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Begumana Daniel

As seen in: Dove Medical Press
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Articles

Diagnosis and Management of Pheochromocytoma in Pregnancy: A Multidisciplinary Approach to Treatment and Outcomes at Mbarara Regional Referral Hospital: A Case Report

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By Mohamed EL Bashir, Begumana Daniel, Moses Anyit
| Dove Medical Press
Introduction Pheochromocytoma (PHEO) is a rare metastatic potential neuroendocrine tumor that arises from neural crest-derived tissue and belongs to the broader group of paragangliomas (PGLs).1 Paragangliomas are hormonally active tumors that secrete excess catecholamines such as norepinephrine, epinephrine, and dopamine, resulting in a spectrum of clinical symptoms.2 Although uncommon, PHEO can present during pregnancy, posing significant diagnostic and therapeutic challenges.
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