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两例神经节瘤。

Two cases of ganglioneuroma.

作者信息

Yamaguchi Kouhei, Hara Isao, Takeda Masashi, Tanaka Kazushi, Yamada Yuji, Fujisawa Masato, Kawabata Gaku

机构信息

Division of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

Urology. 2006 Mar;67(3):622.e1-4. doi: 10.1016/j.urology.2005.09.024. Epub 2006 Feb 28.

Abstract

Although ganglioneuroma is a relatively rare tumor of the sympathetic nervous system, detection of this tumor has increased as imaging techniques such as computed tomography and ultrasonography have become prevalent. We report 2 cases of ganglioneuroma found incidentally. Both tumors were 40 to 60 mm in size. Magnetic resonance imaging in 1 patient showed a homogeneous mass with a low signal intensity on T1-weighted imaging and a heterogeneous mass with a high signal intensity on T2-weighted imaging, both characteristic of neurogenic tumor. Therefore, we performed laparoscopic adrenalectomy. Histopathologic examination demonstrated that one tumor was located on the adrenal medulla, with the other in the extra-adrenal retroperitoneal space.

摘要

虽然神经节神经瘤是一种相对罕见的交感神经系统肿瘤,但随着计算机断层扫描和超声等成像技术的普及,这种肿瘤的检出率有所增加。我们报告2例偶然发现的神经节神经瘤。两个肿瘤大小均为40至60毫米。1例患者的磁共振成像显示,在T1加权成像上为均匀低信号强度肿块,在T2加权成像上为不均匀高信号强度肿块,均为神经源性肿瘤的特征。因此,我们进行了腹腔镜肾上腺切除术。组织病理学检查表明,一个肿瘤位于肾上腺髓质,另一个位于肾上腺外腹膜后间隙。

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