Literature DB >> 8957959

Intravenous immunoglobulin, splenectomy, and antibiotic prophylaxis in Wiskott-Aldrich syndrome.

J Litzman1, A Jones, I Hann, H Chapel, S Strobel, G Morgan.   

Abstract

AIM: To assess the results of supportive treatment with intravenous immunoglobulin (IVIG) and antibiotic prophylaxis in combination with splenectomy in patients with Wiskott-Aldrich syndrome. STUDY
DESIGN: Retrospective review of case records of 21 patients from March 1984 to February 1996.
RESULTS: Thrombocytopenia was cured in 14 of 15 patients who had splenectomy, but it recurred intermittently in three. Mean platelet volume (MPV) was normal transiently in some patients, but all MPV values were subnormal 8-23 months after splenectomy. Antibiotic and IVIG prophylaxis may have contributed to the lack of a detectable increase in the number of severe acute bacterial infections in the 451 months after splenectomy. Four patients died in 2205 months of observation before and after splenectomy (median 82, range 16-248): two of cerebral B cell lymphoma, one of progressive multifocal leucoencephalopathy, and one with severe chronic chest disease of pneumonia.
CONCLUSION: Adequate supportive treatment with IVIG and antibiotic prophylaxis together with splenectomy enables good survival and quality of life in the short and medium term in patients with Wiskott-Aldrich syndrome. Persistence of infection, bleeding, and vasculitic and allergic symptoms in a significant minority and the risk of development of lymphoma, however, suggest that bone marrow transplantation may be indicated if an HLA identical donor is available.

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Year:  1996        PMID: 8957959      PMCID: PMC1511781          DOI: 10.1136/adc.75.5.436

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  21 in total

1.  The Wiskott-Aldrich syndrome: studies of platelets, basophils and polymorphonuclear leucocytes.

Authors:  G Marone; F Albini; L di Martino; S Quattrin; S Poto; M Condorelli
Journal:  Br J Haematol       Date:  1986-04       Impact factor: 6.998

Review 2.  Hereditary thrombocytopenia: relation to Wiskott-Aldrich syndrome with special reference to splenectomy. Report of a family and review of the literature.

Authors:  P L Weiden; R M Blaese
Journal:  J Pediatr       Date:  1972-02       Impact factor: 4.406

3.  Wiskott-Aldrich syndrome. An immunologic deficiency disease involving the afferent limb of immunity.

Authors:  M D Cooper; H P Chae; J T Lowman; W Krivit; R A Good
Journal:  Am J Med       Date:  1968-04       Impact factor: 4.965

4.  Platelet size and kinetics in hereditary and acquired thrombocytopenia.

Authors:  S Murphy; F A Oski; J L Naiman; C J Lusch; S Goldberg; F H Gardner
Journal:  N Engl J Med       Date:  1972-03-09       Impact factor: 91.245

5.  Wiskott-Aldrich syndrome: qualitative platelet defects and short platelet survival.

Authors:  K A Gröttum; T Hovig; H Holmsen; A F Abrahamsen; M Jeremic; M Seip
Journal:  Br J Haematol       Date:  1969-10       Impact factor: 6.998

6.  Lack of platelet response to stimulation in the Wiskott-Aldrich syndrome.

Authors:  A Kuramoto; M Steiner; M G Baldini
Journal:  N Engl J Med       Date:  1970-02-26       Impact factor: 91.245

7.  The Wiskott-Aldrich syndrome: studies of lymphocytes, granulocytes, and platelets.

Authors:  H D Ochs; S J Slichter; L A Harker; W E Von Behrens; R A Clark; R J Wedgwood
Journal:  Blood       Date:  1980-02       Impact factor: 22.113

8.  Splenectomy in the management of the thrombocytopenia of the Wiskott-Aldrich syndrome.

Authors:  L G Lum; D G Tubergen; L Corash; R M Blaese
Journal:  N Engl J Med       Date:  1980-04-17       Impact factor: 91.245

9.  Effect of intravenous gammaglobulin (IVIG) on the platelet count in patients with Wiskott-Aldrich syndrome.

Authors:  P Mathew; M E Conley
Journal:  Pediatr Allergy Immunol       Date:  1995-05       Impact factor: 6.377

10.  Platelet-associated immunoglobulin, platelet size, and the effect of splenectomy in the Wiskott-Aldrich syndrome.

Authors:  L Corash; B Shafer; R M Blaese
Journal:  Blood       Date:  1985-06       Impact factor: 22.113

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  24 in total

Review 1.  The Wiskott-Aldrich syndrome.

Authors:  H D Ochs
Journal:  Clin Rev Allergy Immunol       Date:  2001-02       Impact factor: 8.667

Review 2.  The Wiskott-Aldrich syndrome.

Authors:  A J Thrasher; C Kinnon
Journal:  Clin Exp Immunol       Date:  2000-04       Impact factor: 4.330

Review 3.  The Wiskott-Aldrich syndrome.

Authors:  H D Ochs
Journal:  Springer Semin Immunopathol       Date:  1998

Review 4.  An update on the use of immunoglobulin for the treatment of immunodeficiency disorders.

Authors:  Stephanie Albin; Charlotte Cunningham-Rundles
Journal:  Immunotherapy       Date:  2014       Impact factor: 4.196

Review 5.  Eosinophilia Associated with Disorders of Immune Deficiency or Immune Dysregulation.

Authors:  Kelli W Williams; Joshua D Milner; Alexandra F Freeman
Journal:  Immunol Allergy Clin North Am       Date:  2015-08       Impact factor: 3.479

Review 6.  Immunogenetics: changing the face of immunodeficiency.

Authors:  A M Jones; H B Gaspar
Journal:  J Clin Pathol       Date:  2000-01       Impact factor: 3.411

7.  Rapid platelet turnover in WASP(-) mice correlates with increased ex vivo phagocytosis of opsonized WASP(-) platelets.

Authors:  Amanda Prislovsky; Bindumadhav Marathe; Amira Hosni; Alyssa L Bolen; Falk Nimmerjahn; Carl W Jackson; Darryl Weiman; Ted S Strom
Journal:  Exp Hematol       Date:  2008-03-17       Impact factor: 3.084

Review 8.  The thrombocytopenia of WAS: a familial form of ITP?

Authors:  Ted S Strom
Journal:  Immunol Res       Date:  2009       Impact factor: 2.829

9.  Antiplatelet antibodies in WASP(-) mice correlate with evidence of increased in vivo platelet consumption.

Authors:  Bindumadhav M Marathe; Amanda Prislovsky; Alexander Astrakhan; David J Rawlings; Jim Y Wan; Ted S Strom
Journal:  Exp Hematol       Date:  2009-09-03       Impact factor: 3.084

Review 10.  Clinical immunology review series: An approach to the management of pulmonary disease in primary antibody deficiency.

Authors:  M D Tarzi; S Grigoriadou; S B Carr; L M Kuitert; H J Longhurst
Journal:  Clin Exp Immunol       Date:  2009-02       Impact factor: 4.330

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