Brain metastases from papillary thyroid carcinomas

被引:0
|
作者
Farnaz C. Tahmasebi
Peter Farmer
Suzanne Z. Powell
Kenneth D. Aldape
Gregory N. Fuller
Shital Patel
Peter Hollis
David Chalif
Mark B. Eisenberg
Jian Yi Li
机构
[1] North Shore–Long Island Jewish Health System,Department of Pathology and Laboratory Medicine
[2] The Methodist Hospital,Department of Pathology
[3] The University of Texas M.D. Anderson Cancer Center,Department of Pathology
[4] North Shore University Hospital,Department of Radiology
[5] North Shore University Hospital,Department of Neurosurgery
来源
Virchows Archiv | 2013年 / 462卷
关键词
Papillary thyroid carcinoma (PTC); Brain metastasis; Tall cell variant; Oncocytic variant; Columnar cell variant;
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学科分类号
摘要
Brain metastasis from papillary thyroid carcinoma (PTC) is extremely rare and carries a poor prognosis. We report nine cases (five females and four males) of brain metastasis of PTC. The age of patients ranged from 46 to 87 years old. The patients presented with nonspecific symptoms such as headaches. Brain metastasis was the first clinical presentation in three of nine patients; two of which had the aggressive tall cell variant of PTC. Six patients had prior history of PTC (four classic, one oncocytic variant, and one columnar cell variant) for 2 to 17 years with a median of 12 years. Gross total resection of brain metastasis was achieved for eight of our patients. Eight patients were treated with radioactive iodine. The median follow-up time was 12 months, ranging from 1 month to 4 years. Three patients died of their disease in 6 months, 21 months and 4 years, respectively after their first presentation of brain metastasis. It seems that these rare aggressive variants of PTC, such as tall cell variant, not only have higher propensity to develop brain metastasis, but also more frequently present with brain metastasis as their first clinical presentation than classic PTC. Furthermore, patients with PTC can develop brain metastasis even after many years.
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页码:473 / 480
页数:7
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