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Journal of Drug Delivery and Therapeutics

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Open Access Full Text Article                                                  Review Article

Clinical Characteristics of Oral Tuberculosis: A Scoping Review

Nanan Nur’aeny*, Anargya Alfa Fairuz 2, Tiffany Marsha Indrawati 2, Amira Zahida Raihana 2, Marsyanda Fitri 2, Dewi Zakiawati 1, Indah Suasani Wahyuni 1, Wahyu Hidayat 1

Department of Oral Medicine, Faculty of Dentistry, Universitas Padjadjaran, Bandung, Indonesia.

Dentistry Profession Program, Faculty of Dentistry, Universitas Padjadjaran, Bandung, Indonesia.

Article Info:

_____________________________________________Article History:

Received 23 May 2026 

Reviewed 04 July 2026 

Accepted 26 July 2026 

Published 15 August 2026  

_____________________________________________

Cite this article as:

Nur’aeny N, Fairuz AA, Indrawati TM, Raihana AZ, Fitri M, Zakiawati D, Wahyuni IS, Hidayat W, Clinical Characteristics of Oral Tuberculosis: A Scoping Review, Journal of Drug Delivery and Therapeutics. 2026; 16(8):170-178  DOI: https://doi.org/10.22270/jddt.v16i8.7913              _____________________________________________

For Correspondence:  

Nanan Nur’aeny, Department of Oral Medicine, Faculty of Dentistry, Universitas Padjadjaran, Bandung, Indonesia.

Abstract

_______________________________________________________________________________________________________________

Introduction: Oral tuberculosis (TB) is a rare manifestation of Mycobacterium tuberculosis infection, yet it may signal systemic disease. Because oral TB lesions often mimic traumatic ulcers, oral malignancy, or chronic infection, diagnosis is frequently delayed. Objective: To map the clinical characteristics of oral TB lesions, the oral sites most often involved, and the diagnostic approaches reported in recent literature. Methods: A scoping review was conducted in accordance with the PRISMA-ScR guidelines. PubMed and Scopus were searched for English- or Indonesian-language primary reports published between 2020 and 2025 that described oral manifestations of TB. Four reviewers independently screened records and extracted data; findings were synthesized narratively and mapped quantitatively by lesion pattern, anatomical site, and diagnostic pathway. Results: Of 58 records identified, 13 articles were included after deduplication and screening. Oral TB most often presented as chronic ulceration with poorly defined margins and erythematous or grayish-white surfaces, although nodules and tumor-like masses were also described. The tongue was the most frequent main site (5/13; 38.5%), followed by buccal and/or labial mucosa (4/13; 30.8%), palate (2/13; 15.4%), and, less commonly, gingiva or a post-extraction socket (1/13 each; 7.7%). Diagnosis typically combined clinical assessment, imaging when indicated, biopsy with histopathology, and, in several reports, molecular or culture confirmation. Clinical improvement after standard anti-TB therapy was described in the included cases. Conclusion: Across recent case-based reports, oral TB most commonly appears as chronic tongue or mucosal ulceration and requires multimodal confirmation. Greater familiarity with these patterns may help dentists recognize suspicious lesions earlier, particularly in TB-endemic settings. 

Keywords: Tuberculosis, Clinical characteristics, Oral manifestations, Oral lesions, Mycobacterium tuberculosis 

 


 

INTRODUCTION

Tuberculosis (TB) is an infectious disease caused by Mycobacterium tuberculosis, with the lungs being the most common site of infection. The infection can also spread to other parts of the body, including the oral cavity. Although oral tuberculosis is rare, its presence often indicates a systemic infection and can increase morbidity. Oral TB lesions present in various forms, such as chronic ulcers, nodules, granulomas, or soft tissue enlargements, and frequently mimic other conditions like cancer, syphilis, or trauma. These overlapping clinical characteristics often make diagnosis difficult and lead to delays.

Tuberculosis has a significant global impact and a complex etiology involving the immune system, the environment, and socioeconomic conditions. Data from the World Health Organization (WHO) indicate that approximately 10.6 million new TB cases occurred worldwide in 2022, with Indonesia among the countries bearing the highest burden.1 Oral manifestations of tuberculosis frequently occur in individuals with compromised immune function, including patients with TB–HIV coinfection or poor nutritional status. 

The condition of the oral cavity can reflect an individual's systemic health status; thus, the presence of oral TB lesions may serve as an early indicator of active infection or disease dissemination. The presenting symptoms are typically persistent and painful, and they do not respond to conventional local therapy. Establishing a diagnosis requires histopathological examination and confirmation via microbiological testing.

