Focal Spinal Nondisjunctional Disorders: Including a Discussion on the Embryogenesis of Cranial Focal Nondisjunctional Lesions.
Dermal sinus tract
Dermoid
Dysraphism
Encephalocele
Focal cranial nondisjunctional disorders
Focal spinal nondisjunctional disorders
Limited dorsal myeloschisis
Nondisjunction
Journal
Advances and technical standards in neurosurgery
ISSN: 0095-4829
Titre abrégé: Adv Tech Stand Neurosurg
Pays: United States
ID NLM: 7501064
Informations de publication
Date de publication:
2023
2023
Historique:
medline:
31
8
2023
pubmed:
29
8
2023
entrez:
28
8
2023
Statut:
ppublish
Résumé
The publication of a comprehensive report on limited dorsal myeloschisis by the senior author (DP) in 2010 has brought full attention to the concept of limited myeloschisis that he first formulated in 1992 and ignited interests in the whole spectrum of focal spinal nondisjunctional disorders. Now that focal nondisjunctional disorders have become well known, new clinical reports on these conditions or relevant subjects are frequently seen. Here we present an updated review on the full spectrum of focal spinal nondisjunctional disorders and extend the scope to include a discussion on the embryogenesis of cranial focal nondisjunctional malformations.
Identifiants
pubmed: 37640873
doi: 10.1007/978-3-031-34981-2_4
doi:
Types de publication
Review
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
65-128Informations de copyright
© 2023. The Author(s), under exclusive license to Springer Nature Switzerland AG.
Références
Pang D, Zovickian J, Oviedo A, Moes GS. Limited dorsal myeloschisis: a distinctive clinicopathological entity. Neurosurgery. 2010;67:1555–80.
pubmed: 21107187
doi: 10.1227/NEU.0b013e3181f93e5a
Pang D, Zovickian J, Wong ST, Hou YJ, Moes GS. Limited dorsal myeloschisis: a not-so-rare form of primary neurulation defect. Childs Nerv Syst. 2013;29:1459–84.
pubmed: 24013319
doi: 10.1007/s00381-013-2189-2
O'Rahilly R, Müller F. Neurulation in the normal human embryo. Ciba Found Symp. 1994;181:70–82.
pubmed: 8005032
Müller F, O'Rahilly R. The development of the human brain, the closure of the caudal neuropore, and the beginning of secondary neurulation at stage 12. Anat Embryol (Berl). 1987;176(4):413–30.
pubmed: 3688450
doi: 10.1007/BF00310083
Wong ST, Kan A, Pang D. Limited dorsal spinal nondisjunctional disorders: limited dorsal myeloschisis, congenital spinal dermal sinus tract, and mixed lesions. In: Di Rocco C, Pang D, Rutka J, editors. Textbook of pediatric neurosurgery. Cham: Springer; 2019. https://doi.org/10.1007/978-3-319-31512-6_110-1 .
doi: 10.1007/978-3-319-31512-6_110-1
Wong ST, Pang D. Focal spinal nondisjunction in primary neurulation. J Korean Neurosurg Soc. 2021;64(2):151–88.
pubmed: 33715322
pmcid: 7969048
doi: 10.3340/jkns.2020.0117
Cornips EM, Weber JW, Vles JS, van Aalst J. Pseudo-dermal sinus tract or spinal dermal-sinus-like stalk? Childs Nerv Syst. 2011;27:1189–91.
pubmed: 21656011
pmcid: 3141846
doi: 10.1007/s00381-011-1505-y
Eibach S, Moes G, Zovickian J, Pang D. Limited dorsal myeloschisis associated with dermoid elements. Childs Nerv Syst. 2017;33:55–67.
pubmed: 27541864
doi: 10.1007/s00381-016-3207-y
Elton S, Oakes WJ. Dermal sinus tracts of the spine. Neurosurg Focus. 2001;10(1):e4.
pubmed: 16749756
doi: 10.3171/foc.2001.10.1.5
Lee JY, Park SH, Chong S, Phi JH, Kim SK, Cho BK, Wang KC. Congenital dermal sinus and limited dorsal myeloschisis: “spectrum disorders” of incomplete disjunction between cutaneous and neural ectoderms. Neurosurgery. 2019;84:428–34.
pubmed: 29618070
doi: 10.1093/neuros/nyy058
van Aalst J, Beuls EA, Cornips EM, van Straaten HW, Boselie AF, Rijkers K, Weber JW, Vles JS. The spinal dermal-sinus-like stalk. Childs Nerv Syst. 2009;25:191–7.
pubmed: 18618125
doi: 10.1007/s00381-008-0669-6
Wang KC, Yang HJ, Oh CW, Kim HJ, Cho BK. Spinal congenital dermal sinus—experience of 5 cases over a period of 10 years. J Korean Med Sci. 1993;8:341–7.
