A Rare Case of Catecholamine-Secreting Adrenal Myelolipoma
Keywords:
adrenal myelolipoma, hypertension, nor-metanephrineAbstract
Adrenal myelolipoma (AML) is a rare, benign, asymptomatic, nonfunctioning tumor of the adrenal cortex detected incidentally. AML can be accompanied by several other endocrine disorders simultaneously. Here, we report a case of a 36-year-old woman with primary hypothyroidism and metabolic syndrome accompanied by severe hypertension and pheochromocytoma. However, histopathological examination of the excised adrenal gland confirmed myelolipoma. Following surgery, her plasma nor-metanephrine levels decreased to normal values and the patient became normotensive, which suggested that the mass was functioning.
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Copyright (c) 2025 Veenu Jain, Anshita Aggarwal, Bindu Kulshreshtha, Preeti Singh, Hemant Goel
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