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Aortic Sarcoma with Solitary Metastasis to the Right Suprarenal Region Mimicking Pheochromocytoma

Case Report and Literature Review

Department of Surgery, The University of Hong Kong

K.Y. Lam

Department of Pathology, The University of Hong Kong, Queen Mary Hospital, Hong Kong

S.W.K. Cheng

Department of Surgery, The University of Hong Kong

Primary tumor of the aorta is extremely rare. The authors report a case of primary aortic sarcoma presenting with a solitary metastasis to the right suprarenal region and malignant hypertension, mimicking pheochromocytoma, with a review of the literature on this topic.

Vascular and Endovascular Surgery, Vol. 31, No. 2, 205-213 (1997)
DOI: 10.1177/153857449703100215


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