Oral manifestations of systemic disease

S. R. Porter,1 V. Mercadente2 and S. Fedele3 provide a succinct review of oral mucosal and salivary gland disorders that may arise as a consequence of systemic disease.

While the majority of disorders of the mouth are centred upon the direct action of plaque, the oral tissues can be subject to change or damage as a consequence of disease that predominantly affects other body systems. Such oral manifestations of systemic disease can be highly variable in both frequency and presentation. As lifespan increases and medical care becomes ever more complex I and effective it is likely that the numbers of individuals with I oral manifestations of systemic disease will continue to rise. I This article provides a succinct review of oral manifestations I of systemic disease. It focuses upon oral mucosal and salivary I gland disorders that may arise as a consequence of systemic disease.

Credit: ©corbac40/iStock/Getty Images Plus

Disorders of almost any body system can adversely impact upon the mouth. Oral manifestations may be: 1) the first, only or most severe feature of systemic disease; 2) the principle focus of therapy; and/or 3) the dominant cause of a lessening of the affected person's quality of life. The oral features that an oral healthcare provider may witness will often be dependent upon the nature of their clinical practice. For example, specialists of paediatric dentistry and orthodontics are likely to encounter the oral features of patients with congenital disease while those specialties allied to disease of adulthood may see manifestations of infectious, immunologically- mediated or malignant disease. The present article aims to provide a succinct review of the oral manifestations of systemic disease of patients likely to attend oral medicine services. The review will focus upon disorders affecting the oral mucosa and salivary glands - as these are tissues of greatest interest to practitioners of oral medicine. Although systemic disease relevant to oral medicine can impact upon the teeth and periodontal tissues or cause altered orofacial sensory or motor function these fall out of the scope of the present review.

Oral mucosal manifestations

The oral mucosa is perhaps the most likely oral tissue to be compromised by acquired systemic disease. The following sections will focus upon ulceration and white lesions of the oral mucosa - as these are the most likely abnormal signs that will be observed by oral healthcare providers.

Oral ulceration

A plethora of local and systemic disorders can give rise to ulceration of the oral mucosa (Table 1).

Table 1 Systemic causes of oral mucosal or gingival ulceration

Solitary ulcers

Longstanding solitary oral mucosal ulceration should always initially be considered to reflect repeated local trauma or malignancy (usually oral squamous cell carcinoma [OSCC; Fig. 1]). Of course many other disorders that give rise to oral ulceration may initially manifest as single ulcers but over time they evolve into more extensive disease. Local oral mucosal trauma in relation to systemic disease can arise as a consequence of physical, for example, movement disorders,1 or chemical causes, for example, the now rare instances of placing acidic aspirin at sites of oral pain, and the very rare examples of deliberate self-harm by swallowing caustic agents.2

Figure 1
figure1

Oral squamous cell carcinoma - probably one of the most significant causes of solitary ulceratin of the oral mucosa

Other rare causes of traumatic ulceration could be due to reduced pain and/or touch sensation as might occur in trigeminal neuropathy secondary to metastatic deposits in the mandible or less commonly maxilla, multiple sclerosis, connective tissue disease (for example, scleroderma), diabetes mellitus or drug therapy (for example, with anti-malarials and some chemotherapy regimens). In most instances of suspected traumatic ulceration there will be an identifiable local and/or systemic cause, the ulcers will not be causing notable tissue destruction and the surrounding oral mucosa will be normal in appearance.

Malignancy of the mouth is typically OSCC related to lifestyle factors (tobacco, alcohol, some betal nut preparations and Human papillomavirus oncogenic types),3 however, rare congenital disorders such as dyskeratosis congenita,4 Fanconi anaemia,5 as well as the acquired diseases oral lichen planus,6 possibly scleroderma7 and syphilis8 are risk factors for the development of this malignancy. In contrast to traumatic ulceration OSCC does not have any identifiable local cause, may cause local destruction and have abnormal surrounding mucosa (eg speckling). Oral squamous cell carcinoma, and indeed most malignancies of the mouth, may just appear plain odd.

