Paraganglioma in pregnancy, a mimic of preeclampsia: a case report

Abstract Background The new presentation of pheochromocytoma or paraganglioma in pregnancy is very rare and can be life-threatening for mother and child. Case presentation We present the case of a 26-year-old gravida 3 para 2 otherwise healthy Caucasian woman at 34 weeks gestation who presented with...

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Main Authors: Michelle D. Lundholm, Jessica Marquard, Pratibha PR Rao
Format: Article
Language:English
Published: BMC 2023-04-01
Series:Journal of Medical Case Reports
Subjects:
Online Access:https://doi.org/10.1186/s13256-023-03871-8
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author Michelle D. Lundholm
Jessica Marquard
Pratibha PR Rao
author_facet Michelle D. Lundholm
Jessica Marquard
Pratibha PR Rao
author_sort Michelle D. Lundholm
collection DOAJ
description Abstract Background The new presentation of pheochromocytoma or paraganglioma in pregnancy is very rare and can be life-threatening for mother and child. Case presentation We present the case of a 26-year-old gravida 3 para 2 otherwise healthy Caucasian woman at 34 weeks gestation who presented with new onset hypertension associated with headaches, dry heaves, diaphoresis, and palpitations. She was initially diagnosed with preeclampsia and treated with labetalol and an urgent cesarean section, delivering a healthy baby girl. The diagnosis of preeclampsia came into question when, 6 weeks postpartum, she continued to have hypertension with atypical features. Testing revealed metastatic paraganglioma associated with a succinate dehydrogenase B gene mutation. The patient was then started on alpha-adrenergic blockade and has had close blood pressure monitoring while discussion of advances therapies is ongoing. Conclusion This case demonstrates how paraganglioma/pheochromocytoma can be misdiagnosed as preeclampsia due to the overlapping features of new-onset hypertension late in pregnancy accompanied by headache and proteinuria. It is impractical to routinely screen for paraganglioma/pheochromocytoma in all pregnant patients diagnosed with preeclampsia due to the rarity of these tumors and the harm from high false-positive rates. Therefore, it is incumbent on the provider to have a high degree of suspicion for paraganglioma/pheochromocytoma when clinical features are unusual for preeclampsia, such as intermittent palpitations, diaphoresis, orthostatic hypotension, or hyperglycemia. Early detection of paraganglioma/pheochromocytoma with interventions to mitigate the risk of hypertensive crisis greatly reduce maternal and fetal mortality. Fortunately, our patient delivered a healthy baby and did not have any additional pregnancy complications despite the delay in her diagnosis.
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spelling doaj.art-6fd87081aacd485395c8a1c56334f2e42023-04-09T11:17:25ZengBMCJournal of Medical Case Reports1752-19472023-04-011711610.1186/s13256-023-03871-8Paraganglioma in pregnancy, a mimic of preeclampsia: a case reportMichelle D. Lundholm0Jessica Marquard1Pratibha PR Rao2Department of Endocrinology, Diabetes and Metabolism Cleveland ClinicCenter for Personalized Genetic Healthcare, Genomic Medicine Institute, Cleveland ClinicDepartment of Endocrinology, Diabetes and Metabolism Cleveland ClinicAbstract Background The new presentation of pheochromocytoma or paraganglioma in pregnancy is very rare and can be life-threatening for mother and child. Case presentation We present the case of a 26-year-old gravida 3 para 2 otherwise healthy Caucasian woman at 34 weeks gestation who presented with new onset hypertension associated with headaches, dry heaves, diaphoresis, and palpitations. She was initially diagnosed with preeclampsia and treated with labetalol and an urgent cesarean section, delivering a healthy baby girl. The diagnosis of preeclampsia came into question when, 6 weeks postpartum, she continued to have hypertension with atypical features. Testing revealed metastatic paraganglioma associated with a succinate dehydrogenase B gene mutation. The patient was then started on alpha-adrenergic blockade and has had close blood pressure monitoring while discussion of advances therapies is ongoing. Conclusion This case demonstrates how paraganglioma/pheochromocytoma can be misdiagnosed as preeclampsia due to the overlapping features of new-onset hypertension late in pregnancy accompanied by headache and proteinuria. It is impractical to routinely screen for paraganglioma/pheochromocytoma in all pregnant patients diagnosed with preeclampsia due to the rarity of these tumors and the harm from high false-positive rates. Therefore, it is incumbent on the provider to have a high degree of suspicion for paraganglioma/pheochromocytoma when clinical features are unusual for preeclampsia, such as intermittent palpitations, diaphoresis, orthostatic hypotension, or hyperglycemia. Early detection of paraganglioma/pheochromocytoma with interventions to mitigate the risk of hypertensive crisis greatly reduce maternal and fetal mortality. Fortunately, our patient delivered a healthy baby and did not have any additional pregnancy complications despite the delay in her diagnosis.https://doi.org/10.1186/s13256-023-03871-8ParagangliomaPheochromocytomaPregnancy careHypertensionCase report
spellingShingle Michelle D. Lundholm
Jessica Marquard
Pratibha PR Rao
Paraganglioma in pregnancy, a mimic of preeclampsia: a case report
Journal of Medical Case Reports
Paraganglioma
Pheochromocytoma
Pregnancy care
Hypertension
Case report
title Paraganglioma in pregnancy, a mimic of preeclampsia: a case report
title_full Paraganglioma in pregnancy, a mimic of preeclampsia: a case report
title_fullStr Paraganglioma in pregnancy, a mimic of preeclampsia: a case report
title_full_unstemmed Paraganglioma in pregnancy, a mimic of preeclampsia: a case report
title_short Paraganglioma in pregnancy, a mimic of preeclampsia: a case report
title_sort paraganglioma in pregnancy a mimic of preeclampsia a case report
topic Paraganglioma
Pheochromocytoma
Pregnancy care
Hypertension
Case report
url https://doi.org/10.1186/s13256-023-03871-8
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AT pratibhaprrao paragangliomainpregnancyamimicofpreeclampsiaacasereport