Diagnosis of Lingual Atrophic Conditions: Associations with Local and Systemic Factors. A Descriptive Review
M. Erriu1, *, F.M.G. Pili1, S. Cadoni2, V. Garau1
Identifiers and Pagination:Year: 2016
First Page: 619
Last Page: 635
Publisher ID: TODENTJ-10-619
Article History:Received Date: 03/04/2016
Revision Received Date: 09/10/2016
Acceptance Date: 15/10/2016
Electronic publication date: 16/11/2016
Collection year: 2016
open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
Atrophic glossitis is a condition characterised by absence of filiform or fungiform papillae on the dorsal surface of the tongue. Consequently, the ordinary texture and appearance of the dorsal tongue, determined by papillary protrusion, turns into a soft and smooth aspect.
Throughout the years, many factors, both local and systemic, have been associated with atrophic glossitis as the tongue is currently considered to be a mirror of general health. Moreover, various tongue conditions were wrongly diagnosed as atrophic glossitis. Oral involvement can conceal underlying systemic conditions and, in this perspective, the role of clinicians is fundamental.
Early recognition of oral signs and symptoms, through a careful examination of oral anatomical structures, plays a crucial role in providing patients with a better prognosis.
Due to its proximity to the respiratory tract and its continuity with gastrointestinal system, as well as its participation in speech articulation, the oral cavity assumes a crucial role in many physiologic processes [1, 2]. Additionally, a great variety of systemic disorders have been associated with specific or nonspecific oral changes and, in many circumstances, the oral cavity becomes an important diagnostic area. Oral involvement may precede systemic manifestations and symptoms, providing clinicians with early diagnosis of an underlying condition. In particular, its careful examination can reveal signs and symptoms of metabolic disorders, endocrinopathies, gastrointestinal diseases, hematologic, autoimmune, and neoplastic pathologies [1, 3].
From this perspective, the systematic investigation of the oral mucosa and the dorsum of the tongue appears fundamental. Any variation of oral anatomical structures may be indicative of a systemic disease and should be thoroughly investigated. However, in order to generate differential diagnoses, since the aetiology of many oral conditions remains unknown, defining a univocal classification system is still arduous and clinicians should firstly discern local and generalized systemic conditions [1-5]. Afterwards, having collected all clinical findings and formed a first opinion, clinicians should determine what additional tests might be necessary before establishing the definitive therapy.
This article focuses mainly on local and systemic conditions associated with atrophy of the dorsum of the tongue, currently considered a potential indicator of general health. At the same time other tongue conditions, determining a clinical aspect similar to a atrophic glossitis, will be examined in order to give a guidance to the differential diagnosis In this context, the differential diagnosis between primary atrophic glossitis and the conditions related to atrophic. tongue appears indispensable.
The ordinary texture and appearance of the dorsal tongue are related to the protrusion of a large number of papillae, which are responsible for the roughness of the surface, (Fig. 1). Absence of filiform or fungiform papillae on the dorsal surface of the tongue produces a soft and smooth aspect, known as atrophic glossitis (AG) .
|Fig. (1). Graphical representation of the tongue in physiological conditions. (A. Vallate papillae, B. Foliate papillae, C. Filiform papillae, D. Fungiform papillae).|
Throughout the years, numerous factors have been taken into consideration for the aetiology of AG. In particular, papillary atrophy has been correlated to both local and generalized systemic conditions. Local lesions are more often attributed to congenital or developmental affections, infections, neoplasia; or they may be idiopathic. Lesions of systemic origins are more frequently associated to metabolic disorders, blood dyscrasias and immunological diseases [6, 7]. AG can also be correlated with protein deficiency and a hypocaloric diet; as well as deficiency of iron, vitamin B12, folic acid, riboflavin, and niacin [3, 8, 9].
A literature search was done to identify all reports specifically regarding a condition of atrophy of the papillae of the tongue, regardless of their publication status. Medline, Pubmed and Cochrane Library were searched systematically for all published literature from January 1975 (year of the first published paper regarding the AG) to April 2016, which included the following terms in their titles, abstracts, or keyword lists: atrophic glossitis, benign migratory glossitis and median romboid glossitis. Reviews, case reports, editorials, letters and commentaries were excluded, as well as articles lacking an abstract preview or not written in English.
