Year 2022,
Volume: 1 Issue: 1, 24 - 26, 30.12.2022
Mustafa Ercüment Önder
,
Berkan Altay
,
Fethi Atıl
,
Umut Tekin
,
Doruk Koçyiğit
,
Özkan Özgül
References
- 1. Sowerwine KJ, Holland SM, Freeman AF. Hyper-IgE
syndrome update. Ann N Y Acad Sci. 2012;1250:25.
- 2. Davis SD, Schaller J, Wedgwood RJ. Job’s syndrome:
recurrent, “cold”, staphylococcal abscesses. Lancet
1966;1:1013- 15.
- 3. Grimbacher B, Holland SM, Gallin JI, et al: Hyper-IgE
syndrome with recurrent infections—An autosomal
dominant multisystem disorder. N Engl J Med.
1999;340:692.
- 4. DeWitt CA, Bishop AB, Buescher LS, et al:
Hyperimmunoglobulin E syndrome: Two cases and a
review of the literature. J Am Acad Dermatol. 2006;54:855.
5. Freeman AF, Domingo DL, Holland SM. Hyper IgE (Job’s)
syndrome: A primary deficiency with oral manifestations.
Oral Dis. 2009;15:2.
- 6. Donabedian H, Gallin, JI. The hyperimmunoglobulin E
recurrent- infection (Job’s) syndrome: A review of the NIH
experience and the literature. Medicine.1983;62:195.
- 7. Shyur SD, Hill HR: Job’s syndrome of hyperimmunoglobulin
E and recurrent infections, in Lichtenstein LM, Fauci
AS, (eds). Current Therapy in Allergy, Immunology, and
Rheumatology. St Louis, MO: Mosby-Year Book, 1992. p
322
8. O’Connell AC, Puck JM, Grimbacher B, et al. Delayed
eruption of permanent teeth in hyperimmunoglobulinemia
E recurrent infection syndrome. Oral Surg Oral Med Oral
Pathol Oral Radiol Endod. 2000;89:177-85.
- 9. Domingo DL, Freeman AF, Davis J, et al. Novel intraoral
phenotypes in hyperimmunoglobulin E syndrome. Oral
Dis. 2008;14:73-81.
- 10. Mass E, Kaplan I, Hirshberg A. A clinical and
histopathological study of radicular cysts associated with
primary molars. J Oral Pathol Med. 1995; 24(10):458–61
- 11. Shetty S, Angadi PV, Rekha K. Radicular cyst in deciduous
maxillary molars: a rarity. Head Neck Pathol. 2010;4(1):27–
30.
- 12. Nair PN. New perspectives on radicular cysts: do they
heal?. Int Endod J. 1998;31(3):155–60.
- 13. Nagata T, Nomura J, Matsumura Y, Yanase S, Fujii T, Oka
T, et al. Radicular cyst in a deciduous tooth: a case report
and review of literature. J Dent Child. 2008;75:80–4.
- 14. Behrman RE, Kliegman RM, Jenson HB: Nelson Textbook
of Pediatrics. Philadelphia, PA, Saunders, 2000
- 15. Burg FD, Ingelfinger JR, Wald ER, et al. Gellis and Kagan’s
Current Pediatric Therapy. Philadelphia, PA, Saunders,
1999
- 16. Vigliante CE, Costello BJ, Quinn PD. Life-
Threatening Cervicofacial Infection in a Child With
Hyperimmunoglobulin-E Syndrome. J Oral Maxillofac
Surg. 2001;59:561-565
Unusual Radicular Cyst Formation Derived From Primary Teeth in Hyper Immunoglobulin E Syndrome
Year 2022,
Volume: 1 Issue: 1, 24 - 26, 30.12.2022
Mustafa Ercüment Önder
,
Berkan Altay
,
Fethi Atıl
,
Umut Tekin
,
Doruk Koçyiğit
,
Özkan Özgül
Abstract
Introduction
Hyperimmunoglobulin E syndrome (HIES) is a rare genetic based multi-system disorder. It is characterized by high serum
levels of IgE, pulmonary and recurrent skin infection except for these conditions abnormalities of the dentition, bones and
connective tissue could be seen. The etiology of HIES is considered to be dominant-negative alterations in signal transducer
and activator of transcription 3 (STAT3). STAT3 is integral to signal transduction for multiple cytokines. STAT3 is well expressed
across tissue types.