Other malignancies related to systemic disease include several types of non-Hodgkin's lymphoma (NHL) and Kaposi's sarcoma (KS). Non-Hodgkin's lymphoma usually presents as a mass or area of destructive ulceration of the pharynx, palate or gingivae, sometimes being driven by a background of immunodeficiency (for example, HIV disease, iatrogenic immunosuppression).9 Some types of oral NHL are almost specific for certain situations, for example, plasmablastic lymphoma tends to be associated with HIV disease,10,11 or may arise without obvious underlying cause, for example, Natural Killer T cel lymphoma (NKTCL).12 Oral KS tends to arise on the palate and/or gingivae, is blue, red or purple and does not blanche with local pressure. Prior to the advent of anti-retroviral therapy (ART) KS was the most common oral malignancy of HIV disease, but as the numbers of patients receiving this therapy have climbed there has been a substantial fall in the prevalence of this oral tumour.13 Nevertheless, oral KS can be the first clinical manifestation of unknown (and advanced) HIV disease and can arise in patients receiving long-term immunosuppressive therapy. Metastatic disease generally does not give rise to ulcers of the mouth, although as noted above can manifest within the mandible as a swelling and/ or paraesthesia/anaesthesia.14

Other rare causes of solitary ulceration of possible systemic origin include syphilis (eg tertiary disease), primary or secondary infection of Mycobacteria tuberculosis or mycobacteria other than tuberculosis (MOTT)15,16 and systemic mycoses (eg mucormycosis, aspergillosis, histoplasmosis and paracoccidiodomycosis).17 Solitary ulceration secondary to neutropenias are also possible, although extensive ulceration might be more likely than single ulcers.18

Multiple ulcers

Recurrent aphthous stomatitis is the most common cause of multiple superficial ovoid ulcers of the oral mucosa,19 but this is characterised by the patients being otherwise well (Fig. 2). The multisystem inflammatory disorder Behcet's disease (BD) gives rise to near identical oral ulcers as RAS but also comprises genital ulceration, uveitis, erythema nodosum and other cutaneous features, as well as a plethora of other gastrointestinal, urogenital, neural, musculoskeletal, cutaneous and vascular features.20 The uncommon autoinflammatory syndrome of periodic fever, aphthous ulceration pharyngitis and adenitis (PFAPA) that usually arises in pre-pubertal children gives rise to episodes of superficial aphthous-like ulceration. Unlike RAS this disorder tends to spontaneously remit in the teenage years.21 Other autoinflammatory diseases (that is, periodic fevers) such as familial Mediterranean fever (FMF) may also sometimes give rise to superficial oral ulceration.22

Figure 2
figure2

Recurrent aphthous stomatitis - episodic superficial oral mucosal ulceration in otherwise well children and adults

Ulceration similar to RAS, but without the same periodicity, can be a feature of anaemia of almost any cause. An important diagnostic rule is to always investigate for anaemia as being the cause of sudden onset superficial ulceration in an adult who does not have a history of RAS and has no signs of common bullous disease (see later in article).23

Several mucocutaneous disorders give rise to multiple areas of oral ulceration, lichen planus being without doubt the most common to do so. The ulceration of oral LP (OLP) is usually bilateral, has a background of different white patches and arises bilaterally on the buccal, lingual and/or gingival surfaces. Up to 40% of patients with OLP will also have cutaneous or other mucosal features of LP.24,25 Lichen planus usually arises without identifiable cause although may rarely be secondary to medication - for example, β blockers, sulphonylureas, some anti-malarials (eg, hydroxychloroquine for the management of lupus disease) and a spectrum of other agents - when disease is termed lichenoid drug reaction (LDR), or is a manifestation of graft versus host disease (GvHD).24 Associations between LP and HCV disease are tenuous. Regardless of any association with systemic disorders or therapy, OLP-like disease is considered potentially malignant, this cancer risk being independent of known causative factors of OSCC or therapy of OLP.6 Lupus disease (for example, discoid and systemic) may give rise to oral mucosal and/or gingival features similar to those of OLP, although lesions of lupus may not be bilateral and may be more likely to affect the palate than OLP. Sun-ray pattern lesions that comprise a central area of erosion or ulceration from which white linear areas radiate have been described on the oral mucosa of patients with lupus disease.26,27

The pemphigoid group of immunobullous disorders can give rise to bullae and/or ulceration of the palatal, buccal or lingual surfaces.28 Desquamative gingivitis is common.29 Intact blood or fluid-filled bullae may be observed in patients with pemphigoid disease as the immune-mediated attack is targeting antigens of the basement membrane zone (BMZ).30 Depending upon the type of pemphigoid, patients may have blistering and/or ulceration of other mucocutaneous sites with oral involvement being most likely with mucous membrane pemphigoid.31 The IgA dermatoses (for example, dermatitis herpetiformis [DH; often associated with gluten sensitive enteropathy] and linear IgA disease) can give rise to oral features similar to those of pemphigoid.3235 Dapsone, often employed for the treatment of DH (and sometimes for pemphigoid) may rarely cause blue discolouration of the tongue secondary to methaemoglobinaemia.

