Kawamoto Yuki, Harada Atsuko, Ikura Yoshihiro, Fujinaga Takahiro, Utsunomiya Hidetsuna
Department of Pediatric Neurosurgery, Takatsuki General Hospital, Takatsuki, Japan.
Department of Pathology, Takatsuki General Hospital, Takatsuki, Japan.
Childs Nerv Syst. 2023 Feb;39(2):511-515. doi: 10.1007/s00381-022-05631-3. Epub 2022 Aug 8.
Limited dorsal myeloschisis (LDM) is characterized by a fibroneural tethering stalk linking the skin lesion to the underlying spinal cord. LDM without an extradural stalk is rare. A full-term boy was noted at birth to have a dimple in the upper back (dorsal skin of the lower thoracic region). Computed tomographic scan showed spina bifida at the T9-12 vertebral level and osteochondral tissue at the T10 level. Magnetic resonance imaging (MRI) demonstrated a tiny dorsal lipoma at the T8 vertebral level, but the intradural tethering tract was not apparent. At 18 days of age, the congenital dermal sinus (CDS) tract started from the dimple and terminated at the osteochondral tissue, without continuity of the dura mater, and the osteochondral tissues were resected. At age 2 years 8 months, he developed spastic paresis of the right foot. On MRI, the tethering tract from the dorsal lipoma became apparent. During the second surgery at age 2 years 11 months, the intradural stalk started from the dorsal lipoma and joined the inner surface of the dura mater was untethering from the cord. Postoperatively, right spastic paresis was improved. Histological examination of the intradural stalk revealed the distribution of S100-immunopositive peripheral nerve fibers, which is one of the histopathological hallmarks of LDM. We speculated that the extradural stalk with coexisting CDS originally linked from the skin lesion subsequently regressed and was replaced by fibroadipose tissue with osteochondral tissue migration. Intradural exploration should always be seriously considered in these disorders of persisting neurocutaneous connection.
局限性脊髓脊膜膨出(LDM)的特征是有一条纤维神经束带将皮肤病变与下方的脊髓相连。没有硬膜外束带的LDM很罕见。一名足月儿出生时被发现上背部(下胸部区域的背部皮肤)有一个酒窝。计算机断层扫描显示T9 - 12椎体水平存在脊柱裂以及T10水平有骨软骨组织。磁共振成像(MRI)显示T8椎体水平有一个微小的背部脂肪瘤,但硬膜内束带不明显。在18日龄时,先天性皮肤窦道(CDS)从酒窝处起始并终止于骨软骨组织,硬脑膜无连续性,骨软骨组织被切除。在2岁8个月时,他出现了右脚痉挛性轻瘫。MRI显示来自背部脂肪瘤的束带变得明显。在2岁11个月进行第二次手术时,硬膜内束带从背部脂肪瘤起始并连接到硬脑膜内表面,从脊髓上松解下来。术后,右侧痉挛性轻瘫有所改善。对硬膜内束带的组织学检查显示有S100免疫阳性的周围神经纤维分布,这是LDM的组织病理学特征之一。我们推测,原本从皮肤病变处连接的伴有CDS的硬膜外束带随后退化,并被伴有骨软骨组织迁移的纤维脂肪组织所取代。对于这些持续存在的神经皮肤连接障碍,应始终认真考虑进行硬膜内探查。