Literature DB >> 26318181

Profound Reversible Hypogammaglobulinemia Caused by Celiac Disease in the Absence of Protein Losing Enteropathy.

Rohan Ameratunga1,2, Russell William Barker3, Richard Henderson Steele3, Maneka Deo4, See-Tarn Woon3, Mee Ling Yeong5, Wikke Koopmans3.   

Abstract

When patients with hypogammaglobulinemia are encountered, a vigorous search should be undertaken for secondary treatable causes. Here we describe the first case of a patient with severe asymptomatic hypogammaglobulinemia where the underlying cause was undiagnosed celiac disease. A strict gluten free diet resulted in resolution of her mild long-standing abdominal symptoms and correction of her hypogammaglobulinemia. There was corresponding improvement in her duodenal histology and normalisation of her celiac serology. Protein losing enteropathy was unlikely to have been the mechanism of her profound hypogammaglobulinemia, as her albumin was within the normal range and she had a normal fecal alpha 1 antitrypsin level. Application of the Ameratunga et al. (2013) diagnostic criteria was helpful in confirming this patient did not have Common Variable Immunodeficiency Disorder (CVID). Celiac disease must now be considered in the differential diagnosis of severe hypogammaglobulinemia. There should be a low threshold for undertaking celiac serology in patients with hypogammaglobulinemia, even if they have minimal symptoms attributable to gut disease.

Entities:  

Keywords:  CVID; Celiac disease; hypogammaglobulinemia

Mesh:

Substances:

Year:  2015        PMID: 26318181     DOI: 10.1007/s10875-015-0189-6

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  39 in total

1.  Characterization of immunologic defects in patients with common variable immunodeficiency (CVID) with intestinal disease.

Authors:  Shradha Agarwal; Paul Smereka; Noam Harpaz; Charlotte Cunningham-Rundles; Lloyd Mayer
Journal:  Inflamm Bowel Dis       Date:  2011-01       Impact factor: 5.325

2.  New diagnostic criteria for CVID.

Authors:  Rohan Ameratunga; See-Tarn Woon; David Gillis; Wikke Koopmans; Richard Steele
Journal:  Expert Rev Clin Immunol       Date:  2014-02       Impact factor: 4.473

3.  Lymphocytic interstitial pneumonia of common variable immunodeficiency.

Authors:  V Popa
Journal:  Ann Allergy       Date:  1988-03

Review 4.  New diagnostic criteria for common variable immune deficiency (CVID), which may assist with decisions to treat with intravenous or subcutaneous immunoglobulin.

Authors:  R Ameratunga; S-T Woon; D Gillis; W Koopmans; R Steele
Journal:  Clin Exp Immunol       Date:  2013-11       Impact factor: 4.330

5.  The simultaneous presentation of sarcoidosis and common variable immune deficiency.

Authors:  R Ameratunga; D M Becroft; W Hunter
Journal:  Pathology       Date:  2000-11       Impact factor: 5.306

6.  The enteropathy associated with common variable immunodeficiency: the delineated frontiers with celiac disease.

Authors:  Georgia Malamut; Virginie Verkarre; Felipe Suarez; Jean-François Viallard; Anne-Sophie Lascaux; Jacques Cosnes; Yoram Bouhnik; Olivier Lambotte; Dominique Béchade; Marianne Ziol; Anne Lavergne; Olivier Hermine; Nadine Cerf-Bensussan; Christophe Cellier
Journal:  Am J Gastroenterol       Date:  2010-06-15       Impact factor: 10.864

7.  Immunological and clinical profile of adult patients with selective immunoglobulin subclass deficiency: response to intravenous immunoglobulin therapy.

Authors:  F Abrahamian; S Agrawal; S Gupta
Journal:  Clin Exp Immunol       Date:  2009-12-14       Impact factor: 4.330

8.  Prevalence of celiac disease in Egyptian children disputes the east-west agriculture-dependent spread of the disease.

Authors:  M Abu-Zekry; D Kryszak; M Diab; C Catassi; A Fasano
Journal:  J Pediatr Gastroenterol Nutr       Date:  2008-08       Impact factor: 2.839

Review 9.  Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions.

Authors:  Helen Chapel; Charlotte Cunningham-Rundles
Journal:  Br J Haematol       Date:  2009-03-30       Impact factor: 6.998

Review 10.  Comparison of diagnostic criteria for common variable immunodeficiency disorder.

Authors:  Rohan Ameratunga; Maia Brewerton; Charlotte Slade; Anthony Jordan; David Gillis; Richard Steele; Wikke Koopmans; See-Tarn Woon
Journal:  Front Immunol       Date:  2014-09-15       Impact factor: 7.561

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  4 in total

Review 1.  Review: Diagnosing Common Variable Immunodeficiency Disorder in the Era of Genome Sequencing.

Authors:  Rohan Ameratunga; Klaus Lehnert; See-Tarn Woon; David Gillis; Vanessa L Bryant; Charlotte A Slade; Richard Steele
Journal:  Clin Rev Allergy Immunol       Date:  2018-04       Impact factor: 8.667

2.  Bronchiectasis is associated with delayed diagnosis and adverse outcomes in the New Zealand Common Variable Immunodeficiency Disorders cohort study.

Authors:  R Ameratunga; A Jordan; A Cavadino; S Ameratunga; T Hills; R Steele; M Hurst; B McGettigan; I Chua; M Brewerton; N Kennedy; W Koopmans; Y Ahn; R Barker; C Allan; P Storey; C Slade; A Baker; L Huang; S-T Woon
Journal:  Clin Exp Immunol       Date:  2021-04-12       Impact factor: 5.732

3.  The Natural History of Untreated Primary Hypogammaglobulinemia in Adults: Implications for the Diagnosis and Treatment of Common Variable Immunodeficiency Disorders (CVID).

Authors:  Rohan Ameratunga; Yeri Ahn; Richard Steele; See-Tarn Woon
Journal:  Front Immunol       Date:  2019-07-17       Impact factor: 7.561

4.  All Patients With Common Variable Immunodeficiency Disorders (CVID) Should Be Routinely Offered Diagnostic Genetic Testing.

Authors:  Rohan Ameratunga; Klaus Lehnert; See-Tarn Woon
Journal:  Front Immunol       Date:  2019-11-22       Impact factor: 7.561

  4 in total

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