[朗格汉斯细胞组织细胞增多症与婴儿肌无力有关]。

Pediatrie Pub Date : 1993-01-01
Y Bertrand, A Dutour, A M Manel, G Souillet, N Philippe
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引用次数: 0

摘要

朗格汉斯细胞组织细胞增多症(LCH)的发病机制尚不清楚,但越来越多的证据表明存在免疫功能障碍。我们描述了一个婴儿谁提出了LCH与重症肌无力。胸腺在重症肌无力的病理生理中起着重要的作用,并经常参与LCH。婴儿期和器官功能障碍的迹象预示着预后不良:免疫治疗(胸腺激素、环孢素、α干扰素)以及同种异体骨髓移植将被研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Langerhans cell histiocytosis associated with myasthenia in an infant].

The pathogenesis of Langerhans cell histiocytosis (LCH) is unclear, but there is increasing evidence that an immunological dysfunction is present. We describe an infant who presented a LCH associated with myasthenia gravis. The thymus is known to play an important role in the pathophysiology of myasthenia gravis and is often involved in LCH. Infancy and signs of organ dysfunction are predictive of poor prognosis: immunotherapy is to be investigated (thymic hormone, cyclosporin, alpha interferon), as well as allogeneic bone marrow transplantation.

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