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婴儿型多动脉炎和川崎病。

Infantile polyarteritis and Kawasaki disease.

作者信息

Smith A D

出版信息

Acta Paediatr Scand. 1977 May;66(3):381-4. doi: 10.1111/j.1651-2227.1977.tb07911.x.

Abstract

Polyarteritis in infancy is very rare, difficult to diagnose and invariably fatal. A 6-month-old girl who presented with a prolonged unexplained fever and was subsequently demonstrated at post-mortem examination to have polyarteritis is described. The combination of polyarterits with some unusual presenting features suggests that the case described is one of the Mucocutaneous Lymph Node Syndrome (M.L.N.S.) or Kawasaki Disease. Polyarteritis and Kawasaki Disease are discussed with reference to the case described.

摘要

婴儿期的结节性多动脉炎非常罕见,难以诊断,且无一例外会致命。本文描述了一名6个月大的女孩,她出现了持续不明原因的发热,死后尸检显示患有结节性多动脉炎。结节性多动脉炎与一些不寻常的临床表现相结合,提示所描述的病例是皮肤黏膜淋巴结综合征(M.L.N.S.)或川崎病之一。结合所描述的病例对结节性多动脉炎和川崎病进行了讨论。

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