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Erschienen in: Pediatric Radiology 8/2021

30.03.2021 | Original Article

Taenia–tela choroidea complex and choroid plexus location help distinguish Dandy-Walker malformation and Blake pouch cysts

verfasst von: Matthew T. Whitehead, Gilbert Vezina, Sarah D. Schlatterer, Sarah B. Mulkey, Adre J. du Plessis

Erschienen in: Pediatric Radiology | Ausgabe 8/2021

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Abstract

Background

Dandy-Walker malformation and Blake pouch cysts can have overlapping imaging features. The choroid plexus and associated taenia–tela choroidea complex are displaced inferolaterally in Dandy-Walker malformation and below the vermis in Blake pouch cysts.

Objective

To determine the normal fetal and postnatal MR appearance of the choroid plexus and taenia–tela choroidea complex, and whether their location can help distinguish Dandy-Walker malformation from Blake pouch cysts.

Materials and methods

In this retrospective study, we evaluated brain MR exams from normal-appearing fetuses (gestational age 19–38 weeks) and infants, fetal and postnatal exams in Blake pouch cysts and Dandy-Walker malformation, and ambiguous cases equivocal for mild Dandy-Walker malformation and Blake pouch cysts. We documented choroid plexus and the taenia–tela choroidea complex location and axial and sagittal angles in each case. Then we contrasted and compared the original and updated fetal diagnoses based on taenia–tela choroidea complex and choroid plexus positions.

Results

The choroid plexus location and the taenia–tela choroidea complex location and angles varied significantly among normal exams, Blake pouch cyst exams and Dandy-Walker malformation exams (P<0.01). Dandy-Walker malformation showed inferolateral displacement of the taenia–tela choroidea complex and choroid plexus distant from the vermis. Adding the taenia–tela choroidea complex and choroid plexus into the assessment improved diagnostic accuracy, especially in ambiguous cases.

