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Multiple giant cell lesions in a patient with Noonan syndrome with multiple lentigines
Henk van den Berg1, Willem Hans Schreuder2, Marjolijn Jongmans3
1Department of Pediatric Oncology, Emma Children Hospital/Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
Abstract:
A patient with Noonan syndrome with multiple lentigines (NSML) and multiple giant cell lesions (MGCL) in mandibles and maxillae is described. A mutation p.Thr468Met in the PTPN11-gene was found. This is the second reported NSML patient with MGCL. Our case adds to the assumption that, despite a different molecular pathogenesis and effect on the RAS/MEK pathway, NSML shares the development of MGCL, with other RASopathies.