The pemphigus group, in particular pemphigus vulgaris (PV), characterised by the generation of a series of anti-epithelial antibodies, gives rise to highly superficial ragged-bordered ulcers of the palatal, lingual and buccal mucosa as well as desquamative gingivitis (Fig. 3). The mouth is the first site of involvement of PV in about 50% of affected individuals and without therapy perhaps 95% of patients will develop oral lesions.36,37

Figure 3
figure3

Superficial ulceration of pemphigus vulgaris - the most common type of pemphigus to affect the oral mucosae or gingivae

Of concern has been the realisation that bullous disease can arise on a background of systemic malignancy, this group of disorders being termed paraneoplastic pemphigus (PNP; sometimes also termed paraneoplastic autoimmune multi-organ syndrome [PAMS]). About two thirds of the associated cancers are haematological (for example, non-Hodgkin's lymphoma, chronic lymphocytic leukaemia and Castleman's disease) although PNP has been observed in association with sarcomas, thymoma, lung cancer and OSCC. The mouth, pharynx and larynx are usually the first sites of involvement, although the conjunctivae and genitals may also be affected. The oral features are similar to those of PV, although there can be notable labial involvement. Desquamative gingivitis presumably occurs. Confusingly, oral lichen planus-like features can sometimes arise in PAMS. Of concern PAMS can cause bronchiolitis obliterans and early death. The variable presentation of PAMS reflects the wide range of autoantibodies with different epithelial targets that may be generated.38 Finally, several groups of drugs may cause pemphigus-like disease, for example angiotensin converting enzyme (ACE) inhibitors.39

Erythema multiforme (EM) can often give rise to areas of irregular superficial ulceration of the mouth particularly the anterior oral mucosa. There can also be areas of non-specific erythema, occasional vesicles or blisters or desquamative-like gingivitis. Target-like lesions may very rarely arise on the oral mucosa. This group of disorders includes EM minor, EM major, Stevens Johnson syndrome and toxic epidermal necrolysis syndrome (TENS) that often, but not always, are secondary to an increasingly wide range of medications. The risk of EM type disease clearly increases with the numbers of different drugs that a patient receives - but in some instances EM disease can arise in the absence of drug therapy.40

White patches

White patches of the oral mucosa can be categorised clinically into adherent (that is, do not easily wipe off) and non-adherent. The range of systemic disorders that can give rise to oral mucosal (and sometimes gingival) white patches is summarised in Table 2.

Table 2 Oral mucosal white patches associated with systemic disease

Non-adherent white patches

Pseudomembranous candidiasis (thrush) is a non-adherent white or cream coloured non-adherent pseudomembrane that tends to arise on the posterior palate or pharynx, although when disease is severe almost any oral surface can be affected (Fig. 4). Thrush is usually painless and typically reflects present or recent therapy with broad spectrum antibiotics, corticosteroids or other immunosuppressants, other immunodeficiencies or long standing oral dryness (for example, medication induced or Sjögren's syndrome). Thrush is perhaps most commonly observed in patients receiving long-term corticosteroid inhaler therapy (for example, for the management of asthma). While Candida albicans is the most common species associated with oral thrush, several other types may also give rise to this clinical feature, some of which can be particularly insensitive or indeed resistant to antifungal therapy.41,42

Figure 4
figure4

Pseudomembranous candidiasis (thrush) of the oral mucosa

Adherent white patches

The most common causes of white patches of the mouth are local physical trauma, oral lichen planus (discussed earlier), hyperkeratosis of unknown cause, epithelial dysplasia or neoplasia. Some of these can arise in association with systemic disease (for example, traumatic keratosis secondary to cerebral palsy or oral lichen planus due to medication) and white patches of the oral mucosa and to a lesser extent the gingivae may be a significant feature of systemic disease. Perhaps the most important of these is chronic mucocutaneous candidiasis (CMC), a group of often congenitally driven disorders characterised by recurrent mucocutaneous candidal infection.43 In CMC the complete spectrum of presentations of oral candidal infection can occur (for example, pseudomembraneous, erythematous, chronic hyperplastic). Patients with autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED) not only have chronic candidal infection but may have diabetes mellitus (which presumably will increase the risk or severity of periodontitis), enamel hypocalcification (secondary to hypoparathyroidism) and hypermelanotic pigmentation of the oral mucosa (secondary to autoimmune-driven destruction of the adrenal cortex).4447 Late-onset chronic mucocutaneous candidiasis (Good's syndrome) is accompanied by thymoma, myasthenia gravis and bone marrow abnormalities and thus affected individuals may have abnormal movement of the eyes, mouth and/or face.48 Chronic mucocutaneous candidiasis may be considered to be a rare risk factor for OSCC.49

There are many other potential oral mucosal manifestations of systemic disease, as summarised in Table 3. Perhaps the most notable of these is Addisonian pigmentation. This is actually very rare but manifests as areas of hypermelanotic pigmentation of the buccal mucosae. A similar appearance (together with palatal pigmentation) can arise with some small cell carcinomas of the lung.

