Malignant pheochromocytoma with ganglioneuroblastomatous elements in a patient with von recklinghausen's disease
- 15 June 1985
- Vol. 55 (12) , 2794-2798
- https://doi.org/10.1002/1097-0142(19850615)55:12<2794::aid-cncr2820551213>3.0.co;2-l
Abstract
A 14-year-old girl with numerous café-au-lait spots in her skin was hospitalized because of fever, weight loss, and a mass of the right upper quadrant of the abdomen. Despite intensive chemotherapy, she died 6 months after admission. The autopsy revealed a right adrenal tumor with metastases to liver, lungs, vertebrae, and lymph nodes. Histologically the tumor was a pheochromocytoma with small foci of ganglioneuroblastoma. The catecholamine contents of the tumor were markedly elevated, as confirmed by the catecholamine fluorescence technique. Electron microscopically, the tumor cells contained intracytoplasmic membrane-bound chromaffin granules of varying sizes and shapes. This may be the first report of the concomitant occurrence of malignant catecholamine-secreting pheochromocytoma with ganglioneuroblastomatous elements in a patient with von Recklinghausen's disease.This publication has 9 references indexed in Scilit:
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