pubmed: 8305142
pmcid: 3053715
doi: 10.3346/jkms.1993.8.5.341
Colas JF, Schoenwolf GC. Towards a cellular and molecular understanding of neurulation. Dev Dyn. 2001;221:117–45.
pubmed: 11376482
doi: 10.1002/dvdy.1144
O'Rahilly R, Gardner E. The timing and sequence of events in the development of the human nervous system during the embryonic period proper. Z Anat Entwicklungsgesch. 1971;134(1):1–12.
pubmed: 5088332
doi: 10.1007/BF00523284
Martins-Green M. Origin of the dorsal surface of the neural tube by progressive delamination of epidermal ectoderm and neuroepithelium: implications for neurulation and neural tube defects. Development. 1988;103:687–706.
pubmed: 3073935
doi: 10.1242/dev.103.4.687
Schoenwolf GC, Smith JL. Mechanisms of neurulation: traditional viewpoint and recent advances. Development. 1990;109:243–70.
pubmed: 2205465
doi: 10.1242/dev.109.2.243
van Straaten HW, Jaskoll T, Rousseau AM, et al. Raphe of the posterior neural tube in the chick embryo: its closure and reopening as studied in living embryos with a high definition light microscope. Dev Dyn. 1993;198:65–76.
pubmed: 8292832
doi: 10.1002/aja.1001980107
Silver MH, Kerns JM. Ultrastructure of neural fold fusion in chick embryos. Scan Electron Microsc. 1978;2:209–15.
Schoenwolf GC. On the morphogenesis of the early rudiments of the developing central nervous system. Scan Electron Microsc. 1982;1:289–308.
Martins-Green M, Erickson CA. Basal lamina is not a barrier to neural crest cell emigration: documentation by TEM and by immunofluorescent and immunogold labelling. Development. 1987;101:517–33.
pubmed: 3332260
doi: 10.1242/dev.101.3.517
Wang S, Garcia MD, Lopez AL 3rd, Overbeek PA, Larin KV, Larina IV. Dynamic imaging and quantitative analysis of cranial neural tube closure in the mouse embryo using optical coherence tomography. Biomed Opt Express. 2016;8(1):407–19.
pubmed: 28101427
pmcid: 5231309
doi: 10.1364/BOE.8.000407
Müller F, O'Rahilly R. Somitic-vertebral correlation and vertebral levels in the human embryo. Am J Anat. 1986;177(1):3–19.
pubmed: 3535481
doi: 10.1002/aja.1001770103
O'Rahilly R, Müller F. Somites, spinal ganglia, and centra. Enumeration and interrelationships in staged human embryos, and implications for neural tube defects. Cells Tissues Organs. 2003;173(2):75–92.
pubmed: 12649586
doi: 10.1159/000068948
O'Rahilly R, Müller F. The two sites of fusion of the neural folds and the two neuropores in the human embryo. Teratology. 2002;65(4):162–70.
pubmed: 11948562
doi: 10.1002/tera.10007
Dady A, Havis E, Escriou V, Catala M, Duband JL. Junctional neurulation: a unique developmental program shaping a discrete region of the spinal cord highly susceptible to neural tube defects. J Neurosci. 2014;34(39):13208–21.
pubmed: 25253865
pmcid: 6608335
doi: 10.1523/JNEUROSCI.1850-14.2014
Eibach S, Moes G, Hou YJ, Zovickian J, Pang D. Unjoined primary and secondary neural tubes: junctional neural tube defect, a new form of spinal dysraphism caused by disturbance of junctional neurulation. Childs Nerv Syst. 2017;33(10):1633–47.
pubmed: 27796548
doi: 10.1007/s00381-016-3288-7
O'Rahilly R, Müller F. Bidirectional closure of the rostral neuropore in the human embryo. Am J Anat. 1989;184(4):259–68.
pubmed: 2756902
doi: 10.1002/aja.1001840402
Müller F, O'Rahilly R. Cerebral dysraphia (future anencephaly) in a human twin embryo at stage 13. Teratology. 1984;30(2):167–77.
pubmed: 6388010
doi: 10.1002/tera.1420300203
O'Rahilly R, Müller F. The embryonic human brain. 3rd ed. Wiley; 2006. p. 337.
doi: 10.1002/0471973084
Hoving EW, Vermeij-Keers C, Mommaas-Kienhuis AM, Hartwig NG. Separation of neural and surface ectoderm after closure of the rostral neuropore. Anat Embryol (Berl). 1990;182(5):455–63.
pubmed: 2291490
doi: 10.1007/BF00178910
Puelles L, Domenech-Ratto G, Martinez-de-la-Torre M. Location of the rostral end of the longitudinal brain axis: review of an old topic in the light of marking experiments on the closing rostral neuropore. J Morphol. 1987;194(2):163–71.
