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经扩大经蝶窦入路成功治疗与冯·希佩尔-林道病无关的鞍上血管母细胞瘤:冯·希佩尔-林道病基因衍生蛋白的诊断价值

Suprasellar Hemangioblastoma Unrelated to von Hippel-Lindau Disease Successfully Treated through Extended Transsphenoidal Approach: Diagnostic Value of Von Hippel-Lindau Disease Gene-Derived Protein.

作者信息

Wenting Jia, Ogawa Yoshikazu, Ito Jun, Tominaga Teiji

机构信息

Department of Neurosurgery, Kohnan Hospital, Sendai, Miyagi, Japan.

Department of Neurosurgery, Hachinohe City Hospital, Hachinohe, Aomori, Japan.

出版信息

J Neurol Surg A Cent Eur Neurosurg. 2017 May;78(3):296-301. doi: 10.1055/s-0036-1582016. Epub 2016 Apr 28.

Abstract

Hemangioblastoma tends to occur in the infratentorial regions and rarely in the supratentorial regions. This tumor is strongly associated with von Hippel-Lindau disease (VHLD), especially in the supratentorial regions, with only 12 cases of suprasellar hemangioblastoma unrelated to VHLD. However, all these cases were diagnosed based on clinical screening and confirmation of family history. We report a case of suprasellar hemangioblastoma that was successfully removed through an extended transsphenoidal approach and diagnosed as a sporadic case unrelated to VHLD by immunohistochemical examination.A 67-year-old woman had mild diabetes insipidus and a visual field defect. Head magnetic resonance imaging revealed a suprasellar tumor compressing the optic chiasm upward. The tumor was totally removed without complication through an extended transsphenoidal approach. Postoperative histologic examination disclosed large vacuolated stromal cells and rich capillary networks, and the diagnosis was established as hemangioblastoma. Clinical screening and confirmation of family history revealed no specific results, and additional immunohistochemical staining showed diffuse cytoplasmic expression of anti-VHLD gene-derived protein (pVHL).We emphasize that pVHL immunohistochemical evaluation would be wise to adopt, especially for patients with a high risk of VHLD related to younger age and supratentorial lesions.

摘要

血管母细胞瘤倾向于发生在幕下区域,很少发生在幕上区域。这种肿瘤与冯·希佩尔-林道病(VHLD)密切相关,尤其是在幕上区域,仅有12例鞍上血管母细胞瘤与VHLD无关。然而,所有这些病例都是基于临床筛查和家族史确认而诊断的。我们报告一例鞍上血管母细胞瘤,通过扩大经蝶窦入路成功切除,并经免疫组化检查诊断为与VHLD无关的散发病例。一名67岁女性患有轻度尿崩症和视野缺损。头部磁共振成像显示鞍上肿瘤向上压迫视交叉。通过扩大经蝶窦入路将肿瘤完全切除,无并发症。术后组织学检查发现大量空泡状基质细胞和丰富的毛细血管网,诊断为血管母细胞瘤。临床筛查和家族史确认未发现特异性结果,进一步的免疫组化染色显示抗VHLD基因衍生蛋白(pVHL)弥漫性细胞质表达。我们强调,对于与年轻和幕上病变相关的VHLD高风险患者,采用pVHL免疫组化评估是明智的。

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