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A rare presentation of pheochromocytoma in pregnancy: a case report

BACKGROUND: Early diagnosis of pheochromocytoma and its proper management can lessen its mortality and morbidity. This case report describes a 24-year-old pregnant woman with an unusual presentation of pheochromocytoma. CASE PRESENTATION: An Iranian 24-year-old primigravid woman from Kordistan provi...

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Autores principales: Ghalandarpoor-Attar, Seyedeh Noushin, Ghalandarpoor-Attar, Seyedeh Mojgan, Borna, Sedigheh, Ghotbizadeh, Fahimeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806440/
https://www.ncbi.nlm.nih.gov/pubmed/29422092
http://dx.doi.org/10.1186/s13256-017-1549-z
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author Ghalandarpoor-Attar, Seyedeh Noushin
Ghalandarpoor-Attar, Seyedeh Mojgan
Borna, Sedigheh
Ghotbizadeh, Fahimeh
author_facet Ghalandarpoor-Attar, Seyedeh Noushin
Ghalandarpoor-Attar, Seyedeh Mojgan
Borna, Sedigheh
Ghotbizadeh, Fahimeh
author_sort Ghalandarpoor-Attar, Seyedeh Noushin
collection PubMed
description BACKGROUND: Early diagnosis of pheochromocytoma and its proper management can lessen its mortality and morbidity. This case report describes a 24-year-old pregnant woman with an unusual presentation of pheochromocytoma. CASE PRESENTATION: An Iranian 24-year-old primigravid woman from Kordistan province was referred to our center with left flank pain at 37 weeks of gestation. She had a history of gestational diabetes mellitus since the 12th week of gestation which was managed by insulin administration. She also had a history of pulsatile bi-temporal headache for 2 years prior to her referral to us. She underwent complete abdominal and pelvic ultrasound imaging for her flank pain. This examination revealed a heterogeneous mass of 119 × 87 × 79 mm above her left kidney, highly suspicious of being an adrenal-originating tumor. Subsequently, we consulted an endocrinologist. She underwent abdominopelvic magnetic resonance imaging and her 24-hour urine metanephrine, normetanephrine, and vanillylmandelic acid were assessed. Finally, the diagnosis of pheochromocytoma was confirmed. She underwent a cesarean section and adrenal mass excision at the 40th week of gestation. This timely diagnosis resulted in her proper management and good maternal and neonatal treatment outcomes. CONCLUSIONS: Our patient had pheochromocytoma during pregnancy. She had no complaints about hypertension before or during pregnancy until giving birth to her child; her only symptoms were a vague left flank pain, gestational diabetes, and headaches for the past 2 years. The unusual symptom of flank pain led to timely diagnosis and a good treatment outcome.
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spelling pubmed-58064402018-02-15 A rare presentation of pheochromocytoma in pregnancy: a case report Ghalandarpoor-Attar, Seyedeh Noushin Ghalandarpoor-Attar, Seyedeh Mojgan Borna, Sedigheh Ghotbizadeh, Fahimeh J Med Case Rep Case Report BACKGROUND: Early diagnosis of pheochromocytoma and its proper management can lessen its mortality and morbidity. This case report describes a 24-year-old pregnant woman with an unusual presentation of pheochromocytoma. CASE PRESENTATION: An Iranian 24-year-old primigravid woman from Kordistan province was referred to our center with left flank pain at 37 weeks of gestation. She had a history of gestational diabetes mellitus since the 12th week of gestation which was managed by insulin administration. She also had a history of pulsatile bi-temporal headache for 2 years prior to her referral to us. She underwent complete abdominal and pelvic ultrasound imaging for her flank pain. This examination revealed a heterogeneous mass of 119 × 87 × 79 mm above her left kidney, highly suspicious of being an adrenal-originating tumor. Subsequently, we consulted an endocrinologist. She underwent abdominopelvic magnetic resonance imaging and her 24-hour urine metanephrine, normetanephrine, and vanillylmandelic acid were assessed. Finally, the diagnosis of pheochromocytoma was confirmed. She underwent a cesarean section and adrenal mass excision at the 40th week of gestation. This timely diagnosis resulted in her proper management and good maternal and neonatal treatment outcomes. CONCLUSIONS: Our patient had pheochromocytoma during pregnancy. She had no complaints about hypertension before or during pregnancy until giving birth to her child; her only symptoms were a vague left flank pain, gestational diabetes, and headaches for the past 2 years. The unusual symptom of flank pain led to timely diagnosis and a good treatment outcome. BioMed Central 2018-02-09 /pmc/articles/PMC5806440/ /pubmed/29422092 http://dx.doi.org/10.1186/s13256-017-1549-z Text en © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Ghalandarpoor-Attar, Seyedeh Noushin
Ghalandarpoor-Attar, Seyedeh Mojgan
Borna, Sedigheh
Ghotbizadeh, Fahimeh
A rare presentation of pheochromocytoma in pregnancy: a case report
title A rare presentation of pheochromocytoma in pregnancy: a case report
title_full A rare presentation of pheochromocytoma in pregnancy: a case report
title_fullStr A rare presentation of pheochromocytoma in pregnancy: a case report
title_full_unstemmed A rare presentation of pheochromocytoma in pregnancy: a case report
title_short A rare presentation of pheochromocytoma in pregnancy: a case report
title_sort rare presentation of pheochromocytoma in pregnancy: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806440/
https://www.ncbi.nlm.nih.gov/pubmed/29422092
http://dx.doi.org/10.1186/s13256-017-1549-z
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