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Adrenocortical carcinoma with cerebral metastasis in a child: case report and review of the literature
R L Romaguera1, A Minagar, J H Bruce
1Department of Pathology, University of Miami, Jackson Memorial Hospital, East Tower Room # 2142, 1611 NW 12th Ave., Miami, FL 33136, USA. rromague@med.miami.edu
Objective And Importance:
Adrenocortical carcinoma (ACC) is rare in the pediatric population, and brain metastasis seldom occurs.
Clinical Presentation:
The authors report a case of metastatic ACC to the brain in a 9-year-old patient who had an adrenal cortex neoplasm removed at 4 years of age, and was free of symptoms for 5 years. Two weeks before admission she complained of blurred vision in both eyes.
Intervention:
Examination revealed bilateral papilledema, and a Magnetic Resonance Imaging (MRI) of the brain revealed a mass in the left lateral ventricle with extensive vasogenic edema and hydrocephalus. The tumor was removed, and histopathologic examination demonstrated metastatic ACC.
Conclusion:
Although ACC is a rare neoplasm it must be considered in the differential diagnosis of cerebral lesions in patients with a history of this tumor. Periodic long-term brain imaging is suggested as part of the follow up in patients with adrenocortical neoplasms.
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