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Myelofibrosis in a patient with pachydermoperiostosis
C Bachmeyer1, L Blum, J-F Cadranel
1Service de Médecine Interne, Hôpital Tenon, Paris, France. claude.bachmeyer@tnn.ap-hop-paris.fr
Clinical and Experimental Dermatology
|October 4, 2005
Abstract:
Pachydermoperiostosis (idiopathic or primary hypertrophic osteoarthropathy) is a rare condition of unknown origin involving the skin and the skeleton, with an autosomal dominant transmission. We report a case of anaemia in a patient with pachydermoperiostosis indicating myelofibrosis, and review the literature and the pathogenetic mechanisms.