Conclusion

The location of the taenia–tela choroidea complex and choroid plexus provided additional diagnostic neuroimaging clues that could be used in conjunction with other conventional findings to distinguish Dandy-Walker malformation and Blake pouch cysts. Normal, Blake pouch cyst, and Dandy-Walker malformation cases differed with regard to taenia–tela choroidea complex and choroid plexus position. Inferolateral taenia–tela choroidea complex displacement distant from the vermian margin was characteristic of Dandy-Walker malformation.
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Literatur
1.
Zurück zum Zitat Barkovich AJ, Raybaud CA (2018) Congenital malformations of the brain and skull. In: Barkovich AJ, Raybaud CA (eds) Pediatric neuroimaging, 6th edn. Lippincott Williams & Wilkins, Philadelphia, p 531 Barkovich AJ, Raybaud CA (2018) Congenital malformations of the brain and skull. In: Barkovich AJ, Raybaud CA (eds) Pediatric neuroimaging, 6th edn. Lippincott Williams & Wilkins, Philadelphia, p 531
2.
Zurück zum Zitat Hart MN, Malamud N, Ellis WG (1972) The Dandy-Walker syndrome: a clinicopathological study based on 28 cases. Neurology 22:771–780CrossRef Hart MN, Malamud N, Ellis WG (1972) The Dandy-Walker syndrome: a clinicopathological study based on 28 cases. Neurology 22:771–780CrossRef
3.
Zurück zum Zitat Raybaud C (1982) Cystic malformations of the posterior fossa. Abnormalities associated with the development of the roof of the fourth ventricle and adjacent meningeal structures. J Neuroradiol 9:103–133PubMed Raybaud C (1982) Cystic malformations of the posterior fossa. Abnormalities associated with the development of the roof of the fourth ventricle and adjacent meningeal structures. J Neuroradiol 9:103–133PubMed
4.
Zurück zum Zitat Aldinger KA, Timms AE, Thomson Z et al (2019) Redefining the etiologic landscape of cerebellar malformations. Am J Hum Genet 105:606–615CrossRef Aldinger KA, Timms AE, Thomson Z et al (2019) Redefining the etiologic landscape of cerebellar malformations. Am J Hum Genet 105:606–615CrossRef
5.
Zurück zum Zitat D’Antonio F, Khalil A, Garel C et al (2016) Systemic review and meta-analysis of isolated posterior fossa malformations on prenatal imaging (part 2): neurodevelopmental outcome. Ultrasound Obstet Gynecol 48:28–37CrossRef D’Antonio F, Khalil A, Garel C et al (2016) Systemic review and meta-analysis of isolated posterior fossa malformations on prenatal imaging (part 2): neurodevelopmental outcome. Ultrasound Obstet Gynecol 48:28–37CrossRef
6.
Zurück zum Zitat Limperopoulos C, Robertson RL, Khawaja OS et al (2008) How accurately does current fetal imaging identify posterior fossa anomalies. AJR Am J Roentgenol 190:1637–1643CrossRef Limperopoulos C, Robertson RL, Khawaja OS et al (2008) How accurately does current fetal imaging identify posterior fossa anomalies. AJR Am J Roentgenol 190:1637–1643CrossRef
7.
Zurück zum Zitat Griffiths PD, Brackley BM et al (2017) Anatomical subgroup analysis of the MERIDIAN cohort: posterior fossa abnormalities. Ultrasound Obstet Gynecol 50:745–752CrossRef Griffiths PD, Brackley BM et al (2017) Anatomical subgroup analysis of the MERIDIAN cohort: posterior fossa abnormalities. Ultrasound Obstet Gynecol 50:745–752CrossRef
8.
Zurück zum Zitat Robinson AJ, Blaser S, Toi A et al (2007) The fetal cerebellar vermis: assessment for abnormal development by ultrasonography and magnetic resonance imaging. Ultrasound Q 23:211–223CrossRef Robinson AJ, Blaser S, Toi A et al (2007) The fetal cerebellar vermis: assessment for abnormal development by ultrasonography and magnetic resonance imaging. Ultrasound Q 23:211–223CrossRef
9.
Zurück zum Zitat Adamsbaum C, Moutard ML, André C et al (2004) MR imaging of the fetal cerebellar vermis in utero: criteria for abnormal development, with ultrasonographic and clinicopathologic correlation. Pediatr Radiol 34:S02–S135 Adamsbaum C, Moutard ML, André C et al (2004) MR imaging of the fetal cerebellar vermis in utero: criteria for abnormal development, with ultrasonographic and clinicopathologic correlation. Pediatr Radiol 34:S02–S135
10.
Zurück zum Zitat Dovjak GO, Brugger PC, Gruber GM et al (2018) Prenatal assessment of cerebellar vermian lobulation: fetal MRI with 3-tesla postmortem validation. Ultrasound Obstet Gynecol 52:623–630CrossRef Dovjak GO, Brugger PC, Gruber GM et al (2018) Prenatal assessment of cerebellar vermian lobulation: fetal MRI with 3-tesla postmortem validation. Ultrasound Obstet Gynecol 52:623–630CrossRef
11.
