Blastomycosis was first described by Gilchrist in 1894 as a form of chronic dermatitis. Since that time, many articles have appeared in the literature dealing with the chronic cutaneous lesions (11). Numerous reports have been published describing secondary pulmonary invasion (4, 11), and a few on primary chronic pulmonary blastomycosis (11, 12). Review of the literature reveals only one case which can be interpreted as an acute primary pulmonary blastomycosis. Healy and Morrison, in 1931 (9), described an acute pneumonic process in a patient with persistent blastomycetes in the sputum. A roentgenogram showed a left basal infiltration with associated hilar lymphadenopathy. In the absence of follow-up, however, we do not know whether the disease process subsided or became chronic. Primary pulmonary lesions due to other fungi have been described since 1935. Dickson, in 1937 (5), discussed the primary lesions of coccidioidomycosis, which subsided spontaneously. Carter (2, 3) and Jamison and Carter (10) added to the earlier description. The clinical picture is similar to that of other primary infections, with headache, chest pain, temperature of 100–102°, slight elevation of the white blood count, and a moderately productive cough predominating. Roentgenograms early reveal a pulmonary infiltration varying from thickening of the hilar shadows to almost complete consoUdation. About 33 per cent of the cases in which the disease persists for any period of time show some degree of mediastinal or hilar lymphadenopathy; parenchymal infiltrations tend to become nodose, and in some instances cavitation develops. Pleural effusion appears in approximately 20 per cent of all cases. Death is rarely due to the primary invasion except when dissemination occurs. Zwerling and Palmer, in 1946 (13), postulated an acute benign form of histoplasmosis on the basis of pulmonary calcifications associated with a negative response to tuberculin and a positive response to histoplasmin skin tests. Furcolow, Mantz, and Lewis, in 1947 (6), reported 72 asymptomatic cases of pulmonary infiltration with positive histoplasmin skin tests. They divided the infiltrates into three groups. Nodular foci were present in 49 of the 72 cases. These foci varied from 0.5 cm. to 3.5 cm. in diameter and occasionally had calcific centers. In 39 cases of this group there was associated mediastinal or hilar lymphadenopathy. Pneumonic infiltration was present in 17 cases, and in 14 of these there was associated hilar lymphadenopathy. This lesion is described as a single, persistent patch of pneumonitis about 2 cm. in diameter. Disseminated infiltrates occurred in 3 cases, in 2 of which there was associated lymphadenopathy. The lesions in this group varied from the size of a millet seed to large patchy areas. No deaths are reported in the series and follow-up on many of the cases revealed calcification replacing the active process.
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