Avenia Nicola, Ragusa Mark, Cirocchi Roberto, Puxeddu Efisio, Cavaliere Antonio, De Feo Pierpaolo, Sidoni Angelo, Roila Fausto, Sanguinetti Alessandro, Puma Francesco
Endocrine Surgical Unit, University of Perugia, Perugia, Italy.
Tumori. 2009 Nov-Dec;95(6):712-9. doi: 10.1177/030089160909500613.
Primitive thyroid lymphoma, although rare, is becoming more frequent. Its incidence is increasing, from 0.5% in the sixties to 1-5% of all thyroid neoplasms today. The diagnosis of such neoplasms is not always straightforward. In fact, it is often the result of pathologic findings on a gland resected for an apparently benign disease. Surgical dissection may prove more complicated than in standard cases of thyroidectomy for the possible tight adhesions existing between the gland's capsule and the surrounding structures. In cases of capsular infiltration, postoperative external local radiotherapy is indicated.
A retrospective observational analysis was performed to establish whether patients with incidental thyroid lymphomas who underwent total thyroidectomy for another pathology had major surgical complications and worse prognostic results than patients with an accurate preoperative diagnosis.
Six cases of thyroid lymphoma were retrospectively reviewed: 4 diffuse large B-cell lymphomas and 2 MALT lymphomas. Of these, 2 were correctly preoperatively identified by fine-needle aspiration biopsy and 4 were an unexpected finding at histology: 3 cases of total thyroidectomy carried out for huge hypothyroid goiter in patients affected by Hashimoto's thyroiditis and in 1 case of total thyroidectomy carried out for anaplastic carcinoma in a patient affected by Hashimoto's thyroiditis.
In our experience, a correct preoperative diagnosis was extremely difficult (33%). In patients who underwent fine-needle aspiration, a correct diagnosis was made in 66% of cases. All patients with stage IE lymphoma who underwent total thyroidectomy had equivalent surgical complications and prognosis.
原发性甲状腺淋巴瘤虽罕见,但发病率正逐渐上升,从六十年代的0.5%增至如今占所有甲状腺肿瘤的1 - 5%。此类肿瘤的诊断并非总是一目了然。实际上,其诊断往往源于对因看似良性疾病而切除的腺体进行病理检查的结果。由于甲状腺包膜与周围结构之间可能存在紧密粘连,手术解剖可能比标准甲状腺切除术更为复杂。若存在包膜浸润,术后需进行局部外照射放疗。
进行一项回顾性观察分析,以确定因其他病理情况接受全甲状腺切除术的偶发性甲状腺淋巴瘤患者,是否比术前准确诊断的患者有更多的手术主要并发症及更差的预后结果。
回顾性分析了6例甲状腺淋巴瘤病例:4例弥漫性大B细胞淋巴瘤和2例黏膜相关淋巴组织淋巴瘤。其中,2例通过细针穿刺活检在术前得到正确诊断,4例在组织学检查时意外发现:3例因巨大甲状腺功能减退性甲状腺肿而进行全甲状腺切除术的患者患有桥本甲状腺炎,1例因间变性癌而进行全甲状腺切除术的患者患有桥本甲状腺炎。
根据我们的经验,术前正确诊断极为困难(33%)。接受细针穿刺的患者中,66%的病例得到了正确诊断。所有接受全甲状腺切除术的IE期淋巴瘤患者的手术并发症和预后相当。