Oral Diseases as a Manifestation of Inborn Errors of Immunity

被引:0
作者
Napiorkowska-Baran, Katarzyna [1 ]
Darwish, Samira [2 ]
Kaczor, Justyna [2 ]
Treichel, Pawel [2 ]
Szymczak, Bartlomiej [2 ]
Szota, Maciej [2 ]
Koperska, Kinga [2 ]
Bartuzi, Zbigniew [1 ]
机构
[1] Nicolaus Copernicus Univ Torun, Dept Allergol Clin Immunol & Internal Dis, Coll Med Bydgoszcz, PL-85067 Bydgoszcz, Poland
[2] Nicolaus Copernicus Univ Torun, Dept Allergol Clin Immunol & Internal Dis, Coll Med Bydgoszcz, Student Res Club Clin Immunol, PL-85067 Bydgoszcz, Poland
关键词
inborn errors of immunity; primary immunodeficiencies; immune defects; oral infection; oral diseases; oral pathology; FAMILIAL MEDITERRANEAN FEVER; PAPILLON-LEFEVRE-SYNDROME; ANTIBIOTIC-PROPHYLAXIS; DEFICIENCY; DIAGNOSIS; COMPLEMENT; IMMUNODEFICIENCY; PATHOGENESIS; INFECTIONS; CHILDREN;
D O I
10.3390/jcm13175079
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Oral findings such as inflammation, ulcerations, or lesions can indicate serious systemic diseases and should prompt suspicion of acquired chronic conditions or inborn errors of immunity (IEIs). Currently, there are approximately 500 disease entities classified as IEIs, with the list expanding annually. The awareness of the existence of such conditions is of paramount importance, as patients with these disorders frequently necessitate the utilization of enhanced diagnostic techniques. This is exemplified by patients with impaired antibody production, in whom conventional serological methods may prove to be undiagnostic. Patients with IEI may require distinct therapeutic approaches or antimicrobial prophylaxis throughout their lives. An accurate diagnosis and, more importantly, early identification of patients with immune deficiencies is crucial to ensure the quality and longevity of their lives. It is important to note that the failure to establish a proper diagnosis or to provide adequate treatment could also have legal implications for medical professionals. The article presents IEIs, which may manifest in the oral cavity, and their diagnosis alongside therapeutic procedures.
引用
收藏
页数:34
相关论文
共 203 条
[31]   Cherubism: a systematic literature review of clinical and molecular aspects [J].
Chrcanovic, B. R. ;
Guimara, L. M. ;
Gomes, C. C. ;
Gomez, R. S. .
INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2021, 50 (01) :43-53
[32]   Complement, infection, and autoimmunity [J].
Conigliaro, Paola ;
Triggianese, Paola ;
Ballanti, Eleonora ;
Perricone, Carlo ;
Perricone, Roberto ;
Chimenti, Maria Sole .
CURRENT OPINION IN RHEUMATOLOGY, 2019, 31 (05) :532-541
[33]  
COPPER MP, 1995, ARCH OTOLARYNGOL, V121, P157
[34]   Inherited CARD9 Deficiency: Invasive Disease Caused by Ascomycete Fungi in Previously Healthy Children and Adults [J].
Corvilain, Emilie ;
Casanova, Jean-Laurent ;
Puel, Anne .
JOURNAL OF CLINICAL IMMUNOLOGY, 2018, 38 (06) :656-693
[35]   Cyclic neutropenia [J].
Dale, DC ;
Bolyard, AA ;
Aprikyan, A .
SEMINARS IN HEMATOLOGY, 2002, 39 (02) :89-94
[36]   Orofacial findings in chronic granulomatous disease: Report of twelve patients and review of the literature [J].
Dar-Odeh N.S. ;
Hayajneh W.A. ;
Abu-Hammad O.A. ;
Hammad H.M. ;
Al-Wahadneh A.M. ;
Bulos N.K. ;
Mahafzah A.M. ;
Shomaf M.S. ;
El-Maaytah M.A. ;
Bakri F.G. .
BMC Research Notes, 3 (1)
[37]   Oral manifestations of Chediak-Higashi syndrome: A systematic review [J].
de Arruda, Jose Alcides Almeida ;
Sousa-Neto, Sebastiao Silverio ;
Abreu, Lucas Guimaraes ;
Schuch, Lauren Frenzel ;
Souza, Vinicius Gomes ;
Alves, Thainara Vitoria Lima ;
Martins-Andrade, Barbara ;
Shetty, Sameep S. ;
Monteiro, Joao Luiz Gomes Carneiro ;
Mendonca, Elismauro Francisco ;
Mesquita, Ricardo Alves ;
Callou, Gerhilde .
DM DISEASE-A-MONTH, 2023, 69 (01)
[38]  
Dinauer MC, 2014, METHODS MOL BIOL, V1124, P501, DOI 10.1007/978-1-62703-845-4_30
[39]   Oral manifestations of primary immunodeficiencies [J].
Dolgikh, M. A. ;
Bolkov, M. A. ;
Tuzankina, I. A. ;
Sarkisyan, N. G. ;
Hovsepyan, N. A. .
BYULLETEN SIBIRSKOY MEDITSINY, 2019, 18 (03) :144-154
[40]  
Dunn CP, 1993, GeneReviews