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神经囊虫病表现为孤立性鞍上病变。

Neurocysticercosis Presenting as an Isolated Suprasellar Lesion.

机构信息

Department of Neurological Surgery, University of Virginia Health System, Charlottesville, Virginia, USA.

Division of Endocrinology and Metabolism, Department of Medicine, University of Virginia Health System, Charlottesville, Virginia, USA.

出版信息

World Neurosurg. 2020 Sep;141:352-356. doi: 10.1016/j.wneu.2020.05.212. Epub 2020 Jun 6.

DOI:10.1016/j.wneu.2020.05.212
PMID:32522639
Abstract

BACKGROUND

Although extraparenchymal neurocysticercosis (NCC) is well established, presentation in the suprasellar space is rare. When presenting in the suprasellar space, the imaging characteristics may mimic more common lesions including craniopharyngioma and Rathke cleft cyst depending on the life cycle of the parasite. Although antiparasitic medical therapy may be effective for viable NCC, it is not routinely employed for calcified NCC.

CASE DESCRIPTION

This report presents a 39-year-old male patient who presented with profound visual decline secondary to a partially calcified suprasellar NCC. Suprasellar NCC was presumed based on specific radiologic findings, which are discussed. Medical therapy was not offered because of the proximity to the optic chiasm and the partial calcification of the lesion leading to the presumption that the mass was nonviable. The patient underwent successful endoscopic endonasal resection of the suprasellar NCC and experienced significant improvement in vision. Despite the calcification, pathological evaluation revealed that a portion remained viable.

CONCLUSIONS

Regardless of the life cycle stage, endonasal resection offers a minimally invasive approach for suprasellar NCC; treatment can be tailored to the patient's presentation and stage of infection.

摘要

背景

虽然脑实质外神经囊虫病(NCC)已得到广泛认识,但发生于鞍上区者较为罕见。当发生于鞍上区时,根据寄生虫的生命周期,其影像学特征可能类似于更常见的病变,包括颅咽管瘤和 Rathke 裂囊肿。尽管针对活的囊尾蚴,抗寄生虫药物治疗可能有效,但对于钙化的囊尾蚴通常不采用该方法。

病例描述

本报告介绍了 1 例 39 岁男性患者,因部分钙化的鞍上 NCC 而出现严重视力下降。根据特定的影像学发现推测为鞍上 NCC,这些发现将在文中讨论。由于病变靠近视交叉且部分钙化,认为该肿块已无活力,故未采用药物治疗。患者接受了成功的经鼻内镜下鞍上 NCC 切除术,视力显著改善。尽管存在钙化,但病理评估显示部分仍具有活力。

结论

无论生命周期阶段如何,经鼻内镜手术为鞍上 NCC 提供了一种微创方法;可根据患者的表现和感染阶段来定制治疗方案。

相似文献

1
Neurocysticercosis Presenting as an Isolated Suprasellar Lesion.神经囊虫病表现为孤立性鞍上病变。
World Neurosurg. 2020 Sep;141:352-356. doi: 10.1016/j.wneu.2020.05.212. Epub 2020 Jun 6.
2
Giant suprasellar Rathke's cleft cyst mimicking craniopharyngioma: implications for a spectrum of cystic epithelial lesions of ectodermal origin.酷似颅咽管瘤的巨大鞍上Rathke裂囊肿:对一系列外胚层起源的囊性上皮病变的启示
J Neurol Surg A Cent Eur Neurosurg. 2012 Sep;73(5):324-9. doi: 10.1055/s-0032-1304814. Epub 2012 Jul 30.
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Outcomes following endoscopic endonasal resection of sellar and supresellar lesions in pediatric patients.小儿患者经鼻内镜蝶鞍和鞍上病变切除术的术后结果。
Childs Nerv Syst. 2019 Nov;35(11):2099-2105. doi: 10.1007/s00381-019-04258-1. Epub 2019 Jun 18.
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Neuroendoscopic transventricular surgery for suprasellar cystic mass lesions such as cystic craniopharyngioma and Rathke cleft cyst.神经内镜经脑室手术治疗鞍上囊性肿物,如囊性颅咽管瘤和拉克氏囊肿。
Neurol Med Chir (Tokyo). 2004 Aug;44(8):408-13; discussion 414-5. doi: 10.2176/nmc.44.408.
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Suprasellar and recurrent pediatric craniopharyngiomas: expanding indications for the extended endoscopic transsphenoidal approach.鞍上及复发性儿童颅咽管瘤:扩大经鼻内镜扩大经蝶入路的适应证
J Neurosurg Pediatr. 2018 Jan;21(1):72-80. doi: 10.3171/2017.7.PEDS17295. Epub 2017 Nov 10.
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Endoscopic, endonasal extended transsphenoidal, transplanum transtuberculum approach for resection of suprasellar lesions.内镜下经鼻扩大经蝶、经筛板经结节入路切除鞍上病变。
J Neurosurg. 2007 Mar;106(3):400-6. doi: 10.3171/jns.2007.106.3.400.
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Entirely Suprasellar Rathke Cleft Cysts: Clinical Features and Surgical Efficacy of Endoscopic Endonasal Transtuberculum Sellae Approach.鞍上完全性 Rathke 裂囊肿:经鼻蝶鞍内入路的临床特点和手术疗效。
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A giant suprasellar Rathke cleft cyst with psychiatric manifestations: case report.一例伴有精神症状的巨大鞍上Rathke裂囊肿:病例报告
Clin Neurol Neurosurg. 2014 Jun;121:27-9. doi: 10.1016/j.clineuro.2014.03.011. Epub 2014 Mar 19.
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The endoscopic endonasal transsphenoidal approach to the suprasellar cistern.经鼻内镜经蝶窦入路至鞍上池
Clin Neurosurg. 2007;54:226-35.

引用本文的文献

1
Neurocysticercosis mimicking craniopharyngioma: A case report.酷似颅咽管瘤的神经囊尾蚴病:一例报告
Clin Case Rep. 2023 Nov 30;11(12):e8166. doi: 10.1002/ccr3.8166. eCollection 2023 Dec.
2
Endoscopic endonasal approach for isolated subarachnoid neurocysticercosis in basal cisterns and its complications: illustrative case.经鼻内镜入路治疗基底池孤立性蛛网膜下腔神经囊尾蚴病及其并发症:病例报告
J Neurosurg Case Lessons. 2022 Apr 11;3(15). doi: 10.3171/CASE2229.