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脾性腺融合——阴囊肿胀的罕见原因:一例报告

Splenogonadal fusion - a rare cause of scrotal swelling: a case report.

作者信息

Karray O, Oueslati A, Chakroun M, Ayed H, Bouzouita A, Cherif M, Ben Slama M R, Derouiche A, Chebil M

机构信息

Urology department, Charles Nicolle hospital, Tunis, Tunisia.

出版信息

J Med Case Rep. 2018 Jun 20;12(1):172. doi: 10.1186/s13256-018-1712-1.

Abstract

BACKGROUND

Splenogonadal fusion is a rare and benign condition. Diagnosis is challenging for clinicians. Despite its indolence, diagnosis is often confirmed after orchidectomy. Surgery is mandatory, particularly to rule out the extremely rare association with malignancy.

CASE PRESENTATION

We report a case of splenogonadal fusion in a 38-year-old North African man presenting a palpable scrotal mass. We describe clinical aspects, pathogenic hypothesis, radiological features, as well as surgical management principles.

CONCLUSIONS

Splenogonadal fusion is rarely suspected and diagnosed preoperatively. A diagnosis is made once an ectopic testicular mass is associated with cryptorchidism and suggestive radiological signs. A better knowledge of the clinical and radiological features of splenogonadal fusion provides an opportunity for conservative surgery.

摘要

背景

脾性腺融合是一种罕见的良性病症。对临床医生而言,诊断颇具挑战性。尽管其进展缓慢,但通常在睾丸切除术后才能确诊。手术是必要的,尤其是为了排除与恶性肿瘤极其罕见的关联。

病例报告

我们报告一例38岁北非男性的脾性腺融合病例,该患者阴囊可触及肿块。我们描述了临床症状、发病假说、影像学特征以及手术治疗原则。

结论

脾性腺融合术前很少被怀疑和诊断。一旦发现异位睾丸肿块伴有隐睾症且有提示性影像学征象,即可作出诊断。对脾性腺融合的临床和影像学特征有更深入的了解可为保守手术提供机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71cd/6011191/7183120cb21e/13256_2018_1712_Fig1_HTML.jpg

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