Roelens F A, Barth P G, van der Harten J J
Departments of Neurology and Pediatrics (Pediatric Neurology), University Hospital of Amsterdam, Amsterdam, The Netherlands.
Eur J Paediatr Neurol. 1999;3(2):59-63. doi: 10.1053/ejpn.1999.0183.
Only incidental mention has been made to date of the combined occurrence of subependymal heterotopia and posterior encephalocele. We evaluated the presence of disseminated nodular subependymal heterotopia in two series of patients with posterior encephalocele. The first series consisted of all six patients who were treated in our hospital for encephalocele during the last 11 years and who underwent magnetic resonance imaging (MRI). In three, subependymal nodular heterotopia was found by MRI. The second series consisted of eight autopsy cases with encephalocele, representing all cases of encephalocele that came to autopsy during a 10-year period on whom full microscopic examination could be performed. Nodular heterotopia was found in four. The combined occurrence of these two rare conditions may not be accidental.
迄今为止,仅偶然提及室管膜下异位与后脑膨出合并出现的情况。我们评估了两组后脑膨出患者中弥漫性结节性室管膜下异位的存在情况。第一组包括过去11年内在我院接受后脑膨出治疗并接受磁共振成像(MRI)检查的所有6例患者。其中3例通过MRI发现了室管膜下结节性异位。第二组包括8例后脑膨出尸检病例,代表了10年内所有进行了全面显微镜检查的后脑膨出尸检病例。其中4例发现有结节性异位。这两种罕见情况的合并出现可能并非偶然。