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Concurrent eosinophilia and IgG4-related disease in a child: A case report and review of the literature
The current study presents the case of a 9-year-old Chinese boy who presented with eosinophilia and elevated serum levels of immunoglobulin G4 (IgG4). A bone marrow puncture identified an elevated eosinophil rate of 23% (normal range,
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Published in: | Experimental and therapeutic medicine 2018-03, Vol.15 (3), p.2739-2748 |
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creator | Chen, Can Chen, Kuang Huang, Xilian Wang, Kaile Qian, Shenxian |
description | The current study presents the case of a 9-year-old Chinese boy who presented with eosinophilia and elevated serum levels of immunoglobulin G4 (IgG4). A bone marrow puncture identified an elevated eosinophil rate of 23% (normal range, |
doi_str_mv | 10.3892/etm.2018.5743 |
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hybridization and other examinations, including bone marrow aspiration, blood routine, auto-antibody tests and parasitic and allergens screening, contradicted a diagnosis of secondary or clonal eosinophilia. Furthermore, the patient exhibited multiple lymph node swelling and a lymph biopsy strongly indicted a pathological diagnosis of IgG4-related disease (IgG4-RD). His peripheral blood flow cytometry confirmed an elevated count of plasmablasts, which is specific to IgG4-RD. The patient responded well to therapy with prednisone and remained healthy in all follow-ups. By taking all these factors into consideration, the boy was diagnosed with IgG4-RD. It is difficult to distinguish IgG4-RD from hypereosinophilic syndrome and the potential association between the two remains unclear. However, the present case study serves as a reminder that IgG4-RD may occur in children and medical professionals should not neglect this possibility.</description><identifier>ISSN: 1792-0981</identifier><identifier>EISSN: 1792-1015</identifier><identifier>DOI: 10.3892/etm.2018.5743</identifier><identifier>PMID: 29456677</identifier><language>eng</language><publisher>Greece: Spandidos Publications</publisher><subject>Abdomen ; Allergies ; Blood diseases ; Blood platelets ; Bone marrow ; Care and treatment ; Case reports ; Case studies ; Development and progression ; Disease ; Eosinophilia ; Growth factors ; Leukemia ; Lymphatic system ; Pathogenesis ; Patients ; Polymerase chain reaction ; Ultrasonic imaging</subject><ispartof>Experimental and therapeutic medicine, 2018-03, Vol.15 (3), p.2739-2748</ispartof><rights>COPYRIGHT 2018 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2018</rights><rights>Copyright: © Chen et al. 2018</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c548t-7716ab6942da2e5b1535f0f45d235cda19eda4361ce2c0ff85a6ed906a9b1103</citedby><cites>FETCH-LOGICAL-c548t-7716ab6942da2e5b1535f0f45d235cda19eda4361ce2c0ff85a6ed906a9b1103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5795490/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5795490/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29456677$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Can</creatorcontrib><creatorcontrib>Chen, Kuang</creatorcontrib><creatorcontrib>Huang, Xilian</creatorcontrib><creatorcontrib>Wang, Kaile</creatorcontrib><creatorcontrib>Qian, Shenxian</creatorcontrib><title>Concurrent eosinophilia and IgG4-related disease in a child: A case report and review of the literature</title><title>Experimental and therapeutic medicine</title><addtitle>Exp Ther Med</addtitle><description>The current study presents the case of a 9-year-old Chinese boy who presented with eosinophilia and elevated serum levels of immunoglobulin G4 (IgG4). A bone marrow puncture identified an elevated eosinophil rate of 23% (normal range, <5%), which indicated eosinophilia. However, gene analysis, fluorescent
