Okamoto Akio, Namura Kyoko, Uchiyama Hitoji, Kajita Yoshihiro, Inaba Tohru, Nakamura Shigeo, Shimazaki Chihiro
Department of Medicine, Nantan General Hospital, Yagi, Japan.
Am J Hematol. 2005 Sep;80(1):77-8. doi: 10.1002/ajh.20393.
An 86-year-old female was diagnosed with peripheral T-cell lymphoma, unspecified, which affected only her thyroid gland. Lymphoma cells were TIA-1(+), suggesting cytotoxic T-cell origin. She had not suffered from autoimmune thyroiditis and showed normal thyroid function. Without any specific therapies, the lymphomatous lesion showed the partial spontaneous regression before diagnostic hemithyroidectomy, and she had been well for 2 years without relapse. This is the first case of primary thyroid lymphoma of cytotoxic T-cell origin that showed spontaneous regression.
一名86岁女性被诊断为未特定的外周T细胞淋巴瘤,该淋巴瘤仅累及甲状腺。淋巴瘤细胞TIA-1(+),提示为细胞毒性T细胞来源。她未曾患过自身免疫性甲状腺炎,甲状腺功能正常。在诊断性甲状腺半切术前,未经任何特殊治疗,淋巴瘤病灶出现部分自发消退,且她已健康生存2年无复发。这是首例细胞毒性T细胞来源的原发性甲状腺淋巴瘤出现自发消退的病例。