Plaque Morphea at Distance from Breast Cancer Radiotherapy: A Cost of the Treatment?

E. Dobrica, L. Banciu, C. Soare, A. Malciu, V. Voiculescu
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Abstract

Introduction. Morphea is a rare dermatological disease with no known cause, characterized by persistent inflammation, collagen deposition, fibrosis, and atrophy, as well as a considerable reduction in quality of life. Case presentation. An 89-year-old female patient, with a history of arterial hypertension, right mastectomy, and radiation therapy for breast cancer 10 years before, presented for the appearance of two erythematous plaques in the right submammary groove and right flank. The plaques are well-defined, with irregular margins, and have dimensions of 10/5 cm, and 13/8 cm respectively, were infiltrated, with areas of skin retraction and visible capillary network, itchy and painful. They were observed six months before presentation, as a single hyperpigmented lesion that gradually evolved into its current appearance and was treated as a subcutaneous hematoma, without resolution. Laboratory tests showed a nonspecific inflammatory syndrome and an increase in antinuclear antibodies. By corroborating the clinical and paraclinical data, the diagnosis of plaque morphea was made, and the systemic treatment with Penicillin G 2mil IU/12h, 311nm UVB phototherapy was initiated, with favorable evolution. At the subsequent hospitalization, after noticing the increase in the size of the plaques, with their extension to the left hemiabdomen, it was decided to start treatment with Methotrexate 7.5 mg/week, with a favorable evolution and the disappearance of fibrous bands. Conclusions. Although radiotherapy may be the trigger factor of morphea, the time until the onset of the disease (9 years) is consistent with the data presented in the literature (9.4 years).
乳腺癌放疗远处斑块坏死:治疗成本?
介绍。Morphea是一种罕见的皮肤病,病因不明,以持续炎症、胶原沉积、纤维化和萎缩为特征,并可显著降低生活质量。案例演示。89岁女性患者,既往有动脉高血压病史,右侧乳房切除术,10年前曾接受乳腺癌放疗。因右侧乳下沟及右侧腹部出现2个红斑斑块。斑块边界清晰,边缘不规则,尺寸分别为10/ 5cm和13/ 8cm,浸润,皮肤收缩区,可见毛细血管网,瘙痒,疼痛。他们在发病前6个月被观察到,作为一个单一的色素沉着病变,逐渐演变成目前的外观,并作为皮下血肿治疗,没有解决。实验室检查显示非特异性炎症综合征和抗核抗体增加。根据临床及临床旁资料,诊断为斑块坏死,并开始采用青霉素G 2mil IU/12h, 311nm UVB光疗进行全身治疗,进展良好。在随后的住院治疗中,在注意到斑块的大小增加并扩展到左半腹后,决定开始使用甲氨蝶呤7.5 mg/周治疗,进展良好,纤维带消失。结论。虽然放疗可能是嗜睡的触发因素,但直到发病的时间(9年)与文献数据(9.4年)一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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