Orbital Waldenström Macroglobulinemia With Angiopathic Paraprotein Deposition: A Case Report

Ocular manifestations of Waldenström macroglobulinemia (WM) are most frequently related to hyperviscosity-related retinopathy but may also include conjunctival infiltration and vitritis. Orbital and ocular adnexal lymphomatous deposition, including within the orbit, is exceedingly rare. We report a unique case of a 66-year-old female with orbital infiltration from WM presenting with recurrent episodes of transient vision loss secondary to angiopathic deposition of eosinophilic hyaline paraprotein in the absence of hyperviscosity syndrome. Right orbital biopsy demonstrated adipose tissue with deposition of eosinophilic hyaline material, outlining adipocytes and deposited within walls of blood vessels. The material was strongly PAS positive, weakly metachromatic with crystal violet but was negative for apple-green birefringence on Congo red staining. IgM immunohistochemistry strongly decorated the orbital eosinophilic material, suggesting macroglobulinosis paraprotein deposition and not amyloid. There was an associated patchy infiltrate of low-grade lymphoplasmacytic B-cell lymphoma with kappa light chain restriction demonstrated in the neoplastic plasma cell population, consistent with her known WM.

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Publication Details

Journal
Ophthalmic Plastic and Reconstructive Surgery
Published
2025-12-19
DOI
https://doi.org/10.1097/iop.0000000000003160
Primary Topic
Chronic Lymphocytic Leukemia Research
Type
article
Field-Weighted Citation Impact
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article

Orbital Waldenström Macroglobulinemia With Angiopathic Paraprotein Deposition: A Case Report

Terence Ang, Dinesh Selva, Abdullah I. Almater, Craig James
Ophthalmic Plastic and Reconstructive Surgery
Chronic Lymphocytic Leukemia Research
article

Orbital Waldenström Macroglobulinemia With Angiopathic Paraprotein Deposition: A Case Report

Terence Ang, Dinesh Selva, Abdullah I. Almater, Craig James
article en

Abstract

Ocular manifestations of Waldenström macroglobulinemia (WM) are most frequently related to hyperviscosity-related retinopathy but may also include conjunctival infiltration and vitritis. Orbital and ocular adnexal lymphomatous deposition, including within the orbit, is exceedingly rare. We report a unique case of a 66-year-old female with orbital infiltration from WM presenting with recurrent episodes of transient vision loss secondary to angiopathic deposition of eosinophilic hyaline paraprotein in the absence of hyperviscosity syndrome. Right orbital biopsy demonstrated adipose tissue with deposition of eosinophilic hyaline material, outlining adipocytes and deposited within walls of blood vessels. The material was strongly PAS positive, weakly metachromatic with crystal violet but was negative for apple-green birefringence on Congo red staining. IgM immunohistochemistry strongly decorated the orbital eosinophilic material, suggesting macroglobulinosis paraprotein deposition and not amyloid. There was an associated patchy infiltrate of low-grade lymphoplasmacytic B-cell lymphoma with kappa light chain restriction demonstrated in the neoplastic plasma cell population, consistent with her known WM.

Ophthalmic Plastic and Reconstructive Surgery
Royal Adelaide Hospital (AU), King Saud Medical City (SA), King Saud University (SA), The University of Adelaide (AU)
Openalex Percentile: Top 38%
Chronic Lymphocytic Leukemia Research
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