Skip to main content
Top
Published in: Journal of Medical Ultrasonics 1/2017

01-01-2017 | Case Report

Hemiatrophy of brain: antenatal ultrasonography and MRI/postnatal MRI diagnosis with the introduction of “shifted falx sign”

Authors: Abhinav Aggarwal, Aakriti Kapoor Aggarwal, Aakaar Kapoor, Ravi Kapoor, Ashutosh Bansal

Published in: Journal of Medical Ultrasonics | Issue 1/2017

Login to get access

Abstract

Dyke–Davidoff–Masson syndrome (DDMS) is an uncommon congenital/pediatric disorder diagnosed only with the help of imaging. Clinical features associated with it are hemiparesis, seizures, facial asymmetry, and mental retardation. We here present a case of DDMS diagnosed antenatally at 29 weeks gestational age during routine antenatal ultrasound examination. The patient was further evaluated and followed using both ultrasound and magnetic resonance imaging during antenatal and postnatal periods. The infant had unilateral hemiatrophy with the absence of anterior and middle cerebral arteries. We hereby also want to coin the term “shifted falx sign” as a diagnostic indicator for DDMS for the first time. To our knowledge, this is the earliest antenatally sonologically diagnosed case of the said pathology.
Literature
1.
go back to reference Goyal J, Shaha V, Rao S, et al. Dyke Davidoff Masson syndrome in Children. Internet J Pediatr Neonatol. 2008;10:2. Goyal J, Shaha V, Rao S, et al. Dyke Davidoff Masson syndrome in Children. Internet J Pediatr Neonatol. 2008;10:2.
2.
go back to reference Dyke CG, Davidoff LM, Masson LB. Cerebral hemiatrophy hypertrophy of skull and sinus. Surg Gynecol Obstet. 1933;57:588–600. Dyke CG, Davidoff LM, Masson LB. Cerebral hemiatrophy hypertrophy of skull and sinus. Surg Gynecol Obstet. 1933;57:588–600.
3.
go back to reference Piro E, Piccione M, Marrone G, et al. Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral artery. Ital. J Pediatr. 2013;39:32.CrossRefPubMedPubMedCentral Piro E, Piccione M, Marrone G, et al. Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral artery. Ital. J Pediatr. 2013;39:32.CrossRefPubMedPubMedCentral
4.
go back to reference Solomon GE, Hilal SK, Gold AP, et al. Natural history of acute hemiplegia of childhood. Brain. 1970;93:107–20.CrossRefPubMed Solomon GE, Hilal SK, Gold AP, et al. Natural history of acute hemiplegia of childhood. Brain. 1970;93:107–20.CrossRefPubMed
5.
go back to reference Sharma S, Goyal D, Negi A, et al. Dyke-davidoff masson syndrome. Indian J Radiol Imaging. 2006;16:165–6.CrossRef Sharma S, Goyal D, Negi A, et al. Dyke-davidoff masson syndrome. Indian J Radiol Imaging. 2006;16:165–6.CrossRef
7.
go back to reference Shen WC, Chen CC, Lee SK, et al. Magnetic resonance imaging of cerebral hemiatrophy. J Formos Med Assoc. 1993;92:995–1000.PubMed Shen WC, Chen CC, Lee SK, et al. Magnetic resonance imaging of cerebral hemiatrophy. J Formos Med Assoc. 1993;92:995–1000.PubMed
8.
go back to reference Teixeira RA, Li LM, Santos SLM, et al. Lateralization of epileptiform discharges in patients with epilepsy and precocious destructive brain insults. Arq Neuropsiquiatr. 2004;62:1–8.CrossRefPubMed Teixeira RA, Li LM, Santos SLM, et al. Lateralization of epileptiform discharges in patients with epilepsy and precocious destructive brain insults. Arq Neuropsiquiatr. 2004;62:1–8.CrossRefPubMed
9.
go back to reference Griffiths PD, Reeves MJ, Morris JE, et al. A prospective study of fetuses with isolated ventriculomegaly investigated by antenatal sonography and in utero MR imaging. AJNR. 2010;31:106–11.CrossRefPubMed Griffiths PD, Reeves MJ, Morris JE, et al. A prospective study of fetuses with isolated ventriculomegaly investigated by antenatal sonography and in utero MR imaging. AJNR. 2010;31:106–11.CrossRefPubMed
10.
go back to reference Unal O, Tombul T, Cirak B, et al. Left hemisphere and male sex dominance of cerebral hemiatrophy (Dyke-Davidoff-Masson Syndrome). Clin Imaging. 2004;28:163–5.CrossRefPubMed Unal O, Tombul T, Cirak B, et al. Left hemisphere and male sex dominance of cerebral hemiatrophy (Dyke-Davidoff-Masson Syndrome). Clin Imaging. 2004;28:163–5.CrossRefPubMed
11.
go back to reference Malik P, Garg R, Gulia AKD, et al. Dyke-Davidoff-Masson syndrome—a rare cause of refractory epilepsy. Iran J Psychiatry. 2014;9:42–4.PubMedPubMedCentral Malik P, Garg R, Gulia AKD, et al. Dyke-Davidoff-Masson syndrome—a rare cause of refractory epilepsy. Iran J Psychiatry. 2014;9:42–4.PubMedPubMedCentral
12.
go back to reference Alpers BJ, Dear RB. Hemiatrophy of the brain. J Nerv Ment Dis. 1939;89:651–3. Alpers BJ, Dear RB. Hemiatrophy of the brain. J Nerv Ment Dis. 1939;89:651–3.
13.
go back to reference Hageman G, Gooskens RHJM, Willemse J. A cerebral cause of arthrogryposis: unilateral cerebral hypoplasis. Clin Neurol Neurosurg. 1985;87:119–22.CrossRefPubMed Hageman G, Gooskens RHJM, Willemse J. A cerebral cause of arthrogryposis: unilateral cerebral hypoplasis. Clin Neurol Neurosurg. 1985;87:119–22.CrossRefPubMed
Metadata
Title
Hemiatrophy of brain: antenatal ultrasonography and MRI/postnatal MRI diagnosis with the introduction of “shifted falx sign”
Authors
Abhinav Aggarwal
Aakriti Kapoor Aggarwal
Aakaar Kapoor
Ravi Kapoor
Ashutosh Bansal
Publication date
01-01-2017
Publisher
Springer Japan
Published in
Journal of Medical Ultrasonics / Issue 1/2017
Print ISSN: 1346-4523
Electronic ISSN: 1613-2254
DOI
https://doi.org/10.1007/s10396-016-0744-7

Other articles of this Issue 1/2017

Journal of Medical Ultrasonics 1/2017 Go to the issue