Suppr超能文献

子宫平滑肌肉瘤皮肤孤立转移:病例报告及文献复习。

Isolated cutaneous metastasis of uterine leiomyosarcoma: case report and review of literature.

机构信息

Department of Surgery, Mayo General Hospital, Castlebar, Co Mayo, Ireland.

出版信息

Diagn Pathol. 2012 Jul 18;7:85. doi: 10.1186/1746-1596-7-85.

Abstract

UNLABELLED

A 54 year old lady presented for routine excision of a scalp lesion thought clinically to represent a sebaceous cyst of the right occiput. 4 years earlier she underwent total abdominal hysterectomy and right salpingo-oophorectomy for 3 large uterine fibroids. Histo-pathological examination of the hysterectomy specimen revealed an incidental low-grade leiomyosarcoma. Staging imaging was negative for metastatic disease. She made an uneventful recovery and was treated further by adjuvant pelvic radiotherapy.She noticed an uncomfortable and unsightly cystic swelling on her occiput four years after hysterectomy and was referred for routine excision of what was believed to be a benign lesion. The lesion was excised and sent for histopathological examination. Microscopic analysis including immuno-histochemistry demonstrated an ER and PR positive metastatic deposit of leiomyosarcoma. The margins of excision were histologically clear of disease.At Multi-Disciplinary Team (MDT) discussion a diagnosis of metastatic scalp deposit from previous uterine leiomyosarcoma was made. Re-staging CT brain, thorax, abdomen and pelvis and MRI brain were negative for local recurrence or distant metastases. She is currently undergoing radiotherapy to the scalp and surrounding tissues and will be followed up closely by the involved teams.To the best of our knowledge, this is the first case described in the worldwide literature of isolated cutaneous metastasis to the scalp of uterine leiomyosarcoma without evidence of disseminated disease at other sites.

VIRTUAL SLIDES

The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1311834987345566.

摘要

未注明

一位 54 岁的女士因头皮病变前来就诊,临床诊断为右枕部的皮脂腺囊肿。4 年前,她因 3 个大的子宫肌瘤行全子宫切除术和右输卵管卵巢切除术。子宫切除标本的组织病理学检查显示为偶然的低度平滑肌肉瘤。分期影像学检查未见转移性疾病。她恢复顺利,并进一步接受辅助盆腔放疗。她在子宫切除后 4 年注意到头枕部出现一个不舒服且难看的囊性肿胀,并被转诊行常规切除,认为这是一个良性病变。切除的病变进行了组织病理学检查。包括免疫组织化学在内的显微镜分析显示为 ER 和 PR 阳性的转移性平滑肌肉肉瘤。切除边缘在组织学上无疾病。在多学科团队(MDT)讨论中,诊断为先前子宫平滑肌肉瘤的头皮转移灶。重新分期 CT 脑、胸部、腹部和骨盆以及 MRI 脑均未发现局部复发或远处转移。她目前正在接受头皮和周围组织的放疗,相关团队将密切随访。据我们所知,这是首例在全球文献中描述的子宫平滑肌肉瘤孤立性皮肤转移至头皮,且无其他部位播散性疾病的证据。

虚拟幻灯片

本文的虚拟幻灯片可在此处找到:http://www.diagnosticpathology.diagnomx.eu/vs/1311834987345566.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验