A Pheochromocytoma with Liver Metastasis: What about Curative Surgery?
Choukri Elm’hadi, Meryem Zerrik, Yassir Benameur, Imad Taleb, Rachid Tanz
Journal of Advances in Medicine and Medical Research · pp. 17–22 · Published 8 Mar 2023
10.9734/jammr/2023/v35i74985Abstract
Introduction: 35% of pheochromocytomas are malignant and generally have a poor prognosis.Visceral metastases are associated with shorter survival. Treatments for advanced pheochromocytomas are essentially palliative. Surgery is potentially curative; however, tumor extension limits the chance for a curative resection. Case Presentation: A 21-year-old women presented to our hospital with severe hypertension associated with Ménard's triad and heaviness of the left flank.The abdominal CT scan discovered a left adrenal mass with liver metastases. The diagnosis of pheochromocytoma was confirmed biochemically by the elevated catecholamine and metanephrine levels in the blood and urine. After preparation by the alpha-adrenergic blockade, she underwent left adrenalectomy and resection of left liver metastases followed by right hepatectomy. A pathology examination was performed and the final report was a metastatic pheochromocytoma with negative margins. She was discharged on postoperative without complications, and no evidence of recurrence occurred 48 months postoperatively. Conclusion: complete resection of liver metastases from metastatic pheochromocytoma can improve survival and should also be considered in the event of predominant secreting symptoms.
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