Myelodysplastic syndrome occurring in a patient with gorlin syndrome

Jamie L. Mull, Lisa M. Madden, Susan J. Bayliss

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

We report a case of myelodysplastic syndrome (MDS) occurring in an African American boy with Gorlin syndrome with a novel PTCH1 mutation. Before developing MDS, the patient had been treated with chemotherapy and radiation for a medulloblastoma. He received a bone marrow transplant for the MDS and eventually died of treatment complications. Secondary hematologic malignancies are a known complication of certain chemotherapeutics, although whether a patient with Gorlin syndrome has a greater propensity for the development of such malignancies is unclear.

Original languageEnglish
Pages (from-to)e256-e257
JournalPediatric Dermatology
Volume33
Issue number4
DOIs
StatePublished - Jul 1 2016

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