Two Cases of γ-Heavy Chain Disease and a Review of the Literature

Gamma heavy chain disease (γ-HCD) is a rare lymphoproliferative disorder characterised by the production of a truncated immunoglobulin heavy chain. Fewer than 200 cases have been reported in the literature. In some cases, γ-HCD occurs with other lymphoid neoplasms. This study reports clinical, bioch...

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Main Authors: I. Ramasamy, Z. Rudzki
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Case Reports in Hematology
Online Access:http://dx.doi.org/10.1155/2018/4832619
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author I. Ramasamy
Z. Rudzki
author_facet I. Ramasamy
Z. Rudzki
author_sort I. Ramasamy
collection DOAJ
description Gamma heavy chain disease (γ-HCD) is a rare lymphoproliferative disorder characterised by the production of a truncated immunoglobulin heavy chain. Fewer than 200 cases have been reported in the literature. In some cases, γ-HCD occurs with other lymphoid neoplasms. This study reports clinical, biochemical, haematological, and histological findings in two cases of γ-HCD. We describe newer biochemical diagnostic tools (HevyLite measurement, capillary electrophoresis, and immunotyping) that can aid in the characterisation of γ-HCD. The first case is an 88-year-old woman with γ-HCD. The second case is an 81-year-old woman who developed γ-HCD during treatment for Waldenstrom’s macroglobulinemia. In the second patient, histopathology identified a separate clone responsible for the secretion of the gamma heavy chain. Studies on the clonal evolution of the disease may provide insight into therapeutic implications and the genomic complexity of the disease.
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series Case Reports in Hematology
spelling doaj-art-4b923b55cf6c43fb9f0849ecfd14556d2025-02-03T06:01:44ZengWileyCase Reports in Hematology2090-65602090-65792018-01-01201810.1155/2018/48326194832619Two Cases of γ-Heavy Chain Disease and a Review of the LiteratureI. Ramasamy0Z. Rudzki1Department of Biochemistry, Worcester Royal Hospital, Worcester, UKHeart of England NHS Trust, Birmingham, UKGamma heavy chain disease (γ-HCD) is a rare lymphoproliferative disorder characterised by the production of a truncated immunoglobulin heavy chain. Fewer than 200 cases have been reported in the literature. In some cases, γ-HCD occurs with other lymphoid neoplasms. This study reports clinical, biochemical, haematological, and histological findings in two cases of γ-HCD. We describe newer biochemical diagnostic tools (HevyLite measurement, capillary electrophoresis, and immunotyping) that can aid in the characterisation of γ-HCD. The first case is an 88-year-old woman with γ-HCD. The second case is an 81-year-old woman who developed γ-HCD during treatment for Waldenstrom’s macroglobulinemia. In the second patient, histopathology identified a separate clone responsible for the secretion of the gamma heavy chain. Studies on the clonal evolution of the disease may provide insight into therapeutic implications and the genomic complexity of the disease.http://dx.doi.org/10.1155/2018/4832619
spellingShingle I. Ramasamy
Z. Rudzki
Two Cases of γ-Heavy Chain Disease and a Review of the Literature
Case Reports in Hematology
title Two Cases of γ-Heavy Chain Disease and a Review of the Literature
title_full Two Cases of γ-Heavy Chain Disease and a Review of the Literature
title_fullStr Two Cases of γ-Heavy Chain Disease and a Review of the Literature
title_full_unstemmed Two Cases of γ-Heavy Chain Disease and a Review of the Literature
title_short Two Cases of γ-Heavy Chain Disease and a Review of the Literature
title_sort two cases of γ heavy chain disease and a review of the literature
url http://dx.doi.org/10.1155/2018/4832619
work_keys_str_mv AT iramasamy twocasesofgheavychaindiseaseandareviewoftheliterature
AT zrudzki twocasesofgheavychaindiseaseandareviewoftheliterature