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具有乳头状特征的中分化松果体实质肿瘤:原发性松果体肿瘤的连续体?

Pineal parenchymal tumor of intermediate differentiation with papillary features: a continuum of primary pineal tumors?

机构信息

Department of Neurological Surgery, Weill Cornell Brain Tumor Center, Weill Medical College of Cornell University, New York Presbyterian Hospital, 525 E 68th Street, Box 99, New York, NY 10021, USA.

出版信息

J Neurooncol. 2011 Jan;101(2):301-6. doi: 10.1007/s11060-010-0242-5. Epub 2010 Jun 3.

Abstract

Pineal parenchymal tumors comprise a rare group of primary neoplasms of the pineal gland. We describe a case involving a 29-year-old woman who presented with signs and symptoms of hydrocephalus secondary to a pineal region tumor obstructing the third ventricle. Surgical resection was performed and pathological analysis revealed a novel diagnosis consistent with a pineal parenchymal tumor of intermediate differentiation (PPTID) with transition to a papillary tumor of the pineal region (PTPR). To our knowledge, this particular pineal region tumor pathology has not yet been reported in the literature and highlights the continuum with which primary pineal tumors exist. We provide a review of the existing literature on pineal region tumors, specifically PTPR and PPTID, and offer insight into the management of these rare neoplasms.

摘要

松果体实质肿瘤包括一组罕见的松果体原发性肿瘤。我们描述了一例 29 岁女性患者,因松果体区域肿瘤阻塞第三脑室而出现脑积水的体征和症状。进行了手术切除,病理分析显示了一种新的诊断,符合中间分化的松果体实质肿瘤(PPTID),并向松果体区域的乳头状肿瘤(PTPR)转化。据我们所知,这种特定的松果体区域肿瘤病理学尚未在文献中报道,突显了原发性松果体肿瘤之间存在的连续性。我们回顾了松果体区域肿瘤的现有文献,特别是 PTPR 和 PPTID,并深入了解了这些罕见肿瘤的治疗。

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