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局限性背侧脊髓纵裂,硬膜外茎干与并存的先天性皮样窦无连续性。

Limited dorsal myeloschisis without extradural stalk continuity to coexisting congenital dermal sinus.

作者信息

Kawamoto Yuki, Harada Atsuko, Ikura Yoshihiro, Fujinaga Takahiro, Utsunomiya Hidetsuna

机构信息

Department of Pediatric Neurosurgery, Takatsuki General Hospital, Takatsuki, Japan.

Department of Pathology, Takatsuki General Hospital, Takatsuki, Japan.

出版信息

Childs Nerv Syst. 2023 Feb;39(2):511-515. doi: 10.1007/s00381-022-05631-3. Epub 2022 Aug 8.

DOI:10.1007/s00381-022-05631-3
PMID:35939129
Abstract

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.

摘要

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。

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本文引用的文献

1
Congenital Dermal Sinus Elements in Each Tethering Stalk of Coexisting Thoracic Limited Dorsal Myeloschisis and Retained Medullary Cord.共存的胸段局限性背部脊髓脊膜膨出和脊髓栓系中每个牵系索中的先天性皮窦成分。
Pediatr Neurosurg. 2020;55(6):380-387. doi: 10.1159/000511876. Epub 2020 Dec 3.
2
Neurosurgical Pathology and Management of Limited Dorsal Myeloschisis Associated with Congenital Dermal Sinus in Infancy.婴儿先天性皮窦相关局限性背侧脊髓脊膜膨出的神经外科病理和处理
Pediatr Neurosurg. 2020;55(2):113-125. doi: 10.1159/000507867. Epub 2020 Jul 2.
3
Human tail-like cutaneous appendage with a contiguous stalk of limited dorsal myeloschisis.
具有连续茎且伴有有限背部脊髓裂的人尾状皮肤附属器。
Childs Nerv Syst. 2019 Jun;35(6):973-978. doi: 10.1007/s00381-019-04071-w. Epub 2019 Feb 6.
4
Slender Stalk with Combined Features of Saccular Limited Dorsal Myeloschisis and Congenital Dermal Sinus in a Neonate.新生儿中具有囊状局限性背侧脊髓裂和先天性皮窦联合特征的细长茎状物。
Pediatr Neurosurg. 2019;54(2):125-131. doi: 10.1159/000495810. Epub 2019 Jan 17.
5
Limited dorsal myeloschisis with no extradural stalk linking to a flat skin lesion: a case report.有限性背侧脊髓裂而无硬膜外茎连于扁平皮肤损害:病例报告
Childs Nerv Syst. 2018 Dec;34(12):2497-2501. doi: 10.1007/s00381-018-3938-z. Epub 2018 Aug 6.
6
Bony and Cartilaginous Tissues in Lumbosacral Lipomas.腰骶部脂肪瘤中的骨组织和软骨组织
Pediatr Neurosurg. 2018;53(5):305-310. doi: 10.1159/000490391. Epub 2018 Jul 4.
7
Surgical histopathology of limited dorsal myeloschisis with flat skin lesion.伴有扁平皮肤病变的局限性背侧脊髓裂的手术组织病理学
Childs Nerv Syst. 2019 Jan;35(1):119-128. doi: 10.1007/s00381-018-3870-2. Epub 2018 Jun 22.
8
Congenital Dermal Sinus and Limited Dorsal Myeloschisis: "Spectrum Disorders" of Incomplete Dysjuction Between Cutaneous and Neural Ectoderms.先天性皮肤窦和有限的背侧脊髓脊膜膨出:表皮外胚层和神经外胚层不完全分离的“谱系障碍”。
Neurosurgery. 2019 Feb 1;84(2):428-434. doi: 10.1093/neuros/nyy058.
9
Neurosurgical pathology of limited dorsal myeloschisis.有限性背侧脊髓纵裂的神经外科病理学
Childs Nerv Syst. 2018 Feb;34(2):293-303. doi: 10.1007/s00381-017-3625-5. Epub 2017 Oct 23.
10
Modification of surgical procedure for "probable" limited dorsal myeloschisis.“可能的”局限性脊髓背侧闭合不全手术方法的改良
J Neurosurg Pediatr. 2017 May;19(5):616-619. doi: 10.3171/2016.12.PEDS16171. Epub 2017 Feb 17.