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Erschienen in: Journal of Clinical Immunology 1/2019

10.01.2019 | Letter to Editor

Successful Treatment with SCIG of a Child with Refractory Chronic ITP

verfasst von: Anna Karastaneva, Daniela S. Klobassa, Milen Minkov, Martin Benesch, Markus G. Seidel

Erschienen in: Journal of Clinical Immunology | Ausgabe 1/2019

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Excerpt

To the Editor …
Literatur
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Zurück zum Zitat Seidel MG. Autoimmune and other cytopenias in primary immunodeficiencies: pathomechanisms, novel differential diagnoses, and treatment. Blood. 2014;124(15):2337–44.CrossRefPubMedPubMedCentral Seidel MG. Autoimmune and other cytopenias in primary immunodeficiencies: pathomechanisms, novel differential diagnoses, and treatment. Blood. 2014;124(15):2337–44.CrossRefPubMedPubMedCentral
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Zurück zum Zitat Ballow M. The IgG molecule as a biological immune response modifier: mechanisms of action of intravenous immune serum globulin in autoimmune and inflammatory disorders. J Allergy Clin Immunol. 2011;127(2):315–23 quiz 24-5.CrossRefPubMed Ballow M. The IgG molecule as a biological immune response modifier: mechanisms of action of intravenous immune serum globulin in autoimmune and inflammatory disorders. J Allergy Clin Immunol. 2011;127(2):315–23 quiz 24-5.CrossRefPubMed
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Zurück zum Zitat Iuliano F, Iuliano E, Luci M, Perricelli A, Pomillo A, Abruzzese E. Subcutaneous immunoglobulin (SCIG) in responders to intravenous therapy with chronic immune thrombocytopenia (ITP). Blood. 2014;124(21):5012. Iuliano F, Iuliano E, Luci M, Perricelli A, Pomillo A, Abruzzese E. Subcutaneous immunoglobulin (SCIG) in responders to intravenous therapy with chronic immune thrombocytopenia (ITP). Blood. 2014;124(21):5012.
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Zurück zum Zitat Pedini V, Savore I, Danieli MG. Facilitated subcutaneous immunoglobulin (fSCIg) in autoimmune cytopenias associated with common variable immunodeficiency. Isr Med Assoc J. 2017;19(7):420–3.PubMed Pedini V, Savore I, Danieli MG. Facilitated subcutaneous immunoglobulin (fSCIg) in autoimmune cytopenias associated with common variable immunodeficiency. Isr Med Assoc J. 2017;19(7):420–3.PubMed
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Zurück zum Zitat Scheuerlein P, Pietsch L, Camacho-Ordonez N, Reiser V, Patel S, Burns SO, et al. Is it safe to switch from intravenous immunoglobulin to subcutaneous immunoglobulin in patients with common variable immunodeficiency and autoimmune thrombocytopenia? Front Immunol. 2018;9:1656.CrossRefPubMedPubMedCentral Scheuerlein P, Pietsch L, Camacho-Ordonez N, Reiser V, Patel S, Burns SO, et al. Is it safe to switch from intravenous immunoglobulin to subcutaneous immunoglobulin in patients with common variable immunodeficiency and autoimmune thrombocytopenia? Front Immunol. 2018;9:1656.CrossRefPubMedPubMedCentral
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Zurück zum Zitat Chapdelaine H, Decaluwe H, Levasseur MC, De Deist F, Haddad E. Experience with subcutaneous immunoglobulin therapy in two pediatric cases of immune thrombocytopenia purpura. Allergy, Asthma Clin Immunol. 2012;8(Suppl 1):A23.CrossRef Chapdelaine H, Decaluwe H, Levasseur MC, De Deist F, Haddad E. Experience with subcutaneous immunoglobulin therapy in two pediatric cases of immune thrombocytopenia purpura. Allergy, Asthma Clin Immunol. 2012;8(Suppl 1):A23.CrossRef
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Zurück zum Zitat Cuker A, Neunert CE. How I treat refractory immune thrombocytopenia. Blood. 2016;128(12):1547–54.CrossRefPubMed Cuker A, Neunert CE. How I treat refractory immune thrombocytopenia. Blood. 2016;128(12):1547–54.CrossRefPubMed
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Zurück zum Zitat DiMaggio D, Anderson A, Bussel JB. Cytomegalovirus can make immune thrombocytopenic purpura refractory. Br J Haematol. 2009;146(1):104–12.CrossRefPubMed DiMaggio D, Anderson A, Bussel JB. Cytomegalovirus can make immune thrombocytopenic purpura refractory. Br J Haematol. 2009;146(1):104–12.CrossRefPubMed
Metadaten
Titel
Successful Treatment with SCIG of a Child with Refractory Chronic ITP
verfasst von
Anna Karastaneva
Daniela S. Klobassa
Milen Minkov
Martin Benesch
Markus G. Seidel
Publikationsdatum
10.01.2019
Verlag
Springer US
Erschienen in
Journal of Clinical Immunology / Ausgabe 1/2019
Print ISSN: 0271-9142
Elektronische ISSN: 1573-2592
DOI
https://doi.org/10.1007/s10875-018-0583-y

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