韩国垂体偶发瘤的特点及自然病程

You Jin Lee, Sun Wook Cho, S. W. Kim, C. Shin, K. Park, B. Cho, Hong-Kyu Lee, S. Kim
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引用次数: 3

摘要

背景:垂体偶发瘤是指在诊断不相关疾病时,在患者未表现出神经或内分泌体征和症状的情况下,通过计算机断层扫描(CT)或磁共振扫描(MRI)偶然发现的垂体肿块。尽管发病率越来越高,但只有少数研究报道了其特征、自然史、治疗或随访策略。此外,尚无韩国垂体偶发瘤的流行病学资料。方法:回顾性纳入1992年1月至2006年8月在首尔国立大学医院诊断为垂体偶发瘤的患者。我们回顾了基线人口统计学发现和基线和随访期间的基础激素测试、视野测试和MRI(或CT)结果。结果:1310例垂体腺瘤患者中,161例诊断为偶发瘤。诊断时受试者年龄49.7±15.5岁,男性84例。大腺瘤更常见(n = 110, 68.3%)。微腺瘤和拉克氏裂囊肿分别为21例和30例。肿瘤平均直径1.75 cm。功能性偶发瘤如催乳素瘤或肢端肥大症在31例(19.3%)中发现,尽管没有症状或视野缺损。在61例1年以上未接受手术或其他治疗的偶发瘤患者中,仅有3例患者在平均38.0±24.9个月的随访期间肿瘤体积增大。结论:垂体偶发瘤虽高发病率(68.3%),但总体呈良性发展。然而,由于约20%的患者存在功能性肿瘤,诊断时必须进行垂体激素评估。此外,我们在随访中发现3例肿瘤体积增大,包括1例垂体微腺瘤,因此有必要对垂体偶发瘤进行长期仔细的随访。对更多患者的长期、前瞻性研究将揭示韩国垂体偶发瘤的特点和自然史。(韩医师学报23:111~116,2008)
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Characteristics and Natural Course of Pituitary Incidentaloma in Korea
Background: A pituitary incidentaloma is a pituitary mass discovered incidentally by computed tomography (CT) or magnetic resonance (MRI) of the brain performed for evaluation of an unrelated disease, and when the patient did not show neurological or endocrine signs and symptoms. Despite of increasing incidence, only a few studies have reported on characteristics, natural history, treatment, or follow-up strategy. Moreover no epidemiologic data exist on pituitary incidentaloma in Korean. Methods: We retrospectively enrolled subjects diagnosed as pituitary incidentaloma in Seoul National University Hospital from January 1992 to August 2006. We reviewed baseline demographic findings and the results of basal hormone tests, visual field test, and MRI (or CT) at baseline and during follow-up. Results: Among 1310 patients with pituitary adenoma, 161 subjects were diagnosed with incidentaloma. The subject age at diagnosis was 49.7 ± 15.5 years, with 84 males. Macroadenoma was more frequent (n = 110, 68.3%). with microadenomas and Rathke's cleft cysts found in 21 and 30 cases, respectively. The mean diameter of the tumor was 1.75 cm. Functional incidentalomas such as prolactinoma or acromegaly were found in 31 cases (19.3%) although there were no symptoms or visual field defects. Of 61 incidentaloma patients who did not undergo surgery or other treatment over one year, only 3 patient showed an increase in tumor size during the mean 38.0 ± 24.9 months follow-up. Conclusion: Pituitary incidentaloma generally showed a benign course despite the high prevalence of macroadenoma (68.3%). However, as about 20% of the patients had functioning tumors, pituitary hormonal evaluation at diagnosis is mandatory. Furthermore, as we experienced 3 cases with increased tumor size during follow up, including a case of pituitary microadenoma, long-term careful follow-up of pituitary incidentaloma seems necessary. A long-term, prospective study with more patients would reveal the characteristics and the natural history of pituitary incidentalomas in Korea. (J Korean Endocr Soc 23:111~116, 2008)
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