The search strategy generated 50 records for the AG, 297 records for the benign migratory glossitis and 83 records for the median romboid glossitis. After application of the inclusion/exclusion criteria and the analysis of full-text articles, 40 records were discarded for AG, (Fig. 2), 278 for the benign migratory glossitis and 69 for the median romboid glossitis. Finally, 10 studies for the AG, 19 studies for the benign migratory glossitis and 14 studies for the median romboid glossitis were chosen to write the review. Due to the lack of articles that specifically deal with the subject of this review, most of the data were taken from publications in which the observation of tongue atrophy condition was secondary to the main outcome of the work. Additional sources were hand-searched, including: bibliographies from previous reviews on the subject, bibliography of all publications cited in these articles and chapter from various English textbooks regarding the oral pathology.
|Fig. (2). Study flow chart.|
The tongue is continuously exposed to chemical, mechanical and physical stimuli that, when too strong or chronic, may cause atrophic lesions. Among these kind of aetiological factors are alcohol abuse, traumas and drug collateral effects. At the same time, an incorrect diet with nutritional deficiency can determine atrophy of the dorsum of the tongue leading to a diagnosis of AG.
2.1. AG and Idiopathic Condition (Fissured Tongue)
Typically AG is not a physiological condition; despite this, it has been associated with another tongue disease such as the fissured tongue, also in the absence of a systemic disease . Fissured tongue is typically associated with aging and is considered the most common lingual defect with a prevalence of 5-11% [2, 5, 10-13]. The principal clinical manifestation of this condition, that is not always associated with an atrophy of the lingual dorsum, is the presence of grooves with varying degree of depth along the dorsal surface of the tongue [10, 14]. The fissured tongue is usually asymptomatic, unless a secondary inflammation was determined by a low-grade infection, bacterial overgrowth or trapped food debris. Other than being correlated with older age, this is a condition observed in patients affected by Down's syndrome, Acromegaly, Sjogren syndrome, Psoriasis and Melkersson-Rosenthal syndrome [2, 5, 12].
2.2. AG Related to Nutritional Deficiencies
The association of nutritional deficiencies and AG was first described in 1975 in the first US National Health and Nutritional Examination Survey, and it is considered the principal aetiological factor determining the atrophy of the tongue mucosa [2, 5, 15]. Deficiency of various nutrients, usually several of them rather than one at a time, is described to be correlated with AG [9, 16-19] (Table 1). Those recognised are riboflavin (vitamin B2), niacin (vitamin B3), pyridoxine (vitamin B6), folic acid (vitamin B9), cobalamin (vitamin B12), iron and zinc [2, 5, 8, 9, 16, 17, 20-31] (Table 2). Lately, mechanisms involving cellular oxygenation and/or the iron concentration in tongue's cells have been associated to AG due to nutritional deficiencies. Deficiency of each one of the nutrients listed above determines one of the conditions described, with a direct or an indirect mechanism (poor diet, malabsorption, excessive consumption).
