Yaakup H, Sagap I, Fadilah S A
Department of Medicine, Faculty of Medicine, Universiti Kebangsaan Malaysia, Jalan Yaacob Latif, Bandar Tun Razak, Kuala Lumpur 56000, Malaysia.
Singapore Med J. 2008 Oct;49(10):e289-92.
Primary oesophageal lymphoma is a very rare entity, with fewer than 30 reported cases worldwide. It represents an important cause of dysphagia. Most of the oesophageal lymphomas are diffuse large B-cell type, with only one reported case of anaplastic large cell lymphoma (ALCL) of T-cell phenotype. Primary oesophageal lymphomas that are not associated with an immunocompromised state tend to affect elderly patients. We describe the first case of primary oesophageal Ki (CD30)-positive ALK+ALCL of T-cell phenotype in a 34-year-old immunocompetent woman, who presented with a two-year history of dysphagia. She was treated with chemotherapy and endoscopic oesophageal dilations and stenting, resulting in complete remission of the lymphoma and resolution of the dysphagia. She then underwent autologous peripheral blood haematopoietic stem cell transplantation and remained disease-free two years after the diagnosis.
原发性食管淋巴瘤是一种极为罕见的疾病,全球报告病例少于30例。它是吞咽困难的一个重要原因。大多数食管淋巴瘤为弥漫性大B细胞型,仅有1例报告的T细胞表型间变性大细胞淋巴瘤(ALCL)。非免疫功能低下状态相关的原发性食管淋巴瘤往往影响老年患者。我们描述了首例原发性食管T细胞表型的Ki(CD30)阳性ALK+ALCL病例,患者为一名34岁免疫功能正常的女性,有两年吞咽困难病史。她接受了化疗以及内镜下食管扩张和支架置入治疗,淋巴瘤完全缓解,吞咽困难症状消失。随后她接受了自体外周血造血干细胞移植,诊断后两年无病生存。