SciELO - Scientific Electronic Library Online

 
vol.12 número6Prostatic adenocarcinoma with mandibular metastatic lesion: Case report índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • En proceso de indezaciónCitado por Google
  • No hay articulos similaresSimilares en SciELO
  • En proceso de indezaciónSimilares en Google

Compartir


Medicina Oral, Patología Oral y Cirugía Bucal (Internet)

versión On-line ISSN 1698-6946

Med. oral patol. oral cir.bucal (Internet) vol.12 no.6  oct. 2007

 

 

 

Oral Candidiasis in children and adolescents with cancer. Identification of Candida spp

 

 

Haylen González Gravina1, Evelyn González de Morán2, Olga Zambrano3, María Lozano Chourio4, Sofía Rodríguez de Valero2, Sandra Robertis2, Luz Mesa2

(1) Dentist of the Dentistry Service of the Venezuelan Institute of the Social Security, Ciudad Guayana
(2) Professor of Mycology of the School of Bioanalysis of the Faculty of Medicine of the University of Zulia, Maracaibo
(3) Researcher of the Clinic and Pathology Area of the Institute of Dental Research of the Faculty of Dentistry, University of Zulia, Maracaibo
(4) Student of the PhD program in Dental Sciences of the Faculty of Dentistry University of Zulia, Maracaibo. Venezuela

Correspondence

 

 


ABSTRACT

Oral candidiasis represents a serious problem for children with cancer. The mortality rate of this infection has increased due to fungal septicemia, associated with a primary buccal infection.
Objective: Identify the Candida spp. in buccal lesions of patients with cancer, establish the predominant species and correlate them to age and sex of the patient, clinical presentation, type of neoplasic disease and cytostatic therapy received. Study design: 62 patients, between 0-16 years, were investigated in a cross sectional study.
Sample inclusion criteria: Patients with malignant neoplasic disease that were receiving cytostatic treatment and had suspicious lesions of oral candidiasis. Patients with antifungal therapy, active caries, calculus or intraoral appliances were excluded. A clinical evaluation was carried out. The lesion sample was taken and studied by direct exam and culture in CHROMagar-Candida and Sabouraud-Dextrose Agar with chloramphenicol. The identification of the isolated yeast was done by the filamentation test, carbohydrate fermentation and assimilation.
Results: Most of the cases (69.35%) were positive to oral candidiasis, C. albicans was the most frequent species found, followed by C. parapsilosis (14.89%), C. tropicalis (12.77%), C. krusei (4.26%), C. glabrata (2.13%) and C. lusitaniae (2.13 %). In some cases more than one specie were isolated (9.30%). The most frequent location of the lesion was in the tongue (72.70%). The pseudomembranous candidiasis was the most frequent clinical presentation found (78.71%). There were not significant statistically differences with regard to sex and age of the patient, type of neoplasic disease and cytostatic agent received.
Conclusion: The results suggest that oral candidiasis is a frequent complication in the pediatric oncological population, being C. albicans the main etiological agent, however, there is an important participation of other Candida species.

Key words: Oral Candidiasis, Candida, children, cancer.


 

Introduction

Oral candidiasis, a frequent and important nosologic entity of the buccal cavity; is caused by the pathogenic action of Candida species (1). There are diverse local factors that make the buccal tissues susceptible to Candida infection, such as acid saliva, xerostomia, night use of prosthetic dentures, tobacco, carbohydrate rich-diets and patients that receive radio- and chemotherapies in maxillofacial structures (2).

The colonization for species of Candida genus in patients with cancer and their later dissemination, associated with long term episodes of neutrophenia, use wide spectrum antibiotics, treatment with corticosteroids and cytostatic substances, invasive surgical procedures (central and bladder catheters), xerostomia and prolonged hospitalization time (3). The mortality rate due to fungal septicemia, associated with a primary buccal infection, is a relevant problem in children with cancer (4). Candida species, existing in the mouth, have high probability to infect the digestive pathways and disseminate through the circulation, developing systemic infection that is life threatening for the patient (5). The detection and identification of Candida spp. involved in oral candidiasis are important for the treatment of patients with cancer (6). C. krusei, C. glabrata, C. tropicalis and C. dubliniensis species have shown their resistance to certain antifungal drugs (6-8). The proposal of this study was the identification and frequency of the isolated Candida species from buccal lesions in children and adolescents with cancer, according to age and sex of patients, clinical presentation, type of neoplasic disease and cytostatic therapy received.

