Paratesticular aggressive angiomyxoma: A rare case.
Paratesticular aggressive angiomyxoma: A rare case.
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DOI：
10.4103/ua.ua_168_16
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发表时间：
2017-04
期刊：
影响因子：
0.7
通讯作者：
Fam XI
中科院分区：
文献类型：
--
作者：
Ismail MI;Wong YP;Tan GH;Fam XI
摘要侵袭性血管黏液瘤是一种罕见的良性间叶黏液瘤，尤其是起源于睾丸。它主要发生在育龄女性中，在男性中非常罕见。AMM的特殊睾丸起源在文献中尚未报道。这是一位65岁的男性，他有右侧阴囊肿胀。阴囊超音波检查显示右侧睾丸有一软组织肿瘤。患者接受了根治性右侧睾丸切除术，组织病理学证实为睾丸旁AAM，切除边缘清晰。术后2年未见局部复发或转移。
Aggressive angiomyxoma (AAM) particularly testicular origin is a rare benign mesenchymal myxoid tumor which is locally aggressive, blatant for local recurrence, and may metastasize. It occurs mostly in females of childbearing age and extremely rare in males. AMM particular testicular origin is not reported in literature yet. This is a 65-year-old man who had a right scrotal swelling. Ultrasound scrotum showed a soft tissue tumor of the right testis. The patient underwent radical right orchidectomy of which histopathologically confirmed to be a paratesticular AAM with clear resection margins. There were no signs of local recurrence or metastasis 2 years postsurgical resection.