Kucera J C, Davis R B
Am J Clin Pathol. 1983 May;79(5):644-6. doi: 10.1093/ajcp/79.5.644.
A patient with primary pulmonary histoplasmosis, symptomatic thrombocytopenia, and an associated elevation of platelet associated IgG during the acute phase of the illness is described. Whereas thrombocytopenia has been reported previously in patients with disseminated histoplasmosis, it appears that thrombocytopenia in a patient with nondisseminated histoplasmosis has not been described. Although certain clinical findings suggested idiopathic thrombocytopenic purpura, corticosteroids were not administered, and lymph node biopsy documented the presence of Histoplasma capsulatum. Similarly, elevated platelet associated IgG levels apparently have not been reported previously in thrombocytopenic patients with histoplasmosis. Possible mechanisms for thrombocytopenia associated with histoplasmosis are discussed.
本文描述了一名患有原发性肺组织胞浆菌病、症状性血小板减少症且在疾病急性期伴有血小板相关IgG升高的患者。虽然先前已有播散性组织胞浆菌病患者出现血小板减少症的报道,但非播散性组织胞浆菌病患者出现血小板减少症的情况似乎尚未见报道。尽管某些临床发现提示为特发性血小板减少性紫癜,但未给予皮质类固醇治疗,且淋巴结活检证实存在荚膜组织胞浆菌。同样,血小板减少的组织胞浆菌病患者血小板相关IgG水平升高的情况此前显然也未见报道。文中讨论了与组织胞浆菌病相关的血小板减少症的可能机制。