 

Materials and Methods

-Origin of the sample:

A cross sectional study was carried out in a sample (110 patients) in a given age (0–16 years).These patients were admitted to the Pediatric Oncology Unit at University Hospital of Maracaibo (40 patients) and the Oncohematology Unit at Pediatric Specialities Hospital (70 patients), Maracaibo, Venezuela, from February to May, 2003. Patients with a diagnosis of malignant neoplasic disease, under treatment with cytostatics agents and with oral candidiasis lesions were chosen for this study (62 patients). Patients that received antifungal therapy, ten days prior to the study, had either active extensive caries, dental calculus or intraoral appliances were excluded.

This investigation was carried out according to the norms proposed in the Declaration of Helsinki. The ethics committee of each one of the hospitals involved approved the development of this study. All the parents or legal guardians of the selected children signed a consent report after explaining the purpose of the study.

-Isolation and identification of Candida species

The samples were taken by scaling the lesions with a sterile wooden spatula, a direct exam was done to verify the microscopic characteristic of the Candida spp. (presence of pseudomycelia and blastoconidia) and were cultured on CHROMagar Candida (CHROMagar Candida, Paris, France) and Sabouraud Dextrose Agar with chloramphenicol for yeast isolation. The cultures were incubated at 37ºC for 3 to 7 days.

The CHROMagar -Candida medium contains chromogenic substances that allow a presumptive diagnosis and identification of some species of Candida genus. It was prepared according to the manufacturer indications. The macroscopic study, after 72 hours, considered: number, consistency and color of the colonies. The isolates that developed a green color were identified presumably as Candida albicans, the blue ones as Candida tropicalis and the pink as Candida krusei.

The colonies developed on Agar Sabouraud Dextrose Agar were identified on the basis of their micromorphology on Rice Tween 80(Dalmau Technique) and biochemical tests: carbohydrate fermentation by the Wickerham technique (glucose, galactose, lactose, maltose, sucrose, trehalose (2%), raffinose (4%)) and carbohydrate assimilation by the auxanographic technique in plaque (glucose, cellobiose, galactose, maltose, saccharose, lactose, sorbose, erythritol, trehalose, raffinose, inositol, xylose, melibiose, melezitose, rhamnose, mannitol), according to traditional methodology (9).

-Statistical analysis

Descriptive Statistics were used to present data in absolute and percent values, and summarized in tables. The Chi square test and the exact test of Fisher the tests were used for the statistical analysis. A 95% statistical confidence index was established (p<0,05) and the statistical package used was SPSS 10.0 (SPSS Inc., Chicago, IL, USA).

 

Results

The samples studied (62 patients) showed that most of the patients were positive to oral candidiasis (43; 69.35%) both female (24; 38.70%) and male (19; 30.65%). The group of children (23 patients) between 7 and 12 years presented the highest number of positive cases (20 patients).The sample (8 patients) of the group between 0 and 2 years showed a relatively high number (6 cases) of oral candidiasis.

The distribution of Candida species isolated from oral candidiasis in children and adolescents with cancer, according to clinical presentation and type of cancer, are shown in Tables 1 and 2. Candida albicans was the most frequent species isolated in the malignant neoplasic disease.

 

Discussion

Oral candidiasis represents a problem for children with cancer due to the possibility of a systemic infection that may be life threatening for the patient. It has been reported that the use of preventive therapy, before the establishment of chemotherapy, may decrease the incidence of oral candidiasis (10).

Most of the patients (69.35%) of the studied sample had oral candidiasis as has been previosuly reported (11). The highest incidence was observed in children with ages between 7 and 12 years old. This finding could be due to the mixed dentition and the concomitant presence of the salivary pellicle that could favor the adherence of Candida species to the epithelial surface (12). Also the physical conditions of these children may contribute to an unsuitable buccal hygiene. The prevalence of positive cases in female population as previously observed (13,14), did not represent any significant difference.

The pseudomembranous clinical presentation was mainly observed (78.71%) in the positive cases while the erythematous ones were lower (21.29%). The relationship between clinical presentations and the isolated Candida spp is shown in Table 1. C. albicans was predominantly isolated (42.55%), as was observed previously (6, 15, 16), followed by C. parapsilosis (14.89%), C. tropicalis (12.76%), C. krusei (4.26%), C. glabrata and C. lusitaniae (2.13%). These findings have been previuosly reported (6,17,18) . The high frequency of these species may be related to the patients’ immunosuppression status and the empirical treatment with antibiotic and wide spectrum antimycotics that may cause mutation phenomenon (19, 20).

