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Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case Report
Joint Authors
Shera, Irfan Ali
Khurshid, Sheikh Mudassir
Bhat, Mohd Shafi
Source
Issue
Vol. 2017, Issue 2017 (31 Dec. 2017), pp.1-3, 3 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2017-01-10
Country of Publication
Egypt
No. of Pages
3
Main Subjects
Abstract EN
Agammaglobulinemia is a rare form of B-cell primary immunodeficiency disease characterized by reduced levels of IgG, IgA, or IgM and recurrent bacterial infections.
Agammaglobulinemia is most commonly associated with diffuse nodular lymphoid hyperplasia.
Duodenal polyps are a rare entity; however, due to wide use of esophagogastroduodenoscopy, incidental diagnosis of duodenal polyps appears to be increasing.
Although inflammatory duodenal polyposis has been reported in the literature, its association with common variable immunodeficiency has not been reported till date to the best of our knowledge.
We report a case of a 59-year-old male with chronic symptoms of agammaglobulinemia associated with inflammatory duodenal polyposis.
American Psychological Association (APA)
Shera, Irfan Ali& Khurshid, Sheikh Mudassir& Bhat, Mohd Shafi. 2017. Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case Report. Case Reports in Medicine،Vol. 2017, no. 2017, pp.1-3.
https://search.emarefa.net/detail/BIM-1146817
Modern Language Association (MLA)
Shera, Irfan Ali…[et al.]. Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case Report. Case Reports in Medicine No. 2017 (2017), pp.1-3.
https://search.emarefa.net/detail/BIM-1146817
American Medical Association (AMA)
Shera, Irfan Ali& Khurshid, Sheikh Mudassir& Bhat, Mohd Shafi. Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case Report. Case Reports in Medicine. 2017. Vol. 2017, no. 2017, pp.1-3.
https://search.emarefa.net/detail/BIM-1146817
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1146817