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放射诱导的乳腺未分化多形性肉瘤:保乳治疗后一种罕见但严重的并发症。病例报告及文献综述

Radiation-induced undifferentiated pleomorphic sarcoma of the breast: a rare but serious complication following breast-conserving therapy. A case report and literature review.

作者信息

Komaei I, Guccione F, Sarra F, Palmeri E, Ieni A, Cardia R, Currò G, Navarra G, Palmeri R

出版信息

G Chir. 2019 Nov-Dec;40(6):544-550.

PMID:32007118
Abstract

BACKGROUND

Undifferentiated pleomorphic sarcoma (UPS) of the breast is an extremely rare, but aggressive subtype of sarcoma that can develop in radiotherapy (RT)-treated breast cancer patients. Due to the low incidence, there are many uncertainties regarding the adequate management of these tumors. We present a rare case of radiation-induced UPS in a 63-year-old woman who had undergone breast conserving therapy for invasive ductal carcinoma of the left breast, six years prior to presentation.

CASE PRESENTATION

A 63-year-old woman presented with a rapidly growing left breast mass. She had been diagnosed with invasive ductal carcinoma of the left breast for which she underwent a left upper outer quadrantectomy and ipsilateral axillary dissection followed by RT, six years previously. During her routine oncologic follow-up, the mammography revealed a dense, nodular opacity with microcalcifications. The breast ultrasound (US) confirmed the presence of the nodule. US-guided fine needle aspiration biopsy was performed and the diagnosis of UPS was made, the reason for which the patient underwent wide local excision of the left breast.

CONCLUSION

The diagnosis of RT-induced UPS is challenging and often missed due to the low incidence, long latency period, unspecific imaging findings, and difficulties in clinical and histological detection of these lesions. These tumors should be considered in differential diagnoses of rapidly-growing breast masses in previously RT-treated breast cancer patients, as they can mimic the local recurrence of the primary tumor. Since the prevalence of breast-conserving surgery followed by RT has been increasing, the careful monitoring of at risk patients is of utmost importance, as UPSs are highly aggressive tumors associated with very poor outcomes.

摘要

背景

乳腺未分化多形性肉瘤(UPS)是一种极其罕见但具有侵袭性的肉瘤亚型,可发生于接受过放射治疗(RT)的乳腺癌患者。由于发病率低,这些肿瘤的恰当管理存在许多不确定性。我们报告一例罕见的放射性诱发的UPS病例,患者为一名63岁女性,在就诊前6年曾因左乳腺浸润性导管癌接受保乳治疗。

病例介绍

一名63岁女性因左乳肿块迅速增大就诊。她6年前被诊断为左乳腺浸润性导管癌,接受了左上象限切除术和同侧腋窝清扫术,随后进行了放疗。在她的常规肿瘤学随访期间,乳腺X线摄影显示一个致密的、有微钙化的结节状不透明区。乳腺超声(US)证实了结节的存在。进行了超声引导下细针穿刺活检,诊断为UPS,因此患者接受了左乳广泛局部切除术。

结论

放射性诱发的UPS的诊断具有挑战性,由于其发病率低、潜伏期长、影像学表现不特异以及临床和组织学检测这些病变存在困难,常被漏诊。在既往接受过放疗的乳腺癌患者中,对于迅速增大的乳腺肿块进行鉴别诊断时应考虑到这些肿瘤,因为它们可能酷似原发肿瘤的局部复发。由于保乳手术加放疗的患病率一直在增加,对高危患者进行仔细监测至关重要,因为UPS是具有高度侵袭性且预后极差的肿瘤。

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