Myelofibrosis in a patient with pachydermoperiostosis

被引：12

作者：

Bachmeyer, C

Blum, L

Cadranel, JF

Delfraissy, JF

机构：

[1] Hop Tenon, Serv Med Interne, F-75020 Paris, France

[2] Hop Rene Dubos, Pontoise, France

[3] Hop Laennec, Serv Hepatogastroenterol & Diabetol, Creil, France

[4] CHU Bicetre, Le Kremlin Bicetre, France

来源：

CLINICAL AND EXPERIMENTAL DERMATOLOGY | 2005年 / 30卷 / 06期

关键词：

D O I：

10.1111/j.1365-2230.2005.01891.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

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.

引用

页码：646 / 648

页数：3

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