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本文引用的文献

1
Rhabdomyosarcoma of the Breast in Adolescent and Young Adult (AYA) Women.青少年及年轻成年(AYA)女性乳腺横纹肌肉瘤
J Pediatr Hematol Oncol. 2017 Jan;39(1):62-66. doi: 10.1097/MPH.0000000000000710.
2
The role of radiotherapy in the management of localized soft tissue sarcomas.放射治疗在局限性软组织肉瘤治疗中的作用。
Cancer Biol Med. 2016 Sep;13(3):373-383. doi: 10.20892/j.issn.2095-3941.2016.0028.
3
Breast relapse after metastatic alveolar rhabdomyosarcoma: Is it an incurable entity?转移性肺泡横纹肌肉瘤后的乳腺复发:它是一种无法治愈的疾病吗?
Indian J Med Paediatr Oncol. 2016 Apr-Jun;37(2):119-21. doi: 10.4103/0971-5851.180139.
4
Radiation therapy may increase metastatic potential in alveolar rhabdomyosarcoma.放射治疗可能会增加肺泡横纹肌肉瘤的转移潜能。
Pediatr Blood Cancer. 2015 Sep;62(9):1550-1554. doi: 10.1002/pbc.25516. Epub 2015 Mar 19.
5
Rhabdomyosarcoma of the breast - a rare malignancy.乳腺横纹肌肉瘤——一种罕见的恶性肿瘤。
Am J Case Rep. 2013 Jul 15;14:250-2. doi: 10.12659/AJCR.883976. Print 2013.
6
Nonepithelial malignancies of the breast.乳腺非上皮性恶性肿瘤。
Oncology (Williston Park). 2004 May;18(5):665-73; discussion 673-6.
7
Primary and metastatic rhabdomyosarcoma in the breast: report of two pediatric cases.乳腺原发性及转移性横纹肌肉瘤:两例儿科病例报告
Eur J Radiol. 2003 Dec;48(3):282-4. doi: 10.1016/s0720-048x(03)00041-x.
8
Prognostic factors for patients with localized soft-tissue sarcoma treated with conservation surgery and radiation therapy: an analysis of 1225 patients.采用保肢手术和放射治疗的局限性软组织肉瘤患者的预后因素:1225例患者的分析
Cancer. 2003 May 15;97(10):2530-43. doi: 10.1002/cncr.11365.
9
Response to chemotherapy and predictors of survival in adult rhabdomyosarcoma.成人横纹肌肉瘤对化疗的反应及生存预测因素
Ann Surg. 2001 Aug;234(2):215-23. doi: 10.1097/00000658-200108000-00012.
10
Strong immunostaining for myogenin in rhabdomyosarcoma is significantly associated with tumors of the alveolar subclass.横纹肌肉瘤中肌生成素的强免疫染色与肺泡亚类肿瘤显著相关。
Am J Pathol. 2000 Feb;156(2):399-408. doi: 10.1016/S0002-9440(10)64743-8.

乳腺横纹肌肉瘤:一种罕见恶性肿瘤的报告。

Rhabdomyosarcoma of the breast: Report of a rare malignancy.

机构信息

a Department of Pathology , Anyang Tumor Hospital , Anyang , Henan , China.

b Department of Pulmonary Medicine , The First Affiliated Hospital of Zhengzhou University , Zhengzhou , Henan , China.

出版信息

Cancer Biol Ther. 2017 Sep 2;18(9):676-680. doi: 10.1080/15384047.2017.1360440.

DOI:10.1080/15384047.2017.1360440
PMID:28795902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5663407/
Abstract

Rhabdomyosarcoma (RMS) is an uncommon type of soft-tissue malignancy which mainly influences children. RMS rarely occurs in breast and little of the clinical behavior and treatment strategies were reported. Here, we describe a case of adult female patient with breast RMS. A 34-years-old Chinese woman visited to our hospital complaining palpable mass in her left breast. Seven months ago, the patient was diagnosed as lymphocytic mastitis and received surgical excision in the left breast. Five months later, she noticed a palpable mass again in the left breast. Ultrasonography suspected a malignant lesion and a diagnosis of RMS was made after segmental mastectomy and immunohistochemical staining. Therapy consisted of mastectomy and following neoadjuvant chemotherapy. The patient has remained disease free 30 months post-operatively. We should consider RMS when we see a breast mass. Tissue biopsy and immunohistochemical staining are recommended for diagnosis of RMS in young women. Oncologists should take immediate and active treatment on RMS.

摘要

横纹肌肉瘤(RMS)是一种罕见的软组织恶性肿瘤,主要影响儿童。RMS 在乳房中很少见,报道的临床行为和治疗策略也很少。在这里,我们描述了一例成年女性乳房 RMS 的病例。一位 34 岁的中国女性因左乳房可触及肿块就诊于我院。7 个月前,该患者被诊断为淋巴细胞性乳腺炎,并接受了左乳房的手术切除。5 个月后,她再次发现左乳房可触及肿块。超声怀疑为恶性病变,经节段性乳房切除术和免疫组织化学染色诊断为 RMS。治疗包括乳房切除术和随后的新辅助化疗。患者术后 30 个月无病生存。当我们看到乳房肿块时,应考虑 RMS。对于年轻女性,建议进行组织活检和免疫组织化学染色以诊断 RMS。肿瘤学家应立即对 RMS 进行积极治疗。