A Case of Erythroderma Secondary to Hypereosinophilia

Hypereosinophilic syndrome (HES) is a myeloproliferative disorder characterised by marked peripheral eosinophilia and end organ damage attributable to eosinophilia without secondary cause. Early recognition and treatment are essential to prevent morbidity and mortality. Cytoreduction with Steroids,...

Full description

Saved in:

Bibliographic Details
Published in:	Journal of clinical and diagnostic research Vol. 10; no. 5; pp. OD15 - OD16
Main Authors:	Abdulsalam, Mohammed Shafi, Ghanta, Hari Chandana, Pandurangan, Prabu, Menon, Maya, Jacob, Sheba S K
Format:	Journal Article
Language:	English
Published:	India JCDR Research and Publications Private Limited 01-05-2016
Subjects:	adrenal insufficiency cytoreduction lymphangioma of spleen tissue eosinophilia Cytoreduction Lymphangioma of spleen Adrenal insufficiency Tissue eosinophilia
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Abstract	Hypereosinophilic syndrome (HES) is a myeloproliferative disorder characterised by marked peripheral eosinophilia and end organ damage attributable to eosinophilia without secondary cause. Early recognition and treatment are essential to prevent morbidity and mortality. Cytoreduction with Steroids, Hydroxyurea and Imatinib are the main stay of treatment. Molecular studies like Fip1-like-1 fused with platelet derived growth factor receptor alpha (FIP1L1-PDGFRα) etc., are recommended in view of therapeutic implication. In this paper we report a rare case of HES developing in a lady 6 months after surgical removal of lymphangioma of spleen, which in itself is rare.
AbstractList	Hypereosinophilic syndrome (HES) is a myeloproliferative disorder characterised by marked peripheral eosinophilia and end organ damage attributable to eosinophilia without secondary cause. Early recognition and treatment are essential to prevent morbidity and mortality. Cytoreduction with Steroids, Hydroxyurea and Imatinib are the main stay of treatment. Molecular studies like Fip1-like-1 fused with platelet derived growth factor receptor alpha (FIP1L1-PDGFRα) etc., are recommended in view of therapeutic implication. In this paper we report a rare case of HES developing in a lady 6 months after surgical removal of lymphangioma of spleen, which in itself is rare.
Author	Abdulsalam, Mohammed Shafi Menon, Maya Jacob, Sheba S K Ghanta, Hari Chandana Pandurangan, Prabu
Author_xml	– sequence: 1 givenname: Mohammed Shafi surname: Abdulsalam fullname: Abdulsalam, Mohammed Shafi organization: Post Graduate Student, Department of Internal Medicine, Greams Road, Apollo Main Hospital , Chennai, Tamil Nadu, India – sequence: 2 givenname: Hari Chandana surname: Ghanta fullname: Ghanta, Hari Chandana organization: Associate Consultant Physician, Department of Internal Medicine, Greams Road, Apollo Main Hospital , Chennai, Tamil Nadu, India – sequence: 3 givenname: Prabu surname: Pandurangan fullname: Pandurangan, Prabu organization: Consultant Haematologist, Department of Haematology, Greams Road, Apollo Main Hospital , Chennai, Tamil Nadu, India – sequence: 4 givenname: Maya surname: Menon fullname: Menon, Maya organization: Senior Consultant Pathologist, Department of Pathology, Greams Road, Apollo Main Hospital , Chennai, Tamil Nadu, India – sequence: 5 givenname: Sheba S K surname: Jacob fullname: Jacob, Sheba S K organization: Consultant Pathologist, Department of Pathology, Greams Road, Apollo Main Hospital , Chennai, Tamil Nadu, India
BackLink	https://www.ncbi.nlm.nih.gov/pubmed/27437281$$D View this record in MEDLINE/PubMed
BookMark	eNo9kNtqwkAQQJfSUi_tH5SSH4hO9pp9FGurRSj0Ar4tm-xsjWhWNvbBv2-irU8DA-cwcwbkug41EvKQwUjlEsav06f3MYVMjjMNQo2UUnBF-qAVSxXo1TXpU8p1qnK66pFB02wApJRM3pIeVZwpmmd9IibJ1DaYBJ_M4vGwjsFh3NnkA8tQOxuPySEk8-MeI4amqsN-XW0re0duvN02eP83h-TrefY5nafLt5fFdLJMS8bEIS1Bgsx17hEFUiekdhpRckdLbx1o6TQvMZeZLajQVPuCFZSxggOTGQPHhmRx9rpgN2Yfq117kQm2MqdFiN_GxkNVbtHk3AsmPPMckIMVOQhdtv8zq6V3BWtd_OwqY2iaiP7iy8B0RU1X1HRFzamo6Yq22OMZ2_8UO3QX6D8h-wW16nJl
