Wöckel W, Hofmann W J, Rolle A, Thetter O, Schmölder A, Schopohl J, Suren H
Pathologisches Institut, Zentralkrankenhaus Gauting der LVA Oberbayern.
Dtsch Med Wochenschr. 1990 Mar 16;115(11):412-7. doi: 10.1055/s-2008-1065023.
A large mediastinal tumour was discovered radiologically in a 50-year-old man, with at times blood-tinged sputum and dyspnoea. Parasternal needle biopsy revealed a thymic carcinoid. After surgical excision of the tumour, which had argyrophilic foci (total weight of tumour 1,605 g), histochemical analysis demonstrated neuron-specific enolase, synaptophysin and chromogranin, as well as calcitonin (as the only hormone). For the first time in a thymic carcinoid, radioimmunoassay demonstrated growth-hormone-releasing hormone (2 micrograms/g tumour tissue). Post-operative radiotherapy (total dosage 50.5 Gy) was instituted because histological examination had shown invasion of the capsule and blood vessels. There has been no local recurrence or metastases after three years.
一名50岁男性经放射检查发现纵隔有一个大肿瘤,有时伴有痰中带血和呼吸困难。胸骨旁穿刺活检显示为胸腺类癌。肿瘤切除术后(肿瘤总重1605克,有嗜银灶),组织化学分析显示有神经元特异性烯醇化酶、突触素、嗜铬粒蛋白以及降钙素(作为唯一激素)。在胸腺类癌中首次通过放射免疫分析检测到生长激素释放激素(2微克/克肿瘤组织)。由于组织学检查显示肿瘤侵犯包膜和血管,因此术后进行了放射治疗(总剂量50.5 Gy)。三年后未出现局部复发或转移。