Dergiler / Turkish Journal of Gastroenterology / 2019 / Cilt: 30 - Sayı: 9

Gastrointestinal findings in 26 adults with common variable immunodeficiency: The fickle nature of the disease manifests in gastrointestinal biopsies

Sayfa
789–800
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The association betweenduodenal NLH and eosinophil infiltration deserves further investigation.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Background/Aims: The aim of the present study was to demonstrate the histopathological findings in gastrointestinal (GI) biopsies inadults with common variable immunodeficiency (CVID).Materials and Methods: A total of 172 GI biopsies of 26 patients with CVID obtained over a 16-year period were reevaluated.
📊
Temel Bulgular & Veri:Findingswere analyzed using descriptive analyzes and χ2 test.Results: Female-to-male ratio was 1.36.
💡
Sonuç & Katkı:The association betweenduodenal NLH and eosinophil infiltration deserves further investigation.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Background/Aims: The aim of the present study was to demonstrate the histopathological findings in gastrointestinal (GI) biopsies inadults with common variable immunodeficiency (CVID).Materials and Methods: A total of 172 GI biopsies of 26 patients with CVID obtained over a 16-year period were reevaluated. Findingswere analyzed using descriptive analyzes and χ2 test.Results: Female-to-male ratio was 1.36. The median age at diagnosis was 36±13.94 (16-72) years. Chronic esophagitis was noted in 3patients. The absence of plasma cells in the stomach, duodenum, and colon was observed in 16, 14, and 9 patients, respectively. Divergent results for the presence of plasma cells in concurrent stomach and duodenum samples were found in 11 (44%) patients. Nodularlymphoid hyperplasia (NLH) was notable in the duodenum (56%). The mean number of eosinophils in one high-power field was significantly higher in duodenal biopsies with NLH (27.21 vs. 14.37, p=0.002). Active inflammation was more prominent in the colon (91%) thanin the stomach (65%) and duodenum (60%). Helicobacter pylori infection was found in 57.6%, including a case with persistent infectionby the coccoid form. Celiac-like villous blunting and increased intraepithelial lymphocytes were seen in 40% and 24%, respectively. Inaddition, 23% had giardiasis associated with acute duodenitis and duodenal NLH (p<0.05).Conclusion: CVID gastroenteropathy is a challenging entity, and due to the heterogeneity in the presence and distribution of plasmacells throughout the GI tract and diverse disease course, multiple concurrent biopsies may be needed for tissue diagnosis. Duodenal CVIDmay present with villous alterations and giardiasis, and NLH appears to be an important clue in the duodenum. The association betweenduodenal NLH and eosinophil infiltration deserves further investigation.

🔖

Bu Makaleye Atıf Yap

PEHLİVANOĞLU, B., ARDENİZ, Ö., HASSOY, H., SEZAK, M., ÖZDEMİR, H., ÜNAL, N. G., ONAY, H., DOĞANAVŞARGİL, B. (2019). Gastrointestinal findings in 26 adults with common variable immunodeficiency: The fickle nature of the disease manifests in gastrointestinal biopsies. Turkish Journal of Gastroenterology, Cilt: 30 - Sayı: 9, 789–800. https://ajindex.com/articles/409265

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (12)

  1. Al-Herz W, Bousfiha A, Casanova JL, et al. Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency. Front Immunol 2014
  2. [CrossRef] 2. Notarangelo LD, Fischer A, Geha RS, et al. Primary immunodeficiencies: 2009 update. J Allergy Clin Immunol 2009
  3. [CrossRef] 3. Unger S, Seidl M, Schmitt-Graeff A, et al. Ill-defined germinal centers and severely reduced plasma cells are histological hallmarks of lymphadenopathy in patients with common variable immunodeficiency. J Clin Immunol 2014
  4. [CrossRef] 4. van Schouwenburg PA, Davenport EE, Kienzler AK, et al. Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders. Clin Immunol 2015
  5. [CrossRef] 5. Baldovino S, Montin D, Martino S, Sciascia S, Menegatti E, Roccatello D. Common variable immunodeficiency: crossroads between infections, inflammation and autoimmunity. Autoimmun Rev 2013
  6. [CrossRef] 6. Poodt AE, Driessen GJ, de Klein A, van Dongen JJ, van der Burg M, de Vries E. TACI mutations and disease susceptibility in patients with common variable immunodeficiency. Clin Exp Immunol 2009
  7. [CrossRef] 7. Khodadad A, Aghamohammadi A, Parvaneh N, et al. Gastrointestinal manifestations in patients with common variable immunodeficiency. Digest Dis Sci 2007
  8. [CrossRef] 8. Jorgensen SF, Reims HM, Frydenlund D, et al. A Cross-Sectional Study of the Prevalence of Gastrointestinal Symptoms and Pathology in Patients with Common Variable Immunodeficiency. Am J Gastroenterol 2016
  9. [CrossRef] 9. Zullo A, Romiti A, Rinaldi V, et al. Gastric pathology in patients with common variable immunodeficiency. Gut 1999
  10. [CrossRef] 10. Daniels JA, Lederman HM, Maitra A, Montgomery EA. Gastrointestinal tract pathology in patients with common variable immunodeficiency (CVID): a clinicopathologic study and review. Am J Surg Pathol 2007
  11. [CrossRef] 11. Conley ME, Notarangelo LD, Etzioni A. Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies). Clin Immunol 1999
  12. [CrossRef] 12. Malamut G, Verkarre V, Suarez F, et al. The enteropathy associated with common variable immunodeficiency: the delineated frontiers with celiac disease.