Immune Thrombocytopenic Purpura (ITP) as an Uncommon Extraintestinal Complication of Crohn’s Disease: Case Vignette and Systematic Literature Review

While the association of immune thrombocytopenic purpura (ITP) and inflammatory bowel disease (IBD) has been described in a few case reports, management of ITP as an extraintestinal manifestation of Crohn’s disease (CD) is less studied. There are approximately a dozen cases describing the management...

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Main Authors: Raisa Epistola, Tiffanie Do, Ritika Vankina, Daniel Wu, James Yeh, Michael W. Fleischman, Jennifer M. Lee
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Case Reports in Hematology
Online Access:http://dx.doi.org/10.1155/2020/4785759
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author Raisa Epistola
Tiffanie Do
Ritika Vankina
Daniel Wu
James Yeh
Michael W. Fleischman
Jennifer M. Lee
author_facet Raisa Epistola
Tiffanie Do
Ritika Vankina
Daniel Wu
James Yeh
Michael W. Fleischman
Jennifer M. Lee
author_sort Raisa Epistola
collection DOAJ
description While the association of immune thrombocytopenic purpura (ITP) and inflammatory bowel disease (IBD) has been described in a few case reports, management of ITP as an extraintestinal manifestation of Crohn’s disease (CD) is less studied. There are approximately a dozen cases describing the management of patients dually diagnosed with CD/ITP. Previous reports postulated that the mechanism of ITP in CD was through the presence of circulating immune complexes in the serum and antigenic mimicry due to increased mucosal permeability in active colitis, versus increased mucosal production of TH1-type proinflammatory cytokines during CD flares, which may account for remission of ITP with surgery for CD. We present a case of a 27-year-old man who presented with medically refractory CD and ITP who responded to surgical management with colectomy and splenectomy, along with a systematic review of the literature. These cases suggest that colectomy should be considered in the treatment of medically refractory ITP among patients with concomitant CD.
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institution Kabale University
issn 2090-6560
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language English
publishDate 2020-01-01
publisher Wiley
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series Case Reports in Hematology
spelling doaj-art-6fcaf94ece2141f6b07d84e003b138ee2025-02-03T01:04:59ZengWileyCase Reports in Hematology2090-65602090-65792020-01-01202010.1155/2020/47857594785759Immune Thrombocytopenic Purpura (ITP) as an Uncommon Extraintestinal Complication of Crohn’s Disease: Case Vignette and Systematic Literature ReviewRaisa Epistola0Tiffanie Do1Ritika Vankina2Daniel Wu3James Yeh4Michael W. Fleischman5Jennifer M. Lee6Harbor-UCLA Medical Center, Department of Medicine, Torrance, CA, USAHarbor-UCLA Medical Center, Department of Medicine, Torrance, CA, USAHarbor-UCLA Medical Center, Department of Medicine, Division of Hematology & Medical Oncology, Torrance, CA, USAHarbor-UCLA Medical Center, Department of Medicine, Division of Hematology & Medical Oncology, Torrance, CA, USAHarbor-UCLA Medical Center, Department of Medicine, Division of Hematology & Medical Oncology, Torrance, CA, USAHarbor-UCLA Medical Center, Department of Medicine, Division of Gastroenterology, Torrance, CA, USAHarbor-UCLA Medical Center, Department of Medicine, Division of Hematology & Medical Oncology, Torrance, CA, USAWhile the association of immune thrombocytopenic purpura (ITP) and inflammatory bowel disease (IBD) has been described in a few case reports, management of ITP as an extraintestinal manifestation of Crohn’s disease (CD) is less studied. There are approximately a dozen cases describing the management of patients dually diagnosed with CD/ITP. Previous reports postulated that the mechanism of ITP in CD was through the presence of circulating immune complexes in the serum and antigenic mimicry due to increased mucosal permeability in active colitis, versus increased mucosal production of TH1-type proinflammatory cytokines during CD flares, which may account for remission of ITP with surgery for CD. We present a case of a 27-year-old man who presented with medically refractory CD and ITP who responded to surgical management with colectomy and splenectomy, along with a systematic review of the literature. These cases suggest that colectomy should be considered in the treatment of medically refractory ITP among patients with concomitant CD.http://dx.doi.org/10.1155/2020/4785759
spellingShingle Raisa Epistola
Tiffanie Do
Ritika Vankina
Daniel Wu
James Yeh
Michael W. Fleischman
Jennifer M. Lee
Immune Thrombocytopenic Purpura (ITP) as an Uncommon Extraintestinal Complication of Crohn’s Disease: Case Vignette and Systematic Literature Review
Case Reports in Hematology
title Immune Thrombocytopenic Purpura (ITP) as an Uncommon Extraintestinal Complication of Crohn’s Disease: Case Vignette and Systematic Literature Review
title_full Immune Thrombocytopenic Purpura (ITP) as an Uncommon Extraintestinal Complication of Crohn’s Disease: Case Vignette and Systematic Literature Review
title_fullStr Immune Thrombocytopenic Purpura (ITP) as an Uncommon Extraintestinal Complication of Crohn’s Disease: Case Vignette and Systematic Literature Review
title_full_unstemmed Immune Thrombocytopenic Purpura (ITP) as an Uncommon Extraintestinal Complication of Crohn’s Disease: Case Vignette and Systematic Literature Review
title_short Immune Thrombocytopenic Purpura (ITP) as an Uncommon Extraintestinal Complication of Crohn’s Disease: Case Vignette and Systematic Literature Review
title_sort immune thrombocytopenic purpura itp as an uncommon extraintestinal complication of crohn s disease case vignette and systematic literature review
url http://dx.doi.org/10.1155/2020/4785759
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