Suppr超能文献

乳腺多形性小叶原位癌的治疗结果。

Treatment Outcomes for Pleomorphic Lobular Carcinoma In Situ of the Breast.

机构信息

Department of Surgery, Mayo Clinic, Rochester, MN, USA.

Department of Pathology, Mayo Clinic, Rochester, MN, USA.

出版信息

Ann Surg Oncol. 2018 Oct;25(10):3064-3068. doi: 10.1245/s10434-018-6591-6. Epub 2018 Jun 26.

Abstract

BACKGROUND

Pleomorphic lobular carcinoma in situ (PLCIS) is an uncommon high-grade in situ lesion that shares morphologic features of both classic lobular and ductal carcinoma in situ. Data on the natural history of pure PLCIS are limited, and no evidence-based consensus guidelines for management exist.

METHODS

From our prospectively maintained institutional pathology and breast surgery databases, we identified all patients with a diagnosis of PLCIS on core needle biopsy (CNB) or excisional biopsy from 2004 to 2017. Patient, tumor, treatment, and outcome data were abstracted to analyze upstage rates and treatment outcomes.

RESULTS

We identified 18 patients with pure PLCIS: 15 diagnosed on CNB, 2 diagnosed at operation for atypia on CNB, and 1 diagnosed after excisional biopsy without preceding CNB. Of the 15 patients with PLCIS on CNB, 3 (20%) were upgraded to invasive cancer on surgical excision. Overall, 7 patients were treated with mastectomy (all margin-negative) and 11 with lumpectomy (one with a focally positive margin). Eight patients received adjuvant therapy: six endocrine therapy, one radiation therapy, and one received both. Among patients with a final diagnosis of PLCIS, two ipsilateral recurrences were observed at follow-up: one invasive lobular carcinoma at 87 months and one PLCIS at 16 months postoperatively.

CONCLUSION

PLCIS on CNB mandates surgical resection as 20% of patients may be upgraded to invasive cancer, and outcomes following pathologic margin-negative surgical resection were excellent with only one invasive recurrence observed. Larger-scale investigation with longer follow-up is needed to define a role for adjuvant therapy and to develop evidence-based treatment guidelines.

摘要

背景

多形性小叶原位癌(PLCIS)是一种罕见的高级别原位病变,具有经典小叶状和导管原位癌的形态特征。关于纯 PLCIS 的自然病史数据有限,也没有基于循证的管理共识指南。

方法

我们从我们前瞻性维护的机构病理学和乳房外科数据库中,确定了所有 2004 年至 2017 年期间在核心针活检(CNB)或切除活检中诊断为 PLCIS 的患者。提取患者、肿瘤、治疗和结局数据,以分析升级率和治疗结局。

结果

我们确定了 18 例纯 PLCIS 患者:15 例在 CNB 上诊断,2 例在 CNB 上因非典型性手术诊断,1 例在切除活检后诊断,无先前 CNB。在 15 例在 CNB 上诊断为 PLCIS 的患者中,3 例(20%)在手术切除时升级为浸润性癌。总体而言,7 例患者接受了乳房切除术(均为阴性边缘),11 例患者接受了保乳手术(1 例局部阳性边缘)。8 例患者接受了辅助治疗:6 例内分泌治疗,1 例放射治疗,1 例同时接受了两种治疗。在最终诊断为 PLCIS 的患者中,在随访期间观察到 2 例同侧复发:1 例浸润性小叶癌在 87 个月,1 例在术后 16 个月。

结论

CNB 上的 PLCIS 需要手术切除,因为 20%的患者可能升级为浸润性癌,并且在病理阴性边缘手术后,仅观察到 1 例浸润性复发,结局良好。需要更大规模的研究和更长时间的随访,以确定辅助治疗的作用,并制定基于循证的治疗指南。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验