2007
DOI: 10.1055/s-2007-985877
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Severe Combined Immunodeficiency Signalized by Eosinophilia and Lymphopenia in Rotavirus Infected Infants

Abstract: In infants with rotavirus infection, a full blood count should be performed: Eosinophilia and/or lymphopenia raise a high suspicion of SCID.

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Cited by 8 publications
(7 citation statements)
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“…The majority of patients described so far suff ered from opportunistic infections and failure to thrive within the fi rst 6 months of life. Our patient presented several times with classical warning sign for a SCID in a diff erential blood count: a profound lymphopenia of less than 1 500 lymphocytes / μ l. So, as stressed by campaigns to raise the awareness for SCID, also in our patient the diagnosis of SCID could have been established by the thorough analysis of a peripheral diff erential blood count [9] . In addition over all immunoglobulins were within normal range except for elevated IgA, IgG2 and IgE.…”
Section: Treatmentmentioning
confidence: 60%
See 1 more Smart Citation
“…The majority of patients described so far suff ered from opportunistic infections and failure to thrive within the fi rst 6 months of life. Our patient presented several times with classical warning sign for a SCID in a diff erential blood count: a profound lymphopenia of less than 1 500 lymphocytes / μ l. So, as stressed by campaigns to raise the awareness for SCID, also in our patient the diagnosis of SCID could have been established by the thorough analysis of a peripheral diff erential blood count [9] . In addition over all immunoglobulins were within normal range except for elevated IgA, IgG2 and IgE.…”
Section: Treatmentmentioning
confidence: 60%
“…The dysfunction of the T cell compartment can be associated with B cell defi ciency and NK cell defi ciency or both. Diff erent forms of SCID can be characterized by the immunological phenotype and a corresponding underlying molecular defect [1,6,9,11] . The T-B-NKphenotype of SCID is usually caused by adenosine deaminase defi ciency or purine nucleoside phosphorylase defi ciency [10] .…”
mentioning
confidence: 99%
“…Bei jedem Verdacht auf einen Immundefekt müssen ein mikroskopisch differenziertes Blutbild angefertigt und die IgG-, IgA-, IgM-und IgE-Spiegel be- Eine Eosinophilie und/oder die Erhö-hung von IgE können auf Immundefekte wie SCID (Eosinophilie in Fall 1, IgE-Erhöhung in Fall 2), Wiskott-Aldrich-Syndrom, Hyper-IgE-Syndrom, IPEX-Syndrom ("immunodysregulation polyendocrinopathy enteropathy X-linked syndrome") oder Comèl-Netherton-Syndrom hinweisen [1,4,13,21]. Eine Thrombozytopenie und kleine Thrombozyten sind bei einem Jungen verdächtig für ein Wiskott-Aldrich-Syndrom [1].…”
Section: Stellenwert Der Immunologischen Basisdiagnostikunclassified
“…2 500 bekannten Salmonella -Serovaren [12] oder Ausdruck einer kongenitalen Abwehrschw ä che sein k ö nnen. So k ö nnen persistierende Infektionen mit den wenig lebensbedrohlichen Rotaviren Ausdruck eines schweren kombinierten Immundefekts sein [14] . Andererseits kommt es fernzuhalten.…”
Section: Schlussfolgerungen Und Empfehlungenunclassified