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脾性腺融合:睾丸肿块鉴别诊断中一种非常罕见的先天性异常。

Splenogonadal fusion: a very rare congenital anomaly in the differential diagnosis of a testicular mass.

作者信息

Bal Kaan, Ermete Murat, Balcı Uğur, Dinçel Çetin

机构信息

Department of Urology, İzmir Katip Çelebi University, Atatürk Research and Training Hospital, İzmir, Turkey.

Department of Pathology, İzmir Katip Çelebi University, Atatürk Research and Training Hospital, İzmir, Turkey.

出版信息

Turk J Urol. 2014 Mar;40(1):62-4. doi: 10.5152/tud.2014.90757.

Abstract

Splenogonadal fusion is a rare congenital anomaly characterized by congenital fusion between the spleen and testicular tissue. In the literature, there are approximately 175 reported cases, and most of them are associated with cryptorchidism. In this article, we report an unusual case of splenogonadal fusion that was pre-diagnosed as a solid testicular mass in a patient who underwent orchiectomy.

摘要

脾性腺融合是一种罕见的先天性异常,其特征为脾脏与睾丸组织之间的先天性融合。在文献中,大约有175例报道病例,其中大多数与隐睾症相关。在本文中,我们报告了一例不寻常的脾性腺融合病例,该病例在接受睾丸切除术的患者中被预先诊断为实性睾丸肿块。

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本文引用的文献

2
Sonographic and CT features of splenogonadal fusion.脾肾融合的超声和CT特征。
Pediatr Radiol. 2007 Sep;37(9):916-9. doi: 10.1007/s00247-007-0526-x. Epub 2007 Jun 21.
3
Splenogonadal fusion: case presentation and literature review.脾性腺融合:病例报告及文献综述
J Pediatr Surg. 2005 Aug;40(8):1357-60. doi: 10.1016/j.jpedsurg.2005.05.027.
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Splenicgonadal fusion.脾性腺融合。
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Splenogonadal fusion: report of 2 cases and review of the literature.
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