Table 3 Other oral mucosal manifestations of systemic disease

Salivary gland manifestations

Disease of the salivary glands broadly manifests as local swelling and/or oral dryness (the symptom of xerostomia). The disorders likely to give rise to salivary gland manifestations are summarised in Tables 4 and 5.

Table 4 Non-neoplastic systemic causes of salivary gland swelling
Table 5 Other oral signs and symptoms of systemic disease relevant to oral medicine

Salivary gland swelling

Mucoceles of the minor salivary glands of the lower lip and sialolithiasis of the submandibular gland are probably the most common causes of swelling of the salivary glands. Mucoceles have no association with systemic disease and ranulas, swellings of the submandibular and/or sublingual glands akin to that of mucoceles, do not seem to have any consistent association with systemic disease, although have been observed in patients receiving ART. Sialolithiasis tends to arise de novo but a number of systemic disorders or therapies have been linked to this disorder including diabetes mellitus, hypertension and/or chronic liver disease, nephrolithiasis, hyperparathyroid disease and therapy with the anti-HIV agent atazanavir.50

Acute suppurative sialadenitis that usually manifests as a painful swelling of one parotid gland is typically secondary to longstanding oral dryness such as Sjögren's syndrome or radiotherapy-associated salivary gland disease. However, neonatal disease has been reported in association with prematurity, orogastric feeding and/or immunodeficiency. In adults links with systemic disease have included diabetes mellitus, HIV disease and a plethora of surgical interventions, as well as the very rare coprophagia (the consumption of faeces).

Mumps will often cause short-term salivary gland swelling although, hopefully, the return of the high compliance with appropriate vaccination will lessen the frequency of this and the much more significant consequences of this disorder. Hepatitis C virus (HCV) infection can cause both salivary gland enlargement (typically the parotid glands) and reduced salivary output and importantly there is a risk of NHL of salivary glands.50

Salivary gland disease associated with HIV infection tends to arise in late advanced disease although it may rarely be the first manifestation of a previously unknown HIV infection. There can be swelling and/or xerostomia, the former being most common in the parotid glands. Within the gland there is inflammation (sialadenitis) that is being driven by infection with BK polyomavirus (BKPyV).51,52 Multicystic lymphoepithelial lesions, sometimes termed cystic lymphoid hyperplasia (CLH) or benign lymphoepithelial lesion (BLEL) or benign lymphoepithelial cysts (BLEC), may also occur in 6% of adults and 10% of children infected with HIV. Transformation to non-Hodgkin's lymphoma is a rare complication of CLH. Other causes of salivary swellings of patients with HIV disease include intraglandular lymphadenopathy, Kaposi's sarcoma, NHL and acute suppurative sialadentis. As noted above sialolithiasis possibly secondary to ART has been documented and some HIV protease inhibitors can cause salivary gland enlargement of unknown cause.

Salivary gland swelling (often only of the submandibular glands), sometimes with xerostomia, can arise in IgG4-related disease. This is a rare fibroinflammatory disorder characterised by elevated serum levels of IgG4 and multi-organ inflammation (lacrimal glands, pituitary gland, thyroid, pancreas, biliary tract, lungs, prostate gland and retroperitoneal cavity). The disease has predominantly been described in Asian patients (particularly from Japan) but affected individuals have been reported in the Western World. In the past the features were termed ‘Mikulicz’ disease’ ‘Kuttner tumour’ or ‘chronic sclerosing sialadenitis’.50,53

Sialosis (sometimes termed sialoadenosis) is an uncommon non-neoplastic and non-inflammatory disorder possibly associated with some systemic disorders that give rise to bilateral non-painful enlargement of the major salivary glands - typically the parotids. Xerostomia is not a common or dominant accompanying symptom. The precise cause is unknown although it may reflect a neuropathy by which unopposed sympathetic drive causes an increase in protein content within the acinar cells.54 This would perhaps explain the association of sialosis with diabetes mellitus and perhaps hypothyroidism, malnutrition, alcoholism and other causes of hepatic cirrhosis. Sialosis has also been observed in bulimia nervosa, the degree of salivary gland enlargement possibly correlating with the frequency of bulimic symptoms and with levels of serum amylase.