Dentists play an important role in early detection, particularly through recognition of oral TB lesion characteristics, and interdisciplinary collaboration between medical and dental professionals can strengthen overall case management. Earlier reviews have discussed clinical features and diagnostic considerations of oral TB.2,3 However, a focused scoping review that systematically maps recent case-based evidence (2020–2025) on lesion characteristics, oral sites, and diagnostic pathways remains limited. 

This gap is clinically relevant because oral TB lesions frequently resemble traumatic ulcers, chronic infections, or malignancy and may therefore go unrecognized for months, particularly in TB-endemic regions where a dentist may be the first health professional to examine the oral mucosa. The present scoping review was undertaken to address this gap by assembling and quantitatively summarizing case-based literature published between 2020 and 2025, with particular attention to lesion morphology, anatomical distribution, and diagnostic pathways. 

The aim of this study is to map the oral manifestations of tuberculosis reported in the recent scientific literature, covering clinical presentations, lesion locations, and diagnostic methods in greater detail. In addition, the review seeks to surface secondary knowledge gaps that remain after this mapping exercise, so that future research can be directed more purposefully toward strengthening early detection in dental practice.

The research questions are, first: what clinical characteristics of oral TB lesions have been reported in recent primary literature, then second: which oral tissue sites are most frequently involved, and third: what diagnostic approaches are used to confirm oral TB.

METHODS

This study is a scoping review conducted to identify, characterize, map, and synthesize evidence from diverse primary designs, following the methodological guidance of PRISMA-ScR.4 The stages of the review comprised identifying the research questions, searching information sources, selecting evidence, charting the data, and collating and reporting the results (Figure 1).

The articles used as literature eligibility criteria for this thesis are those that meet the following criteria: a) PCC Criteria (Population, Concept, Context), the PCC criteria are employed to formulate questions, facilitate the search process, and frame the research question. In this study, the criteria format used is as follows: Population: patients diagnosed with TB (pulmonary or extrapulmonary), Concept: Oral manifestations or oral lesions associated with TB, and Context: Original research articles, including case reports, case series, and observational studies; b) Inclusion criteria were: articles reporting cases or data regarding oral manifestations of TB, published between 2020 and 2025, and full-text articles available in Indonesian or English Exclusion criteria were: articles in non-human studies and that are not primary research (e.g., reviews, editorials, letters to the editor).

Search Strategy

PubMed and Scopus databases were used as the Information sources and literature search strategy. Boolean operators were used to combine search terms. The search string used in this review was: (("oral tuberculosis" OR "oral lesion" OR "oral ulcer") AND ("tuberculosis" OR "Mycobacterium tuberculosis") AND ("case report" OR "original research")). 

 

Research Procedure

The research procedure follows the PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews) flow diagram.5 The literature selection process was conducted through the following steps: Formulate the research question and define the topic; Establish PCC, inclusion, and exclusion criteria; Search database journals using specific keywords; Limit the initial screening to publications from 2020 to 2025; Remove duplicate records across all database results; Screen titles and abstracts to exclude irrelevant studies; Read full-text articles to confirm eligibility based on inclusion criteria; Extract, analyze, and present data from the final set of articles. Title/abstract and full-text screening were performed by three reviewers working independently. Disagreements were resolved by discussion or adjudication by a senior reviewer. Figure 1 shows the PRISMA-ScR Diagram Flowchart in this review. 

                  image

Figure 1. PRISMA-ScR Diagram Flowchart

Data Extraction

Data were extracted from articles that met the inclusion criteria. The extracted variables included the author(s), year of publication, study design, title, type of TB, diagnostic method, clinical findings, and main conclusions.

RESULTS

A comprehensive literature search using PubMed and Scopus yielded an initial total of 58 articles. After removing three duplicate entries, 55 unique records remained for screening. Initial title and abstract screening identified 20 relevant articles. These articles were then assessed for full-text availability and eligibility based on the inclusion criteria. Seven articles were excluded due to full-text unavailability or non-alignment with the inclusion criteria. Consequently, 13 articles fulfilled all criteria and were included in the final analysis (Table 1)

.


 

 

Table 1. Sample characteristics

Article Code

Author

Year

Title

Types of TB

Type of Study

Diagnostic Methods

1

Juan Tang, et al.6

2023

A case of oral tuberculous ulcer and literature review

Primary oral tuberculosis

Case reports with literature review

Clinical examination, PPD test, chest imaging, immunology, bacteriology, histopathological examination (H&E stain), with histopathological examination considered the gold standard.

