We report nasopharyngeal angiofibroma in a 13 year old boy treated with embolization, surgical excision and radiotherapy, which recurred 13 years later. No features of sarcomatous transformation were found, but the tumor had a locally aggressive course, possibly due to the HIV-posltivity of the patient who then died of AIDS. The relations between the clinical course of the tumor and severe immunodeficiency are discussed.
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3.
BasakisJ.G., KloppG.T., NewmanW.: Fibrosarcoma arising in a « juvenile » nasopharyngeal angiofibroma following extensive radiation therapy.Am. Surg., 21: 786–793, 1976.
ChenK.T.K., BauerF.W.: Sarcomatous transformation of nasopharyngeal angiofibroma.Cancer, 49: 369–371, 1982.
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EnzingerF.M., WeissS.W.: Soft Tissue Tumors, pp. 127–129. C.V. Mosby Comp., St. Louis, Washington DC, Toronto, 1988.
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PerkochaL.A., RodgersG.M.: Haematologic aspects of human immunodeficency virus infection: laboratory and clinical considerations.Am. J. Haematol., 29: 94–105, 1988.