A wide range of drugs can cause salivary gland enlargement. Transient and mild acute sialadenitis (sometimes termed ‘iodide mumps’) can arise in response to iodine based contrast media (for example, for percutaneous coronary interventions).5558 Similarly radioactive iodine, used for the treatment of thyroid cancer, can cause salivary gland swelling and xerostomia that may arise within 24 hours of therapy and persist for a few weeks. Other agents that may cause salivary gland enlargement include l-asparaginase, clozapine, phenylbutazone, methyldopa, interferon alpha, oxyphenbutazone, ramipril, trimethoprim/sulfamethoxazole, nicardipine, nifedipine, chlormethiazole, methimazole, naproxen, nitrofurantoin, sulfadiazine, captopril, cytarabine, cimetidine, ranitidine, and thioridazine.59

Oral dryness

The symptom of oral dryness does not always accord with loss of salivary gland function, indeed many individuals report some degree of usually transient or mild oral dryness without objective evidence of reduced salivary gland function. Reduced salivary function gives rise to dysarthria, dysphagia, dysgeusia, some mucosal soreness, an increased liability to caries, gingivitis (but perhaps not periodontitis), candida infection (for example, pseudomembranous, erythematous and angular chielitis), acute suppurative sialadenitis and reduced retention of upper full dentures. It can thus greatly lessen quality of life.50

The most common cause of persistent oral dryness is drug therapy - with late-aged patients receiving polypharmacy being at greatest risk of this problem (Box 1). Medication-related xerostomia reflects anti-cholinergic and/or sympathomimetic actions, hence the drugs most commonly implicated in xerostomia are tricyclic antidepressants, benzodiazepines, atropinics, beta-blockers and anti-histamines. Morphine-derived agents cause oral dryness and while often promoted as having less anticholinergic actions than the tricyclics, the selective serotonin reuptake inhibitors (SSRIs) still cause some dry mouth. Some other newer drug therapies including omeprazole, anti-HIV protease inhibitors, the nucleoside analogue HIV reverse transcriptase inhibitor didanosine, trospium chloride, elliptinium, and new generation antihistamines may also cause drug-induced xerostomia.

Xerostomia is the most common persistent adverse side effect of radiotherapy (RT) of the head and neck, affecting up to 85% of patients.60 The prevalence of RT-induced xerostomia varies with respect to RT field, dose, regimen, and technique. Although the introduction of intensity modulated RT has led to a significant reduction in the frequency and severity of this iatrogenic problem, many patients still experience the consequences of irreversible salivary gland dysfunction as a fall in salivary outflow and altered salivary content.

Oral dryness is a dominant symptom of Sjögren's syndrome (Fig. 5). This disorder is classified as primary disease in which there are symptoms and signs of ocular and oral dryness and secondary Sjögren's syndrome in which there is also a connective tissue disorder - most frequently rheumatoid arthritis or systemic lupus erythematosus. However, patients with primary Sjögren's syndrome have a spectrum of other systemic, and often autoimmune phenomena, while those with secondary Sjögren's syndrome may also have oral manifestations of any accompanying connective tissue disease.61

Figure 5
figure5

Oral dryness secondary to Sjögren's syndrome - this tongue is notably fissured and also has signs of mild oral lichen planus

The oral features of primary or secondary SS are those of oral dryness (as described previously) and salivary gland enlargement due to the inflammation of the actual disease, episodes of acute suppurative sialadenitis and NHL. With regard to this last feature it is important to appreciate that SS is a potentially malignant disorder having a 4.3% risk of malignancy with a standardised incident rate of 18.9. The tumours are usually low grade marginal zone lymphoma (MALT), but can also be follicle centre, diffuse B cell lymphoma (DBCL) or lymphoplasmacytoid lymphoma.62,63

Other oral manifestations

The present article has focused upon the impact of systemic disease on the oral mucosa and salivary glands but a very wide range of other symptoms and/or signs of systemic disease can arise in the mouth or adjacent face as a consequence of disorders of non-oral structures (summarised briefly in Table 5).

Conclusion

Oral features of systemic disease can be helpful in the diagnosis and management of the underlying disorder - and indeed the oral symptoms may be those that most lessen the quality of life of affected individuals. The providers of primary oral healthcare have an essential role in the management of patients who may have oral consequences of systemic disease, as they are often likely to be the first clinicians to observe such abnormalities. They may not know exactly what the disease is but timely referral of patients to specialist oral medicine units will ensure that any potential oral manifestation of systemic disease is managed quickly and appropriately to improve the patient's quality of life. A simple rule to perhaps apply is: ‘it looks different thus I will refer the patient to someone who may know what to do.’

