Chiang Homer H, Wieland Rebekah S, Rogers Thomas S, Gibson Pamela C, Atweh George, McCormick Gregory
University of Vermont College of Medicine Department of Pathology and Laboratory Medicine Department of Hematology and Oncology, University of Vermont Medical Center Ophthalmic Consultants of Vermont, South Burlington, VT.
Medicine (Baltimore). 2017 Dec;96(50):e8649. doi: 10.1097/MD.0000000000008649.
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.
A 74 year old female recently diagnosed with monoclonal gammopathy undetermined significance presented with progressive blurry vision bilaterally.
Examination revealed corneal opacities consistent with paraproteinemic keratopathy.
Corneal transplantation with the Boston Type I keratoprosthesis was performed on the right and, a year later, on the left.
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.
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.
我们报告一例与意义未明的单克隆丙种球蛋白病相关的副蛋白血症性角膜病变,采用角膜移植术作为主要的穿透性手术进行治疗。本文呈现了组织病理学发现及对世界文献的综述。
一名74岁女性,近期被诊断为意义未明的单克隆丙种球蛋白病,双侧视力渐进性模糊。
检查发现角膜混浊与副蛋白血症性角膜病变相符。
右眼及一年后左眼均进行了波士顿I型角膜移植术。
视力结果良好。宿主角膜植片的组织病理学染色符合单克隆性,电子显微镜检查显示在正常间质中存在纤维状细胞外聚集体。
角膜沉积物可能是意义未明的单克隆丙种球蛋白病在其他方面无全身症状患者中的唯一表现。遇到角膜混浊的眼科医生可安排适当的诊断性检查以确定隐匿性全身疾病的存在。穿透性角膜移植术后因复发性混浊导致移植失败的风险很高,因此角膜移植术作为主要的穿透性手术可能会带来更好的长期效果。从穿透性角膜移植术或角膜活检获取的宿主角膜植片可送去进行组织病理学检查以确诊。