hybridization and other examinations, including bone marrow aspiration, blood routine, auto-antibody tests and parasitic and allergens screening, contradicted a diagnosis of secondary or clonal eosinophilia. Furthermore, the patient exhibited multiple lymph node swelling and a lymph biopsy strongly indicted a pathological diagnosis of IgG4-related disease (IgG4-RD). His peripheral blood flow cytometry confirmed an elevated count of plasmablasts, which is specific to IgG4-RD. The patient responded well to therapy with prednisone and remained healthy in all follow-ups. By taking all these factors into consideration, the boy was diagnosed with IgG4-RD. It is difficult to distinguish IgG4-RD from hypereosinophilic syndrome and the potential association between the two remains unclear. However, the present case study serves as a reminder that IgG4-RD may occur in children and medical professionals should not neglect this possibility.</description><subject>Abdomen</subject><subject>Allergies</subject><subject>Blood diseases</subject><subject>Blood platelets</subject><subject>Bone marrow</subject><subject>Care and treatment</subject><subject>Case reports</subject><subject>Case studies</subject><subject>Development and progression</subject><subject>Disease</subject><subject>Eosinophilia</subject><subject>Growth factors</subject><subject>Leukemia</subject><subject>Lymphatic system</subject><subject>Pathogenesis</subject><subject>Patients</subject><subject>Polymerase chain reaction</subject><subject>Ultrasonic imaging</subject><issn>1792-0981</issn><issn>1792-1015</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNptks1rHCEYxofQkoQkx16L0Esvs_VzZuyhsCxtGgjkkru4-rprmNGtOin97-s025CU6kF5_T2PvvI0zTuCV2yQ9BOUaUUxGVai5-ykOSe9pC3BRLw57rEcyFlzlfMDrkN0ZBjEaXNGJRdd1_fnzW4Tg5lTglAQxOxDPOz96DXSwaKb3TVvE4y6gEXWZ9AZkA9II1Mh-xmtkVlKCQ4xlT-SBI8efqLoUNkDGn2BpMuc4LJ56_SY4eq4XjT3377eb763t3fXN5v1bWsEH0rb96TT205yajUFsSWCCYcdF5YyYawmEqzmrCMGqMHODUJ3YCXutNwSgtlF8-XJ9jBvJ7CmtpX0qA7JTzr9UlF79fok-L3axUcleim4XAw-Hg1S_DFDLmry2cA46gBxzopizBmnuKcV_fAP-hDnFGp3lSKcEYbxC2qnR1A-uFjvNYupWgtGpWSSykqt_kPVaWHyJgZwvtZfCdongUkx5wTuuUeC1ZINVbOxvGNQSzYq__7lxzzTf5PAfgN9HrO0</recordid><startdate>20180301</startdate><enddate>20180301</enddate><creator>Chen, Can</creator><creator>Chen, Kuang</creator><creator>Huang, Xilian</creator><creator>Wang, Kaile</creator><creator>Qian, Shenxian</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. 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A bone marrow puncture identified an elevated eosinophil rate of 23% (normal range, <5%), which indicated eosinophilia. However, gene analysis, fluorescent
hybridization and other examinations, including bone marrow aspiration, blood routine, auto-antibody tests and parasitic and allergens screening, contradicted a diagnosis of secondary or clonal eosinophilia. Furthermore, the patient exhibited multiple lymph node swelling and a lymph biopsy strongly indicted a pathological diagnosis of IgG4-related disease (IgG4-RD). His peripheral blood flow cytometry confirmed an elevated count of plasmablasts, which is specific to IgG4-RD. The patient responded well to therapy with prednisone and remained healthy in all follow-ups. By taking all these factors into consideration, the boy was diagnosed with IgG4-RD. It is difficult to distinguish IgG4-RD from hypereosinophilic syndrome and the potential association between the two remains unclear. However, the present case study serves as a reminder that IgG4-RD may occur in children and medical professionals should not neglect this possibility.</abstract><cop>Greece</cop><pub>Spandidos Publications</pub><pmid>29456677</pmid><doi>10.3892/etm.2018.5743</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Allergies Blood diseases Blood platelets Bone marrow Care and treatment Case reports Case studies Development and progression Disease Eosinophilia Growth factors Leukemia Lymphatic system Pathogenesis Patients Polymerase chain reaction Ultrasonic imaging |
title | Concurrent eosinophilia and IgG4-related disease in a child: A case report and review of the literature |
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