This article was originally published in the BDJ in Volume 223 issue 9, pages 683–691.

References

  1. 1

    Compilato D, Corsello G, Campisi G. An unusual traumatic ulceration of the tongue. J Paediatr Child Health 2012; 48: 1104–1105.

  2. 2

    Gilvetti C, Porter S R, Fedele S. Traumatic chemical oral ulceration: a case report and review of the literature. Br Dent J 2010; 208: 297–300.

  3. 3

    Radoï L, Luce D. A review of risk factors for oral cavity cancer: the importance of a standardized case definition. Community Dent Oral Epidemiol 2013; 41: 97–109.

  4. 4

    Ray J G, Swain N, Ghosh R, Richa, Pattanayak Mohanty S. Dyskeratosis congenita with malignant transformation. BMJ Case Rep 2011; 2011: DOI: 10.1136/bcr.03.2010.2848.

  5. 5

    Wong W M, Parvathaneni U, Jewell P D et al. Squamous cell carcinoma of the oral tongue in a patient with Fanconi anemia treated with radiotherapy and concurrent cetuximab: a case report and review of the literature. Head Neck 2013; 35: E292-298.

  6. 6

    Fitzpatrick S G, Hirsch S A, Gordon S C. The malignant transformation of oral lichen planus and oral lichenoid lesions: a systematic review. J Am Dent Assoc 2014; 145: 45–56.

  7. 7

    Kuo C F, Luo S F, Yu K H et al. Cancer risk among patients with systemic sclerosis: a nationwide population study in Taiwan. Scand J Rheumatol 2012; 41: 44–49.

  8. 8

    Michalek A M, Mahoney M C, McLaughlin C C, Murphy D, Metzger B B. Historical and contemporary correlates of syphilis and cancer. Int J Epidemiol 1994; 23: 381–385.

  9. 9

    Triantafillidou K, Dimitrakopoulos J, Iordanidis F, Gkagkalis A. Extranodal non-hodgkin lymphomas of the oral cavity and maxillofacial region: a clinical study of 58 cases and review of the literature. J Oral Maxillofac Surg 2012; 70: 2776–2785

  10. 10

    Porter S R, Diz Dios P, Kumar N, Stock C, Barrett A W, Scully C. Oral plasmablastic lymphoma in previously undiagnosed HIV disease. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1999; 87: 730–734.

  11. 11

    Castillo J J, Bibas M, Miranda R N. The biology and treatment of plasmablastic lymphoma. Blood 2015; 125: 2323–2330.

  12. 12

    Al-Hakeem D A, Fedele S, Carlos R, Porter S. Extranodal NK/T-cell lymphoma, nasal type. Oral Oncol 2007; 43: 4–14.

  13. 13

    Patton L L. Oral lesions associated with human immunodeficiency virus disease. Dent Clin North Am 2013; 57: 673–698.

  14. 14

    Rao R S, Patil S, Sanketh D, Amrutha N. Metastatic tumors of the oral cavity. J Contemp Dent Pract 2014; 15: 263–271.

  15. 15

    Ilyas S E, Chen F F, Hodgson T A, Speight P M, Lacey C J, Porter S R. Labial tuberculosis: a unique cause of lip swelling complicating HIV infection. HIV Med 2002; 3: 283–286.

  16. 16

    Aoun N, El-Hajj G, El Toum S. Oral ulcer: an uncommon site in primary tuberculosis. Aust Dent J 2015; 60: 119–122.

  17. 17

    Iatta R, Napoli C, Borghi E, Montagna M T. Rare mycoses of the oral cavity: a literature epidemiologic review. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2009; 108: 647–655.

  18. 18

    Porter S R, Scully C, Standen G R. Autoimmune neutropenia manifesting as recurrent oral ulceration. Oral Surg Oral Med Oral Pathol 1994; 78: 178–180.

  19. 19

    Jurge S, Kuffer R, Scully C, Porter S R. Mucosal disease series. Number VI. Recurrent aphthous stomatitis. Oral Dis 2006; 12: 1–21.

  20. 20

    Al-Otaibi L M, Porter S R, Poate T W. Behçet's disease: a review. J Dent Res 2005; 84: 209–222.

  21. 21

    Stojanov S, Lapidus S, Chitkara P et al. Periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) is a disorder of innate immunity and Th1 activation responsive to IL1 blockade. Proc Natl Acad Sci USA 2011; 108: 7148–7153.