ContentType	Journal Article
DBID	NPM AAYXX CITATION DOA
DOI	10.7860/JCDR/2016/19057.7770
DatabaseName	PubMed CrossRef Directory of Open Access Journals
DatabaseTitle	PubMed CrossRef
DatabaseTitleList	PubMed
Database_xml	– sequence: 1 dbid: DOA name: Directory of Open Access Journals url: http://www.doaj.org/ sourceTypes: Open Website
DeliveryMethod	fulltext_linktorsrc
Discipline	Medicine
EISSN	0973-709X
EndPage	OD16
ExternalDocumentID	oai_doaj_org_article_84f535f3f40e40a58059c2493a96fdb3 10_7860_JCDR_2016_19057_7770 27437281
Genre	Case Reports
GroupedDBID	--- 2WC 5VS ABDBF ADBBV ALMA_UNASSIGNED_HOLDINGS BAWUL BCNDV DIK E3Z EBD EOJEC ESX GROUPED_DOAJ GX1 HYE KQ8 M~E NPM OBODZ OK1 P6G RNS RPM TR2 TUS ~8M AAYXX CITATION
ID	FETCH-LOGICAL-c335t-c0606898fee5e2d569d9ee64d2cfad096d94ce861ab25929fb3b233b4036130d3
IEDL.DBID	DOA
ISSN	2249-782X
IngestDate	Tue Oct 22 15:14:44 EDT 2024 Fri Aug 23 08:39:52 EDT 2024 Sat Sep 28 08:32:58 EDT 2024
IsDoiOpenAccess	true
IsOpenAccess	true
IsPeerReviewed	true
IsScholarly	true
Issue	5
Keywords	Cytoreduction Lymphangioma of spleen Adrenal insufficiency Tissue eosinophilia
Language	English
LinkModel	DirectLink
MergedId	FETCHMERGED-LOGICAL-c335t-c0606898fee5e2d569d9ee64d2cfad096d94ce861ab25929fb3b233b4036130d3
OpenAccessLink	https://doaj.org/article/84f535f3f40e40a58059c2493a96fdb3
PMID	27437281
ParticipantIDs	doaj_primary_oai_doaj_org_article_84f535f3f40e40a58059c2493a96fdb3 crossref_primary_10_7860_JCDR_2016_19057_7770 pubmed_primary_27437281
PublicationCentury	2000
PublicationDate	2016-05-01
PublicationDateYYYYMMDD	2016-05-01
PublicationDate_xml	– month: 05 year: 2016 text: 2016-05-01 day: 01
PublicationDecade	2010
PublicationPlace	India
PublicationPlace_xml	– name: India
PublicationTitle	Journal of clinical and diagnostic research
PublicationTitleAlternate	J Clin Diagn Res
PublicationYear	2016
Publisher	JCDR Research and Publications Private Limited
Publisher_xml	– name: JCDR Research and Publications Private Limited
SSID	ssj0066636
Score	2.0769227
Snippet	Hypereosinophilic syndrome (HES) is a myeloproliferative disorder characterised by marked peripheral eosinophilia and end organ damage attributable to...
SourceID	doaj crossref pubmed
SourceType	Open Website Aggregation Database Index Database
StartPage	OD15
SubjectTerms	adrenal insufficiency cytoreduction lymphangioma of spleen tissue eosinophilia
Title	A Case of Erythroderma Secondary to Hypereosinophilia
URI	https://www.ncbi.nlm.nih.gov/pubmed/27437281 https://doaj.org/article/84f535f3f40e40a58059c2493a96fdb3
Volume	10
hasFullText	1
inHoldings	1
isFullTextHit
isPrint
link	http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV05T8MwGLWgA2JB3JSj8sBqmsTxNZYeqpBgoCB1i-zYlliSqsfQf8_nOK0QCwtrFDnWs-X3Pcd-D6FHY5hwCbPESpeRcFeSGCEUEWWiTbB3sU0YzHQm3uZyNA42Ofuor3AmLNoDR-D6MveMMk99nrg80UxCPVCCZqBacW9N9PlM-E5MxTUYavImHBD4CT4rs3m8NCckT_ovw9E7SP6U94ELmXgSIgQV_yClxrv_V5XZsM3kFJ20ZSIexO6doQNXnaOj1_ZH-AViAzwE_sG1x-PlNmQd2LDE4lnQt1Yvt3hd4ylozKWrV19VvQj7JvoSfU7GH8MpaRMQSEkpW5MyAX0hlfTOMZdZxpVVzvHcZqXXFtSHVXnpJE-1ARmTKW-oySg1OfASkJOlV6hT1ZW7QTjlIKwYqAmlkxxUlXRGytR7qm2uSu67iOwgKBbR6KIAgRAgKwJkRYCsaCArAmRd9Bxw2r8bbKqbBzB4RTt4xV-D10XXEeV9MyCSqchkevsfzd-h49DreD7xHnXWy417QIcru-k106XXbO58A_7VvfA
link.rule.ids	315,782,786,866,2106,27933,27934
linkProvider	Directory of Open Access Journals
openUrl	ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=A+Case+of+Erythroderma+Secondary+to+Hypereosinophilia&rft.jtitle=Journal+of+clinical+and+diagnostic+research&rft.au=Abdulsalam%2C+Mohammed+Shafi&rft.date=2016-05-01&rft.issn=2249-782X&rft_id=info:doi/10.7860%2FJCDR%2F2016%2F19057.7770&rft.externalDBID=n%2Fa&rft.externalDocID=10_7860_JCDR_2016_19057_7770
thumbnail_l	http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2249-782X&client=summon
thumbnail_m	http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2249-782X&client=summon
thumbnail_s	http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2249-782X&client=summon