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Continuous-type splenogonadal fusion: A case report

机译:连续型脾盂融合术1例

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摘要

Splenogonadal fusion (SGF) is a rare congenital malformation. Since it lacks characteristic features, very few cases of SGF have been diagnosed preoperatively. Laparoscopy was effective in both diagnosing and surgically treating this condition. Herein, we reported left side SGF in a male patient who was diagnosed during laparoscopic exploration, and Fowler-Stephens orchidopexy was implemented at the same time. The patient was followed up for one year. At a 6-month follow-up, the left scrotum demonstrated swelling and the internal contents were hard. An ultrasound of this testicle indicated non-uniform, splenic-like organization. However, at the one-year follow-up, the volume of splenic-like organization was reduced but the testicular size did not exhibit further atrophy.
机译:脾盂融合术(SGF)是一种罕见的先天性畸形。由于缺乏特征性特征,术前很少诊断出SGF。腹腔镜在诊断和手术治疗此病方面均有效。在此,我们报道了一名在腹腔镜探查过程中被诊断出的男性患者的左侧SGF,并且同时实施了Fowler-Stephens兰花科手术。对该患者进行了一年的随访。在六个月的随访中,左阴囊出现肿胀,内部内容物变硬。对该睾丸进行超声检查表明脾脏组织不均匀。但是,在一年的随访中,脾样组织的体积减少了,但睾丸的大小并未显示出进一步的萎缩。

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