2

Tribikram Debata, et al.7

2024

Rare case of extrapulmonary tuberculosis masquerading as an intraoral sinus in association with a nonhealing extraction socket in a teenage girl

Primary oral tuberculosis

Case report

Clinical examination, Oral Panoramic Radiograph (OPG), Routine Blood Investigations (ESR), Excisional Biopsy, Histopathological examination (H&E stain), and CBNAAT testing of pus discharge

3

Cintia Milani, et al.8

2024

Tuberculosis of the tongue in a patient under treatment with adalimumab

Primary oral tuberculosis

Case report

Molecular rapid test (sputum), chest radiography, clinical and immunological examination, microscopy, bacterial cultures, biopsy

4

Paulo S.S. Pina, et al.9

2022

A buccal mucosa ulcer as the first sign of tuberculosis

Oral manifestation of pulmonary TB

Case report

Clinical examination, incisional biopsy, histopathological

5

Priyanka Sachdeva, et al.10

2020

Primary oral tuberculosis - A case report

Primary oral tuberculosis

Case report

Histopathological examination, hematological investigations, radiographic investigations (chest radiograph)

6

Bahaa Razem, et al.11

2021

Lingual primary tuberculosis mimicking malignancy

Primary oral tuberculosis

Case report

Histopathological examination

7

Joana Fragoso, et al.12

2020

Oral ulcer as presentation of cavitating pulmonary tuberculosis

Oral manifestation of pulmonary TB

Case report

Biopsy, CTScan, antibacterial sensitivity test, serology for HIV, HCV, and HBV

8

Sevilla-Fuentes, et al.13

2024

Tongue Tuberculosis as a Complication of Pott’s Disease in a Patient on Systemic Steroid Therapy without Pulmonary Tuberculosis

Oral manifestation of spinal TB

Case report

Biopsy, MRI, histopathological examination, clinical examination and serology

9

Shyamkum ar Sriram, et al.14

2023

Primary Tuberculosis of Buccal and Labial Mucosa Literature

Primary oral tuberculosis

Case reports with literature review

Radiographic imaging, microbiological tests, immunological response tests, histopathology, molecular investigation

10

Nakkeeran Adhithiya, et al.15

2024

Gingiva as the primary site of extrapulmonary tuberculosis: A rare case report with brief review of literature

Primary oral tuberculosis

Case reports with literature review

Histopathological examination, liquid culture, cartridge-based nucleic acid amplification test (CB-NAAT), and clinical correlation with antitubercular therapy (ATT)

11

Ines Kechaou, et al.16

2021

Palate Tuberculosis with Paradoxical Lymphadenitis

Palatine tuberculosis with cervical lymph node involvement

Case report

Biopsy of palatine lesion showing granulomatous tissue with caseous necrosis, cervical ultrasonography, facial CT scan, tuberculin skin test, chest radiography, abdominal ultrasonography

12

Rocío Valenzuela-Narváez, et al.17

2020

An Unusual Granular Ulcer Secondary Oral Tuberculosis

Oral manifestation of pulmonary TB

Case report

Clinical examination, anatomopathological study

13

Aboubakr Mabrouki, et al.18

2022

A Giant Nodule of the Soft Palate Mimicking a Tumor: A Case of Oropharyngeal Tuberculosis

Oral manifestation of pulmonary TB

Case report

Contrast-enhanced cervicofacial scan, magnetic resonance imaging (MRI), and histopathological examination of a biopsy specimen

 

Table 2. Characteristics of Oral Tuberculous Lesions

Article Code

Types of Lesions

Location

Size

Color

Lesion margin

Other Findings

1

Ulcerative nodule

Left dorsal surface of the tongue, possibly extending to the surrounding area.

±2.0 cm diameter

Not specified (possibly erythematous)

Indistinct, boundaries are not clearly defined.

Distinct, worsening pain; a central area of ulceration with raised, indurated surrounding tissue.

2

Post-extraction socket lesion with sinus tract and ulceration

Mandibular first molar region (extracted tooth area)

Not specified

Not specified

Not specified

Pain, swelling, purulent discharge, granulomatous inflammation, irregular alveolar bone destruction, persisting for approximately one month.

3

Multiple ulcerative lesions

Tongue — dorsum, right and left lateral borders, extending to the ventral surface.

Broad, gradually enlarging

Not specified (possibly erythematous/inflammatory)

Irregular, ill-defined borders, indurated.

