Friedrichs F, Kusenbach G, Skopnik H
Kinderklinik der RWTH Aachen.
Klin Padiatr. 1991 Sep-Oct;203(5):395-8. doi: 10.1055/s-2007-1025461.
Mycobacterial infections are rarely reported in Cystic Fibrosis patients although they quite often develop predisposing risk factors such as underweight, secondary diabetes mellitus and chronic inflammatory pulmonary disease. Furthermore glucocorticoid therapy is mandatory in some patients. CF heterozygotes are said to have a selective advantage due to an increased host resistance against Mycobacterium tuberculosis. In this survey 1926 CF patients were investigated for the incidence of tuberculin conversion and manifest infection with mycobacterium tuberculosis in the Federal Republic of Germany (FRG). The results do not support the hypothesis of increased host resistance nor do they show any evidence of a higher risk for tuberculosis in CF. Implications for prophylactic, diagnostic and therapeutic measures are discussed in accordance to the recent epidemiologic data of tuberculosis in the FRG.
尽管囊性纤维化患者常常会出现如体重过轻、继发性糖尿病和慢性炎症性肺病等易感风险因素,但分枝杆菌感染在这些患者中却鲜有报道。此外,部分患者必须接受糖皮质激素治疗。据说,由于宿主对结核分枝杆菌的抵抗力增强,囊性纤维化杂合子具有选择性优势。在这项调查中,对德意志联邦共和国(FRG)的1926例囊性纤维化患者进行了结核菌素转化发生率和结核分枝杆菌显性感染的调查。结果既不支持宿主抵抗力增强的假说,也没有显示出囊性纤维化患者患结核病风险更高的任何证据。根据FRG近期结核病的流行病学数据,对预防、诊断和治疗措施的影响进行了讨论。