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ganglioneuroma相关的网络例句

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MethodsTo retrospectively analyze the CT appearance of 4 cases ganglioneuroma confirmed by operation and pathology,and compare with the pathologic result.

方法回顾性分析4例经手术及病理证实的节细胞神经瘤的CT表现,并与病理结果进行对照分析。

The specific diagnosis of adrenal ganglioneuroma requires either biopsy or surgical removal for documentation.

因此明确的诊断有赖细针穿刺或手术切除以进行病理检查。

The imaging data of B ultrasound, CT and MRI can give helpful information in the diagnosis of ganglioneuroma.

结合本文所总结的B超、CT、MRI影像学特点,术前可获提示性诊断。

Ganglioneuroma is a benign neoplasm that is most commonly seen in the posterior mediastinum or retroperitoneum.

神经节瘤是一个良性瘤,大多常见于纵隔后或腹膜后腔。

Materials and Math- ods: CT and MRI findings of 7 cases with ganglioneuroma and 2 case with ganglioneuroblastoma proved by operation and pathology were analysed retrospectively.

目的:分析后纵隔神经节细胞瘤和神经节神经母细胞瘤的CT和MRI表现及其诊断。

Certain characteristic CT features provide a valuable clue to the diagnosis of adrenal ganglioneuroma.

肾上腺节细胞神经瘤有一定的CT影像特点,CT可正确定位和做出较准确的定性诊断。

Certain characteristic CT features provide a valuable clue to the diagnosis of adrenal ganglioneuroma.

肾上腺节细胞神经瘤有一定的CT影像特点,CT可正确定位和做出较准确的定**诊断。

Methods:The clinical and pathological data of one child case were summarized, and the characteristics of incidence, biology, pathology, diagnosis and surgery were analyzed with literature review. Results: It was diagnosed as ganglioneuroma of lymph node by pathology examination.

回顾分析1例发生在小儿淋巴结的节细胞神经瘤的临床病理资料,结合文献对其发病情况、生物学特性、临床、病理诊断及手术原则进行讨论。

The pathology of tumours included 8 cases of phechoromocytoma(1 case appears malignancy),4 cases of ganglioneuroma,4 cases of adrenal myelolipoma, 2 cases of melanoma,4 cases of other lesions. Current median follow up ,available on 19 patients,was 14 months(ranges 3 to 47),no local recurrence and metastases was observed.

术后病理报告:嗜铬细胞瘤8例其中1例恶性),髓样脂肪瘤4例,神经节细胞瘤4例,脂肪肉瘤2例,其它病变4例。3例失访,19例随访3~47个月,平均14±9个月,未见局部复发和转移。

Ganglioneuroma is a rare, benign tumor. It arises from neural crest cells, similar to pheochromocytoma, and grows slowly.

神经节神紃瘤是一种罕见的良性肿瘤,它和嗜铬细胞瘤一样,都是由神经脊细胞分化而来。

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