Severe pain, difficulty eating, ulcers persisting for >1 year prior to diagnosis.

4

Ulceration

Right buccal mucosa, from the labial commissure to the right buccal mucosa.

± 4 cm

Red with a yellowish area

Irregular

Painful, solitary, chronic for ±4 months, gradually enlarging.

5

Solitary ulceration

Left lower labial mucosa

± 4 cm × 4 cm

Whitish-gray

Irregular, with thin and undermined edges.

Painless, base slightly indurated, unchanged for 2 years, no other symptoms.

6

Ulceration

Tongue (lateral sides, tip, and posterior third)

Varies

Not specified

Irregular

The lesion is typically solitary and painful, accompanied by limited tongue protrusion and trismus; it is of short duration but progressive, resembling a traumatic ulcer or cancer.

7

Papillomatous ulceration

Posterior third of the dorsum of the tongue

±3 cm

Not specified

Not specified

Pain, duration of 4 months, bilateral cervical lymphadenopathy, weight loss >10%

8

Solitary ulceration

Tongue

Covers

±80%

of the tongue's surface

Not explicitly stated

Not explicitly stated

The lesion spread rapidly to both sides of the tongue, causing severe pain that made swallowing impossible; it persisted for several months and did not improve with antifungal therapy. 

9

Chronic, non-healing ulceration

Buccal and labial mucosa (mainly); gingiva and tongue are also frequently affected.

Varies

Granular (Trelat)

Irregular and undermined edges

Painless, indurated ulcer with inflammatory exudate, persisting for >3 weeks, resistant to conservative therapy; may be accompanied by regional lymphadenopathy.

10

Ulcerative lesion with gingival hyperplasia

Right maxillary gingiva and alveolar mucosa (between teeth #11–#14)

Not specified

Erythematous (bright red)

Irregular

Granular surface, resembling gravel; bleeds easily; painless; persists for several weeks; does not improve after periodontal therapy.

11

Multiple ulcerations

Palate

diameter

<1 cm

Not specified

Not specified

No necrosis or ulceration; poor oral hygiene; persistent after tooth extraction; resistant to antibiotics.

12

Chronic granular ulceration

Vestibular mucosa of the left mandibular premolar region (buccal)

Diameter ± 2 cm

Not specified (covered with Trélat's granules)

Irregular edges

Granular surface, deep depression, asymptomatic, no lymphadenopathy, chronic course of 3 years.

13

Tumor-like nodular mass

Right soft palate, pushing the uvula to the left.

Diameter ± 3 cm

Clearly defined, separable

Clearly defined, separable

Firm consistency, odynophagia, nocturnal snoring, without signs of inflammation or ulceration.

 

 

Table 3. Distribution of Included Cases

Domain

Category

n

%

TB type

Primary oral TB

7

53.8%

 

Oral manifestation of pulmonary TB

4

30.8%

 

Oral manifestation of spinal TB (Pott’s disease)

1

7.7%

 

Palatine TB with cervical lymph node involvement

1

7.7%

Main oral site

Tongue

5

38.5%

 

Buccal and/or labial/vestibular mucosa

4

30.8%

 

Palate/soft palate

2

15.4%

 

Gingiva/alveolar mucosa

1

7.7%

 

Post-extraction socket

1

7.7%

Predominant lesion pattern

Ulceration (solitary, multiple, papillomatous, granular, or ulcerative nodule)

11

84.6%

 

Socket lesion with sinus tract

1

7.7%

 

Tumor-like nodular mass

1

7.7%

 


 

DISCUSSION

Oral manifestations of tuberculosis (TB) are rare, accounting for only approximately 0.05% to 5% of total TB cases, thus carrying a high risk of misdiagnosis and delayed treatment.6 Innate immunity against TB infection of the oral mucosa is influenced by the integrity of the oral mucosa and saliva. Minor mucosal lesions resulting from chronic inflammation, trauma, leukoplakia, or poor oral hygiene can serve as sites for Mycobacterium tuberculosis to colonize.20 Oral TB lesions are most often secondary to pulmonary TB infection, but primary cases can also occur, particularly in mucosal areas with trauma or decreased local immunity.9,15 The route of infection spread to the oral cavity is generally not through direct inoculation from sputum, but rather through hematogenous or lymphatic spread, with Mycobacterium tuberculosis reaching the submucosa and causing mucosal ulceration.15,21 The most common clinical manifestation is a painless, non-healing chronic ulceration, often accompanied by regional lymphadenopathy.6,14,15 Because it is non-specific and can mimic other granulomatous or neoplastic lesions, such as sarcoidosis, Crohn’s disease, deep mycoses, cat-scratch disease, foreign-body reactions, tertiary syphilis, and Melkerssone-Rosenthal syndrome, additional special tests including histopathology or microbial culture are required.22

