CEBPA-associated familial acute myeloid leukemia mimicking Werner syndrome: a case report
Tanguy Demaret, Damien Feret, Barbara Lambert, Delphine Pranger, Jean-Louis Dargent, Maria Dolores Martin Martinez, Antonio Renda, Isabelle Maystadt

TL;DR
A family with a CEBPA gene mutation developed leukemia and premature aging symptoms similar to Werner syndrome, but the condition was actually a different genetic disorder.
Contribution
First report of a leukemia predisposition syndrome mimicking a progeroid syndrome.
Findings
A CEBPA gene variant was identified in the patient and affected relatives, causing leukemia and premature aging symptoms.
The patient's symptoms were a phenocopy of Werner syndrome, not caused by the WS gene.
Personalized medical monitoring was implemented for the family based on the genetic diagnosis.
Abstract
CEBPA-associated familial acute myeloid leukemia (AML) is an autosomal dominant leukemia predisposition syndrome associated with germline variants in the CEBPA gene. Werner syndrome (WS) is an autosomal recessive progeroid syndrome causing premature aging and malignancies (e.g., AML). We report a 41-year-old man referred for medical genetic evaluation because of 3 synchronous tumors (colon, kidney, and thyroid) and premature aging. He underwent hematopoietic stem cell transplantation (HSCT) at 12 years of age because of AML diagnosed 3 years earlier. His sister (donor for the HSCT) and his brother later developed AML, as did two of her sister’s three children. The patient met the clinical criteria for a “probable” WS, but duo-based (urine and blood DNA) whole exome sequencing did not confirm this diagnosis. A heterozygous c.350del p.(Gly117Alafs*43) pathogenic variant in the CEBPA gene…
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Taxonomy
TopicsAcute Myeloid Leukemia Research · DNA Repair Mechanisms · Acute Lymphoblastic Leukemia research
