【色霉病的不寻常原因】。

A Tomsíková
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引用次数: 0

摘要

将色霉病的典型临床表现、真菌学和组织学基础与目前较为常见的临床病程进行比较。它也指对血管、呼吸、淋巴系统、脑和播散的影响。因此,色霉病应列为机会性真菌病之一。以皮肤结节为特征的嗜色菌丝病很少发生。皮下脓肿也称为phafiomytic囊肿,尤其在皮质激素和免疫抑制治疗后更为常见。在三个捷克斯洛伐克的病例中,皮尔森的病例可以评估为不常见。它是由褐发菌引起的,并作为皮肤形式的色霉菌病传播。该病变发生在一名从未去过热带国家的患者的右手食指上。她从未患过重病,从未接受过抗生素、化疗或皮质类固醇治疗。组织学检查显示肉芽肿,有组织细胞和许多吞噬典型球形棕色微生物的巨细胞。经碘化钾、碘化钾和x线治疗治愈。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Unusual causes of chromomycosis].

The typical clinical picture and mycological and histological basis of chromomycosis is compared with the clinical course, which is encountered more often nowadays. It refers also to the affection of the vascular, respiratory, lymphatic system, the brain and the dissemination in compromised patients. For this reason chromomycosis should rank among opportunistic mycoses. Chromohyphomycosis characterized by skin nodules occurs very rarely. Subcutaneous abscesses also called phaeomycotic cysts, are more frequent especially after corticoid and immunosuppressive therapy. Among three Czechoslovak cases of chromomycosis, the case in Pilsen can be evaluated as uncommon. It was caused by Phialophora pedrosoi and passed as a skin form of chromomycosis. The lesion developed on the right forefinger of a patient who never visited tropical countries. She never was seriously ill, never treated with antibiotics, chemotherapeutics, or corticosteroids. The histological examination of the excision revealed a granuloma with histiocytes and many giant cells phagocytizing typical spherical brown microorganisms. The patient was cured by KI, intraiodine and X-ray therapy.

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