Hypogammaglobulinemia Observed One Year after Rituximab Treatment for Idiopathic Thrombocytopenic Purpura

We present the case of a 19-year-old female with severe hypogammaglobulinemia after having had treatment with rituximab for idiopathic thrombocytopenic purpura requiring intravenous immunoglobulins. She was admitted with the diagnosis of left-sided pneumonia with parapneumonic effusion. The patient...

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Main Authors: Bilal Ahmad Shoukat, Osama Ali, Dileep Kumar, Muhammad Bilal Gilani, Adeela Zahid, Shaheer Aslam Joiya, Maqsood Anwar Malik
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Case Reports in Medicine
Online Access:http://dx.doi.org/10.1155/2018/2096186
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author Bilal Ahmad Shoukat
Osama Ali
Dileep Kumar
Muhammad Bilal Gilani
Adeela Zahid
Shaheer Aslam Joiya
Maqsood Anwar Malik
author_facet Bilal Ahmad Shoukat
Osama Ali
Dileep Kumar
Muhammad Bilal Gilani
Adeela Zahid
Shaheer Aslam Joiya
Maqsood Anwar Malik
author_sort Bilal Ahmad Shoukat
collection DOAJ
description We present the case of a 19-year-old female with severe hypogammaglobulinemia after having had treatment with rituximab for idiopathic thrombocytopenic purpura requiring intravenous immunoglobulins. She was admitted with the diagnosis of left-sided pneumonia with parapneumonic effusion. The patient was treated with piperacillin/tazobactam after having a poor response to co-amoxiclav. The patient had been tested for immunoglobulin levels, and the levels were very low. She has a history of ITP for which she received steroids. She also received rituximab for the same on four separate occasions, and the last one was about 1 year ago.
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id doaj-art-8d2a54b31ec64c7ab4dd8ce2b3e2c943
institution Kabale University
issn 1687-9627
1687-9635
language English
publishDate 2018-01-01
publisher Wiley
record_format Article
series Case Reports in Medicine
spelling doaj-art-8d2a54b31ec64c7ab4dd8ce2b3e2c9432025-02-03T05:51:03ZengWileyCase Reports in Medicine1687-96271687-96352018-01-01201810.1155/2018/20961862096186Hypogammaglobulinemia Observed One Year after Rituximab Treatment for Idiopathic Thrombocytopenic PurpuraBilal Ahmad Shoukat0Osama Ali1Dileep Kumar2Muhammad Bilal Gilani3Adeela Zahid4Shaheer Aslam Joiya5Maqsood Anwar Malik6Our Lady’s Hospital, Navan, Meath, IrelandOur Lady’s Hospital, Navan, Meath, IrelandOur Lady’s Hospital, Navan, Meath, IrelandProvidence Hospital, Washington, DC, USAOur Lady’s Hospital, Navan, Meath, IrelandOur Lady’s Hospital, Navan, Meath, IrelandOur Lady’s Hospital, Navan, Meath, IrelandWe present the case of a 19-year-old female with severe hypogammaglobulinemia after having had treatment with rituximab for idiopathic thrombocytopenic purpura requiring intravenous immunoglobulins. She was admitted with the diagnosis of left-sided pneumonia with parapneumonic effusion. The patient was treated with piperacillin/tazobactam after having a poor response to co-amoxiclav. The patient had been tested for immunoglobulin levels, and the levels were very low. She has a history of ITP for which she received steroids. She also received rituximab for the same on four separate occasions, and the last one was about 1 year ago.http://dx.doi.org/10.1155/2018/2096186
spellingShingle Bilal Ahmad Shoukat
Osama Ali
Dileep Kumar
Muhammad Bilal Gilani
Adeela Zahid
Shaheer Aslam Joiya
Maqsood Anwar Malik
Hypogammaglobulinemia Observed One Year after Rituximab Treatment for Idiopathic Thrombocytopenic Purpura
Case Reports in Medicine
title Hypogammaglobulinemia Observed One Year after Rituximab Treatment for Idiopathic Thrombocytopenic Purpura
title_full Hypogammaglobulinemia Observed One Year after Rituximab Treatment for Idiopathic Thrombocytopenic Purpura
title_fullStr Hypogammaglobulinemia Observed One Year after Rituximab Treatment for Idiopathic Thrombocytopenic Purpura
title_full_unstemmed Hypogammaglobulinemia Observed One Year after Rituximab Treatment for Idiopathic Thrombocytopenic Purpura
title_short Hypogammaglobulinemia Observed One Year after Rituximab Treatment for Idiopathic Thrombocytopenic Purpura
title_sort hypogammaglobulinemia observed one year after rituximab treatment for idiopathic thrombocytopenic purpura
url http://dx.doi.org/10.1155/2018/2096186
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