Earnest Lisa M, Cooper David S, Sciubba James J, Tufano Ralph P
Division of Head and Neck Surgery, Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Head Neck. 2006 Aug;28(8):765-70. doi: 10.1002/hed.20424.
Mucosa-associated lymphoid tissue (MALT) lymphomas account for less than 1% of all primary thyroid malignancies. They typically arise as neoplastic transformations within areas of autoimmune thyroiditis. Although they tend to have an indolent course, these lymphomas present a diagnostic challenge requiring a high level of suspicion in patients at increased risk of development.
We retrospectively reviewed 3 cases of primary MALT thyroid lymphoma discovered in patients with a compressive goiter. This represents the experience at a single institution from 1996 to 2005. Hospital and clinic records were reviewed to identify the workup, treatment, and outcome.
One of 3 patients underwent preoperative fine-needle aspiration (FNA). All patients underwent total thyroidectomy to relieve compressive symptoms, and the final pathology revealed MALT lymphoma. Two patients subsequently underwent radiation therapy. All patients are alive without evidence of disease recurrence.
These cases are notable for the unexpected presentation of MALT lymphoma within a compressive goiter.
黏膜相关淋巴组织(MALT)淋巴瘤占所有原发性甲状腺恶性肿瘤的比例不到1%。它们通常在自身免疫性甲状腺炎区域内发生肿瘤转化。尽管这些淋巴瘤往往病程进展缓慢,但对其诊断具有挑战性,需要对发病风险增加的患者高度怀疑。
我们回顾性分析了3例在患有压迫性甲状腺肿的患者中发现的原发性MALT甲状腺淋巴瘤病例。这代表了1996年至2005年单一机构的经验。回顾医院和诊所记录以确定检查、治疗和结果。
3例患者中有1例接受了术前细针穿刺活检(FNA)。所有患者均接受了全甲状腺切除术以缓解压迫症状,最终病理显示为MALT淋巴瘤。2例患者随后接受了放射治疗。所有患者均存活,无疾病复发迹象。
这些病例的显著特点是在压迫性甲状腺肿中意外出现MALT淋巴瘤。