|1993||Drinka et al.||Nutritional status of 20 elderly patients with a normal tongue and 10 subjects with various degree of AG||Their results demonstrated a statistically significant association between AG and deficiency of vitamin E, considered as another nutrient responsible for the development of AG.|||
|2000||Bøhmer and Mowe||Nutritional status of 416 old people and the resulting lingual alterations.||The correlation between AG and nutritional indices was statistically significant, and related to low levels of haemoglobin, cholesterol, ascorbic acid, serum iron and serum cobalamin.|||
|2012||Sun et al.||Comparison of blood hemoglobin concentration, iron, cobalamin, folic acid and homocysteine in 176 patient with AG with 176 healthy controls||Their results showed a statistically significant association among AG and low serum concentration of iron, vitamin B12 and haemoglobin. Patients with AG showed high homocysteine levels.|||
|2013||Sun et al.||Evaluation of the reduction of homocysteine levels in 91 patients with an AG||AG healed through supplementation of different vitamins and iron|||
|2014||Wu et al.||Comparison of prevalence of AG studying nutritional status of 75 patient with iron-deficiency anemia and of 150 healthy subjects.||Serum concentration of iron, vitamin B12, folic acid and homocysteine was quantified in the blood samples of all cases. Results showed statistically significant differences in the iron and cobalamin concentrations between the two study groups, while no differences were identified for the other two nutrients|||
|2014||Demir N et al.||Analysis of prevalence of AG in 57 neonatal patients with vitamin B12 deficiency||Determination of a prevalence of AG of 70.17%. The authors concluded that a deficiency of vitamin B12 should be considered in the differential diagnosis of infants who present with skin and mucosal lesions.|||
|2016||Bao ZX et al.||Analysis of serum zinc levels in 368 patients (of which 54 had an AG).||The mean serum zinc level in the healthy control group was significantly higher than that of the AG group.|||
|Factor||Name||Sources||Role||Disease related to the deficiency|
|Vitamin B2||Riboflavin||vegetables, yeast, milk||Factor involved in oxidation-reduction reactions.||Normochromic normocytic anemia|
|Vitamin B3||Niacin||meat, beer yeast, cereals||It is involved particularly in the DNA repair process, in the production of steroid hormones and is necessary for cellular oxidation-reduction reactions.||Pellagra|
|Vitamin B6||Pyridoxin||meat, vegetables||It is a cofactor in several enzymatic reactions involving the metabolism of amino acids, glucose and lipids.||Pellagra (indirectly)|
|Vitamin B9||Folic acid||kidney, liver, green leafy vegetables, legumes, eggs||Its principal biological role is related to the synthesis of DNA and RNA and in the prevention of genetic alterations.||Megaloblastic anemia|
|Vitamin B12||Cobalamin||meat, milk, eggs||It is involved in the cells metabolism with several functions such as DNA synthesis, regulatory functions of the nervous system or in the amino acid metabolism.||Pernicious anemia|
|Iron||Iron||meat, vegetables||It carries oxygen in the hemoglobin, in the myoglobin and is also involved in several enzymatic reactions.||Iron-deficiency anemia|
|Zinc||Zinc||Animal-sourced foods and some vegetables||It is involved in various biological reactions in the human body, from cell growth to normal immune function to wound healing.||Different physiological alterations|
2.2.2. Gastrointestinal Diseases
Gastrointestinal diseases are the most common conditions associated with the development of an atrophy of the tongue's mucosa related to a nutritional aetiology. Among them, celiac disease (CD) is considered one of the main causes in determining the nutritional deficiencies described above .
Celiac disease is caused by an autoimmune intolerance to gliadin, a protein contained in gluten [32, 33]. The main target of this intolerance is represented by the mucosa of the small intestine, with the development of histological lesions characterized by various degrees of villous atrophy, crypt hyperplasia, damage to the surface epithelium, an increased number of lymphocytes and other inflammatory cells in the lamina propria [7, 32-34].
This causes poor absorption of nutrients determining a deficiency of vitamin B12, folic acid and iron . Tongue lesions related to celiac diseases are identified as indirect symptoms. The AG associated with celiac disease, when accompanied by other signs or symptoms, has been recognized as a warning sign of the underlying intestinal pathology [2, 4, 7, 34-37]. Pastore and Lo Muzio highlighted the importance of the recognition of AG to obtain the diagnosis of a celiac disease. The authors cited the National Institutes of Health consensus statement on celiac disease: “the single most important step in diagnosing celiac disease is to first consider the disorder by recognizing its myriad clinical features” [6, 38]. AG has also been described as the only clinical sign leading to suspect the diagnosis of celiac disease .
In 2014, a paper by Park JM et al. described a case of Plummer-Vinson syndrome associated with Crohn's disease. Further works will be needed to confirm this data .
2.3. AG by Alcohol Abuse
Malnutrition is a typical condition of an alcoholic patient. A lack of vitamin B12/A vitamin B12 deficit in particular is usually a sign of this malnutrition. This contradiction is due to an alteration in hepatic enzyme levels, meaning that patients can show symptoms or signs of vitamin B12 deficiency even if its levels are normal . In 2012, Cunha S.F. et al analysed papillary atrophy of the tongue and nutritional status of hospitalized alcoholics . They observed a statistically significant correlation between atrophic glossitis and reduced anthropometric measures, anemia and hypoalbuminemia. They also identified alterations in serum levels of vitamins A, E and B12, but were not been able to determine a correlation with an atrophic condition of the tongue .
