Recurrence of paraproteinemic crystalline keratopathy after corneal transplantation: A case of monoclonal gammopathy of ocular significance

Purpose: To report the long-term follow-up (12 years) of a 36-year-old male patient with crystalline keratopathy of both eyes, diagnosed with monoclonal gammopathy of undetermined significance (MGUS). Complete ophthalmic, systemic, and corneal immunohistochemical evaluations were performed. Observat...

Full description

Bibliographic Details
Main Authors: Siamak Nobacht, Benno Kusters, Myrte B. Breukink, Gerard A. Rongen, Johannes R.M. Cruysberg
Format: Article
Language:English
Published: Elsevier 2020-09-01
Series:American Journal of Ophthalmology Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2451993618303244
_version_ 1819206699725094912
author Siamak Nobacht
Benno Kusters
Myrte B. Breukink
Gerard A. Rongen
Johannes R.M. Cruysberg
author_facet Siamak Nobacht
Benno Kusters
Myrte B. Breukink
Gerard A. Rongen
Johannes R.M. Cruysberg
author_sort Siamak Nobacht
collection DOAJ
description Purpose: To report the long-term follow-up (12 years) of a 36-year-old male patient with crystalline keratopathy of both eyes, diagnosed with monoclonal gammopathy of undetermined significance (MGUS). Complete ophthalmic, systemic, and corneal immunohistochemical evaluations were performed. Observations: Slit-lamp examination revealed bilateral fine iridescent confluent crystalline deposits in all layers of the cornea, both peripherally and centrally. Systemic evaluation revealed abnormal M protein, IgG-kappa type, in blood and urine. Bone marrow aspiration showed a monoclonal plasma cell concentration of 2%. Consequently, the patient was diagnosed with MGUS. Because of progressive bilateral visual loss in the following 10 years, a perforating keratoplasty was performed on the left eye. Immunohistochemical analysis of the native cornea (the corneal button) revealed depositions of the same M protein type as detected in plasma and urine. Electron microscopy showed rhomboid-shaped corneal deposits of various sizes up to 4 μm. Recurrence of crystalline keratopathy was observed 9 months after keratoplasty. The monoclonal protein remained stable and the MGUS did not progress to multiple myeloma nor a related disorder. Conclusions and importance: Crystalline keratopathy may be associated with MGUS in otherwise healthy individuals. If the keratopathy causes binocular visual loss, a corneal transplantation may be required. Unfortunately, recurrence of crystalline deposits in the corneal graft may occur within one year. This suggests that patients with vision impairment due to paraproteinemic keratopathy who are diagnosed as MGUS, in fact, have a monoclonal gammopathy of ocular significance (MGOS).
first_indexed 2024-12-23T05:11:45Z
format Article
id doaj.art-baaeca7772fe4dc39b9097c04adb7196
institution Directory Open Access Journal
issn 2451-9936
language English
last_indexed 2024-12-23T05:11:45Z
publishDate 2020-09-01
publisher Elsevier
record_format Article
series American Journal of Ophthalmology Case Reports
spelling doaj.art-baaeca7772fe4dc39b9097c04adb71962022-12-21T17:58:56ZengElsevierAmerican Journal of Ophthalmology Case Reports2451-99362020-09-0119100803Recurrence of paraproteinemic crystalline keratopathy after corneal transplantation: A case of monoclonal gammopathy of ocular significanceSiamak Nobacht0Benno Kusters1Myrte B. Breukink2Gerard A. Rongen3Johannes R.M. Cruysberg4Department of Ophthalmology, Radboud University Medical Center, Nijmegen, the Netherlands; Corresponding author. Department of Ophthalmology, Radboud University Medical Center, PO Box 9101, 6500, HB, Nijmegen, the Netherlands.Department of Pathology, Radboud University Medical Center, Nijmegen, the NetherlandsDepartment of Ophthalmology, Radboud University Medical Center, Nijmegen, the NetherlandsDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, the NetherlandsDepartment of Ophthalmology, Radboud University Medical Center, Nijmegen, the NetherlandsPurpose: To report the long-term follow-up (12 years) of a 36-year-old male patient with crystalline keratopathy of both eyes, diagnosed with monoclonal gammopathy of undetermined significance (MGUS). Complete ophthalmic, systemic, and corneal immunohistochemical evaluations were performed. Observations: Slit-lamp examination revealed bilateral fine iridescent confluent crystalline deposits in all layers of the cornea, both peripherally and centrally. Systemic evaluation revealed abnormal M protein, IgG-kappa type, in blood and urine. Bone marrow aspiration showed a monoclonal plasma cell concentration of 2%. Consequently, the patient was diagnosed with MGUS. Because of progressive bilateral visual loss in the following 10 years, a perforating keratoplasty was performed on the left eye. Immunohistochemical analysis of the native cornea (the corneal button) revealed depositions of the same M protein type as detected in plasma and urine. Electron microscopy showed rhomboid-shaped corneal deposits of various sizes up to 4 μm. Recurrence of crystalline keratopathy was observed 9 months after keratoplasty. The monoclonal protein remained stable and the MGUS did not progress to multiple myeloma nor a related disorder. Conclusions and importance: Crystalline keratopathy may be associated with MGUS in otherwise healthy individuals. If the keratopathy causes binocular visual loss, a corneal transplantation may be required. Unfortunately, recurrence of crystalline deposits in the corneal graft may occur within one year. This suggests that patients with vision impairment due to paraproteinemic keratopathy who are diagnosed as MGUS, in fact, have a monoclonal gammopathy of ocular significance (MGOS).http://www.sciencedirect.com/science/article/pii/S2451993618303244Crystalline keratopathyParaproteinemiaMonoclonal gammopathyUndetermined significanceOcular significance
spellingShingle Siamak Nobacht
Benno Kusters
Myrte B. Breukink
Gerard A. Rongen
Johannes R.M. Cruysberg
Recurrence of paraproteinemic crystalline keratopathy after corneal transplantation: A case of monoclonal gammopathy of ocular significance
American Journal of Ophthalmology Case Reports
Crystalline keratopathy
Paraproteinemia
Monoclonal gammopathy
Undetermined significance
Ocular significance
title Recurrence of paraproteinemic crystalline keratopathy after corneal transplantation: A case of monoclonal gammopathy of ocular significance
title_full Recurrence of paraproteinemic crystalline keratopathy after corneal transplantation: A case of monoclonal gammopathy of ocular significance
title_fullStr Recurrence of paraproteinemic crystalline keratopathy after corneal transplantation: A case of monoclonal gammopathy of ocular significance
title_full_unstemmed Recurrence of paraproteinemic crystalline keratopathy after corneal transplantation: A case of monoclonal gammopathy of ocular significance
title_short Recurrence of paraproteinemic crystalline keratopathy after corneal transplantation: A case of monoclonal gammopathy of ocular significance
title_sort recurrence of paraproteinemic crystalline keratopathy after corneal transplantation a case of monoclonal gammopathy of ocular significance
topic Crystalline keratopathy
Paraproteinemia
Monoclonal gammopathy
Undetermined significance
Ocular significance
url http://www.sciencedirect.com/science/article/pii/S2451993618303244
work_keys_str_mv AT siamaknobacht recurrenceofparaproteinemiccrystallinekeratopathyaftercornealtransplantationacaseofmonoclonalgammopathyofocularsignificance
AT bennokusters recurrenceofparaproteinemiccrystallinekeratopathyaftercornealtransplantationacaseofmonoclonalgammopathyofocularsignificance
AT myrtebbreukink recurrenceofparaproteinemiccrystallinekeratopathyaftercornealtransplantationacaseofmonoclonalgammopathyofocularsignificance
AT gerardarongen recurrenceofparaproteinemiccrystallinekeratopathyaftercornealtransplantationacaseofmonoclonalgammopathyofocularsignificance
AT johannesrmcruysberg recurrenceofparaproteinemiccrystallinekeratopathyaftercornealtransplantationacaseofmonoclonalgammopathyofocularsignificance