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Eur J Med Genet. 2019 Aug;62(8):103706. doi: 10.1016/j.ejmg.2019.103706. Epub 2019 Jun 21.

Ongoing issues with the management of children with Constitutional Mismatch Repair Deficiency syndrome.

Author information

1
Department of Pediatrics, Saint George Hospital University Medical Center, Beirut, Lebanon. Electronic address: rafarah@stgeorgehospital.org.
2
Department of Pediatrics, Saint George Hospital University Medical Center, Beirut, Lebanon.
3
Department of Surgery, Saint George Hospital University Medical Center, Beirut, Lebanon.
4
Department of Laboratory Medicine, University Medical Center, LAUMCRH-Rizk Hospital, Beirut, Lebanon.
5
The Hospital for Sick Children, Toronto, Canada.
6
Mount Sinai Hospital, Toronto, Canada.

Abstract

Constitutional Mismatch Repair Deficiency (CMMRD) is a rare cancer predisposition syndrome, presenting in childhood, in which affected patients develop various malignancies such as hematological, gastrointestinal and central nervous system tumors. Although guidelines are being increasingly developed for surveillance and early detection of cancers in affected families, there are no clear recommendations regarding choice of therapy and very scarce information about tolerance to chemotherapy and radiation in these patients. We report the pedigree of a consanguineous family with four affected children. Although clinical and molecular tests confirm CMMRD, genetic testing revealed heterogeneous mutations. The index case developed severe toxicity from therapy for glioblastoma and T-cell leukemia and died from an infection while in complete remission. His sister developed a malignant brain tumor while undergoing surveillance for a low grade brain lesion and is still undergoing follow-up. This family illustrates the difficulties and opportunities with challenging diagnosis, surveillance and choice of therapy for children with CMMRD and the need for increased awareness and more information about this rare but important syndrome.

KEYWORDS:

BrainTumor; CMMRD; Constitutional mismatch repair deficiency syndrome; GI malignancies; Genetic predisposition to cancer; Glioblastoma multiforme; Lynch syndrome; Surveillance; T-cell leukemia

PMID:
31233827
DOI:
10.1016/j.ejmg.2019.103706
[Indexed for MEDLINE]

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