Direct damage of tongue tissues caused by alcohol has been analyzed by several authors. In 1985, Valentine J.A. et al. observed the effects of alcohol and tobacco abuse on tongue mucosa in order to identify the alteration in the lingual epithelial structure in an antitumor evaluation . The authors studied the histology of 161 tongue specimens taken from corpses of patients with a history of abuse of alcohol within 5 years before death. Their results showed that epithelial atrophy was frequently present on the lingual dorsum, with an increase in basal cells size and also a decrease in superficial cells . In 1994, Maier H. et al. investigated the role of alcohol as co-carcinogen. Alcohol consumption determined a reduction of epithelial thickness associated to increased cellular proliferation in the basal layer. Alcohol determined a cytotoxic effect, with atrophy of the oral mucosa followed by an hyper-regeneration. All these effects have been associated with an increased susceptibility to carcinogenic substances [44, 45].
2.4. AG Related to Drugs Administration
Drugs determine an AG through several different mechanisms. The AG could derive from drug usage principally in an indirect way, or as a symptom or consequence of a specific adverse reaction to a drug therapy [46, 47]. In fact, specific medicaments can determine a vitamin deficiency that leads to an AG through the mechanisms previously explained. The drugs with an adverse reactionleading to this kind of consequence are very different. It is possible to find drugs for the treatment of type 2 diabetes, contraceptives, acid-lowering agents, anti-cancer medicaments, agents for the treatment of hypertension, neurologic drugs as well as others [28, 48-66] (Table 1). Each one of them could generate an AG related to a vitamin deficiency through two principal mechanisms of action: firstly, they can determine a malabsorption of the nutrient; secondly, they can interfere in the metabolization of a specific vitamin. In addition, there are other mechanisms leading to an atrophic condition such as the development of candidiasis after antibiotic use, xerostomia related to antidepressant consumption or microcirculation alteration after use of chemotherapeutical drugs [67-73]. In addition, a review from 2012 described as a tongue dysesthesia can also be associated with multitargeted tyrosine kinase inhibitors (TKIs) and mammalian target of rapamycin inhibitors (mTORIs) .
2.5. AG as Consequence of Infectious Disease
Tongue crypts, along with tonsils and gingival sulcus, are considered important ecological niches of the oral cavity . In these areas the balance between the environment and oral microorganisms is frail, and regulates the maintenance of the oral ecosystem equilibrium preventing environmental changes [76-78].
The tongue dorsum is always colonized by various microbial colonies without the development of a pathological condition. When the balance of the niches is altered, it is often possible to observe a pathological colonization due to a specific, and often single, microbial strain accompanied by clinical manifestations. Atrophic condition of the tongue has been described in association with candidiasis, colonization of Helicobacter pylori and as consequence of Treponema pallidum infection [2, 12, 79-81].
2.5.1. Candida Albicans
Candida albicans (C. albicans) is one of the normal components of microflora of the oral cavity, with a prevalence between the 30 and the 50% . The development of an oral candidiasis is usually related to an imbalance of the normal oral microbial ecosystem. Determinants of an oral candidiosis are: long-term antibiotic therapy, use of local steroids (i.e. inhaler or mouthwashes), immunodeficiencies (i.e. AIDS, organ transplant, chemotherapy) or favourable environmental conditions (i.e. xerostomia, poor oral hygiene, diabetes) [83-86]. Candida infection promotes different clinical manifestations on the tongue surface, both acute and chronic. Among them, chronic erythematous candidiasis determines an atrophic lesion defined as median rhomboid glossitis [5, 70], while an acute erythematous candidiasis can promote an a specific AG .
2.5.2. Helicobacter Pylori
Helicobacter pylori (H. pylori) is a Gram-negative, microaerophilic bacterium identified among etiologic factors contributing to chronic gastritis and gastric ulcers . Its presence in oral plaque and saliva is controversial, in several studies prevalence fluctuated from 0 to 100% [88-91]. In 2001, Gall-Troselj et al. examined the possible role of H. pylori in determining an AG and the burning mouth syndrome . They examined 87 patients with an AG looking for the presence of H. pylori by cytobrash of the dorsal tongue mucosa. Their results showed a high prevalence of the bacteria of tongues in patients affected by the AG (16%) compared with healthy controls (0%). This statistically higher incidence lead the authors to suspect that H. pylori colonization could have been secondary to the development of the AG, and not its causative agent. They hypotized a change in salivary flow and/or salivary content prior to the development of the AG .
