Extra-adrenal Pheochromocytoma in the Organ of Zuckerkandl: Diagnosis and Treatment Strategies

 

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Abstract

Pheochromocytoma (PHEO) and paraganglioma (PGL) are rare catecholamine-secreting neuroendocrine tumors arising from chromaffin tissue and can occur within the adrenal medulla (PHEO) or extra-adrenal sites (PGL). The most common site for PGL is the organ of Zuckerkandl, extra-adrenal chromaffin tissue near the origin of the inferior mesenteric artery.We here present 2 patients with extra-adrenal PGL in the organ of Zuckerkandl, located by iodine-123-metaiodobenzylguanadine (¹²³I-MIBG) scintigraphy and thereafter treated surgically or with iodine-131-metaiodobenzylguanadine (¹³¹I-MIBG). First, in a 15-year-old boy with clinical suspicion of PHEO, the diagnosis was established by biochemical evaluation and confirmed by further imaging studies, including CT and ¹²³I-MIBG, as PGL in the Zuckerkandl organ. The tumor was completely resected by laparotomy. Second, in a 70-year-old woman presenting with progressive hypertension and palpitations, MR and ¹²³I-MIBG revealed a singular tumor lesion with abnormal ¹²³I-MIBG uptake in the Zuckerkandl organ. Due to severe general vascular disease, surgery was not performed and instead the patient underwent ¹³¹I-MIBG therapy. The patient showed a good symptomatic response with improvement of symptoms and no relevant side-effects of therapy.

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Correspondence

D. KahramanMD 

Department of Nuclear

Medicine, University of Cologne

Kerpener Straße 62

50924 Köln

Phone: +49/221/478 4050

Fax: +49/221/478 6777

Email: deniz.kahraman@uk-koeln.de