-old multigravida woman at 30 weeks of gestation who presented with clinical features consistent with partial HELLP syndrome. Her symptoms were not controlled by pharmacologic therapy, and the patient underwent urgent cesarean section. The patient gave birth to a viable baby, but she sustained an episode of ventricular fibrillation intraoperatively that did not result in any long-term sequelae. The patient's symptoms persisted postoperatively and work-up for secondary etiologies of hypertension demonstrated a right adrenal pheochromocytoma. Following resection, the patient's signs and symptoms resolved, and her lab tests normalized.
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spelling pubmed-45531872015-09-08 Pheochromocytoma Presenting as Partial HELLP Syndrome Daaboul, Yazan Korjian, Serge Khalil, Lamis Nemr, Rita Case Rep Obstet Gynecol Case Report Diagnosis of pheochromocytoma in partial HELLP syndrome is extremely rare. We report a case of a 25-year-old multigravida woman at 30 weeks of gestation who presented with clinical features consistent with partial HELLP syndrome. Her symptoms were not controlled by pharmacologic therapy, and the patient underwent urgent cesarean section. The patient gave birth to a viable baby, but she sustained an episode of ventricular fibrillation intraoperatively that did not result in any long-term sequelae. The patient's symptoms persisted postoperatively and work-up for secondary etiologies of hypertension demonstrated a right adrenal pheochromocytoma. Following resection, the patient's signs and symptoms resolved, and her lab tests normalized. Hindawi Publishing Corporation 2015 2015-08-16 /pmc/articles/PMC4553187/ /pubmed/26351602 http://dx.doi.org/10.1155/2015/294326 Text en Copyright © 2015 Yazan Daaboul et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Daaboul, Yazan
Korjian, Serge
Khalil, Lamis
Nemr, Rita
Pheochromocytoma Presenting as Partial HELLP Syndrome
title Pheochromocytoma Presenting as Partial HELLP Syndrome
title_full Pheochromocytoma Presenting as Partial HELLP Syndrome
title_fullStr Pheochromocytoma Presenting as Partial HELLP Syndrome
title_full_unstemmed Pheochromocytoma Presenting as Partial HELLP Syndrome
title_short Pheochromocytoma Presenting as Partial HELLP Syndrome
title_sort pheochromocytoma presenting as partial hellp syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4553187/
https://www.ncbi.nlm.nih.gov/pubmed/26351602
http://dx.doi.org/10.1155/2015/294326
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