Department of Radiology, Gartnavel General Hospital, Glasgow, UK.
Br J Radiol. 2011 Jan;84(997):e14-7. doi: 10.1259/bjr/91375895.
We present the case of a 73-year-old woman who presented with clinical features of Cushing's syndrome, confirmed biochemically with elevated levels of cortisol and adrenocorticotrophic hormone (ACTH). Petrosal venous sampling showed no ACTH gradient and MRI of pituitary was normal, suggesting ectopic ACTH production. In the course of further investigations, a thoracic CT was carried out to look for evidence of bronchial neoplasm. Although there was no discrete tumour identified, CT revealed widespread fine nodularity in the right middle and lower lobe. Subsequent trans-bronchial and video-assisted thorascopic biopsy showed pulmonary tumourlets and two typical carcinoid tumours on a background of diffuse idiopathic pulmonary neuroendocrine cell neoplasia (DIPNECH). We describe the clinical, radiological and histological features of this rare condition.
我们报告了一例 73 岁女性患者,其临床表现符合库欣综合征,通过检测发现皮质醇和促肾上腺皮质激素(ACTH)水平升高而得以确诊。岩下窦采血未见 ACTH 梯度,垂体 MRI 正常,提示异位 ACTH 产生。在进一步检查过程中,进行了胸部 CT 检查以寻找支气管肿瘤的证据。尽管未发现明显的肿瘤,但 CT 显示右肺中叶和下叶有广泛的细小结节。随后的经支气管和电视辅助胸腔镜活检显示肺类瘤和弥漫性特发性肺神经内分泌细胞肿瘤(DIPNECH)背景下的两个典型类癌肿瘤。我们描述了这种罕见疾病的临床、放射学和组织学特征。