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男性患者右乳内下象限的神经鞘瘤:一例罕见病例报告。

Schwannoma in the lower inner quadrant of the right breast in a male patient: A rare case report.

作者信息

Chen Jingjing, Huang Yan, Liu Haofeng, Sun Yuanyuan, Liu Fufeng

机构信息

Department of Pathology, Taizhou People's Hospital of Jiangsu Province, Taizhou, Jiangsu, China.

Department of Pathology, First People's Hospital of Linping District, Hangzhou, China.

出版信息

Medicine (Baltimore). 2025 Jan 31;104(5):e41309. doi: 10.1097/MD.0000000000041309.

Abstract

RATIONALE

Lower inner-quadrant breast schwannomas are exceedingly rare, with no reports of their occurrence in male patients in the literature. In this report, we describe a male patient with a schwannoma in the lower inner quadrant of the right breast.

PATIENT CONCERNS

A 26-year-old man presented at our hospital with a 6-month history of a lump in the right breast and reported pain in the area 3 days prior to presentation. Ultrasonography identified a 0.86 × 0.64 cm hypoechoic nodule 0.41 cm beneath the skin in the lower inner quadrant of the right breast. The nodule exhibited clear boundaries and uniform internal echogenicity with no signs of significant blood flow on color Doppler flow imaging. The patient was concerned that the nodule was benign or malignant.

DIAGNOSES

Histopathological and immunohistochemical analyses after complete surgical excision confirmed that the lesion was breast schwannoma. The postoperative course was unremarkable and the tumor did not recur during 7 years of follow-up.

INTERVENTIONS

Biochemical parameters were examined preoperatively. The radiological examination of breast color Doppler ultrasound was performed.

OUTCOMES

A well-shaped, 0.86 × 0.64 cm mass, complete capsule in the lower inner quadrant of the right breast was surgically resected. The postoperative course was unremarkable and the tumor did not recur during 7 years of follow-up.

LESSONS

Breast schwannoma is an extremely rare tumor that is very difficult to preoperatively diagnose. Preoperative biochemical examination and ultrasonography can only provide diagnostic ideas. Histological and immunohistochemical analyses are required for confirmation. It can transform into malignant peripheral nerve sheath tumors, but not often. Consequently, regular postoperative follow-up is required for such patients, especially ultrasonography.

摘要

理论依据

乳腺内下象限的神经鞘瘤极为罕见,文献中尚无男性患者发生此类肿瘤的报道。在本报告中,我们描述了一名右乳腺内下象限患有神经鞘瘤的男性患者。

患者情况

一名26岁男性因右乳肿块6个月就诊于我院,就诊前3天该区域出现疼痛。超声检查发现右乳腺内下象限皮下0.41厘米处有一个0.86×0.64厘米的低回声结节。该结节边界清晰,内部回声均匀,彩色多普勒血流成像未见明显血流信号。患者担心该结节是良性还是恶性。

诊断

完整手术切除后,组织病理学和免疫组织化学分析证实病变为乳腺神经鞘瘤。术后恢复顺利,随访7年肿瘤未复发。

干预措施

术前检查生化指标。进行乳腺彩色多普勒超声影像学检查。

结果

手术切除了右乳腺内下象限一个形状规整、大小为0.86×0.64厘米、有完整包膜的肿块。术后恢复顺利,随访7年肿瘤未复发。

经验教训

乳腺神经鞘瘤是一种极其罕见的肿瘤,术前很难诊断。术前生化检查和超声检查只能提供诊断思路。确诊需要组织学和免疫组织化学分析。它可转变为恶性周围神经鞘膜瘤,但并不常见。因此,此类患者术后需要定期随访,尤其是超声检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5bc/11789902/992f1fd4c6e4/medi-104-e41309-g001.jpg

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