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Pheochromocytoma in Pregnancy

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A Case-Based Guide to Clinical Endocrinology

Abstract

Pheochromocytoma in pregnancy is a rare condition; however, its early diagnosis significantly decreases maternal and fetal mortality. Overall, diagnosis and treatment of pheochromocytoma are similar to that in the nonpregnant patient except for certain challenges and exceptions such as the following: Some imaging studies are contraindicated in pregnancy, surgery is only recommended during the second trimester, and the laparoscopic surgical approach is limited to transperitoneal/transabdominal. Biochemical diagnosis with plasma metanephrines and/or 24-hour urinary fractionated metanephrines and catecholamines have the same reference range in pregnancy as in the general nonpregnant population. The only imaging modality considered safe in pregnancy is MRI without gadolinium, while nuclear imaging is contraindicated. Adrenergic receptor blockers can be effective in pregnancy, and the benefits of using them outweigh the risks of not doing so. In instances where pheochromocytoma is diagnosed later than the second trimester of pregnancy, surgical excision of pheochromocytoma should be considered concomitantly with C-section or postpartum. Either C-section or vaginal delivery can be considered in pregnant women with pheochromocytoma based on individualized decision-making.

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Correspondence to Anand Vaidya .

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Vodopivec, D.M., Vaidya, A. (2022). Pheochromocytoma in Pregnancy. In: Davies, T.F. (eds) A Case-Based Guide to Clinical Endocrinology. Springer, Cham. https://doi.org/10.1007/978-3-030-84367-0_36

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  • DOI: https://doi.org/10.1007/978-3-030-84367-0_36

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