Tongue microbiota and pathological processes: a pilot autopsy study

Autores/as

  • Sanivia Aparecida de Lima Pereira University of Uberaba
  • Vitorino Modesto dos Santos Catholic University Medical Course and Armed Forces Hospital
  • Denise Bertulucci Rocha Rodrigues University of Uberaba
  • Dalmo Correia Filho Infectious Disease Division, Federal University of Triângulo Mineiro, Uberaba
  • Eumênia da Costa Cunha Castro General Pathology Division, Federal University of Triângulo Mineiro, Uberaba
  • Marlene Antônia dos Reis General Pathology Division, Federal University of Triângulo Mineiro, Uberaba
  • Vicente de Paula Antunes Teixeira General Pathology Division, Federal University of Triângulo Mineiro, Uberaba

Resumen

Context: Human general health may be mirrored in oral changes, and oral lesions can hallmark systemic diseases.
Diverse pathological processes and numerous infectious agents have been described in the human oral cavity.
Autopsy reports of the association among oral pathogens, tongue pathological changes, and systemic diseases are still lacking.
Aim: To describe pathological processes and infectious agents found in the tongues of necropsied patients, and comment the data from coexistent systemic disease.
Design: Cross sectional study.
Setting and Participants: Twenty-four complete autopsies of adults were randomly selected in a Brazilian University Hospital.
Main Outcomes Measures: After macroscopic evaluation, the tongues were longitudinally sectioned and the tissue samples were submitted to the histological routine.
Results: The histopathology changes were: hydropic degeneration (83.3%), atrophy (75%), inflammation (70.8%), necrosis with ulceration (70.8%), hypertrophy (58.3%), necrosis without ulceration (16.6%) and arteriolar hyalinosis (4.2%). The microbiota consisted of: bacteria (54.2%), Candida sp (25%), Cryptococcus sp (4.2%) and Malassezia furfur (4.2%). Bacteria were found on the tongues from all the patients with rheumatic cardiopathy or pyelonephritis, in 44.4% of the patients with bronchopneumonia and in 40% of the patients with esophagitis. Half of AIDS patients presented Candida sp hyphae associated with tongue inflammation, necrosis and ulceration.
Conclusions: Although not always associated to gross lesions, the tongue microbiota can cause pathological processes. As oral pathology has been associated with systemic diseases, workers in health care should develop a higher awareness about the role of tongue changes in the general health.

Descargas

Los datos de descargas todavía no están disponibles.

Métricas

Cargando métricas ...

Citas

1. Axéll T. The oral mucosa as a mirror of general health or disease. Eur J Oral Sci 1992; 100: 9-16.

2. Nashi N, Kang S, Barkdull GC, Lucas J, Davidson TM. Lingual fat at autopsy. Laryngoscope 2007; 117: 1467-73.

3. Parks ET, Lancaster H. Oral manifestations of systemic diseases. Dermatol Clin 2003; 21: 171-82.

4. Demmer RT, Desvarieux M. Periodontal infections and cardiovascular disease: the heart of the matter. J Am Dent Assoc 2006; 137: 14S-20S.

5. Aas JA, Paster BJ, Stokes LN, Olsen I, Dewhirst FE. Defining the normal bacterial flora of the oral cavity. J Clin Microbiol 2005; 43: 5721-32.

6. Starke EM, Smoot JC, Smoot LM, Liu WT, Chandler DP, Lee HH, Stahl DA. Technology development to explore the relationship between oral health and the oral microbial community. BMC Oral Health 2006; 6 Suppl 1: S10.

7. Chen T, Hudnall SD. Anatomical mapping of human herpesvirus reservoirs of infection. Mod Pathol 2006; 19: 726-37.

8. de Faria P, Vargas PA, Saldiva PH, Böhm GM, Mauad T, de Almeida OP. Tongue disease in advanced AIDS. Oral Dis 2005; 11: 72-80.

9. Rocha ML, Dias EP, Fonseca EC. Patologia da língua: estudo prospectivo de 100 necropsias. RPG Rev Pós Grad 1999; 6: 139-46.

10. Ramirez-Amador V, Anaya-Saavedra G, Gonzalez-Ramirez I, Mosqueda-Gómez JL, Esquivel-Pedraza L, Reyes-Gutiérrez E, Sierra- Madero J. Lingual ulcer as the only sign of recurrent mycobacterial infection in an HIV/AIDSinfected patient. Med Oral Patol Oral Cir Bucal 2005; 10: 109-14.

