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本文引用的文献

1
Splenogonadal fusion and testicular cancer: case report and review of the literature.脾性腺融合与睾丸癌：病例报告及文献综述
Einstein (Sao Paulo). 2012 Jan-Mar;10(1):92-5. doi: 10.1590/s1679-45082012000100019.
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.
4
Splenicgonadal fusion.脾性腺融合。
Am J Pathol. 1956 Jan-Feb;32(1):15-33.
5
The pathogenesis of cryptorchidism and splenogonadal fusion: a new hypothesis.隐睾症与脾性腺融合的发病机制：一种新假说。
Br J Urol. 1996 Feb;77(2):285-90. doi: 10.1046/j.1464-410x.1996.89022.x.
6
Splenogonadal fusion: report of 2 cases and review of the literature.
J Urol. 1996 Jan;155(1):309-11. doi: 10.1016/s0022-5347(01)66651-5.
7
The spectrum of splenogonadal fusion. Case report and review of 84 reported cases.脾肾融合的谱系。病例报告及84例报告病例的综述。
Eur J Pediatr. 1985 Nov;144(4):316-23. doi: 10.1007/BF00441771.

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.

DOI:10.5152/tud.2014.90757
PMID:26328150
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4548637/
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。