A case of Constitutional Mismatch Repair Deficiency (CMMRD)
Journal of the Philippine Medical Association
;
: 75-81, 2023.
Article
Dans Anglais
| WPRIM
| ID: wpr-1006367
ABSTRACT
@#Constitutionalmismatch repair deficiency(CMMRD) is a hereditary predisposition of malignancy evident in childhood leukemias, lymphomas, and malignant tumors of the brain, GI tract. It is a very rare condition that affects 1 per 1 million patients. Patients with CMMRD syndrome may also manifest with Neurofibromatosis Type 1 (NF1) phenotypic features, and benign masses, particularly in the gastrointestinal tract. This is a case of a 12-year old male who presented with phenotypic features of NF1, developed Acute Lymphoblastic Leukemia at 7 years old and went into remission. He subsequently developed synchronous Glioblastoma and Poorly differentiated Adenocarcinoma of the rectum.This report aims to raise awareness regarding the possibility of a CMMRD syndrome in pediatric patients who present with phenotypic features of NF1, and in those patients who present with two or more malignancies in their lifetime.
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Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Glioblastome
/
Leucémie-lymphome lymphoblastique à précurseurs B et T
langue:
Anglais
Texte intégral:
Journal of the Philippine Medical Association
Année:
2023
Type:
Article
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