睾丸旁动静脉畸形:1例报告及文献复习。

Rawa Bapir, Fahmi H Kakamad, Ismaeel Aghaways, Ari M Abdullah, Marwan N Hassan, Ayoob Asaad Mohammed Abid, Sabah Jalal Hasan, Karzan M Salih, Hussein M Hamasalih
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摘要

睾丸旁结构引起的动静脉畸形非常罕见,文献中报道的病例数量有限。本文报告一例罕见的睾丸旁动静脉畸形。一名6岁男童,阴囊无痛性肿胀6个月。经检查,在睾丸下方的右半阴囊可见无压痛性、无搏动性囊性肿胀。阴囊超声显示一个独立的囊性病变,质地正常,双睾丸血管通畅。在全身麻醉下,通过一个小的阴囊切口,切除了一个囊性的、充满血液的肿块。组织病理学检查的结果提示血管畸形。在本研究中描述的病例旨在阐明血管畸形。许多血管畸形被错误地称为血管瘤,许多患者因这种错误分类而接受不适当的治疗。虽然睾丸旁动静脉畸形是一种非常罕见的疾病,但它应该包括在睾丸旁病变的鉴别诊断中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Para‑testicular arteriovenous malformation: A case report and mini‑review of the literature.

Arteriovenous malformations from para-testicular structures are very rare, with only a limited number of cases reported in the literature. The present study reports a rare case of para-testicular arteriovenous malformation. A 6-year-old boy presented with painless swelling in the scrotum for 6 months. Upon examination, a non-tender and non-pulsatile cystic swelling was observed in the right hemi-scrotum below the testis. A scrotal ultrasound revealed a separate cystic lesion with a normal texture and the vascularity of both testes. Under general anesthesia, via a small scrotal incision, a cystic, blood-filled mass was excised. The results of a histopathological examination were suggestive of vascular malformation. The case described in the present study aims to shed light on vascular malformations. A number of vascular malformations are incorrectly referred to as hemangiomas, and numerous patients undergo inappropriate therapy due to this misclassification. Although para-testicular arteriovenous malformation is a very rare condition, it should be included in the differential diagnosis of para-testicular lesions.

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