pubmed: 3430632
doi: 10.1002/jmor.1051940205
ten Donkelaar HJ, Bekker M, Renier WO, Hori A, Shiota K. Neurulation and neural tube defects. In: Clinical neuroembryology. Berlin: Springer; 2014. https://doi.org/10.1007/978-3-642-54687-7_4 .
doi: 10.1007/978-3-642-54687-7_4
Barkovich AJ, Vandermarck P, Edwards MS, Cogen PH. Congenital nasal masses: CT and MR imaging features in 16 cases. AJNR Am J Neuroradiol. 1991;12(1):105–16.
pubmed: 1903239
pmcid: 8367564
Kim JW, Wang KC, Chong S, Kim SK, Lee JY. Limited dorsal myeloschisis: reconsideration of its embryological origin. Neurosurgery. 2020;86:93–100.
pubmed: 30690520
doi: 10.1093/neuros/nyy632
Müller F, O'Rahilly R. The prechordal plate, the rostral end of the notochord and nearby median features in staged human embryos. Cells Tissues Organs. 2003;173:1–20.
pubmed: 12566624
doi: 10.1159/000068214
Müller F, O'Rahilly R. The primitive streak, the caudal eminence and related structures in staged human embryos. Cells Tissues Organs. 2004;177:2–20.
pubmed: 15237191
doi: 10.1159/000078423
Quon JL, Grant GA. Commentary: Limited dorsal myeloschisis: reconsideration of its embryological origin. Neurosurgery. 2020;86:E13–4.
pubmed: 30715453
doi: 10.1093/neuros/nyz011
Selleck MA, Bronner-Fraser M. Origins of the avian neural crest: the role of neural plate–epidermal interactions. Development. 1995;121:525–38.
pubmed: 7768190
doi: 10.1242/dev.121.2.525
Theveneau E, Mayor R. Neural crest delamination and migration: from epithelium-to-mesenchyme transition to collective cell migration. Dev Biol. 2012;366:34–54.
pubmed: 22261150
doi: 10.1016/j.ydbio.2011.12.041
Nikolopoulou E, Galea GL, Rolo A, Greene ND, Copp AJ. Neural tube closure: cellular, molecular and biomechanical mechanisms. Development. 2017;144:552–66.
pubmed: 28196803
doi: 10.1242/dev.145904
Rolo A, Escuin S, Greene NDE, Copp AJ. Rho GTPases in mammalian spinal neural tube closure. Small GTPases. 2018;9:283–9.
pubmed: 27768516
doi: 10.1080/21541248.2016.1235388
Abdul-Aziz NM, Turmaine M, Greene ND, Copp AJ. EphrinA-EphA receptor interactions in mouse spinal neurulation: implications for neural fold fusion. Int J Dev Biol. 2009;53(4):559–68.
pubmed: 19247962
doi: 10.1387/ijdb.082777na
Yamaguchi Y, Shinotsuka N, Nonomura K, et al. Live imaging of apoptosis in a novel transgenic mouse highlights its role in neural tube closure. J Cell Biol. 2011;195:1047–60.
pubmed: 22162136
pmcid: 3241723
doi: 10.1083/jcb.201104057
Pang D. Surgical management of spinal dysraphism. In: Fessler R, Sekhar L, editors. Atlas of neurosurgical techniques. New York: Thieme Medical and Scientific Publishers; 2006. p. 729–58.
Pang D, Dias M, Ahdab-Barmada M. Split cord malformation part I: a unified theory of embryogenesis for double spinal cord malformation. Neurosurgery. 1992;31:451–80.
pubmed: 1407428
doi: 10.1227/00006123-199209000-00010
Pang D, Devadass A, Thompson D. Limited dorsal myeloschisis involving one hemicord of a split cord malformation—a “hemi-LDM”. Childs Nerv Syst. 2022;38(11):2223–30.
pubmed: 35794361
doi: 10.1007/s00381-022-05599-0
Wong ST, Moes GS, Yam KY, Fong D, Pang D. Intrinsic brainstem neurenteric cyst with extensive squamous metaplasia in a child. J Neurosurg Imaging Tech. 2016;1(1):26–37.
