Nouira Cyrine, Ghazal Wassim, Panthier Christophe, Saad Alain, Gatinel Damien
Department of Anterior Segment and Refractive Surgery, Adolphe de Rothschild Foundation Hospital, Paris, France.
BMC Ophthalmol. 2025 Jul 1;25(1):356. doi: 10.1186/s12886-025-04161-1.
Paraproteinemic keratopathy (PPK) is a rare ocular manifestation of monoclonal gammopathies such as monoclonal gammopathy of undetermined significance (MGUS), smoldering multiple myeloma (SMM), and multiple myeloma (MM). Although these hematologic conditions are relatively common in older adults, their ocular presentations remain underrecognized or misdiagnosed. We report a case of PPK where anterior segment optical coherence tomography (AS-OCT) revealed a unique mixed-layer deposition pattern, contributing new imaging insights to the clinical spectrum of PPK and underscoring the importance of ophthalmic findings in prompting systemic evaluation.
A 52 -year-old man with no prior medical or family history presented with incidental discovery of bilateral corneal white lesions. Visual acuity was 20/20 in both eyes. Slit-lamp examination showed bilateral peripheral white nummular stromal opacities with limbal sparing. AS-OCT revealed mid-peripheral hyperreflective lesions affecting Bowman's layer, anterior and posterior stroma, and endothelium, with a clear intermediate stroma separating the lesions, an imaging feature not previously documented in PPK. Hematologic workup revealed an IgG kappa monoclonal gammopathy, and bone marrow biopsy confirmed smoldering multiple myeloma without systemic symptoms. The patient received nine courses of chemotherapy leading to hematologic remission and progressive improvement of corneal changes on slit-lamp examination and AS-OCT.
This case illustrates the potential of AS-OCT to identify subtle and layered patterns of corneal paraprotein deposition in PPK. While findings are limited to a single patient, the imaging features expand current understanding of the disease and support the integration of AS-OCT into diagnostic and follow-up strategies. Ophthalmologists should consider monoclonal gammopathies in unexplained bilateral interstitial keratitis, as timely diagnosis may influence both ocular and systemic outcomes.
副蛋白血症性角膜病变(PPK)是意义未明的单克隆丙种球蛋白病(MGUS)、冒烟型多发性骨髓瘤(SMM)和多发性骨髓瘤(MM)等单克隆丙种球蛋白病罕见的眼部表现。尽管这些血液系统疾病在老年人中相对常见,但其眼部表现仍未得到充分认识或误诊。我们报告一例PPK病例,其中前段光学相干断层扫描(AS-OCT)显示出独特的混合层沉积模式,为PPK的临床谱提供了新的影像学见解,并强调了眼科检查结果在促使进行全身评估方面的重要性。
一名52岁男性,既往无病史及家族史,偶然发现双侧角膜白色病变。双眼视力均为20/20。裂隙灯检查显示双侧周边白色钱币状基质混浊,角膜缘未受累。AS-OCT显示中周边高反射性病变累及Bowman层、前基质和后基质以及内皮,病变之间有清晰的中间基质分隔,这是PPK中以前未记录的影像学特征。血液学检查显示IgG κ单克隆丙种球蛋白病,骨髓活检证实为无全身症状的冒烟型多发性骨髓瘤。患者接受了九个疗程的化疗,导致血液学缓解,裂隙灯检查和AS-OCT显示角膜病变逐渐改善。
本病例说明了AS-OCT在识别PPK中角膜副蛋白沉积的细微和分层模式方面的潜力。虽然研究结果仅限于一名患者,但影像学特征扩展了目前对该疾病的认识,并支持将AS-OCT纳入诊断和随访策略。眼科医生在无法解释的双侧间质性角膜炎中应考虑单克隆丙种球蛋白病,因为及时诊断可能会影响眼部和全身的预后。