 The diagnosis of oral TB requires a multidisciplinary approach with histopathological confirmation, liquid culture, and molecular examinations such as cartridge-based nucleic acid amplification tests (CB-NAAT).6,15 The CB-NAAT testing technology was endorsed by the World Health Organization (WHO) in December 2010 and recognized as a major advancement in global TB control. Cartridge-based nucleic acid amplification testing (CBNAAT) is a real-time polymerase chain reaction (PCR) assay that enables the simultaneous detection of the Mycobacterium tuberculosis complex and rifampicin resistance from biological specimens within two hours.23

Clinical characteristics of oral TB lesions across the included reports, chronic ulceration was the dominant morphological pattern, accounting for 11 of 13 cases (84.6%). Ulcers were described as solitary or multiple, occasionally papillomatous or granular, and sometimes combined with nodularity.6,8,10,12,13 This distribution is broadly consistent with earlier observations that ulcerative forms predominate in oral TB.19 At the same time, non-ulcerative presentations should not be dismissed: a firm, tumor-like soft-palate mass was reported and initially suggested neoplastic disease,18 while an extraction-socket lesion with sinus tract illustrated a further atypical route of presentation.7 Lesion size ranged from small palatal ulcers less than 1 cm in diameter to extensive involvement covering most of the tongue surface.13,16 Color, when recorded, was most often erythematous or whitish-gray, and several reports emphasized irregular or undermined margins together with a granular surface resembling Trélat granules, a finding that may help distinguish tuberculous ulceration from more banal chronic ulcers.10,14,17 Pain was strikingly inconsistent: some lesions were painless for long periods, whereas others produced severe odynophagia, trismus, or feeding difficulty.10,11,13,15 Within this small case-based sample, chronicity, resistance to local therapy, and morphological irregularity appeared more consistent clinical prompts than pain intensity alone; this interpretation should be tested in larger series.

Anatomical sites of involvement the tongue was the most frequent main site (5/13; 38.5%), followed by buccal, labial, or vestibular mucosa (30.8%) and palate (15.4%), with single reports involving gingiva and a post-extraction socket (Table 3). Predilection for the tongue has been linked to repeated microtrauma from teeth or rough dental surfaces and to the rich vascular supply of lingual muscle, which may facilitate either local implantation or hematogenous seeding.3,11 Involvement of buccal mucosa, gingiva, and palate confirms that oral TB is not confined to one anatomical niche. The post-extraction socket case is particularly instructive for dental practice, because disruption of mucosal integrity after extraction may allow local colonization or reactivation and present as a non-healing sinus with suppuration.7

Oral tuberculosis are rare and are difficult to diagnose, so every chronic, abnormal looking lesion should be examined cautiously for early diagnosis and prompt treatment.24 Diagnostic approaches because clinical features are nonspecific and may mimic granulomatous or neoplastic disease, confirmation in the included reports generally followed a multimodal pathway. Suspicious chronic lesions prompted biopsy; hematoxylin–eosin staining frequently revealed granulomatous inflammation with caseous necrosis, sometimes supported by acid-fast staining.6,9,13 Molecular assays such as GeneXpert MTB/RIF, PCR, or CB-NAAT on tissue or pus, and liquid culture in selected cases, provided microbiological confirmation.7,8,15 Imaging (plain radiography, CT, or MRI) and immunologic tests (tuberculin skin testing or IGRA) were used mainly to evaluate systemic involvement or to support the overall diagnostic context rather than as stand-alone proof of oral disease.10,11,13 In practical terms, the included reports most often combined clinical suspicion with tissue diagnosis and, where available, microbiological confirmation, while systemic work-up was guided by pulmonary or extrapulmonary clues.

Of the thirteen cases recorded, the most common types of lesions as a manifestation of oral tuberculosis are ulceration in various forms, such as single ulceration,10,13  multiple ulceration,8 and papillomatous ulceration.12  This is in accordance with previous reports which stated that 93% of lesions in oral manifestations of TB were ulcerated.19,25 There are also ulcerative nodular lesions6 and hard, painless nodular masses that resemble tumors,18 indicating that oral tuberculosis does not always act as an ulcer alone but can resemble mass lesions or nodules.