Hiraoka A, Morioka T, Murakami N, Suzuki SO, Mizoguchi M. Limited dorsal myeloschisis with no extradural stalk linking to a flat skin lesion: a case report. Childs Nerv Syst. 2018;34:2497–501.
pubmed: 30083799
doi: 10.1007/s00381-018-3938-z
Martínez-Lage JF, Almagro MJ, Ferri-Ñiguez B, et al. Spinal dermal sinus and pseudo-dermal sinus tracts: two different entities. Childs Nerv Syst. 2011;27:609–16.
pubmed: 20978770
doi: 10.1007/s00381-010-1308-6
van Aalst J, Beuls EA, Cornips EM, Vanormelingen L, Vandersteen M, et al. Anatomy and surgery of the infected dermal sinus of the lower spine. Childs Nerv Syst. 2006;22:1307–15.
pubmed: 16708253
doi: 10.1007/s00381-006-0106-7
Girishan S, Rajshekhar V. Rapid onset paraparesis and quadriparesis in patients with intramedullary spinal dermoid cysts: report of 10 cases. J Neurosurg Pediatr. 2016;17:86–93.
pubmed: 26431244
doi: 10.3171/2015.5.PEDS1537
De Vloo P, Lagae L, Sciot R, Demaerel P, van Loon J, Van Calenbergh F. Spinal dermal sinuses and dermal sinus-like stalks analysis of 14 cases with suggestions for embryologic mechanisms resulting in dermal sinus-like stalks. Eur J Paediatr Neurol. 2013;17:575–84.
pubmed: 23711910
doi: 10.1016/j.ejpn.2013.04.003
Tisdall MM, Hayward RD, Thompson DN. Congenital spinal dermal tract: how accurate is clinical and radiological evaluation? J Neurosurg Pediatr. 2015;15:651–6.
pubmed: 26030333
doi: 10.3171/2014.11.PEDS14341
Pang D, Dias MS. Cervical myelomeningoceles. Neurosurgery. 1993;33:363–72.
pubmed: 8413865
Steinbok P. Dysraphic lesions of the cervical spinal cord. Neurosurg Clin N Am. 1995;6(2):367–76.
pubmed: 7620360
doi: 10.1016/S1042-3680(18)30469-8
Steinbok P, Cochrane DD. The nature of congenital posterior cervical or cervicothoracic midline cutaneous mass lesions. Report of eight cases. J Neurosurg. 1991;75:206–12.
pubmed: 2072156
doi: 10.3171/jns.1991.75.2.0206
Rossi A, Piatelli G, Gandofolo C, Pavanello M, et al. Spectrum of nonterminal myelocystoceles. Neurosurgery. 2006;58:509–15.
pubmed: 16528191
doi: 10.1227/01.NEU.0000197122.92954.82
Suneson A, Kalimo H. Myelocystocele with cerebellar heterotopia. J Neurosurg. 1979;51:392–6.
pubmed: 469585
doi: 10.3171/jns.1979.51.3.0392
Schoenwolf GC. Observations on closure of the neuropores in the chick embryo. Am J Anat. 1979;155:445–66.
pubmed: 484511
doi: 10.1002/aja.1001550404
Morioka T, Suzuki SO, Murakami N, Mukae N, et al. Surgical histopathology of limited dorsal myeloschisis with flat skin lesion. Childs Nerv Syst. 2019;35:119–28.
pubmed: 29934704
doi: 10.1007/s00381-018-3870-2
Morioka T, Suzuki SO, Murakami N, Shimogawa T, et al. Neurosurgical pathology of limited dorsal myeloschisis. Childs Nerv Syst. 2018;34:293–303.
pubmed: 29063264
doi: 10.1007/s00381-017-3625-5
Lee JY, Chong S, Choi YH, Phi JH, Cheon JE, Kim SK, Park SH, Kim IO, Wang KC. Modification of surgical procedure for “probable” limited dorsal myeloschisis. J Neurosurg Pediatr. 2017;19:616–9.
pubmed: 28291421
doi: 10.3171/2016.12.PEDS16171
Asiri A, Dimpudus F, Atcheson N, Al-Najjar A, McMahon K, Kurniawan ND. Comparison between 2D and 3D MEDIC for human cervical spinal cord MRI at 3T. J Med Radiat Sci. 2021;68(1):4–12.
pubmed: 32931647
doi: 10.1002/jmrs.433
Lee SM, Cheon JE, Choi YH, Kim IO, Kim WS, Cho HH, Lee JY, Wang KC. Limited dorsal myeloschisis and congenital dermal sinus: comparison of clinical and MR imaging features. AJNR. 2017;38:176–82.
pubmed: 27765739
pmcid: 7963655
doi: 10.3174/ajnr.A4958
Pang D, Zovickian J, Wong ST, Hou YJ, Moes GS. Surgical treatment of complex spinal cord lipomas. Childs Nerv Syst. 2013;29:1485–513.
pubmed: 24013320
doi: 10.1007/s00381-013-2187-4
Ackerman LL, Menezes AH. Spinal congenital dermal sinuses: a 30-year experience. Pediatrics. 2003;112(3 Pt 1):641–7.
pubmed: 12949296
doi: 10.1542/peds.112.3.641