Wain E M, Setterfield J, Judge M R, Harper J I, Pemberton M N, Russell-Jones R
Skin Tumour Unit, St John's Institute of Dermatology, St Thomas' Hospital, London.
Clin Exp Dermatol. 2003 Sep;28(5):499-501. doi: 10.1046/j.1365-2230.2003.01348.x.
Involvement of the oral mucosa in cutaneous T-cell lymphoma is uncommon and is usually associated with a poor prognosis (the majority of patients dying from the disease within 3 years of the diagnosis of oral involvement). We report the first case of intraoral mycosis fungoides occurring in a child. In addition, our patient has had intraoral disease for 3 years and is currently systemically well with no evidence of cutaneous or systemic disease progression.
口腔黏膜受累于皮肤T细胞淋巴瘤并不常见，且通常与预后不良相关（大多数患者在口腔受累诊断后的3年内死于该疾病）。我们报告了首例发生在儿童中的口腔蕈样肉芽肿病例。此外，我们的患者口腔疾病已持续3年，目前全身状况良好，无皮肤或全身疾病进展的迹象。