Zurück zum Zitat Dovjak GO, Diogo MC, Brugger PC et al (2020) Quantitative fetal MRI assessment of cystic posterior fossa malformations. Ultrasound Obstet Gynecol 56:78–85CrossRef Dovjak GO, Diogo MC, Brugger PC et al (2020) Quantitative fetal MRI assessment of cystic posterior fossa malformations. Ultrasound Obstet Gynecol 56:78–85CrossRef
12.
Zurück zum Zitat Bernardo S, Vinci V, Saldari M et al (2015) Dandy-Walker malformation: is the 'tail sign' the key sign? Prenat Diagn 35:1358–1364CrossRef Bernardo S, Vinci V, Saldari M et al (2015) Dandy-Walker malformation: is the 'tail sign' the key sign? Prenat Diagn 35:1358–1364CrossRef
13.
Zurück zum Zitat Kau T, Marterer R, Kottke R et al (2020) Blake's pouch cysts and differential diagnoses in prenatal and postnatal MRI: a pictorial review. Clin Neuroradiol 30:435–445CrossRef Kau T, Marterer R, Kottke R et al (2020) Blake's pouch cysts and differential diagnoses in prenatal and postnatal MRI: a pictorial review. Clin Neuroradiol 30:435–445CrossRef
14.
Zurück zum Zitat Pertl B, Eder S, Stern C, Verheyen S (2019) The fetal posterior fossa on prenatal ultrasound imaging: normal longitudinal development and posterior fossa anomalies. Ultraschall Med 40:692–721CrossRef Pertl B, Eder S, Stern C, Verheyen S (2019) The fetal posterior fossa on prenatal ultrasound imaging: normal longitudinal development and posterior fossa anomalies. Ultraschall Med 40:692–721CrossRef
15.
Zurück zum Zitat Kau T, Birnbacher R, Schwärzler P et al (2019) Delayed fenestration of Blake's pouch with or without vermian hypoplasia: fetal MRI at 3 tesla versus 1.5 tesla. Cerebellum Ataxias 6:4CrossRef Kau T, Birnbacher R, Schwärzler P et al (2019) Delayed fenestration of Blake's pouch with or without vermian hypoplasia: fetal MRI at 3 tesla versus 1.5 tesla. Cerebellum Ataxias 6:4CrossRef
16.
Zurück zum Zitat Volpe P, Contro E, De Musso F et al (2012) Brainstem-vermis and brainstem-tentorium angles allow accurate categorization of fetal upward rotation of cerebellar vermis. Ultrasound Obstet Gynecol 39:632–635CrossRef Volpe P, Contro E, De Musso F et al (2012) Brainstem-vermis and brainstem-tentorium angles allow accurate categorization of fetal upward rotation of cerebellar vermis. Ultrasound Obstet Gynecol 39:632–635CrossRef
17.
Zurück zum Zitat Pinto J, Paladini D, Severino M et al (2016) Delayed rotation of the cerebellar vermis: a pitfall in early second-trimester fetal magnetic resonance imaging. Ultrasound Obstet Gynecol 48:121–124CrossRef Pinto J, Paladini D, Severino M et al (2016) Delayed rotation of the cerebellar vermis: a pitfall in early second-trimester fetal magnetic resonance imaging. Ultrasound Obstet Gynecol 48:121–124CrossRef
18.
Zurück zum Zitat Paladini D, Quarantelli M, Pastore G et al (2012) Abnormal or delayed development of the posterior membranous area of the brain: anatomy, ultrasound diagnosis, natural history and outcome of Blake's pouch cyst in the fetus. Ultrasound Obstet Gynecol 39:279–287CrossRef Paladini D, Quarantelli M, Pastore G et al (2012) Abnormal or delayed development of the posterior membranous area of the brain: anatomy, ultrasound diagnosis, natural history and outcome of Blake's pouch cyst in the fetus. Ultrasound Obstet Gynecol 39:279–287CrossRef
19.
Zurück zum Zitat Conte G, Caschera L, Parazzini C et al (2020) Prenatal magnetic resonance imaging within the 26th week of gestation may predict the fate of isolated upward rotation of the cerebellar vermis: insights from a multicentre study. Eur Radiol 30:2161–2170CrossRef Conte G, Caschera L, Parazzini C et al (2020) Prenatal magnetic resonance imaging within the 26th week of gestation may predict the fate of isolated upward rotation of the cerebellar vermis: insights from a multicentre study. Eur Radiol 30:2161–2170CrossRef
20.
Zurück zum Zitat Whitehead MT, Vezina G (2020) The fetal falx cerebelli. Pediatr Radiol 50:984–989CrossRef Whitehead MT, Vezina G (2020) The fetal falx cerebelli. Pediatr Radiol 50:984–989CrossRef
21.
Zurück zum Zitat Nelson MD, Maher K, Gilles FH (2004) A different approach to cysts of the posterior fossa. Pediatr Radiol 34:720–732CrossRef Nelson MD, Maher K, Gilles FH (2004) A different approach to cysts of the posterior fossa. Pediatr Radiol 34:720–732CrossRef
22.
Zurück zum Zitat Paladini D, Donarini G, Parodi S et al (2019) Hindbrain morphometry and choroid plexus position in differential diagnosis of posterior fossa cystic malformations. Ultrasound Obstet Gynecol 54:207–214CrossRef Paladini D, Donarini G, Parodi S et al (2019) Hindbrain morphometry and choroid plexus position in differential diagnosis of posterior fossa cystic malformations. Ultrasound Obstet Gynecol 54:207–214CrossRef
23.