This finding may explain the reason why some isolated Candida species (21.28%) were not identified by the used methodology. It is important to note that two different species were identified in four cases of oral candidiasis, i.e., C. albicans and C. tropicalis (2 cases); C. albicans with C. krusei (1 case) and C. tropicalis and C. parapsilosis (1 case).

After chemotherapy, candidiasis pseudomembranous was the most frequent clinical presentation in oral candidiasis in children and adolescents with cancer, as has been previously observed (21-23). The clinical presentations were observed mainly in the tongue (72.70%) followed by the inside cheeks (12.70%), soft palate (10.90%) and lips (3.60%) as was observed previously (24) but differ in the preferential location, hard palate, found in the buccal cavity (25). It is important to note that the positive cases (90.70%) were presented as non painful lesions.

The distribution of Candida species according to type of cancer (Table 2), showed that the patients that suffered acute lymphoid leukemia presented the highest number of positive cases , in accordance with some reports (26, 27) but differed from the predominant oral candidiasis in patients with acute myeloid leukemia and sarcoma (4, 11). The incidence of oral candidiasis in patients with leukemia may be due to the alteration of the mediated-immunity by cells in this pathology and the processes that participate in the maturation of lymphocyte and plasmatic cells, generating serious alterations in the mediated-immunity by antibodies (humoral). These conditions favour the susceptibility to fungal infections (28). C. albicans was presented as the most frequent specie, either in the acute lymphoid leukemia or in the rest of the oncological pathologies evaluated in this study; similar results have been reported (21).

The combination of cytostatic treatments and isolated Candida spp. showed not significant statistically evidences. However, the combination methotrexate-purinethol presented the highest number of cases of Candida species. This behavior may be due to the oral complications of the pediatric patients with malignant neoplasic pathologies and the potential immunosuppressive effect of therapies used in this disease that has a direct cytotoxic effect on oral mucosa (29,30). The epithelial cells of the buccal mucosa are very sensitive to chemotherapeutic drugs, they inhibit the cellular cycle, attacking the tissues with more mitotic activity. Nevertheless this cellular inhibition is unspecific, therefore, tissues of rapid renovation like the gastrointestinal mucosa are equally affected (31).

There are certain specific toxic drugs that affect the buccal mucosa, such as methotrexate, doxorubicin, cyclophosphamide and vincristine, which are frequently used in oncological therapies protocols for infants patients (19,20). The cytotoxic result of these drugs: are epithelial atrophy and necrosis, favoring the colonization by fungus, bacteria and viruses.

Oral candidiasis is a frequent complication in pediatric oncology. C. albicans is the main etiologic agent, however, there is an important participation of other Candida species.

 

References

1. Roseff Shelly, Sugar Alan. Oral and esophageal candidiasis. In: Gerald Bodey, editor. Candidiasis, pathogenesis, diagnosis and treatment. New York: Raven Press; 1993. p. 185.        [ Links ]

2. Saap P, Eversole L, Wysoci G. Patología Maxilofacial Contemporánea. Madrid: Harcourt Brace; 1998. p. 433.        [ Links ]

3. Durango H, Hernández M, Zapata C, Sierra M, Peña J, Aristizábal M et al. Colonización por especies de Candida en orofaringe y tracto gastrointestinal en niños. Infection 2002;63:156-61.        [ Links ]

4. Childers NK, Stinnett EA, Wheeler P, Wright JT, Castleberry RP, Dasanayake AP. Oral complications in children with cancer. Oral Surg Oral Med Oral Pathol. 1993 Jan;75(1):41-7.        [ Links ]

5. Tish K, Fisher D, Welch M. Cancer chemotherapy: treatment and care. Boston: Hall Medical Pulishers Co;1993.        [ Links ]

6. Safdar A, Chaturvedi V, Cross EW, Park S, Bernard EM, Armstrong D, et al. Prospective study of Candida species in patients at a comprehensive cancer center. Antimicrob Agents Chemother. 2001 Jul;45(7):2129-33.        [ Links ]

7. Safdar A, Chaturvedi V, Koll BS, Larone DH, Perlin DS, Armstrong D. Prospective, multicenter surveillance study of Candida glabrata: fluconazole and itraconazole susceptibility profiles in bloodstream, invasive, and colonizing strains and differences between isolates from three urban teaching hospitals in New York City (Candida Susceptibility Trends Study, 1998 to 1999). Antimicrob Agents Chemother. 2002 Oct;46(10):3268-72.        [ Links ]

8. Pfaller MA, Diekema DJ, Rinaldi MG, Barnes R, Hu B, Veselov AV, et al. Results from the Artemis Disk Global Antifungal Surveillance Study: a 6.5-year analysis of susceptibilities of Candida and other yeast species to fluconazole and voriconazole by standardized disk diffusion testing. J Clin Microbiol. 2005 Dec;43(12):5848-59.        [ Links ]