2.5.3. Treponema Pallidum (Syphilis)
Treponema pallidum is an anaerobic spirochete causing the sexually transmitted systemic disease named syphilis. Oral manifestations are uncommon but can be present in all the three stages of the disease. The importance of mouth examination for the diagnosis has been recognized long ago .
The review analyzing the literature from 1950 to 2011 about oral manifestation of syphilis, determined the atrophic condition of the tongue as the sign of a secondary and tertiary stages of the disease. In particular, tongues were shown to be affected in 37% of cases, while the prevalence of the atrophic conditions is not clear .
2.6. Atrophic Tongue Condition as Consequence of Systemic Diseases
An atrophic condition of the tongue can be related to a systemic disorder that leads to nutritional deficiency, with the determination of an AG as described in 2.2. section, to direct damage following autoimmunity mechanisms or through neoplastic degeneration that brings to an atrophic aspect of the tongue, but that doesn't determine a diagnosis of AG.
There are several other systemic conditions or pathologies that can lead to the formation of an atrophic aspect of the tongue, not always classifiable as AG: autoimmune diseases, pre-neoplastic and neoplastic conditions, direct damage, genetic pathologies and metabolic disorders [1, 3, 12].
2.6.1. Gastroesophageal Reflux
Gastroesophageal reflux disease (GERD) is a pathological condition typically represented by the regurgitation of gastric acid with damage to the esophagus. Symptoms of GERD are distinguished into classic and extra-esophageal, the latter being the only symptoms in about fifty percent of cases . Oral signs can be distinguished on the basis of their aetiological cause. Direct damage provoked by gastric acid reflux from the stomach is represented mainly by dental erosions . Mucosal damages, in particular on the palatine mucosa, are often described as hyperaemic, erythematous areas along with an alteration in salivary gland functions. Atrophic lesions of the tongue are frequently described in association with GERD. It is often difficult to determine if they are a direct consequence of the acid ph or if they are secondary to the alteration of the saliva (often with a xerostomic condition) leading to infection (e.g. candidiosis) or, more frequently, originating from drug administration (see Table 3) [95, 96].
|Drug name||Application||Side effect potentially producing an atrophic tongue||Ref|
|Metformin||Type 2 diabetes treatment||Vitamin B12 and folic acid deficiency (in association with proton-pump inhibitor)|||
|Proton-pump inhibitor (omeoprazole, lansoprazole)||Acid-lowering agent||Vitamin B12 deficiency (in association with metformin)|||
|Histamine antagonist||Acid-lowering agents||Vitamin B12 deficiency|||
|Isoniazid||Anti-tuberculosis agent||Vitamin B3 and vitamin B6 deficiency|||
|Chloramphenicol||Antibiotic||Vitamin B3 deficiency|||
|Fluorouracil||Cancer treatment (antimetabolite)||Vitamin B3 deficiency|||
|Oral contraceptives||Contraceptive||Vitamin B6 and folic acid deficiency|||
|Anticonvulsants (carbamazepine, valproic acid, gabapentin, phenobarbital, phenytoin and primidone)||Treatment of epilepsy and neuropathic pain||Vitamin B6 and folic acid deficiency|||
|Cycloserine||Anti-tuberculosis agent||Vitamin B6 deficiency|||
|Penicillamine||Immunosuppression to treat rheumatoid arthritis||Vitamin B6 deficiency|||
|Hydrocortisone||Immune system suppression||Vitamin B6 deficiency|||
|Mercaptopurine||Immunesuppressive agent||Vitamin deficiency|||
|Methotrexate||Treatment of cancer and autoimmune diseases||Folic acid deficiency|||
|Sulfasalazine||Rheumatoid arthritis treatment||Folic acid deficiency|||
|Triamterene||Treatment of hypertension and edema||Folic acid deficiency|||
|Chemotherapy||Cancer treatment||Changes of oral microcirculation||[69, 70]|