Lesions can vary in size from small lesions less than 1 cm on the palate to extensive lesions covering 80% of the tongue surface.13,16 Large and progressive lesions are often associated with long-term lesion duration or delayed diagnosis, as in one case where the lesion progressed from the size of a sorghum grain to the size of a coin over four months.6

The color of the lesions is mostly described as erythematous (red) or whitish-gray, such as a single ulcerated lesion on the labial mucosa,10 which has a whitish-gray color with thin, undermined edges. Some lesions exhibit a granular surface resembling "Trelat granules," which is a characteristic finding and helps distinguish tuberculosis from other chronic ulcers.14,17 Lesion borders are often irregular and ill-defined, for example in ulcerative nodules6 and some multiple ulcerated lesions, indicating active infiltration and widespread inflammation. These ill-defined borders can make it difficult to assess the extent of lesion spread clinically. Another characteristic finding is the presence of pain of varying degrees, ranging from painless10,15 to severe pain and functional impairment such as difficulty swallowing and trismus.11,13 This indicates that pain is not always the primary parameter in assessing oral tuberculosis.

Of the thirteen cases, all received WHO standard therapy in the form of a combination regimen of HRZE (isoniazid, rifampicin, pyrazinamide, and ethambutol), with a duration of therapy ranging from 6 to 12 months. In cases of glanular ulceration and Pott's disease, additional management in the form of periodontal surgery17 or cervical fixation13 was performed to restore function and prevent deformity. Treatment outcomes were generally good; almost all patients showed improvement within the first 4–6 weeks of therapy and fully recovered after 6–12 months.

Overall, the characteristics of oral TB lesions are highly variable and sometimes resemble other pathological conditions such as traumatic ulcers, malignancies, or other chronic infections. Therefore, establishing a correct diagnosis requires a thorough evaluation of the clinical features and diagnostic support, which includes a combined clinical, radiographic, histopathological, and molecular testing approach. The diagnosis of oral tuberculosis in existing cases generally begins with the clinical identification of suspicious lesions, followed by tissue biopsy as the primary step. Routine histopathological examination with hematoxylin-eosin (H&E) staining reveals granulomas with caseous necrosis, which is then confirmed by Ziehl–Neelsen (ZN) staining for acid-fast bacilli.6,9,13 Several reports also utilize molecular tests such as GeneXpert MTB/RIF or PCR from biopsy tissue or pus as definitive confirmation of the presence of Mycobacterium tuberculosis.7,8,13 In addition, liquid cultures are performed in some cases to confirm the diagnosis.15 Other supporting examinations such as X-rays, CT scans, and MRI are used if there is suspicion of involvement of other organs such as bones.13 The tuberculin test (Mantoux) and IGRA are also used in some cases as additional screening.10,11

Several cases indicate that the initial manifestations of systemic TB were first detected in dental clinics through complaints of chronic ulcers. Dentists play a crucial role as first-line providers in detecting oral lesions, thus contributing to the identification of tuberculosis cases, especially in patients who are unaware of their disease status. Early detection by dentists is crucial, not only to prevent the development of potentially fatal disease but also to reduce the risk of transmission to both the general public and the medical team, including the dentists themselves.10 Therefore, in patients with complaints of lesions limited to the oral mucosa, dentists need to be aware that these abnormalities could be manifestations of systemic diseases such as tuberculosis.9 Furthermore, tuberculosis should always be considered as a differential diagnosis in cases of atypical oral ulcers that do not show improvement with conventional therapy, especially in patients from areas with a high TB incidence.14 Comparison with prior literature and research gaps when set against earlier clinical overviews of oral TB,2,3  the contribution of this review lies less in claiming an entirely new clinical entity than in offering a structured and quantified reading of recent case material (2020–2025), from which patterns of lesion site and morphology become more visible to the practicing clinician. The predominance of ulceration accords with older series such as Dogra et al. (2013)19, while the present map additionally summarizes diagnostic approaches reported in the included cases. Even so, several secondary gaps remain apparent once the included reports are examined side by side: lesion descriptors are applied inconsistently across publications; epidemiological estimates specific to oral TB continue to be scarce; diagnostic algorithms are often incompletely described; and prospective evidence on diagnostic delay, or on dentist-initiated case finding in high-burden settings, is still rare.

