Kong Joshua, Shahait Awni D, Kim Steve, Choi Lydia
General Surgery, Wayne State University School of Medicine, Detroit, Michigan, USA.
General Surgery, Wayne State University School of Medicine, Detroit, Michigan, USA
BMJ Case Rep. 2020 Feb 10;13(2):e232616. doi: 10.1136/bcr-2019-232616.
Breast sarcoma is a rare form of malignancy that arises from connective tissue within the breast, comprising less than 5% of all sarcomas. They develop as primary tumours or as secondary following radiation therapy. Diagnosis can be challenging as breast sarcomas are often asymptomatic and resemble benign breast tissue changes. Radiation-induced breast sarcomas present in various forms with an average latency period of 10-20 years following initial radiation therapy. Angiosarcomas are the most common form, while other types such as undifferentiated pleomorphic sarcomas remain rare. Here, we report a case of radiation-induced undifferentiated pleomorphic breast sarcoma in a 75-year-old woman that developed nearly 20 years following breast conserving surgery and radiation for invasive ductal carcinoma. The patient initially noticed a mass in 2017 on self-examination. The mammogram, ultrasound and biopsy at the time showed a benign 2.2 cm nodular fasciitis without malignancy. The mass grew rapidly in the next 6 months to 5.6 cm and repeat biopsy diagnosed undifferentiated pleomorphic sarcoma. The mass abutted the pectoralis muscle but staging workup ruled out distant metastasis and the patient underwent wide local resection of the mass with clear margins. The patient subsequently underwent further postoperative radiation due to insufficient posterior margin width on wide local excision, as chest wall resection would have been required for a wider posterior margin. Prognosis for postradiation sarcomas is generally poor with 27%-36% 5-year survival, with surgical resection as the main line of treatment. The patient currently remains disease-free after 15 months of surveillance.
乳腺肉瘤是一种罕见的恶性肿瘤,起源于乳腺内的结缔组织,占所有肉瘤的比例不到5%。它们可作为原发性肿瘤出现,也可在放射治疗后作为继发性肿瘤出现。由于乳腺肉瘤通常无症状且类似良性乳腺组织变化,因此诊断具有挑战性。放射诱导的乳腺肉瘤呈现出多种形式,在初次放射治疗后的平均潜伏期为10至20年。血管肉瘤是最常见的形式,而其他类型如未分化多形性肉瘤仍然罕见。在此,我们报告一例75岁女性的放射诱导未分化多形性乳腺肉瘤病例,该病例在保乳手术和针对浸润性导管癌的放疗后近20年发生。患者最初在2017年自我检查时发现一个肿块。当时的乳房X光检查、超声检查和活检显示为一个2.2厘米的良性结节性筋膜炎,无恶性病变。该肿块在接下来的6个月内迅速增大至5.6厘米,重复活检诊断为未分化多形性肉瘤。肿块紧邻胸大肌,但分期检查排除了远处转移,患者接受了肿块的广泛局部切除,切缘清晰。由于广泛局部切除时后缘宽度不足,患者随后接受了进一步的术后放疗,因为要获得更宽的后缘需要进行胸壁切除。放射后肉瘤的预后通常较差,5年生存率为27%至36%,主要治疗方法为手术切除。在15个月的随访后,患者目前仍无疾病。