NORTH AMERICAN BLASTOMYCOSIS: A STUDY OF 40 PATIENTS
NORTH AMERICAN BLASTOMYCOSIS: A STUDY OF 40 PATIENTS
复制标题
北美芽生菌病:对 40 名患者的研究
DOI:
10.1097/00005792-196805000-00001
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发表时间:
1968
期刊:
影响因子:
1.6
通讯作者:
J. Utz
中科院分区:
文献类型:
--
作者:
P. Witorsch;J. Utz
North American blastomycosis is a systemic fungal disease produced by the dimorphic micro-organism, Blastomyces dermatitidis. The first patient was described by Gilchrist in 1894 (64). Subsequently, Gil-christ and Stokes (65, 67, 68) isolated, identi-fied, and named the causative fungus. Originally thought to be a localized infection of the skin, the disease was soon recognized to have extracutaneous manifestations (40, 51, 66, 113, 119, 166), and by 1916, 47 cases with such involvement had been reported (164). A review of the literature in 1939 (100) revealed 347 reported cases of this disease. Of these, 80 were regarded as “unquestionably” proved and 163 as “presumptively” so. The remaining 104 reports were found to have in-sufficient evidence to support the diagnosis. These and other authors (148) classified the disease into two forms, cutaneous and systemic, based on the then prevalent concept that there were two natural portals of entry, the lungs and the skin. This dual pathogenesis was generally accepted until 1951, when Schwarz and Baum (135) presented evidence to support the hypothesis that in most cases, in-