This review has several limitations. First, the evidence base consisted predominantly of case reports, which limits generalizability and introduces potential publication bias toward unusual or severe presentations; the percentages reported here therefore describe the included literature rather than true population frequencies. Second, only PubMed and Scopus were searched, and the publication window was restricted to 2020–2025; relevant studies outside these sources or years may have been missed. Third, only Indonesian- and English-language full texts were included. Fourth, critical appraisal of individual sources was not performed. Fifth, quantitative synthesis or meta-analysis was not feasible because of clinical and methodological heterogeneity. These constraints favor cautious interpretation focused on pattern recognition rather than causal inference.

CONCLUSION

Oral tuberculosis is a rare condition with highly variable lesions, ranging from ulcers and granulomas to intraoral sinuses and tumor-like masses that can mimic other diseases such as cancer or chronic infections. Although lesion locations vary, they are most commonly found on the tongue, buccal mucosa, palate, and post-extraction sockets. Diagnosis requires a thorough evaluation, including medical history, clinical, radiological, and histopathological examinations, along with confirmation through molecular testing.

The dentist plays a crucial role in detecting suspicious oral lesions, especially those that do not resolve with conventional therapy. A high index of suspicion for TB should always be maintained in the differential diagnosis, particularly in patients from endemic areas or those with a history of TB exposure, to prevent delayed diagnosis and break the chain of transmission.

Acknowledgements: We would like to express our sincere gratitude to all individuals who supported this scoping review. 

Author's contribution: All authors contributed equally to this work.

Funding source: No funding was received for the current study.

Competing interests/Conflicts of interest: The author(s) report no conflicts of interest in this work.

REFERENCES

1.     World Health Organization. Global tuberculosis report 2023. Geneva: World Health Organization; 2023.

2. Ewa K, Elzbieta S. Tuberculosis of the oral cavity: An uncommon but still a live issue. Postępy Dermatologii i Alergologii, 2015;32(4):302-306 https://doi.org/10.5114/pdia.2014.43284 PMid:26366156 PMCid:PMC4565830

3. Supriya S, Jyoti B, Pankaj KP, Akshyaya P, Priyanka S, Surya K. Oral tuberculosis - Current concepts. Journal of Family Medicine and Primary Care, 2019;8(4):1308-1312. https://doi.org/10.4103/jfmpc.jfmpc_97_19 PMid:31143712 PMCid:PMC6510082

4. Andrea CT, Erin L, Wasifa Z, Kelly KO, Heather C, Danielle L, et al. PRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation. Annals of Internal Medicine, 2018;169(7):467-473 https://doi.org/10.7326/M18-0850 PMid:30178033

5. Neal RH, Matthew JP, Chris CP, Luke AM. PRISMA2020: An R package and Shiny app for producing PRISMA 2020-compliant flow diagrams, with interactivity for optimised digital transparency and Open Synthesis. Campbell Systematic Reviews, 2022;18(2): e1230: 1-12 https://doi.org/10.1002/cl2.1230 PMid:36911350 PMCid:PMC8958186

6. Juan T, Jinhua Z, Honghai F. A case of oral tuberculous ulcer and literature review, Clinical Case Reports, 2023;11(e8216):1-4 https://doi.org/10.1002/ccr3.8216 PMid:38076017 PMCid:PMC10697859

7. Tribikram D, Anuroopa M, Sujit RS, Upasana D. Rare case of extrapulmonary tuberculosis masquerading as an intraoral sinus in association with a nonhealing extraction socket in a teenage girl-“A case report with Review of literature”. Journal of Oral and Maxillofacial Pathology, 2024;28(2):301-306. https://doi.org/10.4103/jomfp.jomfp_304_23 PMid:39157821 PMCid:PMC11329101

8.     Cintia MM, Rafaela A, Rafaela SM, Antônio ASL, Maria ANM, and Liliane R. Tuberculosis of the tongue in a patient under treatment with adalimumab. Revista Portuguesa de Estomatologia Medicina Dentaria e Cirurgia Maxilofacial, 2024; 65(4): 205-208.

