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Metachronous T-Lymphoblastic Lymphoma and Burkitt Lymphoma in a Child With Constitutional Mismatch Repair Deficiency Syndrome.

Authors :
Alexander TB
McGee RB
Kaye EC
McCarville MB
Choi JK
Cavender CP
Nichols KE
Sandlund JT
Source :
Pediatric blood & cancer [Pediatr Blood Cancer] 2016 Aug; Vol. 63 (8), pp. 1454-6. Date of Electronic Publication: 2016 Apr 01.
Publication Year :
2016

Abstract

Constitutional mismatch repair deficiency (CMMRD) is a cancer predisposition syndrome associated with a high risk of developing early-onset malignancies of the blood, brain, and intestinal tract. We present the case of a patient with T-lymphoblastic lymphoma at the age of 3 years, followed by Burkitt lymphoma 10 years later. This patient also exhibited numerous nonmalignant findings including café au lait spots, lipomas, bilateral renal nodules, a nonossifying fibroma, multiple colonic adenomas, and a rapidly enlarging pilomatrixoma. The spectrum of malignant and nonmalignant neoplasms in this patient highlights the remarkable diversity, and early onset, of lesions seen in children with CMMRD.<br /> (© 2016 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1545-5017
Volume :
63
Issue :
8
Database :
MEDLINE
Journal :
Pediatric blood & cancer
Publication Type :
Academic Journal
Accession number :
27037742
Full Text :
https://doi.org/10.1002/pbc.25989