神經節瘤 的英文怎麼說
中文拼音 [shénjīngjiéliú]
神經節瘤
英文
ganglioma-
Adrenal ganglioneuroma report of 9 cases
腎上腺節細胞神經瘤9例報告Mr imaging revealed an infiltrative enhancing epidural tumor at the dorsum of t2 to t5 levels with foraminal extension
磁振造影影像發現硬腦膜上的腫瘤位於胸椎第二到第五節部位並有向神經孔蔓延現象。Clusters of ganglion cells were scattered throughout the tumor
神經節細胞束被腫瘤徹底的分散。Since the possibility of malignancy can ' t be rule out, a laparoscopic adrenalectomy was performed uneventfully, and pathological findings proved to be a ganglioneuroma
由於無法排除惡性病變的可能，病人接受手術切除腫瘤，病理檢查證實是神經節神經瘤。The diagnosis and treatment of adrenal ganglioneuroma report of 6 cases
腎上腺節細胞神經瘤的診治體會附6例報告Among patients with adrenal incidentalomas, approximately 0 - 6 %, were proved to be ganglioneuromas
在這些腎上腺偶見瘤中，神經節神經瘤約? 0至6 % 。These tumors are rare tumors and originate from the neural crest tissue of the sympathetic nervous system
這些罕見的神經節神經瘤起源於交感神經系統之神經脊組織。Primary intrinsic gangliogliomas of the brainstem are exceedingly unusual
摘要原發性腦干神經節細胞神經膠質瘤是一種非常罕見的腫瘤。Gangliocytoma of temporoparietal lobe : report of one case
顳頂葉神經節細胞瘤1例Understanding this proliferative capacity during environmental change is critical, he says, as adult neural stem cells in this region may sometimes proliferate out of control to form brain tumors
理解這種增殖能力在環境變化時是至關重要的，他說，像該區域的成熟神經幹細胞有時候可能無節制地增殖導致大腦腫瘤形成。The treatment of choice is often surgical resection for most paragangliomas
大部分副神經節瘤的首選治療方式是外科手術切除。Paragangliomas of head and neck are rare tumors that occur sporadically with the prevalence of about 1 in 30, 000 of head and neck tumors
摘要頭頸部副神經節瘤是一罕見偶發的疾病，盛行率約占所有頭頸部腫瘤的三萬分之一。Herein we present a case of malignant retroperitoneal paraganglioma with lung metastasis and the computed tomography ( ct ) findings
本文藉由腹部計算機斷層的發現，我們提出一位罕見的惡性副神經節瘤合併有肺部轉移之病例報告。We reported a case of paraganglioma of head and neck with the treatment of surgery plus postoperative irradiation and reviewed the literatures of paraganglioma
在本文中，我們報告一位以外科手術合併術後放線治療的頭頸部副神經節瘤的患者，並且回顧關于副神經節瘤的文獻。Paragangliomas are rare tumors arising from extraadrenal chromaffin cell and accounting for 10 ~ 48 % of all chromaffin tissue - related tumors and one tenth of pheochromocytomas
摘要副神經節瘤為罕見的原發于腎上腺外嗜鉻細胞的腫瘤，約占所有原發于嗜鉻細胞腫瘤的10 ~ 18 % ；發生率也只有腎上腺嗜鉻細胞瘤的十分之一。The combination of radiological findings and clinical characteristics may be helpful to diagnose retroperitoneal tumors, including paragangliomas and other neurogenic tumors and, to determine the local extent of tumor
因此熟悉副神經節瘤的影像學表現及其可能的臨床特徵，將有利於后腹腔腫瘤的?別診斷及腫瘤局部侵犯的評估。To be considered in the differential diagnosis of nodular fasciitis are seeral other soft tissue tumors arising from fat, muscle, neres, connectie tissue, and blood essels
結節性筋膜炎的鑒別診斷要考慮到其他起源於脂肪、肌肉、神經、結蒂組織和血管的幾種軟組織腫瘤。Sleep / waking cycle is a complex network modulation and many factors such as interleukin - 1 ( il - 1 ), tumor necrosis factor ( tnf ), growth hormone releasing hormone ( ghrh ), vasoactive intestina polypeptide ( vip ) and many conventional neurotransmitters such as serotonin ( 5 - ht ), acetylcholine ( ach ), norepinephrine ( ne ), dopamine ( da ) and gamma - aminobutyric acid ( gaba ) were involved in it. recent evidence has shown that no synthesized in neurons in several areas of the brain can induce the release of neurotransmitters. in the rat central nervous system, the anatomical distribution of nos - containing neurons is now well established, and it was reported that nos is co - localized with neurotransmitters well known for their involvement in sleep mechanisms, i. e. 5 - ht, ach, da and gaba
鄭州大學2003屆碩士畢業論文gaba受體激動劑消除no合成酶抑制劑對大鼠睡/醒周期的影響睡/醒周期的形成是一個復雜的網路調控的結果，體內許多因子都參與了這一調控網路，這些因子如白介素一1 （ il一1 ） 、腫瘤壞死因子（ tnf ） 、生長激素釋放激素（ ghrh ） 、血管活性腸膚（ vip ）以及經典的神經遞質如5一輕色氨（ 5一ht ） 、乙酞膽堿（ ach ） 、去甲腎上腺素（ ne ） 、多巴胺（ da ）和卜氨基丁酸（ gaba ）等，它們在睡眠的發生和調節中也發揮著重要作用。Pathologic features of the ganglioglioma gangliocytoma in the central nervous system
神經節細胞瘤的病理特點Tumors with sparse number of ganglion cells may be misdiagnosed as neurofibroma
帶有許多稀疏的神經節細胞的腫瘤可能會被誤診為神經纖維瘤。分享友人