Zurück zum Zitat Altman NR, Naidich TP, Braffman BH (1992) Posterior fossa malformations. AJNR Am J Neuroradiol 13:691–724PubMed Altman NR, Naidich TP, Braffman BH (1992) Posterior fossa malformations. AJNR Am J Neuroradiol 13:691–724PubMed
24.
Zurück zum Zitat Twickler DM, Reichel T, McIntire DD et al (2002) Fetal central nervous system ventricle and cisterna magna measurements by magnetic resonance imaging. Am J Obstet Gynecol 187:927–931CrossRef Twickler DM, Reichel T, McIntire DD et al (2002) Fetal central nervous system ventricle and cisterna magna measurements by magnetic resonance imaging. Am J Obstet Gynecol 187:927–931CrossRef
25.
Zurück zum Zitat Chapman T, Menashe SJ, Zare M et al (2018) Establishment of normative values for the fetal posterior fossa by magnetic resonance imaging. Prenat Diag 38:1035–1041CrossRef Chapman T, Menashe SJ, Zare M et al (2018) Establishment of normative values for the fetal posterior fossa by magnetic resonance imaging. Prenat Diag 38:1035–1041CrossRef
26.
Zurück zum Zitat Xi Y, Brown E, Bailey A, Twickler DM (2016) MR imaging of the fetal cerebellar vermis: biometric predictors of adverse neurologic outcome. J Magn Reson Imaging 44:1284–1292CrossRef Xi Y, Brown E, Bailey A, Twickler DM (2016) MR imaging of the fetal cerebellar vermis: biometric predictors of adverse neurologic outcome. J Magn Reson Imaging 44:1284–1292CrossRef
27.
Zurück zum Zitat Kline-Faith B, Bulas D, Bahado-Singh R (2015) Fundamental and advanced fetal imaging-ultrasound and MRI. Wolters-Kluwers, Philadelphia Kline-Faith B, Bulas D, Bahado-Singh R (2015) Fundamental and advanced fetal imaging-ultrasound and MRI. Wolters-Kluwers, Philadelphia
28.
Zurück zum Zitat Jandeaux C, Kuchcinski G, Ternynck C et al (2019) Biometry of the cerebellar vermis and brain stem in children: MR imaging reference data from measurements in 718 children. AJNR Am J Neuroradiol 40:1835–1841PubMedPubMedCentral Jandeaux C, Kuchcinski G, Ternynck C et al (2019) Biometry of the cerebellar vermis and brain stem in children: MR imaging reference data from measurements in 718 children. AJNR Am J Neuroradiol 40:1835–1841PubMedPubMedCentral
29.
Zurück zum Zitat Tubbs RS, Shoja MM, Aggarwal A et al (2016) Choroid plexus of the fourth ventricle: review and anatomic study highlighting anatomical variations. J Clin Neurosci 26:79–83CrossRef Tubbs RS, Shoja MM, Aggarwal A et al (2016) Choroid plexus of the fourth ventricle: review and anatomic study highlighting anatomical variations. J Clin Neurosci 26:79–83CrossRef
30.
Zurück zum Zitat Mussi AC, Matushita H, Andrade FG, Rhoton AL (2015) Surgical approaches to IV ventricle — anatomical study. Childs Nerv Syst 31:1807–1814CrossRef Mussi AC, Matushita H, Andrade FG, Rhoton AL (2015) Surgical approaches to IV ventricle — anatomical study. Childs Nerv Syst 31:1807–1814CrossRef
31.
Zurück zum Zitat Benda CE (1954) The Dandy-Walker syndrome or the so-called atresia of the foramen Magendie. J Neuropathol Exp Neurol 13:14–29CrossRef Benda CE (1954) The Dandy-Walker syndrome or the so-called atresia of the foramen Magendie. J Neuropathol Exp Neurol 13:14–29CrossRef
32.
Zurück zum Zitat Taggart JK, Walker AE (1942) Congenital atresia of the foramens of Luschka and Magendie. Arch Neurol Psychiatr 48:583–612CrossRef Taggart JK, Walker AE (1942) Congenital atresia of the foramens of Luschka and Magendie. Arch Neurol Psychiatr 48:583–612CrossRef
33.
Zurück zum Zitat Haldipur P, Aldinger KA, Bernardo S et al (2019) Spaciotemporal expansion of the primary progenitor zones in the developing human cerebellum. Science 366:454–460CrossRef Haldipur P, Aldinger KA, Bernardo S et al (2019) Spaciotemporal expansion of the primary progenitor zones in the developing human cerebellum. Science 366:454–460CrossRef
34.
Zurück zum Zitat Pichiecchio A, Decio A, Di Perri C et al (2016) “Acquired” Dandy-Walker malformation and cerebellar hemorrhage: usefulness of serial MRI. Eur J Paediatr Neurol 20:188–191 Pichiecchio A, Decio A, Di Perri C et al (2016) “Acquired” Dandy-Walker malformation and cerebellar hemorrhage: usefulness of serial MRI. Eur J Paediatr Neurol 20:188–191
Metadaten
Titel
Taenia–tela choroidea complex and choroid plexus location help distinguish Dandy-Walker malformation and Blake pouch cysts
verfasst von
Matthew T. Whitehead
Gilbert Vezina
Sarah D. Schlatterer
Sarah B. Mulkey
Adre J. du Plessis
Publikationsdatum
30.03.2021
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Radiology / Ausgabe 8/2021
Print ISSN: 0301-0449
Elektronische ISSN: 1432-1998
DOI
https://doi.org/10.1007/s00247-021-04991-3

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