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乳腺原发性腺泡细胞癌预后不良:一例报告及文献复习

Primary acinic cell carcinoma of the breast is associated with a poor outcome: A case report and literature review.

作者信息

Sarsiat Ludivine, Watkinson George, Turnbull Arran, Diana Anna, Oikonomidou Olga

机构信息

Department of Pharmaceutical Sciences, University of Bordeaux, 33076 Bordeaux, France.

Cancer Research UK Edinburgh Centre, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh EH4 2XR, UK.

出版信息

Mol Clin Oncol. 2022 Feb;16(2):43. doi: 10.3892/mco.2021.2476. Epub 2021 Dec 22.

Abstract

Primary acinic cell carcinoma (AcCC) is a rare histological type of malignant breast cancer. AcCC was first identified as an entity in 1996, and since then 51 cases have been reported in the literature. The first early case reports and reviews suggested a relatively favourable prognosis for patients with AcCC; however, reports of AcCC recurrent disease have been more recently described in a subset of patients with high-grade disease. The present case report describes an unusual case of estrogen receptor-negative AcCC of the breast in a 59-year-old woman who did not respond to neoadjuvant chemotherapy (NACT), despite imaging revealing a large reduction in tumour volume. Furthermore, 14 months after NACT completion, the patient presented with disease progression comprising peritoneal involvement and linitis plastica. The patient started on first-line chemotherapy with carboplatin and paclitaxel combination, achieving a notable and prolonged response. After 2.5 years and while still on carboplatin and paclitaxel, the patient developed leptomeningeal carcinomatosis disease (LD) and died 6 weeks after LD presentation. The present report is the third case of AcCC in which cancer-associated death was registered. As studies on large series are lacking, further investigations are required to identify predictors of poor outcome. Notably, the prolonged response achieved to first-line chemotherapy suggested that platinum and taxane compounds may offer a potential therapeutic benefit for patients with AcCC. Moreover, the present case report highlights the importance of careful interpretation of follow-up imaging, as an apparent positive response to treatment may not always be a true representation of disease.

摘要

原发性腺泡细胞癌(AcCC)是一种罕见的组织学类型的恶性乳腺癌。AcCC于1996年首次被确认为一种独立的疾病实体,自那时以来,文献中已报道了51例病例。最初的早期病例报告和综述表明,AcCC患者的预后相对较好;然而,最近在一部分高级别疾病患者中描述了AcCC复发病例。本病例报告描述了一名59岁女性的罕见病例,该患者患有雌激素受体阴性的乳腺AcCC,尽管影像学显示肿瘤体积大幅缩小,但对新辅助化疗(NACT)无反应。此外,在完成NACT 14个月后,患者出现疾病进展,包括腹膜受累和皮革胃。患者开始使用卡铂和紫杉醇联合进行一线化疗,取得了显著且持久的缓解。在使用卡铂和紫杉醇2.5年后,患者发生软脑膜癌病(LD),并在出现LD后6周死亡。本报告是第三例记录有癌症相关死亡的AcCC病例。由于缺乏对大量病例系列的研究,需要进一步调查以确定预后不良的预测因素。值得注意的是,一线化疗取得的持久缓解表明铂类和紫杉烷类化合物可能对AcCC患者具有潜在的治疗益处。此外,本病例报告强调了仔细解读随访影像学的重要性,因为对治疗的明显阳性反应可能并不总是疾病的真实表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34d7/8739076/e8f408cd27f0/mco-16-02-02476-g00.jpg

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