Acrometastasis of the Third Finger in Widespread Radiation-Induced Angiosarcoma

IF 2.4 4区 医学 Q2 RHEUMATOLOGY
Etienne Rivière, Pierre Germain
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引用次数: 0

Abstract

An 88-year-old woman with dementia, who previously underwent tumorectomy and radiation for left breast cancer in 2007, developed extensive ulcerated purplish nodular lesions of the left breast (Figure 1A) 5 years later. These lesions were identified as angiosarcoma located in the radiotherapy field. Despite receiving four courses of palliative chemotherapy with taxol, she experienced painful swelling in the third phalanx of her left middle finger, initially treated with rifampicin and ofloxacin for 3 weeks. Distal purplish nodular cutaneous lesions (Figure 1B) and radiological evidence of erosion and destruction of the distal phalanx (Figure 1C) persisted. A biopsy confirmed the presence of angiosarcoma acrometastasis, and the patient was provided with best supportive care but passed away 1 month later.

Acrometastases of the hand are exceptionally rare, comprising less than 0.1% of malignant bone lesions and up to 0.6% in autopsy series [1]. These lesions primarily occur in patients around 60 years of age, often with a history of lung carcinoma, and they carry a poor prognosis, typically averaging around 6 months [2]. In the hand, both metacarpals and phalanges can be affected, with the distal phalanx of the thumb being most commonly involved [3]. These lesions can mimic inflammatory or benign conditions, such as gout or infections, which may lead to misdiagnosis, underreporting, and delayed treatment. Additionally, some patients might overlook their condition due to denial, addiction, or cognitive impairment, resulting in presentation at advanced stages with widespread disease and a poor prognosis, as seen in the patient.

There are several other complications that can occur after chemotherapy or radiotherapy for breast cancer, including localized pain or skin lesions [4], breast lymphedema [5], radiation-induced fibrosis of the breast [6], skeletal muscle dysfunction [7], osteoporosis [8], neuropathic pain [9], valvular heart disease [10] or cardiovascular toxicity [11], amenorrhea and infertility in younger women [12], metabolic alterations [13] or diabetes and cancer-related fatigue [14], cognitive impairment [15] with or without sleep disturbance [16], anxiety or depression [17], radiation-induced pulmonary fibrosis [18] or bronchiolitis obliterans with organizing pneumonia [19], and second malignancies such as leukemia [20].

Radiation-induced angiosarcoma of the breast is a very rare and severe complication of radiotherapy, primarily observed in older women, with an estimated incidence of 0.05%–0.3% [21]. The aggressive nature of this tumor and its propensity for metastasis, although unlikely to the finger, might be attributed to dysregulation of angiogenesis combined with chronic lymphedema, which could facilitate the dissemination of neoplastic cells [22].

E.R. and P.G. were responsible for conceptualization, methodology, writing – original draft, writing – review and editing, supervision, and project administration.

The authors declare no conflicts of interest.

广泛性放射性血管肉瘤中指端转移
一名88岁痴呆女性,2007年因左乳腺癌接受肿瘤切除术和放疗,5年后左乳房出现广泛溃疡性紫色结节病变(图1A)。这些病变被确定为位于放疗场的血管肉瘤。尽管接受了4个疗程的紫杉醇姑息性化疗,但她的左中指第三指骨出现疼痛肿胀,最初使用利福平和氧氟沙星治疗3周。远端紫色结节性皮肤病变(图1B)和远端指骨侵蚀和破坏的放射证据(图1C)持续存在。活检证实了血管肉瘤的存在,患者得到了最好的支持治疗,但在1个月后去世。手部肢端转移异常罕见,占恶性骨病变的不到0.1%,在尸检系列[1]中高达0.6%。这些病变主要发生在60岁左右的患者,通常有肺癌病史,预后较差,通常平均约为6个月。在手部,掌骨和指骨均可受累,拇指远端指骨最常受累。这些病变可以模拟炎症或良性状况,如痛风或感染,这可能导致误诊、漏报和延迟治疗。此外,一些患者可能由于否认、成瘾或认知障碍而忽视了自己的病情,导致疾病扩散到晚期,预后较差,如患者所见。乳腺癌化疗或放疗后还可能出现其他一些并发症,包括局部疼痛或皮肤病变[4]、乳腺淋巴水肿[5]、辐射引起的乳腺纤维化[6]、骨骼肌功能障碍[7]、骨质疏松[8]、神经性疼痛[9]、瓣膜性心脏病[10]或心血管毒性[11]、年轻女性闭经和不孕[12]、代谢改变[13]或糖尿病和癌症相关疲劳[14]。认知障碍[15]伴或不伴睡眠障碍[16],焦虑或抑郁[17],放射性肺纤维化[18]或闭塞性细支气管炎伴组织性肺炎[19],第二恶性肿瘤如白血病[20]。放射诱导的乳腺血管肉瘤是一种非常罕见和严重的放射治疗并发症,主要见于老年妇女,估计发病率为0.05%-0.3%。这种肿瘤的侵袭性及其转移倾向,虽然不太可能转移到手指,但可能归因于血管生成失调并慢性淋巴水肿,这可能促进肿瘤细胞的播散。和P.G.负责构思、方法论、写作原稿、写作审查和编辑、监督和项目管理。作者声明无利益冲突。
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来源期刊
CiteScore
3.70
自引率
4.00%
发文量
362
审稿时长
1 months
期刊介绍: The International Journal of Rheumatic Diseases (formerly APLAR Journal of Rheumatology) is the official journal of the Asia Pacific League of Associations for Rheumatology. The Journal accepts original articles on clinical or experimental research pertinent to the rheumatic diseases, work on connective tissue diseases and other immune and allergic disorders. The acceptance criteria for all papers are the quality and originality of the research and its significance to our readership. Except where otherwise stated, manuscripts are peer reviewed by two anonymous reviewers and the Editor.
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