|Bleomycin||Cancer treatment||Tissutal hypoxia||[69, 70]|
|Bisphosphonates (alendronate, etidronate and risedronate)||Metastatic prevention, treatment of osteoporosis and arthritis rheumatoid||Xerostomia, alteration of cellular turnover|||
|Antidepressants (clomipramine, doxepin)||Tricyclic antidepressants||Xerostomia, anemia (rare)|||
|Fluoxetine||Antidepressant||Xerostomia, gastrointestinal disorders|||
|Venlafaxine||Antidepressant||Xerostomia, gastrointestinal disorders|||
|Fluvoxamine||Treatment of obsessive-compulsive disorder and major depressive disorder||Xerostomia, gastrointestinal disorders|||
|Serteraline||Antidepressant||Gastrointestinal disorders determining malabsorption||[68, 73]|
|Antibiotics||Antibacterial activity||Candidiasis, gastrointestinal disorders|||
|Rivastigmine||Treatment of dementia of the Alzheimer’s type and dementia due to Parkinson's disease.||Gastrointestinal disorders|||
2.6.2. Lichen Planus
Lichen planus is a chronic dermatologic disease that often affects the oral mucosa with two clinical manifestations: reticular and erosive [3, 97, 98]. Erosive lichen is less common than the reticular one, but it is clinically more important because is often symptomatic. The lesion appear as atrophic, erythematous areas with central erosion of varying degrees [3, 97, 98]. The tongue, the third or fourth oral site are more frequently involved after the buccal mucosa, lower lip and, sometime, the gingiva . It is suggested to perform a biopsy in cases in which diagnosis is doubtful (Fig. 3).
2.6.3. Neoplastic Conditions
Squamous cell carcinoma of the tongue is the cancer more frequently diagnosed in the oral cavity, with an incidence between 25 and 40% . This condition is strictly related to the abuse of tobacco and alcohol, and more frequently involves the lateral surface of the tongue [2, 100, 101]. Cancer of the tongue clinically appears as a nodular or ulcerated lesion frequently associated with pain and discomfort. In the premalignant phase, the tongue shows a red or white lesion that leads to the diagnosis of an erythroplakia or a leukoplakia . The erythroplakia is a condition that can determine a misdiagnosis of AG, with the risk of delayed recognition of the tumour [2, 12]. A biopsy is fundamental for the correct diagnosis and subsequent therapy .
|Fig. (3). Tongue lesion related to lichen planus (histological diagnosis).|
2.6.4. Riley-Day Syndrome
First described in 1949 by Conrad Milton Riley and Richard Lawrence Day, this disorder is an autosomal recessive neuropathy of the autonomic nervous system [103, 104]. It is characterised by decreased deep tendon reflexes, impaired perception of temperature and pain, lack of an axon flare following intradermal histamine injection, labile blood pressure and absence of fungiform and filiform papillae in the tongue [5, 12, 105]. This pathology exclusively affects Ashkenazi Jewish children, and presents several oral signs with high rates of dental trauma and self-mutilations. AG represents the most important oral sign that can lead to a suspicion of the underlying syndrome and is based on a degenerative condition caused by a local autoimmune reaction .
Psoriasis is a skin and joint disease affecting between 1 and 2% of the population of the United States . The clinical pattern is represented by an increased proliferation of keratinocytes due to an autoimmune reaction, with activation of T lymphocytes, abnormal production of cytokines, altered molecular adhesion, chemotactic mechanisms and grow factors productions . Specific oral lesions have been associated with this pathology. In particular, fissured tongue and geographical tongue have been observed as consequence of the immunological disorder . Oral mucosal lesion may be associated with psoriasis, but it is not clear if these can be considered pathognomonic of this systemic disease .