Case Report
In this paper, we report a 7-year-old boy with HIES and a rare clinical manifestation regarding radicular cyst which is related
to the deciduous tooth.
Conclusion
Chronic usage of antibiotics in the HIES patients can cause that sup-pressed serious lesion so that radicular cysts may be
missed. Therefore, dentists should be alert on clinical and radiologic examination.
References
- 1. Sowerwine KJ, Holland SM, Freeman AF. Hyper-IgE
syndrome update. Ann N Y Acad Sci. 2012;1250:25.
- 2. Davis SD, Schaller J, Wedgwood RJ. Job’s syndrome:
recurrent, “cold”, staphylococcal abscesses. Lancet
1966;1:1013- 15.
- 3. Grimbacher B, Holland SM, Gallin JI, et al: Hyper-IgE
syndrome with recurrent infections—An autosomal
dominant multisystem disorder. N Engl J Med.
1999;340:692.
- 4. DeWitt CA, Bishop AB, Buescher LS, et al:
Hyperimmunoglobulin E syndrome: Two cases and a
review of the literature. J Am Acad Dermatol. 2006;54:855.
5. Freeman AF, Domingo DL, Holland SM. Hyper IgE (Job’s)
syndrome: A primary deficiency with oral manifestations.
Oral Dis. 2009;15:2.
- 6. Donabedian H, Gallin, JI. The hyperimmunoglobulin E
recurrent- infection (Job’s) syndrome: A review of the NIH
experience and the literature. Medicine.1983;62:195.
- 7. Shyur SD, Hill HR: Job’s syndrome of hyperimmunoglobulin
E and recurrent infections, in Lichtenstein LM, Fauci
AS, (eds). Current Therapy in Allergy, Immunology, and
Rheumatology. St Louis, MO: Mosby-Year Book, 1992. p
322
8. O’Connell AC, Puck JM, Grimbacher B, et al. Delayed
eruption of permanent teeth in hyperimmunoglobulinemia
E recurrent infection syndrome. Oral Surg Oral Med Oral
Pathol Oral Radiol Endod. 2000;89:177-85.
- 9. Domingo DL, Freeman AF, Davis J, et al. Novel intraoral
phenotypes in hyperimmunoglobulin E syndrome. Oral
Dis. 2008;14:73-81.
- 10. Mass E, Kaplan I, Hirshberg A. A clinical and
histopathological study of radicular cysts associated with
primary molars. J Oral Pathol Med. 1995; 24(10):458–61
- 11. Shetty S, Angadi PV, Rekha K. Radicular cyst in deciduous
maxillary molars: a rarity. Head Neck Pathol. 2010;4(1):27–
30.
- 12. Nair PN. New perspectives on radicular cysts: do they
heal?. Int Endod J. 1998;31(3):155–60.
- 13. Nagata T, Nomura J, Matsumura Y, Yanase S, Fujii T, Oka
T, et al. Radicular cyst in a deciduous tooth: a case report
and review of literature. J Dent Child. 2008;75:80–4.
- 14. Behrman RE, Kliegman RM, Jenson HB: Nelson Textbook
of Pediatrics. Philadelphia, PA, Saunders, 2000
- 15. Burg FD, Ingelfinger JR, Wald ER, et al. Gellis and Kagan’s
Current Pediatric Therapy. Philadelphia, PA, Saunders,
1999
- 16. Vigliante CE, Costello BJ, Quinn PD. Life-
Threatening Cervicofacial Infection in a Child With
Hyperimmunoglobulin-E Syndrome. J Oral Maxillofac
Surg. 2001;59:561-565