ten Donkelaar H J, Willemsen M A A P, van der Heijden I, Beems T, Wesseling P
Department of Neurology, University Medical Center St. Radboud Nijmegen, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.
Acta Neuropathol. 2002 Nov;104(5):538-42. doi: 10.1007/s00401-002-0599-4. Epub 2002 Aug 1.
We report a case of a newborn presenting with severe compression of the spinal cord due to a large, solitary mass extending from C4 to T2. Neurosurgical exploration revealed a large intradural, extramedullary cystic lesion, compressing the spinal cord. Slowly progressive respiratory failure due to severe myelopathy led to the death of the child 19 days postpartum. At autopsy, a well-differentiated enterogenous cyst was found, the cyst wall containing gastric and esophageal type mucosa, and a bona fide muscularis propria. The gastrointestinal tract was completely normal. The possible developmental history of intradural enterogenous cysts is discussed.
我们报告一例新生儿病例,该患儿因一个从C4延伸至T2的巨大孤立性肿块导致脊髓严重受压。神经外科探查发现一个巨大的硬膜内、髓外囊性病变,压迫脊髓。由于严重的脊髓病导致的缓慢进行性呼吸衰竭致使患儿在产后19天死亡。尸检时发现一个高分化的肠源性囊肿,囊肿壁包含胃和食管型黏膜以及一层真正的固有肌层。胃肠道完全正常。本文讨论了硬膜内肠源性囊肿可能的发育史。