Sahin Hilal, Ceylan Naim, Bayraktaroglu Selen, Tasbakan Sezai, Veral Ali, Savas Recep
Department of Radiology, Faculty of Medicine, Ege University, Izmir, Turkey.
Iran J Radiol. 2012 Mar;9(1):37-41. doi: 10.5812/iranjradiol.6572. Epub 2012 Mar 25.
Necrotizing sarcoid granulomatosis (NSG) is a rare disease which is classified in the spectrum of pulmonary angiitis and granulomatosis. It is a variant of sarcoidosis and differs from it histologically. Diagnosis is based on the pathological features, but radiology may help in the differential diagnosis. It is characterized by alveolar infiltrates or parenchymal nodules in multidetector computed tomography (MDCT). We report a case of a 50-year-old man with the diagnosis of NSG mimicking lung malignancy. Radiological and pathological findings and also the destructive course of the disease will be discussed.
坏死性结节病样肉芽肿病(NSG)是一种罕见疾病,归类于肺血管炎和肉芽肿病范畴。它是结节病的一种变体,在组织学上与之不同。诊断基于病理特征,但放射学检查可能有助于鉴别诊断。其在多排螺旋计算机断层扫描(MDCT)上的特征为肺泡浸润或实质结节。我们报告一例50岁男性,诊断为NSG,临床表现类似肺癌。将讨论其放射学和病理学表现以及疾病的进展过程。