Ali Mohammad Javed, Mishra Dilip Kumar, Baig Farhana, Lakshman Mekala, Naik Milind N
*Dacryology Service and †Ocular Pathology Service, L.V. Prasad Eye Institute; ‡Department of Pathology, Global Hospitals; and §Ruska Laboratories, College of Veterinary Science, Hyderabad, India.
Ophthalmic Plast Reconstr Surg. 2015 Mar-Apr;31(2):98-102. doi: 10.1097/IOP.0000000000000204.
To study the histologic, immunohistochemical, and electron microscopic features of puncta and proximal vertical canaliculi to understand the etiopathogenesis of punctal stenosis.
Prospective study of 26 stenosed punctae that were collected following a punctoplasty. Sixteen were from lower eyelid and 10 from upper eyelid. Histopathological examination was performed on 20 punctae using hematoxylin-eosin, periodic acid-Schiff, and Masson trichrome staining. Immunohistochemical patterns were analyzed after staining with leukocyte common antigen or CD45, CD3, CD5, CD10, CD20, CD138, and smooth muscle actin. Six punctae (3 upper, 3 lower) were separately processed for electron microscopic studies as per standard protocols.
All punctae showed evidence of subepithelial and subconjunctival fibrosis. Thirty percent (6/20) showed extensive fibrosis. Inflammation was noted in 80% (16/20) of the samples; however, 20% (4/20) showed severe inflammation. Strong immunoreactivity was noted, with CD45 and CD3 in 80% (16/20) with predominance in the subepithelial areas. Focal immunoreactivity was noted for CD10, CD20, and CD138. Immunoreactivity was negative for CD5. Electron microscopic features include blunted epithelial microvilli, numerous fibroblasts, extensive and irregularly arranged collagen bundles, mononuclear infiltration in the vicinity of fibroblasts or in between collagen bundles, and inter- and intracellular edema in areas of inflammation.
Chronic inflammation and subsequent fibrosis appear to be the basic ultrastructural response to various noxious stimuli. Mononuclear inflammatory infiltration in the vicinity of fibroblasts could possibly reflect a close cellular interaction between these 2 cells.
研究泪点及近端垂直小管的组织学、免疫组织化学和电子显微镜特征,以了解泪点狭窄的病因发病机制。
对26例泪点成形术后收集的狭窄泪点进行前瞻性研究。其中16例来自下眼睑,10例来自上眼睑。对20个泪点进行苏木精-伊红、过碘酸-希夫和马森三色染色的组织病理学检查。用白细胞共同抗原或CD45、CD3、CD5、CD10、CD20、CD138和平滑肌肌动蛋白染色后分析免疫组织化学模式。按照标准方案分别对6个泪点(3个上睑,3个下睑)进行电子显微镜研究。
所有泪点均显示上皮下和结膜下纤维化。30%(6/20)显示广泛纤维化。80%(16/20)的样本中观察到炎症;然而,20%(4/20)显示严重炎症。在80%(16/20)的样本中观察到CD45和CD3的强免疫反应性,以上皮下区域为主。CD10、CD20和CD138有局灶性免疫反应性。CD5免疫反应性为阴性。电子显微镜特征包括上皮微绒毛钝圆、大量成纤维细胞、广泛且排列不规则的胶原束、成纤维细胞附近或胶原束之间的单核细胞浸润以及炎症区域的细胞内和细胞间水肿。
慢性炎症及随后的纤维化似乎是对各种有害刺激的基本超微结构反应。成纤维细胞附近的单核细胞炎症浸润可能反映了这两种细胞之间密切的细胞相互作用。