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Unique Complications of MIS-C and Its Treatment: Encephalopathy in a Child with MIS-C Who Developed Life-Threatening Gastrointestinal Hemorrhage

In this case report, we describe a previously healthy eleven-year-old male diagnosed with multisystem inflammatory syndrome in children (MIS-C) associated with coronavirus disease 2019. The patient presented with shock and neurologic symptoms including altered mental status and dysarthria. Brain mag...

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Autores principales: Burton, Luke, Manchikalapati, Ananya, Rutledge, Chrystal, Loberger, Jeremy M., Rockwell, Nicholas, Cooper, Joshua, Lawrence, Maggie, Sasser, William C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617717/
https://www.ncbi.nlm.nih.gov/pubmed/36317092
http://dx.doi.org/10.1155/2022/7244434
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author Burton, Luke
Manchikalapati, Ananya
Rutledge, Chrystal
Loberger, Jeremy M.
Rockwell, Nicholas
Cooper, Joshua
Lawrence, Maggie
Sasser, William C.
author_facet Burton, Luke
Manchikalapati, Ananya
Rutledge, Chrystal
Loberger, Jeremy M.
Rockwell, Nicholas
Cooper, Joshua
Lawrence, Maggie
Sasser, William C.
author_sort Burton, Luke
collection PubMed
description In this case report, we describe a previously healthy eleven-year-old male diagnosed with multisystem inflammatory syndrome in children (MIS-C) associated with coronavirus disease 2019. The patient presented with shock and neurologic symptoms including altered mental status and dysarthria. Brain magnetic resonance imaging, obtained to rule out thromboembolic injury, demonstrated cytotoxic edema of the corpus callosum, an imaging finding similar in nature to several previous reports of MRI abnormalities in children with MIS-C. Following administration of intravenous immunoglobulin and pulse-dose steroids, the patient convalesced and was discharged home. Medications prescribed upon discharge included a steroid taper, daily aspirin, and proton pump inhibitor. Four days later, he was readmitted with shock and life-threatening gastrointestinal (GI) hemorrhage. After extensive evaluation of potential bleeding sources, angiography revealed active bleeding from two arterial vessels supplying the duodenum. The patient demonstrated no further signs of bleeding following successful coil embolization of the two vessels. We hypothesize that the vasculitic nature of MIS-C combined with anti-inflammatory and antithrombotic therapy placed him at risk of GI hemorrhage. This case highlights unique radiologic features of MIS-C as well as potential complications of treatment.
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spelling pubmed-96177172022-10-30 Unique Complications of MIS-C and Its Treatment: Encephalopathy in a Child with MIS-C Who Developed Life-Threatening Gastrointestinal Hemorrhage Burton, Luke Manchikalapati, Ananya Rutledge, Chrystal Loberger, Jeremy M. Rockwell, Nicholas Cooper, Joshua Lawrence, Maggie Sasser, William C. Case Rep Crit Care Case Report In this case report, we describe a previously healthy eleven-year-old male diagnosed with multisystem inflammatory syndrome in children (MIS-C) associated with coronavirus disease 2019. The patient presented with shock and neurologic symptoms including altered mental status and dysarthria. Brain magnetic resonance imaging, obtained to rule out thromboembolic injury, demonstrated cytotoxic edema of the corpus callosum, an imaging finding similar in nature to several previous reports of MRI abnormalities in children with MIS-C. Following administration of intravenous immunoglobulin and pulse-dose steroids, the patient convalesced and was discharged home. Medications prescribed upon discharge included a steroid taper, daily aspirin, and proton pump inhibitor. Four days later, he was readmitted with shock and life-threatening gastrointestinal (GI) hemorrhage. After extensive evaluation of potential bleeding sources, angiography revealed active bleeding from two arterial vessels supplying the duodenum. The patient demonstrated no further signs of bleeding following successful coil embolization of the two vessels. We hypothesize that the vasculitic nature of MIS-C combined with anti-inflammatory and antithrombotic therapy placed him at risk of GI hemorrhage. This case highlights unique radiologic features of MIS-C as well as potential complications of treatment. Hindawi 2022-10-22 /pmc/articles/PMC9617717/ /pubmed/36317092 http://dx.doi.org/10.1155/2022/7244434 Text en Copyright © 2022 Luke Burton et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under 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
Burton, Luke
Manchikalapati, Ananya
Rutledge, Chrystal
Loberger, Jeremy M.
Rockwell, Nicholas
Cooper, Joshua
Lawrence, Maggie
Sasser, William C.
Unique Complications of MIS-C and Its Treatment: Encephalopathy in a Child with MIS-C Who Developed Life-Threatening Gastrointestinal Hemorrhage
title Unique Complications of MIS-C and Its Treatment: Encephalopathy in a Child with MIS-C Who Developed Life-Threatening Gastrointestinal Hemorrhage
title_full Unique Complications of MIS-C and Its Treatment: Encephalopathy in a Child with MIS-C Who Developed Life-Threatening Gastrointestinal Hemorrhage
title_fullStr Unique Complications of MIS-C and Its Treatment: Encephalopathy in a Child with MIS-C Who Developed Life-Threatening Gastrointestinal Hemorrhage
title_full_unstemmed Unique Complications of MIS-C and Its Treatment: Encephalopathy in a Child with MIS-C Who Developed Life-Threatening Gastrointestinal Hemorrhage
title_short Unique Complications of MIS-C and Its Treatment: Encephalopathy in a Child with MIS-C Who Developed Life-Threatening Gastrointestinal Hemorrhage
title_sort unique complications of mis-c and its treatment: encephalopathy in a child with mis-c who developed life-threatening gastrointestinal hemorrhage
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617717/
https://www.ncbi.nlm.nih.gov/pubmed/36317092
http://dx.doi.org/10.1155/2022/7244434
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