Davidorf F H, Anderson J D
Int Ophthalmol Clin. 1975 Fall;15(3):51-63. doi: 10.1097/00004397-197501530-00009.
The relationship between systemic histoplasmosis and this particular clinical picutre of a central choroiditis with peripheral atrophic lesions in the fundus was postulated by Woods in 1960 [19]. Since that time there have been many studies attempting to substantiate his hyptthesis [1, 3-5, 7-18]. In a large study performed in Walkersville, Maryland, which is an area endemic for histoplasmosis [14], the prevalence of the characteristic peripheral histoplasmic lesion in the fundus was 27 per 1000 population. The prevalence was 44 per 1000 population with positive histoplasmosis skin tests. In a similar study done in sothern Ohio, the prevalence of peripheral fundus lesions was 1.6 percent of 1417 patients examined [1]. Several generalizations can be made from the information obtained in studying the students involved in the Willis flu, and these can be compared with information from the control students from Bellingham. First, the acute infection at Willis School did not cause significant ocular abnormalities. This finding is supported by the fact that no significant differences occurred in the fundus lesions seen in the control group of students who lived in the same geographic area but were not clinically ill from histoplasmosis. Our evidence shows that the eyegrounds of the individuals living in this area were different from those of the students who lived outside the central Ohio area. How do we account for the similarity of ocular lesions in the affected students and the Delaware control group? Perhaps by the age of 11 or 12, a person living in the histoplasmosis belt will have already been exposed to histoplasmosis, resulting in the characteristic scars that are seen. If, in fact, histoplasmosis is the etiological agent in the patients who are diagnosed as having presumed ocular histoplasmosis, difficulty arises in understanding why those individuals involved in the epidemic did not have more scars than the control group. Perhaps the numbers of patients examined were not large enough to reflect the difference that really may exist. An interesting observation is that 4 (67 percent) of our control students with significant lesions had negative histoplasmosis skin tests. Of course, other organisms may have caused these lesions which have not yet been implicated as causative agents in the presumed ocular histoplasmosis syndrome.
1960年,伍兹推测全身性组织胞浆菌病与这种伴有眼底周边萎缩性病变的中心性脉络膜炎的特定临床表现之间存在关联[19]。自那时起,有许多研究试图证实他的假说[1,3 - 5,7 - 18]。在马里兰州沃克维尔进行的一项大型研究中(该地区是组织胞浆菌病的流行地区[14]),眼底特征性周边组织胞浆菌病变的患病率为每1000人中有27例。组织胞浆菌素皮肤试验呈阳性的人群中,患病率为每1000人中有44例。在俄亥俄州南部进行的一项类似研究中,在接受检查的1417名患者中,周边眼底病变的患病率为1.6%[1]。从对参与威利斯流感的学生的研究中获得的信息可以得出一些一般性结论,这些结论可以与来自贝灵汉的对照学生的信息进行比较。首先,威利斯学校的急性感染并未导致明显的眼部异常。这一发现得到了以下事实的支持:居住在同一地理区域但临床上没有组织胞浆菌病的学生对照组中,眼底病变没有显著差异。我们的证据表明,居住在该地区的人的眼底与居住在俄亥俄州中部地区以外的学生的眼底不同。我们如何解释受影响学生与特拉华对照组眼部病变的相似性呢?也许到11岁或12岁时,生活在组织胞浆菌病流行带的人已经接触过组织胞浆菌病,从而产生了可见的特征性疤痕。事实上,如果组织胞浆菌病是被诊断为疑似眼组织胞浆菌病患者的病原体,那么就很难理解为什么那些参与疫情的人没有比对照组有更多的疤痕。也许检查的患者数量不够多,无法反映实际可能存在的差异。一个有趣的观察结果是,我们有明显病变的4名(67%)对照学生的组织胞浆菌素皮肤试验呈阴性。当然,其他生物体可能导致了这些病变,而这些生物体尚未被认为是疑似眼组织胞浆菌病综合征的病原体。