Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case Report
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, d...
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| Format: | Article |
| Language: | English |
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Wiley
2017-01-01
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| Series: | Case Reports in Medicine |
| Online Access: | http://dx.doi.org/10.1155/2017/6206085 |
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| _version_ | 1832550325564735488 |
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| author | Irfan Ali Shera Sheikh Mudassir Khurshid Mohd Shafi Bhat |
| author_facet | Irfan Ali Shera Sheikh Mudassir Khurshid Mohd Shafi Bhat |
| author_sort | Irfan Ali Shera |
| collection | DOAJ |
| description | 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. |
| format | Article |
| id | doaj-art-08463943c7104d90a20c2e8e7db4d7f0 |
| institution | Kabale University |
| issn | 1687-9627 1687-9635 |
| language | English |
| publishDate | 2017-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Case Reports in Medicine |
| spelling | doaj-art-08463943c7104d90a20c2e8e7db4d7f02025-02-03T06:07:01ZengWileyCase Reports in Medicine1687-96271687-96352017-01-01201710.1155/2017/62060856206085Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case ReportIrfan Ali Shera0Sheikh Mudassir Khurshid1Mohd Shafi Bhat2Department of Gastroenterology, Max Super Speciality Hospital, Saket, New Delhi 110 007, IndiaDepartment of General Surgery, Fortis Hospital, Mohali, Punjab 160 062, IndiaDepartment of Sports Medicine, Safdarjung Hospital, New Delhi, IndiaAgammaglobulinemia 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.http://dx.doi.org/10.1155/2017/6206085 |
| spellingShingle | Irfan Ali Shera Sheikh Mudassir Khurshid Mohd Shafi Bhat Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case Report Case Reports in Medicine |
| title | Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case Report |
| title_full | Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case Report |
| title_fullStr | Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case Report |
| title_full_unstemmed | Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case Report |
| title_short | Inflammatory Duodenal Polyposis Associated with Primary Immunodeficiency Disease: A Novel Case Report |
| title_sort | inflammatory duodenal polyposis associated with primary immunodeficiency disease a novel case report |
| url | http://dx.doi.org/10.1155/2017/6206085 |
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