9. Paulo SSP, Celso AL, Suzana COMS. A buccal mucosa ulcer as the first sign of tuberculosis. Journal of Oral and Maxillofacial Pathololgy, 2022;26(3):399-403. PMCid:PMC9802504 https://doi.org/10.4103/jomfp.jomfp_443_21 PMid:36588851 

10. Priyanka S, Sukhdeep S, Nitin B. Primary oral tuberculosis - A case report. Contemporary Clinical Dentistry, 2020;11(1):79-82. https://doi.org/10.4103/ccd.ccd_416_19 PMid:33110314 PMCid:PMC7580750

11. Bahaa R, Sami EH, Iro S, Mohamed R, Faical S. Lingual primary tuberculosis mimicking malignancy. Annals of Medicine and Surgery, 2021;67(102525):1-3 PMCid:PMC8226386 https://doi.org/10.1016/j.amsu.2021.102525 PMid:34194736 

12. Joana F, Mariana MO, Celina G, Josefina M, Rui SC. Oral ulcer as presentation of cavitating pulmonary tuberculosis. IDCases, 2020;22(e00976):1-3 https://doi.org/10.1016/j.idcr.2020.e00976 PMid:33083228 PMCid:PMC7554358

13. Samuel SF, Luis ÁMV, José FAR, Bertha BG, Ramcés FV, Brandon B. Tongue Tuberculosis as a Complication of Pott’s Disease in a Patient on Systemic Steroid Therapy without Pulmonary Tuberculosis. Medicina, 2024; 60(8):1-7 https://doi.org/10.3390/medicina60081282 PMid:39202562 PMCid:PMC11355980

14. Shyamkumar S, Shamimul H, Shazina S, Syed AA, Swagatika P. Primary Tuberculosis of Buccal and Labial Mucosa: Literature Review and a Rare Case Report of a Public Health Menace. Case Report Dentistry, 2023; 2023(6543595):1-11 https://doi.org/10.1155/2023/6543595 PMid:37842328 PMCid:PMC10569891

15. Nakkeeran A, Srinivasan PKKB, Grace TP, Kadathanadan VS. Gingiva as the primary site of extrapulmonary tuberculosis: A rare case report with brief review of literature. Indian Society of Periodontology, 2024;28(1):132-137 https://doi.org/10.4103/jisp.jisp_134_23 PMid:38988968 PMCid:PMC11232812

16. Ines K, Rym A, Mohamed SH, Lamie BH. Palate Tuberculosis with Paradoxical Lymphadenitis. Journal of Global Infectious Diseases, 2021;13(2):94-96 https://doi.org/10.4103/jgid.jgid_266_20 PMid:34194177 PMCid:PMC8213087

17. Rocio VN, Daniel AV, Daniel RV, Aguilar B, Heriberto M, Carla M, Maria C, Cris M, Ana E. An Unusual Granular Ulcer Secondary Oral Tuberculosis of Vestibule Mandibular Mucosa. European Journal of Dentistry, 2020;14(2):331-334. https://doi.org/10.1055/s-0040-1709919 PMid:32396968 PMCid:PMC7274836

18.  Aboubakr M, Azzedine L, Adil A, Fahd E. A Giant Nodule of the Soft Palate Mimicking a Tumor: A Case of Oropharyngeal Tuberculosis. Cureus, 2022 ;14(11):e31891:1-5

19. SS Dogra, Bal C, Mani K. Tuberculosis of oral cavity: a series of one primary and three secondary cases. Indian Journal of Otolaryngology and Head Neck Surgery, 2013;65(3):275-279 https://doi.org/10.1007/s12070-012-0489-6 PMid:24427581 PMCid:PMC3696165

20. Singhaniya SB, Barpande SR, Bhavthankar JD. Oral tuberculosis in an asymptomatic pulmonary tuberculosis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 2011;111:8-10. https://doi.org/10.1016/j.tripleo.2010.09.007 PMid:21194989

21.  Pankaj J, Isha J. Oral Manifestations of Tuberculosis: Step towards Early Diagnosis. Journal of Clinical and Diagnostic Research, 2014;8(12):18-21.

22. Sung TL, Seok BJ, Tae GK, So YC. Oral tuberculosis mimicking a traumatic denture ulcer. The Journal of Prosthetic Dentistry, 2014;121(2):225-228. https://doi.org/10.1016/j.prosdent.2018.04.024 PMid:30722984

23.  World Health Organization. Automated Real‑Time Nucleic Acid Amplification Technology for Rapid and Simultaneous Detection of Tuberculosis and Rifampicin Resistance Xpert MTB/RIF System. Geneva: WHO; 2011.

24.  Pulin S, Aparna D, Manpreet A, Ishita S. Primary Oral Tuberculosis Imitating Malignancy- A Rare Case Report. Journal of Clinical and Diagnostic Research, 2023;17(1):22-25

25. Ebenezer J., Samuel R., Mathew GC., et al., Primary oral tuberculosis Report of two cases. Ind J Dent Res,2006; 17(1); 40-44. https://doi.org/10.4103/0970-9290.29893 PMid:16900894