Primary Adrenocortical Carcinoma With Skull Metastasis Case Report and Review of the Literature

被引:0
作者
Bose, Bikash [1 ,2 ]
机构
[1] Christiana Care Hlth Syst, Dept Neurosurg, Newark, DE USA
[2] Thomas Jefferson Univ, Jefferson Med Coll, Dept Neurosurg, Philadelphia, PA 19107 USA
关键词
primary adrenocortical carcinoma; skull metastasis; neoplasm; ADRENAL-CORTICAL CARCINOMA; DISEASE-FREE SURVIVAL; FRENCH-ASSOCIATION; COMPLETE RESECTION; PROGNOSTIC-FACTORS; CLINICAL-FEATURES; POOR-PROGNOSIS; LONG SURVIVAL; UNITED-STATES; MITOTANE;
D O I
10.1097/WNQ.0b013e3182086ae0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Adrenocortical carcinoma (ACC) is a rare but highly aggressive neoplasm. It is not often diagnosed early. At diagnosis, up to 70% of patients have disease that extends beyond the adrenal glands. Although regional disease and/or metastases to the peritoneum, liver, lung, or bone are common, metastasis to the skull is extremely rare. The author believes this to be only the third case reported in the literature. Despite advances in cancer therapy over several decades, prognoses for patients with ACC remain grim. Radical surgical excision is the only approach that may cure localized disease. Thus far, radiation therapy and chemotherapy have shown little impact on the course of ACC.
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页码:63 / 68
页数:6
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