The Central Nervous System Effects and Mimicry of Common Variable Immunodeficiency (CVID): A Case Report with Literature Review

There is a scarceness of information on the central nervous system effects of common variable immunodeficiency (CVID). A 30-year-old woman with a history of recurrent upper respiratory infections, vitiligo, and immune thrombocytopenic purpura presented with right-sided numbness. Magnetic resonance i...

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Main Authors: Sohail Farshad, Fernando Figueroa Rodriguez, Alexandra Halalau, Joseph Skender, Cory Rasmussen, Martin Pevzner
Format: Article
Language:English
Published: Wiley 2019-01-01
Series:Case Reports in Rheumatology
Online Access:http://dx.doi.org/10.1155/2019/7623643
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author Sohail Farshad
Fernando Figueroa Rodriguez
Alexandra Halalau
Joseph Skender
Cory Rasmussen
Martin Pevzner
author_facet Sohail Farshad
Fernando Figueroa Rodriguez
Alexandra Halalau
Joseph Skender
Cory Rasmussen
Martin Pevzner
author_sort Sohail Farshad
collection DOAJ
description There is a scarceness of information on the central nervous system effects of common variable immunodeficiency (CVID). A 30-year-old woman with a history of recurrent upper respiratory infections, vitiligo, and immune thrombocytopenic purpura presented with right-sided numbness. Magnetic resonance imaging (MRI) of the thoracic spine revealed a signal hyperintensity. MRI of the brain demonstrated FLAIR hyperintensity in the right middle frontal gyrus. Cerebral spinal fluid was unremarkable. Serum immunoglobulins revealed hypogammaglobulinemia. Endobronchial and subsequent mediastinum biopsies were all negative for sarcoidosis and malignancy. No infectious etiology was found. She was treated with glucocorticoids and intravenous immunoglobulin (IVIG) replacement therapy for CVID-associated myelitis. Follow-up MRI showed improvement; however, her numbness persisted despite these treatments, which led to an outside physician adding methotrexate for their suspicion of sarcoidosis. Her symptoms remained stable for two years, but when the methotrexate dose was weaned, her numbness worsened. Upon review, the treatment team refuted the diagnosis of sarcoidosis but continued treatment with prednisone, IVIG, and methotrexate for CVID-associated myelitis, from which her symptoms have stabilized. Here, we discuss CVID-associated neurological complications, its similarities to sarcoidosis, and a literature review with treatment regimens and outcomes.
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spelling doaj-art-d64272831ff14b7a99f619a7f5f28b202025-02-03T01:20:29ZengWileyCase Reports in Rheumatology2090-68892090-68972019-01-01201910.1155/2019/76236437623643The Central Nervous System Effects and Mimicry of Common Variable Immunodeficiency (CVID): A Case Report with Literature ReviewSohail Farshad0Fernando Figueroa Rodriguez1Alexandra Halalau2Joseph Skender3Cory Rasmussen4Martin Pevzner5Internal Medicine, Beaumont Hospital, Royal Oak 48073, MI, USAInternal Medicine, Beaumont Hospital, Royal Oak 48073, MI, USAInternal Medicine, Beaumont Hospital, Royal Oak 48073, MI, USARheumatology, Beaumont Hospital, Royal Oak 48073, MI, USAInternal Medicine, Beaumont Hospital, Royal Oak 48073, MI, USARheumatology, Beaumont Hospital, Royal Oak 48073, MI, USAThere is a scarceness of information on the central nervous system effects of common variable immunodeficiency (CVID). A 30-year-old woman with a history of recurrent upper respiratory infections, vitiligo, and immune thrombocytopenic purpura presented with right-sided numbness. Magnetic resonance imaging (MRI) of the thoracic spine revealed a signal hyperintensity. MRI of the brain demonstrated FLAIR hyperintensity in the right middle frontal gyrus. Cerebral spinal fluid was unremarkable. Serum immunoglobulins revealed hypogammaglobulinemia. Endobronchial and subsequent mediastinum biopsies were all negative for sarcoidosis and malignancy. No infectious etiology was found. She was treated with glucocorticoids and intravenous immunoglobulin (IVIG) replacement therapy for CVID-associated myelitis. Follow-up MRI showed improvement; however, her numbness persisted despite these treatments, which led to an outside physician adding methotrexate for their suspicion of sarcoidosis. Her symptoms remained stable for two years, but when the methotrexate dose was weaned, her numbness worsened. Upon review, the treatment team refuted the diagnosis of sarcoidosis but continued treatment with prednisone, IVIG, and methotrexate for CVID-associated myelitis, from which her symptoms have stabilized. Here, we discuss CVID-associated neurological complications, its similarities to sarcoidosis, and a literature review with treatment regimens and outcomes.http://dx.doi.org/10.1155/2019/7623643
spellingShingle Sohail Farshad
Fernando Figueroa Rodriguez
Alexandra Halalau
Joseph Skender
Cory Rasmussen
Martin Pevzner
The Central Nervous System Effects and Mimicry of Common Variable Immunodeficiency (CVID): A Case Report with Literature Review
Case Reports in Rheumatology
title The Central Nervous System Effects and Mimicry of Common Variable Immunodeficiency (CVID): A Case Report with Literature Review
title_full The Central Nervous System Effects and Mimicry of Common Variable Immunodeficiency (CVID): A Case Report with Literature Review
title_fullStr The Central Nervous System Effects and Mimicry of Common Variable Immunodeficiency (CVID): A Case Report with Literature Review
title_full_unstemmed The Central Nervous System Effects and Mimicry of Common Variable Immunodeficiency (CVID): A Case Report with Literature Review
title_short The Central Nervous System Effects and Mimicry of Common Variable Immunodeficiency (CVID): A Case Report with Literature Review
title_sort central nervous system effects and mimicry of common variable immunodeficiency cvid a case report with literature review
url http://dx.doi.org/10.1155/2019/7623643
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