11. Mulliken RA, Casner MJ. Oral manifestations of systemic disease. Emerg Med Clin North Am 2000; 18: 565-75.

12. Ahmad NM, Ahmad KM. Corynebacterium minutissimum pyelonephritis with associated bacteraemia: a case report and review of literature. J Infect 2005; 51: 299-303.

13. Aperis G, Moyssakis I. Corynebacterium minutisimum endocaditis: a report and review. J Infect 2007; 54: 79-81.

14. Ninomyia T, Kubo M, Dói Y, Yonemoto K, Tanizaki Y, Tsuruya K, Sueishi K, et al. Prehypertension increases the risk for renal arteriosclerosis in autopsies: the Hisayama Study. J Am Soc Nephrol 2007; 18: 2135-42.

15. Pei Z, Yang L, Peek RM, Levine SM, Pride DT, Blaser MJ. Bacterial biota in reflux esophagitis and Barrett´s esophagus. World J Gastroenterol 2005; 11: 7277-83.

16. Weerasuriya N, Snape J. A study of candida esophagitis in elderly patients attending a district general hospital in the UK. Dis Esophagus 2006; 19:189-92.

17. Olmos MA; Araya V, Concetti H, Ramallo J, Piskorz E, Pérez H, Cahn P, et al. Oesophageal candidiasis: clinical and mycological analysis. Acta Gastroenterol Latinoam 2005; 35: 211-18.

18. Sumi Y, Miura H, Michiwaki Y, Nagaosa S, Nagaya M. Colonization of dental plaque by respiratory pathogens in dependent elderly. Arch Gerontol Geriatr 2007; 44: 119-24.

19. Sumi Y, Miura H, Nagaya M, Michiwaki Y, Uematsu H. Colonization on the tongue surface by respiratory pathogens in residents of a nursing home - a pilot study. Gerodontology 2006; 23: 55-59.

20. Gonsalves WC, Chi AC, Neville BW. Common oral lesions: Part I. Superficial mucosal lesions. Am Fam Physician 2007; 75: 501-7.

21. Scully C, De Almeida OP. Orofacial manifestations of the systemic mycoses. J Oral Pathol Med 1992; 21: 289-94.

22. Schmidt-Westhausen AM, Bendick C, Reichart PA, Samaranayake LP. Oral candidosis and associated Candida species in HIV-infected Cambodians exposed to antimycotics. Mycoses 2004; 47: 435-41.

23. Yohn JJ, Lucas J, Camisa C. Malassezia folliculitis in immunocompromised patients. Cutis 1985; 35: 536-8.

24. Ferreira MS, Borges AS. Some aspects of protozoan infections in immunocompromised patients- a review. Mem Inst Oswaldo Cruz 2002; 97: 443-57.

25. Guleç AT, Demirbilek M, Seçkin D, Can F, Saray Y, Sarifakioglu E, Haberal M. Superficial fungal infections in 102 renal transplant recipients: a case-control study. J Am Acad Dermatol 2003; 49: 187-92.

26. Sirera G, Videla S, Piñol M, Cañadas MP, Llatjos M, Ballesteros AL, García-Cuyás F, et al. High prevalence of human papillomavirus infection in the anus, penis and mouth in HIV-positive men. AIDS 2006; 20: 1201-4.

27. Faveri M, Feres M, Shibli JA, Hayacibara RF, Hayacibara MM, de Figueiredo LC. Microbiota of the dorsum of the tongue after plaque accumulation: an experimental study in humans. J Periodontol 2006; 77: 1539-46.

29. Ledder RG, Gilbert P, Huws SA, Aarons L, Ashley MP, Hull PS, McBain AJ. Molecular analysis of the subgingival microbiota in health and disease. Appl Environ Microbiol 2007; 73: 516-23.

30. Riggio MP, Lennon A, Rolph HJ, Hodge PJ, Donaldson A, Maxwell AJ, Bagg J. Molecular identification of bacteria on the tongue dorsum of subjects with and without halitosis. Oral Dis 2008; 14: 251-8.

31. Sachdeo A, Haffajee AD, Socransky SS. Biofilms in the edentulous oral cavity. J Prosthodont 2008; Mar 17. [Epub ahead of print]

Descargas

Publicado

2017-05-29

Cómo citar

1.
Aparecida de Lima Pereira S, Modesto dos Santos V, Rocha Rodrigues DB, Correia Filho D, Cunha Castro E da C, dos Reis MA, Antunes Teixeira V de P. Tongue microbiota and pathological processes: a pilot autopsy study. Rev Fac Cien Med (Quito) [Internet]. 29 de mayo de 2017 [citado 4 de mayo de 2024];33(2):17-23. Disponible en: https://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/1040