Perry H D, Donnenfeld E D, Font R L
Department of Ophthalmology, North Shore University Hospital, Manhasset, New York 11030.
Cornea. 1993 Sep;12(5):448-50. doi: 10.1097/00003226-199309000-00012.
A 52-year-old man was first examined because of bilateral superficial punctate keratitis. Slit-lamp examination disclosed numerous intraepithelial minute opacities in both corneas. A corneal biopsy revealed intraepithelial rhomboidal or rectangular crystals that immunohistochemically stained only for IgG-kappa. Serum immunoelectrophoresis demonstrated an IgG-kappa monoclonal gammopathy. Over the ensuing 6 years, the clinical appearance of the crystals changed from small dot-like opacities to polychromatic crystals. At this time, bone marrow examination established the diagnosis of multiple myeloma. Ophthalmologists should be aware of this entity and carefully monitor these patients; the corneal lesions may be the initial manifestation of an asymptomatic monoclonal gammopathy preceding the development of multiple myeloma.
一名52岁男性因双侧浅层点状角膜炎首次接受检查。裂隙灯检查发现双眼角膜上皮内有大量微小混浊。角膜活检显示上皮内有菱形或长方形晶体,免疫组化仅对IgG-κ染色阳性。血清免疫电泳显示IgG-κ单克隆丙种球蛋白病。在接下来的6年里,晶体的临床表现从小点状混浊变为多色晶体。此时,骨髓检查确诊为多发性骨髓瘤。眼科医生应了解这一疾病并仔细监测这些患者;角膜病变可能是多发性骨髓瘤发生前无症状单克隆丙种球蛋白病的初始表现。