Seigel R S, Seeger J F, Gabrielsen T O, Allen R J
Radiology. 1979 Jan;130(1):159-64. doi: 10.1148/130.1.159.
Computed tomography (CT) in patients with oculocraniosomatic disease (OCSD) or Kearns-Sayre syndrome has not been previously reported to the authors' knowledge. CT scans were performed in 6 children and 3 adults with OCSD. Abnormalities in children included: intracranial calcifications (4 patients); white matter disease (3 patients); cerebellar hypoplasia (1 patient); and scattered areas of decreased density in the cerebellar hemispheres, mesencephalon, and thalamus (1 patient). CT scans were normal in all adults. OCSD should be considered in the differential diagnosis in patients with intracranial calcification and white matter disease.
据作者所知,此前尚未有关于眼颅躯体疾病(OCSD)或卡恩斯-塞尔综合征患者的计算机断层扫描(CT)报告。对6名患有OCSD的儿童和3名成人进行了CT扫描。儿童的异常表现包括:颅内钙化(4例);白质疾病(3例);小脑发育不全(1例);小脑半球、中脑和丘脑密度减低的散在区域(1例)。所有成人的CT扫描均正常。对于有颅内钙化和白质疾病的患者,鉴别诊断时应考虑OCSD。