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睾丸内平滑肌瘤:一例病例报告及文献综述

Intratesticular leiomyoma: A case report and a literature review.

作者信息

Zouari Skander, Othmane Mouna Ben, Bouassida Khaireddine, Hmida Wissem, Jaidane Mehdi

机构信息

Urology Department, Sahloul Hospital, Sousse, Tunisia.

Urology Department, Sahloul Hospital, Sousse, Tunisia.

出版信息

Int J Surg Case Rep. 2020;71:217-221. doi: 10.1016/j.ijscr.2020.05.030. Epub 2020 May 23.

DOI:10.1016/j.ijscr.2020.05.030
PMID:32480328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7262370/
Abstract

INTRODUCTION

Leiomyomas are benign tumors that originate from smooth muscles cells. Intratesticular leiomyoma is a very rare type of benign testicular masses. Through the literature, only 11 cases were reported.

PRESENTATION OF CASE

A 36 years old man presented with painless right scrotal mass. Clinical examination showed right upper polar testicular mass, well circumscribed and highly vascularized on sonography. Serum tumor markers were normal. Patient was explained the possibility of an organ sparing surgery if frozen section shows no sign of malignancy. Midline incision with frozen section was performed, with wide local excision. Pathological examination of the specimen confirmed intratesticular leiomyoma. Two years after the surgery, patient showed no sign of recurrence.

DISCUSSION

Intratesticular Leiomyoma is usually revealed as a non-tender firm scrotal mass that increases in size. Sonography is the imaging modality of choice for assessing intrascrotal pathology, and cannot distinguish benign from malignant tumor. Surgical management is subject of debate. While some authors recommend radical orchiectomy, others suggest the use of frozen section intraoperatively, and perform conservative treatment by mass excision in the absence of signs of malignancy.

CONCLUSION

Intratesticular leiomyoma is a very rare finding. When suspected, conservative management using frozen section followed by mass excision can be done, but final diagnosis remains on pathological examination and immunohistochemistry of the specimen.

摘要

引言

平滑肌瘤是起源于平滑肌细胞的良性肿瘤。睾丸内平滑肌瘤是一种非常罕见的良性睾丸肿物类型。通过文献检索,仅报道了11例。

病例介绍

一名36岁男性因右侧阴囊无痛性肿物就诊。临床检查发现右侧睾丸上极肿物,超声检查显示边界清晰且血供丰富。血清肿瘤标志物正常。向患者解释了如果冰冻切片显示无恶性迹象则有可能进行保留器官手术。行中线切口并进行冰冻切片,随后进行广泛局部切除。标本的病理检查证实为睾丸内平滑肌瘤。术后两年,患者无复发迹象。

讨论

睾丸内平滑肌瘤通常表现为无痛性坚实的阴囊肿物,且体积会增大。超声是评估阴囊内病变的首选影像学检查方法,但无法区分良性和恶性肿瘤。手术治疗存在争议。一些作者推荐根治性睾丸切除术,另一些人则建议术中使用冰冻切片,在无恶性迹象时通过肿物切除进行保守治疗。

结论

睾丸内平滑肌瘤是一种非常罕见的发现。当怀疑为此病时,可采用冰冻切片后进行肿物切除的保守治疗方法,但最终诊断仍需依靠标本的病理检查和免疫组织化学检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a745/7262370/0f0a94926c2c/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a745/7262370/08ddaca537b5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a745/7262370/35e9779a9c67/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a745/7262370/cc4899863c82/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a745/7262370/0f0a94926c2c/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a745/7262370/08ddaca537b5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a745/7262370/35e9779a9c67/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a745/7262370/cc4899863c82/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a745/7262370/0f0a94926c2c/gr4.jpg

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引用本文的文献

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