Margo C, Rabinowicz I M, Kwon-Chung K J, Zimmerman L E
Arch Ophthalmol. 1983 Oct;101(10):1580-5. doi: 10.1001/archopht.1983.01040020582017.
A zygomycotic (phycomycotic) orbital cellulitis developed in a healthy 9-year-old boy. Because of the involved tissue's unfamiliar histopathologic features, an initial diagnosis of eosinophilic granuloma was made and appropriate treatment was delayed for more than six months. The patient's slowly progressive form of zygomycosis was clinically and morphologically similar to that described in previously recorded cases. All three cases occurred in otherwise healthy children living within the United States. Their involved tissues had mixed histopathologic features of chronic granulomatous entomophthoramycosis and acute necrotizing mucormycosis; however, unlike entomophthoramycosis, the fungi in these cases may invade the walls of blood vessels and cause severe tissue necrosis. We believe that these three cases represent a distinct clinicopathologic variant of facial-cranial zygomycosis not previously delineated in the literature. Although they are aggressive, these infections are not as fulminant as in classic mucormycosis, but can nevertheless be lethal.
一名健康的9岁男孩发生了接合菌性(藻菌性)眼眶蜂窝织炎。由于受累组织具有不熟悉的组织病理学特征,最初诊断为嗜酸性肉芽肿,适当的治疗被推迟了六个多月。患者接合菌病的缓慢进展形式在临床和形态上与先前记录的病例相似。所有三例均发生在美国境内其他方面健康的儿童中。他们受累组织具有慢性肉芽肿性耳霉病和急性坏死性毛霉病的混合组织病理学特征;然而,与耳霉病不同的是,这些病例中的真菌可能侵入血管壁并导致严重的组织坏死。我们认为这三例代表了文献中先前未描述的一种独特的面颅接合菌病临床病理变体。尽管它们具有侵袭性,但这些感染不像经典毛霉病那样暴发性,但仍可能致命。