Shimizu Kimihiro, Ishii Genichiro, Nagai Kanji, Yokose Tomoyuki, Ishizawa Kenichi, Tamaru Junichi, Yoshida Junji, Nishimura Mituyo, Ochiai Atushi
Pathology Division, National Cancer Center Research Institute East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577, Japan.
Jpn J Clin Oncol. 2005 Jul;35(7):412-6. doi: 10.1093/jjco/hyi105. Epub 2005 Jun 23.
Mucosa-associated lymphoid tissue (MALT) lymphoma in the thymus is extremely rare, and little is known about its clinicopathological features. In this study, we examined four cases of MALT lymphoma in the thymus at our institute in terms of clinicopathological features. Most patients had autoimmune disease or hyperglobulinemia, and they also had cysts in the tumors. Both elevated serum levels of autoantibodies and the polyclonal increase in serum Ig remained almost unchanged after total thymectomy in all patients. We recommend that MALT lymphoma in the thymus should be considered in the differential diagnosis when a cystic thymic mass is found and if the patient is Asian and/or has autoimmune disease or hyperglobulinemia.
胸腺黏膜相关淋巴组织(MALT)淋巴瘤极为罕见,对其临床病理特征了解甚少。在本研究中,我们从临床病理特征方面对我院4例胸腺MALT淋巴瘤病例进行了检查。大多数患者患有自身免疫性疾病或高球蛋白血症,且肿瘤内有囊肿。所有患者全胸腺切除术后,自身抗体血清水平升高和血清Ig多克隆增加均几乎保持不变。我们建议,当发现囊性胸腺肿物且患者为亚洲人和/或患有自身免疫性疾病或高球蛋白血症时,鉴别诊断应考虑胸腺MALT淋巴瘤。