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Research ArticlePediatric Neuroimaging

Multiple Brain Developmental Venous Anomalies as a Marker for Constitutional Mismatch Repair Deficiency Syndrome

S.I. Shiran, L. Ben-Sira, R. Elhasid, J. Roth, U. Tabori, M. Yalon, S. Constantini and R. Dvir
American Journal of Neuroradiology October 2018, 39 (10) 1943-1946; DOI: https://doi.org/10.3174/ajnr.A5766
S.I. Shiran
aFrom the Departments of Radiology (S.I.S., L.B.-S.)
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L. Ben-Sira
aFrom the Departments of Radiology (S.I.S., L.B.-S.)
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R. Elhasid
bPediatric Hematology/Oncology (R.E., R.D.)
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J. Roth
cPediatric Neurosurgery (J.R., S.C.), Dana Children's Hospital, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
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U. Tabori
dDivision of Hematology/Oncology (U.T.), Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada
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M. Yalon
eDepartment of Pediatric Hematology/Oncology (M.Y.), Sheba Medical Center, Tel-Hashomer, Israel.
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S. Constantini
cPediatric Neurosurgery (J.R., S.C.), Dana Children's Hospital, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
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R. Dvir
bPediatric Hematology/Oncology (R.E., R.D.)
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Abstract

BACKGROUND AND PURPOSE: Biallelic constitutional mutations in DNA mismatch repair genes cause a distinct syndrome, constitutional mismatch repair deficiency syndrome (CMMRD), characterized by cancers from multiple organs, most commonly brain tumors, during childhood. Surveillance protocols include total and brain MR imaging among other modalities to enable early detection of tumors. Brain surveillance scans revealed prominent brain developmental venous anomalies (DVAs) in some patients. DVAs are benign vascular anomalies, and their incidence in the general population is 2.6%–6.4%. Most developmental venous anomalies are asymptomatic and are found incidentally. Our purpose was to assess the prevalence of DVAs in CMMRD patients and describe their phenotype.

MATERIALS AND METHODS: A retrospective descriptive analysis of brain MR imaging studies from 10 patients from 3 families with CMMRD was performed. Analysis included the number of developmental venous anomalies, location, draining vessels, and associated vascular anomalies (ie, cavernomas), with clinical correlation of symptoms and tumors.

RESULTS: All 10 patients had ≥2 developmental venous anomalies, and 2 had, in addition, non-therapy-induced cavernomas. There was no clinically symptomatic intracranial bleeding from developmental venous anomalies. Six patients had malignant brain tumors. The location of brain tumors was not adjacent to the developmental venous anomalies. No new developmental venous anomalies developed during follow-up.

CONCLUSIONS: The occurrence of multiple developmental venous anomalies in all our patients with CMMRD suggests that developmental venous anomalies may be a characteristic of this syndrome that has not been previously described. If confirmed, this quantifiable feature can be added to the current scoring system and could result in early implementation of genetic testing and surveillance protocols, which can be life-saving for these patients.

ABBREVIATIONS:

CMMRD
constitutional mismatch repair deficiency syndrome
DVA
developmental venous anomaly
  • © 2018 by American Journal of Neuroradiology
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American Journal of Neuroradiology: 39 (10)
American Journal of Neuroradiology
Vol. 39, Issue 10
1 Oct 2018
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Cite this article
S.I. Shiran, L. Ben-Sira, R. Elhasid, J. Roth, U. Tabori, M. Yalon, S. Constantini, R. Dvir
Multiple Brain Developmental Venous Anomalies as a Marker for Constitutional Mismatch Repair Deficiency Syndrome
American Journal of Neuroradiology Oct 2018, 39 (10) 1943-1946; DOI: 10.3174/ajnr.A5766

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Multiple Brain Developmental Venous Anomalies as a Marker for Constitutional Mismatch Repair Deficiency Syndrome
S.I. Shiran, L. Ben-Sira, R. Elhasid, J. Roth, U. Tabori, M. Yalon, S. Constantini, R. Dvir
American Journal of Neuroradiology Oct 2018, 39 (10) 1943-1946; DOI: 10.3174/ajnr.A5766
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Cited By...

  • Symptomatic Developmental Venous Anomaly: State-of-the-Art Review on Genetics, Pathophysiology, and Imaging Approach to Diagnosis
  • Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group
  • Neonatal Developmental Venous Anomalies: Clinicoradiologic Characterization and Follow-Up
  • Paediatric systemic lupus erythematosus as a manifestation of constitutional mismatch repair deficiency
  • Neuroimaging Findings in Children with Constitutional Mismatch Repair Deficiency Syndrome
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