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源于肩胛舌骨肌的硬纤维瘤:经腋窝机器人甲状腺切除术后罕见并发症的首例报告。

Desmoid tumor arising from omohyoid muscle: The first report for unusual complication after transaxillary robotic thyroidectomy.

作者信息

Cha Wonjae, Kong Il Gyu, Kim Heejin, Hah J Hun, Sung Myung-Whun

机构信息

Department of Otorhinolaryngology - Head and Neck Surgery, Seoul National University Hospital, Seoul, Korea.

出版信息

Head Neck. 2014 May;36(5):E48-51. doi: 10.1002/hed.23518. Epub 2014 Mar 10.

DOI:10.1002/hed.23518
PMID:24115367
Abstract

BACKGROUND

Transaxillary robotic (TAR) thyroidectomy has been performed for better aesthetic results by many surgeons. In this report, we describe a rare case of a desmoid tumor developed after TAR thyroidectomy, which is speculated to be a late-term complication.

METHODS AND RESULTS

A 61-year-old woman with a history of papillary microcarcinoma had experienced a large left neck mass that had grown over 2 years. The patient underwent TAR thyroidectomy (right lobectomy and isthmectomy) via the right axilla almost 2.5 years previously. Physical examination revealed a 6-cm, firm mass fixed to the left anterior neck. The mass was fixed to the omohyoid muscle. The 5.9- × 4.7- × 4.5-cm tumor with the surrounding muscles was excised in an en bloc fashion. Pathologic examination confirmed the diagnosis of a desmoid tumor.

CONCLUSION

This case suggests that desmoid tumors could develop late after TAR thyroidectomy. Thus, careful observation of the surgical wound may be necessary after TAR thyroidectomy.

摘要

背景

许多外科医生已开展经腋窝机器人辅助甲状腺切除术(TAR)以获得更好的美学效果。在本报告中,我们描述了1例TAR甲状腺切除术后发生硬纤维瘤的罕见病例,推测这是一种晚期并发症。

方法与结果

一名有乳头状微癌病史的61岁女性,左侧颈部有一个大肿块,已生长2年多。该患者于近2.5年前经右腋窝接受了TAR甲状腺切除术(右侧叶切除术和峡部切除术)。体格检查发现左侧颈前有一个6厘米的质地坚硬的肿块,该肿块与肩胛舌骨肌固定。将这个5.9×4.7×4.5厘米的肿瘤及其周围肌肉整块切除。病理检查确诊为硬纤维瘤。

结论

该病例提示硬纤维瘤可能在TAR甲状腺切除术后晚期发生。因此,TAR甲状腺切除术后可能需要仔细观察手术伤口。

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引用本文的文献

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A prospective 1-year comparative study of transaxillary total thyroidectomy regarding functional outcomes: Is it really promising?经腋窝全甲状腺切除术功能结局的前瞻性1年比较研究:它真的有前景吗?
Surg Endosc. 2016 Apr;30(4):1599-606. doi: 10.1007/s00464-015-4386-4. Epub 2015 Jul 21.