Ocular complications of plasma cell dyscrasias

Author:

Singh Rohan Bir123ORCID,Singhal Sachi4,Sinha Shruti1,Cho Junsang5,Nguyen Anne Xuan-Lan6ORCID,Dhingra Lovedeep Singh7ORCID,Kaur Snimarjot8,Sharma Vasudha9ORCID,Agarwal Aniruddha1011

Affiliation:

1. Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA, USA

2. Department of Ophthalmology, Great Ormond Street Institute of Child Health, University College London, London, UK

3. Discipline of Ophthalmology and Visual Sciences, Faculty of Health and Medical Sciences, University of Adelaide, Adelaide, Australia

4. Department of Internal Medicine, Crozer-Chester Medical Center, Upland, PA, USA

5. Department of Ophthalmology, Vanderbilt Eye Center, Vanderbilt University Medical Center, Nashville, TN, USA

6. Faculty of Medicine, McGill University, Montreal, Canada

7. Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, CT, USA

8. Department of Pediatrics, Yale-New Haven Hospital, New Haven, CT, USA

9. Department of Internal Medicine, Dayanand Medical College and Hospital, Ludhiana, India

10. Department of Ophthalmology, University of Maastricht, Maastricht, the Netherlands

11. Department of Ophthalmology, The Eye Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates

Abstract

Plasma cell dyscrasias are a wide range of severe monoclonal gammopathies caused by pre-malignant or malignant plasma cells that over-secrete an abnormal monoclonal antibody. These disorders are associated with various systemic findings, including ophthalmological disorders. A search of PubMed, EMBASE, Scopus and Cochrane databases was performed in March 2021 to examine evidence pertaining to ocular complications in patients diagnosed with plasma cell dyscrasias. This review outlines the ocular complications associated with smoldering multiple myeloma and monoclonal gammopathy of undetermined significance, plasmacytomas, multiple myeloma, Waldenström's macroglobulinemia, systemic amyloidosis, Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal gammopathy and Skin changes (POEMS) syndrome, and cryoglobulinemia. Although, the pathological mechanisms are not completely elucidated yet, wide-ranging ocular presentations have been identified over the years, evolving both the anterior and posterior segments of the eye. Moreover, the presenting symptoms also help in early diagnosis in asymptomatic patients. Therefore, it is imperative for the treating ophthalmologist and oncologist to maintain a high clinical suspicion for identifying the ophthalmological signs and diagnosing the underlying disease, preventing its progression through efficacious treatment strategies.

Publisher

SAGE Publications

Subject

Ophthalmology,General Medicine

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