Findler G, Hadani M, Tadmor R, Bubis J J, Shaked I, Sahar A
Neurosurgery. 1985 Sep;17(3):484-6. doi: 10.1227/00006123-198509000-00015.
Spinal intradural ependymal cysts are extremely rare. The case presented is the sixth reported in the literature. The symptoms are consistent clinically and radiologically with a spinal intradural space-occupying lesion. The cyst wall is lined with both ciliated and nonciliated cells, resting directly on connective tissue. The exact embryonal origin of these cysts is obscure.
脊髓硬膜内室管膜囊肿极为罕见。本文报道的病例是文献中第六例。其症状在临床和放射学上与脊髓硬膜内占位性病变相符。囊肿壁由纤毛细胞和非纤毛细胞衬里,直接位于结缔组织上。这些囊肿的确切胚胎起源尚不清楚。