MANIFESTATIONS OF PRIMARY IMMUNODEFICIENTS IN THE REGION OF THE MOUTH AND THE MAXIMUM-FACE REGION

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Abstract

The aim of the work was to describe the nature of various orofascial manifestations of primary immunodeficiency in patients in the register of the Sverdlovsk Region in comparison with data from literature sources. As a result of the study, it was possible to trace the significant correspondence of the detected pathological manifestations with identical PID groups. The most common signs can be called retention of baby teeth, candidiasis of the oral mucosa, angular cheilitis, multiple caries in combination with manifestations of primary immunodeficiency in other organs and systems.

About the authors

M. A. Dolgikh

Institute of Immunology and Physiology, Ural Branch, Russian Academy of Sciences

Author for correspondence.
Email: noemail@neicon.ru
Russian Federation

I. A. Tuzankina

Institute of Immunology and Physiology, Ural Branch, Russian Academy of Sciences; Regional Children Clinical Hospital

Email: noemail@neicon.ru
Russian Federation

N. G. Sarkisyan

Institute of Immunology and Physiology, Ural Branch, Russian Academy of Sciences; Urals State Medical University

Email: noemail@neicon.ru
Russian Federation

N. A. Ovsepyan

Institute of Immunology and Physiology, Ural Branch, Russian Academy of Sciences

Email: noemail@neicon.ru
Russian Federation

M. A. Bolkov

Institute of Immunology and Physiology, Ural Branch, Russian Academy of Sciences

Email: noemail@neicon.ru
Russian Federation

References

  1. https://esid.org/Education/Documents-Reports
  2. Nikfarjam J, et al. Oral manifestations in selective IgA deficiency. Int. J. Dent. Hyg. 2004, 2 (1), 19-25.
  3. Porter S. R., et al. Orofacial manifestations in primary immunodeficiencies: common variable immunodeficiencies. J. Oral. Pathol. Med. 1993, 22 (4), 157-8.
  4. Porter S. R., et al. Orofacial manifestations in primary immunodeficiencies involving IgA deficiency. J Oral Pathol Med. 1993, 22 (3), 117-9.
  5. Ildiko Tar, Csongor Kiss, Laszlo Marodi, Ildiko J. Marton. Oral and dental conditions of children with selective IgA deficiency. Pediatric allergy and immunology 2008, 19 (1), 33-6.
  6. Wu J., Chen J., Tian Z. Q., Zhang H., Gong R. L., et al. Clinical Manifestations and Genetic Analysis of 17 Patients with Autosomal Dominant Hyper-IgE Syndrome in Mainland China: New Reports and a Literature Review. J. Clin. Immunol. 2017, 37 (2), 166-179.
  7. Alexandra F. Freeman, Steven M. Holland. Clinical Manifestations, Etiology, and Pathogenesis of the Hyper-IgE Syndromes. Pediatr. Res. 2009, 65 (5 Pt 2), 32R-37R.
  8. Kofoed E. M., Hwa V., Little B., Woods K. A., Buckway C. K., et al. Growth hormone insensitivity associated with a STAT5b muta- tion. N. Engl. J. Med. 2003, 349(12), 1139-1147.
  9. Sullivan K. E., Mullen C. A., Blaese R. M., Winkelstein J. A. A multiin- stitutional survey of the Wiskott-Aldrich syndrome. J. Pediatr. 1994, 125 (6 Pt 1), 876-885.
  10. Peacock M. E., et al. Periodontal and other oral manifestations of immunodeficiency diseases. 2016 John Wiley & Sons A/S. Published by John Wiley & Sons.
  11. Miranda Muhvic-Urek, Marija Tomac-Stojmenovic, and Brankica MijandrusiC-SinciC.Oral pathology in inflammatory bowel disease. World J. Gastroenterol. 2016, 22 (25), 5655-5667.
  12. Paraskevi V. Voulgari Rheumatological manifestations in inflammatory bowel disease. Annals of Gastroenterology 2011,24,173-180.
  13. Lindor N. M., Arsenault T. M., Solomon H., Seidman C. E., McEvoy MT. A new autosomal dominant disorder of pyogenic sterile arthritis, pyoderma gan-grenosum, and acne: PAPA syndrome. Mayo Clin. Proc. 1997, 72, 611-615.
  14. Jabs D. A., Houk J. L., Bias W. B., Arnett F. C. Familial granulomatous synovitis, uveitis, and cranial neuropathies. Am. J. Med. 1985, 78(5), 801-804.
  15. Atkinson J. C., et al. Oral manifestations and dental management of patients with hereditary angioede-ma. J. Oral. Pathol. Med. 1991, 20 (3), 139-142.
  16. Porter S. R., et al. Orofacial manifestations in primary immunodeficiencies: polymorphonuclear leukocyte defects. J. Oral. Pathol. Med. 1993, 22 (7), 310-311.
  17. Uzel G., Sampaio E.P., Lawrence M.G., Hsu A.P, Hackett M., Dorsey M.J., et al. Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation polyendocrinopathy enteropathy X-linked-like syndrome. J Allergy Clin Immunol. 2013, 131(6), 1611, 23.e3.
  18. Neufeld M., Maclaren N.K., Blizzard R.M. Two types of autoimmune Addison's disease associated with different polyglandular autoim- mune (PGA) syndromes. Medicine (Baltimore) 1981, 60 (5), 355-362.
  19. Musemma Karabel. A Rare Cause of Recurrent Oral Lesions: Chediak-Higashi Syndrome Turk. J. Haematol. 2014, 31(3), 313-314.
  20. Sharfe N.,Dadi H. K.,Shahar M.,Roifman C. M. Human immune disorder arising from mutation of the alpha chain of the interleukin-2 receptor. Proc. Natl. Acad. Sci. 1997, 94 (7), 3168-3171.
  21. Prentice A. G. Oral and gastrointestinal candidosis: prophylaxis during immunosuppressive therapy. Mycoses 1989, 32 (Suppl. l), 42-46.

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Copyright (c) 2017 Dolgikh M.A., Tuzankina I.A., Sarkisyan N.G., Ovsepyan N.A., Bolkov M.A.

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