Schmalzl F, Weiser G, Hüttenberg H, Czarnecki N, Netolitzky G, Skrabal F, Gasser H, Braunsteiner H
Acta Med Austriaca. 1979;6(5):244-7.
The authors report on a woman (34 years old) which was affected by lymphomatoid granulomatosis. During the first periods of the disease the granulomatous lesions were confined to the muscles of the upper extremities. High fever, progressive development of new muscular lesions and later of lesions in the pharynx, larynx, and the lungs characterized the clinical course. Therapeutic approaches included glucocorticoids, chemotherapy, irradiation, plasmapheresis, but induced no relevant beneficial effect. Based on laboratory and experimental data as well as on data from the literature the authors discuss the pathogenesis and differential diagnosis of this disorder.
作者报道了一名34岁患有淋巴瘤样肉芽肿病的女性。在疾病的最初阶段,肉芽肿性病变局限于上肢肌肉。高热、新的肌肉病变的进行性发展以及随后咽部、喉部和肺部的病变是该临床病程的特征。治疗方法包括糖皮质激素、化疗、放疗、血浆置换,但均未产生明显有益效果。基于实验室和实验数据以及文献数据,作者讨论了该疾病的发病机制和鉴别诊断。