A spontaneous paraganglioma-pheochromocytoma syndrome
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Updated: Apr 30, 2026

A Novel Method: Super-selective Adrenal Venous Sampling
Published on: September 15, 2017
Sadegh Toutounchi1, Ryszard Pogorzelski1, Maciej Siński2
1Clinic of General and Thoracic Surgery, Medical University of Warsaw, Warsaw, Poland.
Abstract:
We present a case of a 40-year old woman diagnosed with a four-place spontaneous paraganglioma-pheochromocytoma syndrome, which was treated surgically. The presence of the succinate dehydrogenase complex subunit D (SDHD) mutation that causes the pheochromocytoma was confirmed but no mutations in the family members were found. After the excision of the paragangliomas located in the areas of the division of carotid arteries, and mediastinum, as well as a tumor on the left site of the celiac trunk, the patient remains asymptomatic and is regularly followed-up.
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