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首页> 外文期刊>Medicine. >Paraproteinemic keratopathy in monoclonal gammopathy of undetermined significance treated with primary keratoprosthesis: Case report, histopathologic findings, and world literature review
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Paraproteinemic keratopathy in monoclonal gammopathy of undetermined significance treated with primary keratoprosthesis: Case report, histopathologic findings, and world literature review

机译:具有原发性角膜移植术治疗的意义不明的单克隆丙种球蛋白病副蛋白血症性角膜病:病例报告,组织病理学发现和世界文献综述

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Rationale: We report a case of paraproteinemic keratopathy associated with monoclonal gammopathy of undetermined significance, treated with keratoprosthesis as a primary penetrating procedure. Histopathological findings and a world literature review are presented. Patient concerns: A 74 year old female recently diagnosed with monoclonal gammopathy undetermined significance presented with progressive blurry vision bilaterally. Diagnoses: Examination revealed corneal opacities consistent with paraproteinemic keratopathy. Interventions: Corneal transplantation with the Boston Type I keratoprosthesis was performed on the right and, a year later, on the left. Outcomes: Visual outcomes were good. Histopathological staining of host corneal buttons were consistent with monoclonality, and electron microscopy revealed fibrillar extracellular aggregates within intervening normal stroma. Lessons: Corneal deposits may be the only manifestation of monoclonal gammopathy of undetermined significance in patients who are otherwise systemically asymptomatic. Ophthalmologists who encounter corneal opacities may order the appropriate diagnostic studies to determine the presence of occult systemic disease. Risk of graft failure after penetrating keratoplasty from recurring opacities is high, so keratoprosthesis as a primary penetrating procedure may afford superior long-term outcomes. Host corneal buttons retrieved from penetrating keratoplasty or corneal biopsy may be sent for histopathological examination to confirm the diagnosis.
机译:理由:我们报告了一例伴有副蛋白球蛋白变性的副蛋白血症性角膜病,其意义尚不确定,已将角膜假体作为主要穿透方法进行了治疗。介绍了组织病理学发现和世界文献综述。患者关注:一名74岁的女性最近被诊断出患有单克隆丙种球蛋白病,其不确定的意义尚未确定,双侧进行性视力模糊。诊断:检查发现角膜混浊与副蛋白性角膜病一致。干预措施:右侧进行了波士顿I型角膜假体的角膜移植,一年后,左侧进行了角膜移植。结果:视觉结果良好。宿主角膜纽扣的组织病理学染色与单克隆抗体一致,并且电子显微镜检查显示介入正常基质内的纤维状细胞外聚集体。经验教训:对于那些全身无症状的患者,角膜沉积物可能是唯一的意义不明的单克隆丙种球蛋白病。遇到角膜混浊的眼科医生可以命令进行适当的诊断研究,以确定是否存在隐匿性系统疾病。复发性混浊穿透性角膜移植术后移植失败的风险很高,因此作为主要穿透性方法的角膜移植术可以提供长期的优越疗效。可将穿透性角膜移植术或角膜活检取回的宿主角膜纽扣送去进行组织病理学检查,以确认诊断。

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