Renal hilar pheochromocytoma: A case report

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Abstract

Paraganglioma is a rare tumor arising from undifferentiated cells of the primitive neural crest. These tumors are most commonly found in the adrenal gland, other localisations are also possible. A 58-year-old woman who presented with history of left lumbar pain, headache, hypertension, palpitation and sweating was found to have a secreting left renal hilar pheochromocytoma. Radical excision of the tumor was therefore undertaken and her hypertension was controlled. From the case report and literature review, the authors suggest a diagnostic and therapeutic strategy for the management of ectopic localization of pheochromocytoma. © 2009 Ahallal et al; licensee Cases Network Ltd.

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Ahallal, Y., Tazi, M. F., Elfatemi, H., Znati, K., Tazi, E., Amarti, A., … Moulay, H. F. M. H. (2009). Renal hilar pheochromocytoma: A case report. Cases Journal, 2(6). https://doi.org/10.4076/1757-1626-2-6416

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