单词查询
neurofibromas
释义
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n. 神经纤维瘤；纤维神经瘤；
例句
Benign peripheral nerve sheath tumors can be divided into two major groups: Schwannomas and neurofibromas.
良性外周神经鞘瘤可分为两大类，神经鞘瘤及神经纤维瘤。
Schwannomas and neurofibromas are benign lesions that are thought to arise from neoplastic transformation of nerve sheath cells.
前两者是良性肿瘤，一般认为来自神经鞘细胞的瘤变。
Benign neurogenic tumors originating from the peripheral nervous system usually appear as schwannomas or neurofibromas.
纵隔腔许旺氏细胞瘤或神经纤维瘤为起源于周边神经的良性神经性肿瘤。
Other rare conditions that cause breast enlargement in men include neurofibromas, hematomas, and dermatoid cysts.
其它引起男性乳房增生的罕见情况包括神经纤维瘤，血肿和皮肤样囊肿。
Schwannomas are less common than neurofibromas and constitute about 5% of all benign soft tissue tumors.
神经鞘瘤通常少于神经纤维瘤，大约占良性软组织肿瘤的5%左右。
They can develop in pre-existing neurofibromas or schwannomas, denovo from peripheral nerves, or following radiation therapy.
他们将事先存在的神经纤维瘤或神经鞘瘤，从头从周围神经，或下面的放射治疗。
To explore the molecular pathogenesis of neurofibromas in the patients with neurofibromatosis type 1 (NF1).
探讨1型神经纤维瘤病（NF1）患者神经纤维瘤发生、发展的分子病理机制。
In this report we describe 3 adult patients with SNF who presented with only neurofibromas.
在这个报告中，我们描述了与民阵3只成年患者神经纤维瘤谁主办。
Neurofibromas are well defined and may appear homogeneously hypoechoic to hyperechoic, with posterior enhancement.
平滑肌瘤界限清晰，可表现为均质低回声到高回声，伴后方增强。
Schwannomas are not easily distinguished from other benign tumors such as neurofibromas and leiomyomas .
神经鞘瘤不易和其他良性肿瘤鉴别，比如神经纤维瘤和平滑肌瘤。
良性外周神经鞘瘤可分为两大类，神经鞘瘤及神经纤维瘤。
Schwannomas and neurofibromas are benign lesions that are thought to arise from neoplastic transformation of nerve sheath cells.
前两者是良性肿瘤，一般认为来自神经鞘细胞的瘤变。
Benign neurogenic tumors originating from the peripheral nervous system usually appear as schwannomas or neurofibromas.
纵隔腔许旺氏细胞瘤或神经纤维瘤为起源于周边神经的良性神经性肿瘤。
Other rare conditions that cause breast enlargement in men include neurofibromas, hematomas, and dermatoid cysts.
其它引起男性乳房增生的罕见情况包括神经纤维瘤，血肿和皮肤样囊肿。
Schwannomas are less common than neurofibromas and constitute about 5% of all benign soft tissue tumors.
神经鞘瘤通常少于神经纤维瘤，大约占良性软组织肿瘤的5%左右。
They can develop in pre-existing neurofibromas or schwannomas, denovo from peripheral nerves, or following radiation therapy.
他们将事先存在的神经纤维瘤或神经鞘瘤，从头从周围神经，或下面的放射治疗。
To explore the molecular pathogenesis of neurofibromas in the patients with neurofibromatosis type 1 (NF1).
探讨1型神经纤维瘤病（NF1）患者神经纤维瘤发生、发展的分子病理机制。
In this report we describe 3 adult patients with SNF who presented with only neurofibromas.
在这个报告中，我们描述了与民阵3只成年患者神经纤维瘤谁主办。
Neurofibromas are well defined and may appear homogeneously hypoechoic to hyperechoic, with posterior enhancement.
平滑肌瘤界限清晰，可表现为均质低回声到高回声，伴后方增强。
Schwannomas are not easily distinguished from other benign tumors such as neurofibromas and leiomyomas .
神经鞘瘤不易和其他良性肿瘤鉴别，比如神经纤维瘤和平滑肌瘤。