Department of Neurosurgery, Lausanne University Hospital, Rue du Bugnon 44, 1005, Lausanne, Switzerland.
Department of Clinical Pathology, Institute of Pathology, Lausanne University Hospital, Lausanne, Switzerland.
Endocr Pathol. 2019 Sep;30(3):219-236. doi: 10.1007/s12022-019-09581-6.
The 2017 World Health Organization classification of central nervous system and endocrine tumors have introduced significant changes in the diagnostic criteria for pituitary lesions. The aim of our paper is to describe the epidemiological, clinico-pathological, and radiological features of a single consecutive institutional surgical series of rare pituitary lesions, using these new criteria. Of the 316 endoscopic endonasal trans-sphenoidal approaches performed for pituitary lesions between 2010 and 2018, 15 rare lesions were encountered. These included metastases, pituitary carcinomas, pituicytomas, granular cell tumor, primary pituitary lymphomas, germinoma, mixed gangliocytoma-adenoma, hypophysitis, and pituitary hyperplasia. Their clinical, radiological, and pathological features are herewith presented along with a literature review that enabled us to propose an algorithm to facilitate a diagnosis for rare pituitary lesions.
2017 年世界卫生组织中枢神经系统和内分泌肿瘤分类对垂体病变的诊断标准引入了重大变化。我们的目的是使用这些新标准描述单一连续机构手术系列罕见垂体病变的流行病学、临床病理和影像学特征。在 2010 年至 2018 年间进行的 316 例内镜经鼻蝶窦入路治疗垂体病变中,发现了 15 例罕见病变。这些病变包括转移瘤、垂体癌、垂体细胞瘤、颗粒细胞瘤、原发性垂体淋巴瘤、生殖细胞瘤、混合神经节细胞瘤-腺瘤、垂体炎和垂体增生。本文介绍了它们的临床、放射学和病理学特征,并进行了文献复习,提出了一种诊断罕见垂体病变的算法。