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[恶性甲状腺淋巴瘤——诊断与治疗问题]

[Malignant thyroid lymphoma--diagnostic and treatment problems].

作者信息

Buła Grzegorz, Bichalski Wojciech R, Waler Janusz M, Podwińska Ewa

机构信息

Katedry i Oddziału Klinicznego Chirurgii Ogólnej w Bytomiu.

出版信息

Wiad Lek. 2002;55(3-4):144-9.

Abstract

UNLABELLED

The aim of this study was to present our experience in the diagnostics and treatment of primary malignant thyroid lymphoma (PMTL). Five patients at the age of 48-72 years with PMTL were treated at the Department of General Surgery in Bytom in the years 1988-1999. They made up 0.04% of patients operated on at this time in our Department because of different types of goiter and 1.05% because of thyroid carcinoma. The clinical examinations included ultrasonography, radioisotope diagnostics, preoperative thin needle biopsy and hormonal examination of thyroid gland. All patients were operated on under general anesthesia and with intraoperative histopathological examination. They were treated with chemo- and/or radiotherapy in postoperative period. The appearance of PMTL was preceded by nodular goiter or Hashimoto disease. In three cases we observed neck compression symptoms and in two the dramatic course of disease. Ultrasonography revealed hypoechogenic thyroid gland with nodular structures characterized by the decreased J131 uptake. In one case thin needle biopsy confirmed the diagnosis of PMTL. Evident hypothyreosis was diagnosed in one and subclinical in two patients. Surgical treatment--partial excision of neoplastic tumor--was complicated by tracheostomy in two cases. One case with almost total resection of thyroid gland was complicated by lesion of esophagus which was sutured. After operation one patient was treated with chemotherapy, one with radiotherapy and two cases using both of methods. Three patients died: in 3rd, 32nd day and after 3 months since surgery. We confirmed the remission of the disease in two the youngest patients with not advanced state. One of them was treated with Co 60 therapy and the second one with chemotherapy according to COP and radiotherapy.

CONCLUSIONS

PMTL is a rare disease and difficult to diagnose. The biopsy is useful. The treatment of PMTL combined, including surgical treatment, chemo- and radiotherapy. The prognosis is uncertain and depends on the disease period.

摘要

未标注

本研究的目的是介绍我们在原发性甲状腺恶性淋巴瘤(PMTL)诊断和治疗方面的经验。1988年至1999年期间,比托姆普通外科治疗了5例年龄在48至72岁的PMTL患者。他们占当时因不同类型甲状腺肿在我科接受手术患者的0.04%,因甲状腺癌接受手术患者的1.05%。临床检查包括超声检查、放射性同位素诊断、术前细针穿刺活检和甲状腺激素检查。所有患者均在全身麻醉下进行手术,并进行术中组织病理学检查。术后对他们进行化疗和/或放疗。PMTL出现之前有结节性甲状腺肿或桥本氏病。3例出现颈部压迫症状,2例病情进展迅速。超声检查显示甲状腺低回声,有结节结构,表现为131碘摄取减少。1例细针穿刺活检确诊为PMTL。1例诊断为明显甲状腺功能减退,2例为亚临床甲状腺功能减退。手术治疗——肿瘤部分切除术——2例并发气管切开术。1例几乎全甲状腺切除术后并发食管损伤并进行了缝合。术后1例患者接受化疗,1例接受放疗,2例同时采用两种方法。3例患者死亡:分别在术后第3天、第32天和3个月后。我们证实了2例最年轻、病情未进展患者的病情缓解。其中1例接受钴60治疗,另1例根据COP方案接受化疗和放疗。

结论

PMTL是一种罕见疾病,诊断困难。活检很有用。PMTL的治疗采用综合方法,包括手术治疗、化疗和放疗。预后不确定,取决于疾病分期。

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