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Erschienen in:
03.03.2018 | Images
Acral Hyperpigmentation Resulting from Hydroxyurea Therapy in Primary Myelofibrosis
Erschienen in: Indian Journal of Hematology and Blood Transfusion | Ausgabe 3/2018
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A 77-year-old Asian man with congenital lymphedema had been diagnosed with JAK2-V617F mutation positive primary myelofibrosis for 2 years. After diagnosis, he was treated with hydroxyurea 500 mg/day. The patient has developed palmoplantar hyperpigmentation after receiving 22 months of hydroxyurea therapy (Fig. 1).
Fig. 1
Appearance of the acral skin and nails hyperpigmentation
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