Yuceler Zeyneb, Kantarci Mecit, Karabulut Nevzat, Ogul Hayri, Bayraktutan Ummugulsum, Akman Canan
Department of Radiology (Drs. Bayraktutan, Kantarci, Ogul, and Yuceler), School of Medicine, Ataturk University, 25000 Erzurum; Department of Radiology (Dr. Karabulut), School of Medicine, Pamukkale University, 20000 Denizli; and Department of Radiology (Dr. Akman), Cerrahpasa Medical Faculty, Istanbul University, 34000 Istanbul; Turkey.
Tex Heart Inst J. 2014 Jun 1;41(3):338-40. doi: 10.14503/THIJ-13-3350. eCollection 2014 Jun.
Erdheim-Chester disease is a rarely reported disease that can affect nearly every organ and chiefly infiltrates the connective, perivascular, and adipose tissue. The disease is a form of non-Langerhans-cell histiocytosis characterized by the proliferation of foamy histiocytes; its cardiovascular complications carry a severe prognosis. We present the case of a 29-year-old woman who was admitted for analysis of her angina. Our evaluation with use of cardiac multidetector computed tomographic angiography revealed large mediastinal soft tissue that compressed the patient's left anterior descending coronary artery. To our knowledge, this is the first report of the use of low-dose, dual-source, 256-slice multidetector computed tomography to characterize Erdheim-Chester disease that exclusively caused angina and stenosis of a coronary artery in a young adult.
厄尔德海姆-切斯特病是一种罕见疾病,几乎可累及每个器官,主要浸润结缔组织、血管周围组织和脂肪组织。该疾病是非朗格汉斯细胞组织细胞增多症的一种形式,其特征为泡沫状组织细胞增殖;其心血管并发症预后严重。我们报告一例29岁女性因心绞痛入院分析的病例。我们使用心脏多排螺旋计算机断层血管造影进行评估,发现纵隔有巨大软组织,压迫患者左前降支冠状动脉。据我们所知,这是首例使用低剂量双源256层多排螺旋计算机断层扫描来描述仅在一名年轻成年人中引起心绞痛和冠状动脉狭窄的厄尔德海姆-切斯特病的报告。