Clark B J, Kemp E G, Behan W M, Lee W R
Department of Pathology, Western Infirmary, Glasgow, Scotland.
Arch Ophthalmol. 1995 Nov;113(11):1414-9. doi: 10.1001/archopht.1995.01100110074028.
To determine the pathologic abnormalities of the levator palpebrae superioris in congenital ptosis.
By means of light and electron microscopy and immunohistochemistry, anterior levator tissue specimen from 15 patients with congenital ptosis excised during routine levator resections were examined.
All specimens showed lack of muscle fibers with endomysial and perimysial fibrosis and thickening of the aponeurosis. In addition, in four of the 15 patients, an abnormal extracellular material was present. By light microscopy this appeared as an unusual amorphous material arranged in clumps and bands, and electron microscopy showed it to consist of parallel coarse bundles of fibrillogranular material. Collagen type III and fibronectin were identified within this material by immunohistochemistry. There was no detectable collagen types I, II, IV, V, VI, or VII or laminin, and the material did not stain for actin, myosin, myoglobin, amyloid P component, or amyloid A.
In four of 15 samples of levator palpebrae superioris from patients with congenital ptosis, we identified an unusual amorphous extracellular material that stained positively for collagen type III and fibronectin on immunohistochemistry. This novel material, which we call "amorphocollagenoid," may represent a product of dysgenesis of the levator tissues. The source and full composition of this material merit further study.
确定先天性上睑下垂患者提上睑肌的病理异常情况。
通过光学显微镜、电子显微镜及免疫组织化学方法,对15例先天性上睑下垂患者在常规提上睑肌切除术中切除的提上睑肌前部组织标本进行检查。
所有标本均显示肌纤维缺失,伴有肌内膜和肌束膜纤维化以及腱膜增厚。此外,15例患者中有4例存在异常的细胞外物质。光学显微镜下,其表现为呈团块状和带状排列的异常无定形物质,电子显微镜显示它由平行的粗束状纤维颗粒物质组成。免疫组织化学在该物质中鉴定出Ⅲ型胶原蛋白和纤连蛋白。未检测到Ⅰ型、Ⅱ型、Ⅳ型、Ⅴ型、Ⅵ型或Ⅶ型胶原蛋白或层粘连蛋白,且该物质对肌动蛋白、肌球蛋白、肌红蛋白、淀粉样蛋白P成分或淀粉样蛋白A均无染色反应。
在15例先天性上睑下垂患者的提上睑肌样本中,有4例发现一种异常的无定形细胞外物质,免疫组织化学显示其对Ⅲ型胶原蛋白和纤连蛋白呈阳性染色。这种我们称为“无定形类胶原蛋白”的新型物质,可能代表提上睑肌组织发育异常的产物。该物质的来源和完整组成值得进一步研究。