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IgA/Kappa-restricted crystal storing histiocytosis involving the central nervous system characterized by proteomic analysis

Crystal storing histiocytosis (CSH) is a rare disorder characterized by the accumulation of crystalline material in the cytoplasm of histiocytes. Involvement of the central nervous system (CNS) with CSH is extremely rare. Herein, we report a case of crystal storing histiocytosis involving the CNS. U...

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Autores principales: Orr, Bent A., Gallia, Gary L., Dogan, Ahmed, Rodriguez, Fausto J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dustri-Verlag Dr. Karl Feistle 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199188/
https://www.ncbi.nlm.nih.gov/pubmed/23924753
http://dx.doi.org/10.5414/NP300645
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author Orr, Bent A.
Gallia, Gary L.
Dogan, Ahmed
Rodriguez, Fausto J.
author_facet Orr, Bent A.
Gallia, Gary L.
Dogan, Ahmed
Rodriguez, Fausto J.
author_sort Orr, Bent A.
collection PubMed
description Crystal storing histiocytosis (CSH) is a rare disorder characterized by the accumulation of crystalline material in the cytoplasm of histiocytes. Involvement of the central nervous system (CNS) with CSH is extremely rare. Herein, we report a case of crystal storing histiocytosis involving the CNS. Using immunohistochemistry and mass spectrometry we demonstrate that the disease resulted from an IgA-κ restricted plasma cell dyscrasia. CNS-CSH represents a rare clinicopathologic entity with an indolent course, usually lacking systemic manifestations.
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spelling pubmed-41991882014-10-28 IgA/Kappa-restricted crystal storing histiocytosis involving the central nervous system characterized by proteomic analysis Orr, Bent A. Gallia, Gary L. Dogan, Ahmed Rodriguez, Fausto J. Clin Neuropathol Case Report Crystal storing histiocytosis (CSH) is a rare disorder characterized by the accumulation of crystalline material in the cytoplasm of histiocytes. Involvement of the central nervous system (CNS) with CSH is extremely rare. Herein, we report a case of crystal storing histiocytosis involving the CNS. Using immunohistochemistry and mass spectrometry we demonstrate that the disease resulted from an IgA-κ restricted plasma cell dyscrasia. CNS-CSH represents a rare clinicopathologic entity with an indolent course, usually lacking systemic manifestations. Dustri-Verlag Dr. Karl Feistle 2014 2013-08-07 /pmc/articles/PMC4199188/ /pubmed/23924753 http://dx.doi.org/10.5414/NP300645 Text en © Dustri-Verlag Dr. K. Feistle http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Orr, Bent A.
Gallia, Gary L.
Dogan, Ahmed
Rodriguez, Fausto J.
IgA/Kappa-restricted crystal storing histiocytosis involving the central nervous system characterized by proteomic analysis
title IgA/Kappa-restricted crystal storing histiocytosis involving the central nervous system characterized by proteomic analysis
title_full IgA/Kappa-restricted crystal storing histiocytosis involving the central nervous system characterized by proteomic analysis
title_fullStr IgA/Kappa-restricted crystal storing histiocytosis involving the central nervous system characterized by proteomic analysis
title_full_unstemmed IgA/Kappa-restricted crystal storing histiocytosis involving the central nervous system characterized by proteomic analysis
title_short IgA/Kappa-restricted crystal storing histiocytosis involving the central nervous system characterized by proteomic analysis
title_sort iga/kappa-restricted crystal storing histiocytosis involving the central nervous system characterized by proteomic analysis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199188/
https://www.ncbi.nlm.nih.gov/pubmed/23924753
http://dx.doi.org/10.5414/NP300645
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