Evidence map›Paper›PMID 35939129›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2023

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

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

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed, 0 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Yuki KawamotoDepartment of Pediatric Neurosurgery, Takatsuki General Hospital, Takatsuki, Japan.
Atsuko HaradaDepartment of Pediatric Neurosurgery, Takatsuki General Hospital, Takatsuki, Japan. atsu-ko@qb3.so-net.ne.jp.
Yoshihiro IkuraDepartment of Pathology, Takatsuki General Hospital, Takatsuki, Japan.
Takahiro FujinagaDepartment of Pediatric Neurosurgery, Takatsuki General Hospital, Takatsuki, Japan.
Hidetsuna UtsunomiyaDepartment of Radiology, Teikyo University School of Medicine, Tokyo, Japan.
Takatsuki General Hospital · JPTeikyo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

LipomaMeningomyeloceleSkin DiseasesSpina Bifida OccultaSpinal DysraphismChild, PreschoolHumansIchthyosiform Erythroderma, CongenitalInfant, NewbornLipid Metabolism, Inborn ErrorsMagnetic Resonance ImagingMaleMuscle SpasticityMuscular DiseasesSkinCongenital dermal sinusExtradural stalkLimited dorsal myeloschisisOsteochondral tissueSpinal lipoma

Identifiers

PMID35939129
OpenAlexW4290652290

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.