An Interesting Case of Acute Section Encephalitic Syndrome with Pancytopenia and Splenomegaly

Human Parvovirus infection is a rare condition causing encephalitis as well as pancytopenia. Similarly patient of Wilson disease presenting as hepatic encephalopathy as an initial manifestation is also a rare phenomenon. A previously healthy 20-year-old female patient presented as acute encephalitis...

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Main Authors: Satyendra Kumar Sonkar, Satish Kumar, Neeraj Kumar Singh
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2019-03-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/12677/40432_CE[Ra1]_F(AC)_PF1(AGAK)_PFA(AK)_PB(NC_AG)_PN(SL).pdf
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spelling doaj-d2b2ea1ba7074be480c7fe65092a0a822020-11-25T02:19:50ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2019-03-01133OD08OD1010.7860/JCDR/2019/40432.12677An Interesting Case of Acute Section Encephalitic Syndrome with Pancytopenia and SplenomegalySatyendra Kumar Sonkar0Satish Kumar1Neeraj Kumar Singh2Professor, Department of Medicine, King George’s Medical University, Lucknow, Uttar Pradesh, India.Senior Resident, Department of Medicine, King George’s Medical University, Lucknow, Uttar Pradesh, India.Junior Resident, Department of Medicine, King George’s Medical University, Lucknow, Uttar Pradesh, India.Human Parvovirus infection is a rare condition causing encephalitis as well as pancytopenia. Similarly patient of Wilson disease presenting as hepatic encephalopathy as an initial manifestation is also a rare phenomenon. A previously healthy 20-year-old female patient presented as acute encephalitis syndrome with hepatitis and pancytopenia. Bone marrow examination showed the presence of inclusion bodies and PCR (Polymerase Chain Reaction) showed the presence of DNA of human parvo virus B19. Patient was suspected as a case of Wilson’s disease due to the persistence of splenomegaly and radiological findings and was confirmed by increased 24 hours urinary copper and low level of serum ceruloplasmin. Patient was treated symptomatically and gained consciousness and pancytopenia improved over course of time.https://jcdr.net/articles/PDF/12677/40432_CE[Ra1]_F(AC)_PF1(AGAK)_PFA(AK)_PB(NC_AG)_PN(SL).pdfhuman parvovirus b 19serum ceruloplasminwilson’s disease
collection DOAJ
language English
format Article
sources DOAJ
author Satyendra Kumar Sonkar
Satish Kumar
Neeraj Kumar Singh
spellingShingle Satyendra Kumar Sonkar
Satish Kumar
Neeraj Kumar Singh
An Interesting Case of Acute Section Encephalitic Syndrome with Pancytopenia and Splenomegaly
Journal of Clinical and Diagnostic Research
human parvovirus b 19
serum ceruloplasmin
wilson’s disease
author_facet Satyendra Kumar Sonkar
Satish Kumar
Neeraj Kumar Singh
author_sort Satyendra Kumar Sonkar
title An Interesting Case of Acute Section Encephalitic Syndrome with Pancytopenia and Splenomegaly
title_short An Interesting Case of Acute Section Encephalitic Syndrome with Pancytopenia and Splenomegaly
title_full An Interesting Case of Acute Section Encephalitic Syndrome with Pancytopenia and Splenomegaly
title_fullStr An Interesting Case of Acute Section Encephalitic Syndrome with Pancytopenia and Splenomegaly
title_full_unstemmed An Interesting Case of Acute Section Encephalitic Syndrome with Pancytopenia and Splenomegaly
title_sort interesting case of acute section encephalitic syndrome with pancytopenia and splenomegaly
publisher JCDR Research and Publications Private Limited
series Journal of Clinical and Diagnostic Research
issn 2249-782X
0973-709X
publishDate 2019-03-01
description Human Parvovirus infection is a rare condition causing encephalitis as well as pancytopenia. Similarly patient of Wilson disease presenting as hepatic encephalopathy as an initial manifestation is also a rare phenomenon. A previously healthy 20-year-old female patient presented as acute encephalitis syndrome with hepatitis and pancytopenia. Bone marrow examination showed the presence of inclusion bodies and PCR (Polymerase Chain Reaction) showed the presence of DNA of human parvo virus B19. Patient was suspected as a case of Wilson’s disease due to the persistence of splenomegaly and radiological findings and was confirmed by increased 24 hours urinary copper and low level of serum ceruloplasmin. Patient was treated symptomatically and gained consciousness and pancytopenia improved over course of time.
topic human parvovirus b 19
serum ceruloplasmin
wilson’s disease
url https://jcdr.net/articles/PDF/12677/40432_CE[Ra1]_F(AC)_PF1(AGAK)_PFA(AK)_PB(NC_AG)_PN(SL).pdf
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