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231224s2016 xx |||||o 00| ||chi c |
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|a 10.3760/cma.j.issn.0578-1310.2016.04.013
|2 doi
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|a pubmed24n0863.xml
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|a (DE-627)NLM259180750
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|a (NLM)27055430
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|a DE-627
|b ger
|c DE-627
|e rakwb
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| 041 |
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|a chi
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| 100 |
1 |
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|a Xiao, L
|e verfasserin
|4 aut
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| 245 |
1 |
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|a X-linked lymphoproliferative syndrome type 1 complicated with secondary hemophagocytic lymphohistiocytosis and ileal perforation
|b case report and literature review
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|c 2016
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| 336 |
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 30.01.2017
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|a Date Revised 02.12.2018
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|a published: Print
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|a Citation Status MEDLINE
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|a OBJECTIVE: To analyze and summarize the clinical characteristics, laboratory tests and treatment of X-linked lymphoproliferative syndrome type 1 (XLP-1)
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|a METHOD: A retrospective study was done in 2012 on an XLP-1 patient to collect the data on clinical manifestation, laboratory examination, gene and protein expression, complications and prognosis. Literatures were reviewed in Pubmed with the key word"X-linked lymphoproliferative syndrome"
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| 520 |
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|a RESULT: The patient with persistent high fever, jaundice, abdominal distension, hepatosplenomegaly and lymphadenectasis, rash and suspicious positive family history; the patient eventually died of hemophagocytic lymphohistiocytosis (HLH), with intestinal perforation, intestinal infection and bleeding after being infected with EB virus. This patient with SH2D1A gene exon 1 large fragment of the coding region of the nucleotide deletion and insertion mutations causing missense mutations (p.Leu25Lys) and nonsense mutations (stop codon TAG was inserted after missense mutation so that the protein encoded by the early termination of the 25 amino acids), which led to SAP protein missing. The expression of SAP in his mother was also partly missing. Retrieval of reports on XLP-1 was conducted through literature search (included totally 157 cases) at home and abroad, positive family history accounted for 60.6%(40/66); lymphoma incidence accounted for 49.7%(72/145); low gamma globulin occurred in 24.8%(39/157) of cases; secondary HLH ratio accounted for 43.3%(68/157); XLP-1 in patients with hemorrhagic enteritis and gastritis was low, accounted for only 2.6%(3/116)
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|a CONCLUSION: XLP-1 patients occasionally develop necrotic enteritis complicated with ileal perforation.XLP-1 with large fragment deletion of SH2D1A gene might be associated with serious gastrointestinal manifestations
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|a Case Reports
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|a Journal Article
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|a Review
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|a SH2D1A protein, human
|2 NLM
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| 650 |
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|a Signaling Lymphocytic Activation Molecule Associated Protein
|2 NLM
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| 700 |
1 |
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|a Guan, X M
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Meng, Y
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Zhao, X D
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Xian, Y
|e verfasserin
|4 aut
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| 700 |
1 |
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|a An, Y F
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Yu, J
|e verfasserin
|4 aut
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| 773 |
0 |
8 |
|i Enthalten in
|t Zhonghua er ke za zhi = Chinese journal of pediatrics
|d 1960
|g 54(2016), 4 vom: 07. Apr., Seite 290-3
|w (DE-627)NLM136249191
|x 0578-1310
|7 nnns
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| 773 |
1 |
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|g volume:54
|g year:2016
|g number:4
|g day:07
|g month:04
|g pages:290-3
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| 856 |
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|u http://dx.doi.org/10.3760/cma.j.issn.0578-1310.2016.04.013
|3 Volltext
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|d 54
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