2.6.6. Epidermolysis Bullosa
Epidermolysis bullosa (EB) is a rare genetic disorder represented by various and different subtypes, all based on a fragility of skin and mucosal membranes with the development of blisters and atrophic areas. A strong association between this systemic disease and tongue affections has been described. More than the 50% of patients involved in a study presented AG in various degrees of severity, so that the tongue has been considered the most affected oral site in patients with diagnosed EB . Lingual involvement has also been described by other authors, confirming that the lingual dorsum is the oral site with the most frequent manifestations. Unfortunately, oral lesions are not pathognomonic of EB or of EB sub-types [108-110]. It is hypothesized that the high prevalence of tongue affection can be explained by its size, function and position, so that it is constantly exposed to the risk of traumas .
2.6.7. Melkersson-rosenthal Syndrome
The Melkersson-Rosenthal syndrome (MRS) is a rare granulomatous disease characterised by vesicles, lymphangiomas, facial paralysis and fissured tongue [3, 111, 112]. Tongue lesions were described in a large number of patients, arriving up to 75% in a study by Feng et al. In the MRS there is an alteration of the microcirculation, in addiction to food intolerance determining malabsorption [113-116]. The tongue can develop fissures, edema, paresthesia, erosions or taste alteration [3, 111, 112]. For the reasons explained previously, in addition to the therapy with corticosteroid, clinicians often suggest a specific diet, with the addition of B vitamins. Therefore, the application of tests to determine food allergies will make it easier to identify and eliminate particular foods from a given patient’s diet .
Diabetes mellitus is a disease that causes an alteration in the production of insulin or that determines a tissue resistance to insulin effects . It is divided into two different clinical patterns (Type I and type II). Only type I diabetes is related to oral manifestation through autoimmune aetiology. Oral manifestations are periodontitis, diabetic sialoadenosis, oral candidiasis, xerostomia, fissured tongue and benign migratory glossitis [3, 14, 117-119].
3. DIAGNOSTIC HINTS
The diagnosis of an atrophic condition of the tongue is complicated by the similar, local expression of different clinical presentations. It is usually composed of three different clinical patterns, such as atrophic glossitis, geographic tongue (benign migratory glossitis) and the median rhomboid glossitis (Table 4).
|Median Rhomboid glossitis||It affects 0.001%-1% of the population||Candida infection||Usually asymptomatic,
burning or itching possible
|Application of antifungal medicaments|
|Geographic tongue/benign migratory glossitis||Prevalence range from 1% to 2.5%||Unknown||Often asymptomatic, sometimes burning sensation||None, if associated with burning mouth syndrome it is possible to apply topical steroid|
|Atrophic glossitis||Incidence between 1.3-9%||Nutritional defiencies or underlying disease||Asymptomatic||Treatment of the systemic disease (if present) and administration of nutritional supplement (see Table 1)|
|Fig. (4). Atrophic glossitis related to a celiac disease (histological diagnosis).|
3.1. Atrophic Glossitis
Reamy et al. in 2010 described this clinical as: “Atrophic glossitis is also known as smooth tongue because of the smooth, glossy appearance with a red or pink background. The smooth quality is caused by the atrophy of filiform papillae ,” (Fig. 4). As previously described, the real AG is typically related to a nutritional deficiency status. The lack of vitamin intake can be associated with a poor diet or with a systemic disease. In both cases a blood sample is necessary to identify an alteration in hemoglobin, iron, folic acid and vitamin B group and homocysteine levels, in addition to gastric parietal cell antibody positivity [9, 18, 19, 122]. It can also be useful to perform antigliadin, tissue transglutaminase and the IgA-endomysial antibody tests, and a microbiological analysis of tongue surface [7, 18]. Sometimes, the absence of symptoms makes the diagnosis more difficult because patients are often non-compliant with all the required exams.
3.2. Geographic Tongue/Benign Migratory Glossitis
This disease has been defined as: “[...] the dorsal tongue develops areas of papillary atrophy that appear smooth and are surrounded by raised serpiginous borders. These regions of atrophy spontaneously resolve and migrate, giving the tongue a variegated appearance .” The diagnosis of this condition is easy, because of the tendency of the lesions to change and “move” throughout the day. Two repeat visits in 12-24 hours and a microbiological examination to rule out a Candida infection, will help in identifying with sufficient certainty the disease without the need for further tests [12, 79, 123]. It is often impossible to alleviate patients’ burning sensations. A simple search for nutritional deficiencies is strongly recommended .