  22. 22

    Scully C, Hodgson T, Lachmann H. Auto- inflammatory syndromes and oral health. Oral Dis 2008; 14: 690–699.

  23. 23

    Scully C, Porter S. Orofacial disease: update for the dental clinical team: 2. Ulcers, erosions and other causes of sore mouth. Part II. Dent Update 1999; 26: 31–39.

  24. 24

    Ryan K, Hegarty A M, Hodgson T. Aetiology, diagnosis and treatment of oral lichen planus. Br J Hosp Med (Lond) 2014; 75: 492–496.

  25. 25

    Bidarra M, Buchanan J A, Scully C, Moles D R, Porter S R. Oral lichen planus: a condition with more persistence and extra-oral involvement than suspected? J Oral Pathol Med 2008; 37: 582–586.

  26. 26

    Lourenço S V, de Carvalho F R, Boggio P et al. Lupus erythematosus: clinical and histopathological study of oral manifestations and immunohistochemical profile of the inflammatory infiltrate. J Cutan Pathol 2007; 34: 558–564.

  27. 27

    Nico M M, Vilela M A, Rivitti E A, Lourenço S V . Oral lesions in lupus erythematosus: correlation with cutaneous lesions. Eur J Dermatol 2008; 18: 376–381.

  28. 28

    Xu H H, Werth V P, Parisi E, Sollecito T P. Mucous membrane pemphigoid. Dent Clin North Am 2013; 57: 611–630.

  29. 29

    Leao J C, Ingafou M, Khan A, Scully C, Porter S. Desquamative gingivitis: retrospective analysis of disease associations of a large cohort. Oral Dis 2008; 14: 556–560.

  30. 30

    Chan L S. Ocular and oral mucous membrane pemphigoid (cicatricial pemphigoid). Clin Dermatol 2012; 30: 34–37.

  31. 31

    Kasperkiewicz M, Zillikens D, Schmidt E. Pemphigoid diseases: pathogenesis, diagnosis, and treatment. Autoimmunity 2012; 45: 55–70.

  32. 32

    Lähteenoja H, Irjala K, Viander M, Vainio E, Toivanen A, Syrjänen S. Oral mucosa is frequently affected in patients with dermatitis herpetiformis. Arch Dermatol 1998; 134: 756–758.

  33. 33

    Said S, Golitz L. Vesiculobullous eruptions of the oral cavity. Otolaryngol Clin North Am 2011; 44: 133–160, vi.

  34. 34

    Dan H, Lu R, Li W, Chen Q, Zeng X. Linear IgA disease limited to the oral mucosa. J Am Acad Dermatol 2011; 65: 677–679.

  35. 35

    Eguia del Valle A, Aguirre Urízar J M, Martínez Sahuquillo A. Oral manifestations caused by the linear IgA disease. Med Oral 2004; 9: 39–44.

  36. 36

    Sticherling M, Erfurt-Berge C. Autoimmune blistering diseases of the skin. Autoimmun Rev 2012; 11: 226–230.

  37. 37

    Santoro F A, Stoopler E T, Werth V P. Pemphigus. Dent Clin North Am 2013; 57: 597–610.

  38. 38

    Niimi Y, Ohyama B, Di Zenzo G, Calabresi V, Hashimoto T, Kawana S. Paraneoplastic pemphigus presenting as mild cutaneous features of pemphigus foliaceus and lichenoid stomatitis with antidesmoglein 1 antibodies. Dermatol Res Pract 2010; 2010: DOI: 10.1155/2010/931340.

  39. 39

    Cozzani E, Rosa G M, Drosera M, Intra C, Barsotti A, Parodi A. ACE inhibitors can induce circulating antibodies directed to antigens of the superficial epidermal cells. Arch Dermatol Res 2011; 303: 327–332.

  40. 40

    Al-Johani K A, Fedele S, Porter S R. Erythema multiforme and related disorders. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2007; 103: 642–654.

  41. 41

    Muzyka B C, Epifanio R N. Update on oral fungal infections. Dent Clin North Am 2013; 57: 561–581.

  42. 42

    Stoopler E T, Sollecito T P. Oral mucosal diseases: evaluation and management. Med Clin North Am 2014; 98: 1323–1352.

  43. 43

    Lanternier F, Cypowyj S, Picard C et al. Primary immunodeficiencies underlying fungal infections. Curr Opin Pediatr 2013; 25: 736–747.

