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Multiple Brain Developmental Venous Anomalies as a Marker for Constitutional Mismatch Repair Deficiency Syndrome.
Shiran, S I; Ben-Sira, L; Elhasid, R; Roth, J; Tabori, U; Yalon, M; Constantini, S; Dvir, R.
Afiliação
  • Shiran SI; From the Departments of Radiology (S.I.S., L.B.-S.) shellyshiran@gmail.com.
  • Ben-Sira L; From the Departments of Radiology (S.I.S., L.B.-S.).
  • Elhasid R; Pediatric Hematology/Oncology (R.E., R.D.).
  • Roth J; Pediatric Neurosurgery (J.R., S.C.), Dana Children's Hospital, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Tabori U; Division of Hematology/Oncology (U.T.), Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Yalon M; Department of Pediatric Hematology/Oncology (M.Y.), Sheba Medical Center, Tel-Hashomer, Israel.
  • Constantini S; Pediatric Neurosurgery (J.R., S.C.), Dana Children's Hospital, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Dvir R; Pediatric Hematology/Oncology (R.E., R.D.).
AJNR Am J Neuroradiol ; 39(10): 1943-1946, 2018 10.
Article em En | MEDLINE | ID: mdl-30166433
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Veias Cerebrais / Síndromes Neoplásicas Hereditárias / Neoplasias Encefálicas / Neoplasias Colorretais Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies / Screening_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: AJNR Am J Neuroradiol Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Veias Cerebrais / Síndromes Neoplásicas Hereditárias / Neoplasias Encefálicas / Neoplasias Colorretais Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies / Screening_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: AJNR Am J Neuroradiol Ano de publicação: 2018 Tipo de documento: Article