Sweet's syndrome in a patient with oral cancer associated with radiotherapy

E.H. van der Meij , J.B. Epstein , J. Hay , V. Ho , K. Lerner
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引用次数: 49

Abstract

Approximately 10–20% of the reported patients with acute febrile neutrophilic dermatosis (Sweet's syndrome) have an associated neoplasm. Oral findings of Sweet's syndrome are rarely reported, and no cases in patients with oral cancer have been reported to date. This report describes the clinico- and histopathological findings of Sweet's syndrome in a patient with oral cancer, treated with radiotherapy. After 10 fractions of external beam radiotherapy, treatment was interrupted because of severe oral mucositis which extended beyond the radiation fields. Two days later the patient developed multiple tender skin lesions and the diagnosis Sweet's syndrome was made. Skin and oral lesions resolved without additional treatment and did not recur upon resuming radiotherapy. As suggested in previous case reports, tumour antigens might play a role in the development of Sweet's syndrome. In this case, irradiation therapy may also have been a trigger for this syndrome.

口腔癌放疗患者的Sweet综合征
大约10-20%的报道的急性发热性中性粒细胞皮肤病(Sweet综合征)患者伴有肿瘤。Sweet's综合征的口腔表现很少报道,迄今为止没有口腔癌患者的病例报道。本报告描述了口腔癌患者放疗后出现Sweet综合征的临床和组织病理学结果。经10次体外放射治疗后,因严重的口腔黏膜炎而中断治疗。两天后,患者出现多处皮肤触痛病变,诊断为斯威特综合征。皮肤和口腔病变在没有额外治疗的情况下消退,并且在恢复放疗后没有复发。正如以前的病例报告所表明的那样,肿瘤抗原可能在斯威特综合征的发展中起作用。在这种情况下,放射治疗也可能是这种综合征的触发因素。
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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