Binesh Fariba, Akhavan Ali, Navabii Hossein
Pathology Department, Yazd Shahid Sadoghi University, Yazd, Iran, Islamic Republic of Iran.
BMJ Case Rep. 2011 Nov 1;2011:bcr0520114277. doi: 10.1136/bcr.05.2011.4277.
Primary thyroid gland lymphomas are uncommon tumours that occur in the setting of lymphocytic thyroiditis or Hashimoto's disease in almost all cases. Rarely these tumours show extensive plasmacytic differentiation. In these conditions, a distinction between an inflammatory thyroid infiltrate and extramedullary plasmacytoma may be extremely difficult and precise criteria and ancillary techniques are necessary for a correct diagnosis. The authors report a case of mucosa associated lymphoid tissue (MALT) lymphoma of the thyroid gland in a 69-year-old Iranian man with Hashimoto's thyroiditis which was diagnosed by means of immunohistochemical stains. This case demonstrates that histology may not distinguish between extramedullary plasmacytoma and MALT lymphoma of the thyroid gland and the use of immunohistochemical staining stains were essential to prove definite diagnosis.
原发性甲状腺淋巴瘤是一种罕见肿瘤,几乎所有病例均发生于淋巴细胞性甲状腺炎或桥本氏病背景下。这些肿瘤很少表现出广泛的浆细胞分化。在这些情况下,区分炎性甲状腺浸润和髓外浆细胞瘤可能极其困难,正确诊断需要精确的标准和辅助技术。作者报告了一例69岁患有桥本氏甲状腺炎的伊朗男性甲状腺黏膜相关淋巴组织(MALT)淋巴瘤病例,该病例通过免疫组织化学染色得以诊断。此病例表明,组织学可能无法区分甲状腺的髓外浆细胞瘤和MALT淋巴瘤,使用免疫组织化学染色对于明确诊断至关重要。