New Approach to Addison Disease: Oral Manifestations Due to Endocrine Dysfunction and Comorbidity Burden

被引:46
作者
Bugala, Narcis Mihaita [1 ]
Carsote, Mara [2 ,3 ]
Stoica, Loredana Elena [4 ]
Albulescu, Dana Maria [5 ]
Tuculina, Mihaela Jana [6 ]
Preda, Smaranda Adelina [6 ]
Boicea, Ancuta-Ramona [7 ]
Alexandru, Dragos Ovidiu [1 ]
机构
[1] Univ Med & Pharm Craiova, Dept Med Informat & Biostat, Fac Med, Craiova 200349, Romania
[2] Carol Davila Univ Med & Pharm, Dept Endocrinol, Bucharest 050474, Romania
[3] CI Parhon Natl Inst Endocrinol, Aviatorilor Ave 34-38, Bucharest 011683, Romania
[4] Univ Med & Pharm Craiova, Fac Med, Dept Dermatol, Craiova 200349, Romania
[5] Univ Med & Pharm Craiova, Fac Med, Dept Anat, Craiova 200349, Romania
[6] Univ Med & Pharm Craiova, Fac Med Dent, Dept Odontol, Craiova 200349, Romania
[7] Univ Med & Pharm Craiova, Fac Med, Dept Occupat Med, Craiova 200349, Romania
关键词
Addison disease; cortisol; adrenal insufficiency; oral; tongue; periodontal disease; pigmentation; candidiasis; ACTH; autoimmune; BETA-CELL FUNCTION; ADRENAL INSUFFICIENCY; PERIODONTAL-DISEASE; DENTAL IMPLANTS; BONE LOSS; AUTOIMMUNE; HYPERPIGMENTATION; CANDIDIASIS; MANAGEMENT; PATIENT;
D O I
10.3390/diagnostics12092080
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This review highlights oral anomalies with major clinical impact in Addison disease (AD), including dental health and dermatologic features, through a dual perspective: pigmentation issues and AD comorbidities with oral manifestations. Affecting 92% of AD patients, cutaneomucosal hyperpigmentation is synchronous with or precedes general manifestations by up to a decade, underlying melanocytic infiltration of the basal epidermal layer; melanophages in the superficial dermis; and, rarely, acanthosis, perivascular lymphocytic infiltrate, and hyperkeratosis. Intraoral pigmentation might be the only sign of AD; thus, early recognition is mandatory, and biopsy is helpful in selected cases. The buccal area is the most affected location; other sites are palatine arches, lips, gums, and tongue. Pigmented oral lesions are patchy or diffuse; mostly asymptomatic; and occasionally accompanied by pain, itchiness, and burn-like lesions. Pigmented lingual patches are isolated or multiple, located on dorsal and lateral areas; fungiform pigmented papillae are also reported in AD individuals. Dermoscopy examination is particularly indicated for fungal etiology; yet, it is not routinely performed. AD's comorbidity burden includes the cluster of autoimmune polyglandular syndrome (APS) type 1 underlying AIRE gene malfunction. Chronic cutaneomucosal candidiasis (CMC), including oral CMC, represents the first sign of APS1 in 70-80% of cases, displaying autoantibodies against interleukin (IL)-17A, IL-17F +/- IL-22, and probably a high mucosal concentration of interferon (IFN)-gamma. CMC is prone to systemic candidiasis, representing a procarcinogenic status due to Th17 cell anomalies. In APS1, the first cause of mortality is infections (24%), followed by oral and esophageal cancers (15%). Autoimmune hypoparathyroidism (HyP) is the earliest endocrine element in APS1; a combination of CMC by the age of 5 years and dental enamel hypoplasia (the most frequent dental complication of pediatric HyP) by the age of 15 is an indication for HyP assessment. Children with HyP might experience short dental roots, enamel opacities, hypodontia, and eruption dysfunctions. Copresence of APS-related type 1 diabetes mellitus (DM) enhances the risk of CMC, as well as periodontal disease (PD). Anemia-related mucosal pallor is related to DM, hypothyroidism, hypogonadism, corresponding gastroenterological diseases (Crohn's disease also presents oral ulceration (OU), mucogingivitis, and a 2-3 times higher risk of PD; Biermer anemia might cause hyperpigmentation by itself), and rheumatologic diseases (lupus induces OU, honey-comb plaques, keratotic plaques, angular cheilitis, buccal petechial lesions, and PD). In more than half of the patients, associated vitiligo involves depigmentation of oral mucosa at different levels (palatal, gingival, alveolar, buccal mucosa, and lips). Celiac disease may manifest xerostomia, dry lips, OU, sialadenitis, recurrent aphthous stomatitis and dental enamel defects in children, a higher prevalence of caries and dentin sensitivity, and gingival bleeding. Oral pigmented lesions might provide a useful index of suspicion for AD in apparently healthy individuals, and thus an adrenocorticotropic hormone (ACTH) stimulation is useful. The spectrum of autoimmune AD comorbidities massively complicates the overall picture of oral manifestations.
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