3.3. Median Rhomboid Glossitis
This pathology is described as “[...] a smooth, shiny, erythematous, sharply circumscribed, asymptomatic, plaque-like lesion on the dorsal midline of the tongue ,” (Fig. 5). Clinically it can be asymptomatic or it can determine pain or burning sensation. The aetiology of this disease is controversial, but it is usually considered as a clinical variant of a candida infection. A microbiological analysis of tongue surface and a thorough anamnesis are key to diagnosis .
The tongue can be considered as a mirror of oral and/or systemic health. An oral medicine expert can be the first to observe the lingual status, and should be familiar with the different diagnoses of these conditions, for example being able to link lingual abnormalities with specific etiologic causes. Recognition of alterations relative to tongue’s morphology, in the presence of a negative anamnesis, should lead to more accurate investigations, in order to ascertain if they are manifestations of an underlying systemic condition [1, 12].
|Fig. (5). Median rhomboid glossitis (Microbiological diagnosis).|
Among tongue diseases, AG has the most complex differential diagnosis, because it is associated with several conditions. Atrophy of the filiform papillae, not directly attributable to mechanical damages of the mucosa, can occur in systemic or local conditions. Although seemingly simple, sometimes the recognition of a “real AG” can be very hard. Many local conditions, such as median rhomboid glossitis, of glossite migrans, mediated by infective and idiopathic etiological factors, as well as neoplastic or congenital factors, can complicate the diagnosis. Reamy et al. described and analyzed the most frequent lingual diseases, with a particular attention to the atrophic conditions . They summarized the etiologic conditions responsible for the development of AG; among them it was discovered that nutritional deficiencies and drug reactions are the most frequently encountered. Unfortunately, while drug interactions are almost always detectable with anamnesis, nutritional deficiencies can be related to various and different systemic conditions, and sometimes the etiological factor may be difficult to identify. A typical example is anaemia, in which the cause may be acute or chronic. In some circumstances, however, the outbreak of other symptoms in association with the casual discovery of tongue lesions, as in case of celiac disease, can be decisive for the diagnosis .
The clinician has to identify the clinical and anamnestic conditions that will lead to the diagnosis of the AG and also identify a possible related systemic disease. During the first observation of the lesion it is necessary to apply a strict protocol to achieve the right diagnosis. First of all, after the anamnesis, the clinician has to identify if the lingual condition can be associated with medication taken by the patient (Table 2) or with some already recognised systemic disease (chapter 2.3). In case of a negative anamnesis, it is fundamental to verify if the AG changes during the 12-24 hours after the first observation in order to reject the hypothesis of a geographic tongue (chapter 3.2). If the lesion shows no variation in this time-span, the clinician needs to perform a microbiological analysis of the lingual dorsum to exclude or find a candida infection (that can be classified as primary or secondary to the AG). The presence of a candidiasis is not necessarily the diagnostic answer, because the AG can easily be infected by both local and systemic conditions. It is important to remember that the clinical picture associated with a primary candidiasis is the median rhomboid glossitis (chapter 3.3), while condition such as nutritional deficiencies, diabetes, xerostomia and ph alterations can easily lead to a secondary infection. Anyway, in case of positivity of the microbiological test, it is necessary to treat the infection and to revaluate the patient after the therapy, repeating the microbiological analysis in order to observe possible remission of the atrophic condition (in case of primary candidiasis). If the lesion is still observable after the antimicrobic therapy, or in case the microbiological test was negative, the clinician needs to evaluate specific blood tests (chapter 3.1). Following the results of the blood tests, the pathologist should be able to identify the aetiology of the atrophic condition and to treat it, or ask for a consultation. In the case of unknown or unidentified aetiology, the observation has to be repeated to identify the appearance of other signs (local or systemic).
The early recognition of signs and symptoms relative to systemic conditions through careful analysis of oral anatomical structures appears essential in the perspective of achieving a better prognosis. Atrophic anomalies are related to several conditions, both local and systemic, that clinicians have to know and identify. For these reasons, knowledge of oral diseases and their aetiology is important, requiring a continuous professional education as well as interaction with other medical specialists when necessary.
CONFLICT OF INTEREST
The authors confirm that this article content has no conflict of interest.
Authors are thankful to Laura Armosini for the picture on tongue anatomy.