  44. 44

    Kisand K, Peterson P. Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy and other primary immunodeficiency diseases help to resolve the nature of protective immunity against chronic mucocutaneous candidiasis. Curr Opin Pediatr 2013; 25: 715–721.

  45. 45

    Lindh E, Brännström J, Jones P et al. Autoimmunity and cystatin SA1 deficiency behind chronic mucocutaneous candidiasis in autoimmune polyendocrine syndrome type 1. J Autoimmun 2013; 42: 1–6.

  46. 46

    Capalbo D, Improda N, Esposito A et al. Autoimmune polyendocrinopathycandidiasisectodermal dystrophy from the pediatric perspective. J Endocrinol Invest 2013; 36: 903–912.

  47. 47

    Porter S R, Scully C. Candidiasis endocrinopathy syndrome. Oral Surg Oral Med Oral Pathol 1986; 61: 573–578.

  48. 48

    Kelesidis T, Yang O. Good's syndrome remains a mystery after 55 years: A systematic review of the scientific evidence. Clin Immunol 2010; 135: 347–363.

  49. 49

    Shephard M K, Schifter M, Palme C E. Multiple oral squamous cell carcinomas associated with autoimmune polyendocrinopathycandidiasisectodermal dystrophy. Oral Surg Oral Med Oral Pathol Oral Radiol 2012; 114: e36-e42.

  50. 50

    Porter S R, Mercadante V, Fedele S. Non-neoplastic salivary gland disease. In Scott-Brown's otorhinolaryngology: head & neck surgery, 8th edition. London: Hodder Arnold (in press).

  51. 51

    Jeffers L K, Madden V, Webster-Cyriaque J. BK virus has tropism for human salivary gland cells in vitro: Implications for transmission. Virology 2009; 394: 183–193.

  52. 52

    Burger-Calderon R, Madden V, Hallett R A, Gingerich A D, Nickeleit V, Webster-Cyriaque J. Replication of oral BK virus in human salivary gland cells. J Virology 2014; 88: 559–573.

  53. 53

    Mahajan V S, Mattoo H, Deshpande V, Pillai S S, Stone J H. IgG4-related disease. Ann Rev Pathol 2014; 9: 315–347.

  54. 54

    Deshpande V, Zen Y, Chan J K C et al. Consensus statement on the pathology of IgG4-related disease. Mod Pathol 2012; 25: 1181–1192.

  55. 55

    Mandel L, Khelemsky R. Asymptomatic bilateral facial swelling. J Am Dent Assoc 2012; 143: 1205-1208.

  56. 56

    Capoccia L, Sbarigia E, Speziale F. Monolateral sialadenitis following iodinated contrast media administration for carotid artery stenting. Vascular 2010; 18: 34–36.

  57. 57

    Chau A M T, Suan D. Iodide mumps. Clinical Imaging 2013; 37: 367–368.

  58. 58

    Shacham Y, Havakuk O, Roth A. A rare case of acute contrast-induced sialadenitis after percutaneous coronary intervention. Israel Med Assoc J 2013; 15: 652–653.

  59. 59

    Brooks K G, Thompson D F. A review and assessment of drug-induced parotitis. Ann Pharmacother 2012; 46: 1688–1699.

  60. 60

    Jensen S B, Pedersen A M L, Vissink A et al. A systematic review of salivary gland hypofunction and xerostomia induced by cancer therapies: Prevalence, severity and impact on quality of life. Support Care Cancer 2010; 18: 1039–1060.

  61. 61

    Konings A W T, Coppes R P, Vissink A. On the mechanism of salivary gland radiosensitivity. Int J Radiat Oncol Biol Phys 2005; 62: 1187–1194.

  62. 62

    Reksten T R, Jonsson M V. Sjögren's Syndrome: An update on epidemiology and current insights on pathophysiology. Oral Maxillofac Surg Clin North Am 2014; 26: 1–12.

  63. 63

    Voulgarelis M, Ziakas P D, Papageorgiou A, Baimpa E, Tzioufas A G, Moutsopoulos H M. Prognosis and outcome of non-hodgkin lymphoma in primary Sjögren syndrome. Medicine 2012; 91: 1–9.

  64. 64

    Routsias J G, Goules J D, Charalampakis G, Tzima S, Papageorgiou A, Voulgarelis M. Malignant lymphoma in primary Sjögren's syndrome: An update on the pathogenesis and treatment. Semin Arthritis Rheum 2013; 43: 178–186.

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Porter, S., Mercadente, V. & Fedele, S. Oral manifestations of systemic disease. BDJ Team 5, 18012 (2018). https://doi.org/10.1038/bdjteam.2018.12

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