医学
空单元格
垂体腺瘤
恶性肿瘤
放射治疗
垂体瘤
腺瘤
颅咽管瘤
垂体
病理
海绵窦
脑膜瘤
转移
放射科
癌症
内科学
生物
遗传学
激素
细胞培养
作者
Mustafa Kemal Demir,Özlem Yapıcıer,Aylin Oral,Baran Yılmaz,Türker Kılıç
出处
期刊:Neurochirurgie
[Elsevier BV]
日期:2021-02-27
卷期号:68 (1): 106-112
被引量:2
标识
DOI:10.1016/j.neuchi.2021.02.006
摘要
Abstract Introduction Pituitary carcinomas are rare, with only a few case reports to date. We present a null cell type non-functioning pituitary carcinoma (NFPC) with intracranial metastases and a review of the literature. Case report A 56-year-old male with a history of an aggressive pituitary adenoma was admitted. Initial MRI highlighted a large intracranial mass with leptomeningeal involvement, simulating meningioma. Based on his previous pathology report of the sellar mass, a diagnosis of null cell type non-functioning pituitary carcinoma has been made. Conclusions An aggressive recurrent pituitary tumor with suprasellar and/or cavernous sinus invasion is the main characteristics of the NFPC. Single or multiple enhancing dural-based mass(es) mimicking meningioma is the most common MRI finding. The proof of malignancy is the same histopathological features of the recurrent aggressive pituitary tumor in the metastases. The histology alone is not distinctive in terms of malignancy. Most patients require a combined surgery, radiotherapy and chemotherapy.
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