9. Kurtzman C, Fell V. The yeasts, a taxonomic study. Amsterdam: Elsevier Science. B.V.;1998.p.891-913.        [ Links ]

10. Rojas de Morales T, Zambrano O, Rivera L, Navas R, Chaparro N, Bernardonni C, et al. Oral-disease prevention in children with cancer: testing preventive protocol effectiveness. Med Oral. 2001 Nov-Dec;6(5):326-34.        [ Links ]

11. Sepulveda E, Brethauer U, Morales R, Jimenez M. Oral manifestations in pediatric patients with oncologic pathologic. Med Oral. 2000 May;5(3):193-197.        [ Links ]

12. GhannoumM, Radwan S. Candida adherence to epithelial cells. Boca Ratón: CRC Press Inc;1990.p.270.        [ Links ]

13. Arendorf TM, Walker DM. The prevalence and intra-oral distribution of Candida albicans in man. Arch Oral Biol. 1980;25(1):1-10.        [ Links ]

14. Berdicevsky I, Ben-Aryeh H, Szargel R, Gutman D. Oral Candida in children. Oral Surg Oral Med Oral Pathol. 1984 Jan;57(1):37-40.        [ Links ]

15. Cannon RD, Holmes AR, Mason AB, Monk BC. Oral Candida: clearance, colonization, or candidiasis? J Dent Res. 1995 May;74(5):1152-61.        [ Links ]

16. Fayle SA, Curzon ME. Oral complications in pediatric oncology patients. Pediatr Dent. 1991 Sep-Oct;13(5):289-95.        [ Links ]

17. Kontoyiannis DP, Vaziri I, Hanna HA, Boktour M, Thornby J, Hachem R, et al. Risk Factors for Candida tropicalis fungemia in patients with cancer. Clin Infect Dis. 2001 Nov 15;33(10):1676-81. Epub 2001 Sep 24.        [ Links ]

18. El-Mahallawy HA, Attia I, Ali-el-Din NH, Salem AE, Abo-el-Naga S. A prospective study on fungal infection in children with cancer. J Med Microbiol. 2002 Jul;51(7):601-5.        [ Links ]

19. Panizo M, Reviákina V, Vellorí E. Dificultades en la identificación de levaduras aisladas de pacientes oncológicos. Bol Soc Venez Microbiol 2000;20:104–07.        [ Links ]

20. Odds F. Candida and Candidosis. A review and bibliography. London: Bailliere Tindall; 1988.        [ Links ]

21. Stinnett EA, Childers NK, Wright JT, Rodu BK, Bradley EL Jr. The detection of oral Candida in pediatric leukemia patients. Pediatr Dent. 1992 Jul-Aug;14(4):236-9.        [ Links ]

22. Reichart PA, Samaranayake LP, Philipsen HP. Pathology and clinical correlates in oral candidiasis and its variants: a review. Oral Dis. 2000 Mar;6(2):85-91.        [ Links ]

23. Epstein JB, Freilich MM, Le ND. Risk factors for oropharyngeal candidiasis in patients who receive radiation therapy for malignant conditions of the head and neck. Oral Surg Oral Med Oral Pathol. 1993 Aug;76(2):169-74.        [ Links ]

24. Peterson DE, D’Ambrosio JA. Diagnosis and management of acute and chronic oral complications of nonsurgical cancer therapies. Dent Clin North Am. 1992 Oct;36(4):945-66.        [ Links ]

25. Sepulveda E, Brethauer U, Rojas J, Fernandez E, Le Fort P. Oral ulcers in children under chemotherapy: clinical characteristics and their relation with Herpes Simplex Virus type 1 and Candida albicans. Med Oral Patol Oral Cir Bucal. 2005 Apr 1;10 Suppl 1:E1-8.        [ Links ]

26. Sallah S, Wan JY, Nguyen NP, Vos P, Sigounas G. Analysis of factors related to the occurrence of chronic disseminated candidiasis in patients with acute leukemia in a non-bone marrow transplant setting: a follow-up study. Cancer. 2001 Sep 15;92(6):1349-53.        [ Links ]

27. McElroy TH. Infection in the patient receiving chemotherapy for cancer: oral considerations. J Am Dent Assoc. 1984 Sep;109(3):454-6.        [ Links ]

28. Reviákina V, Panizo M. Inmunopatogénesis de la candidosis sistémica e inmunomodulación. Rev Soc Venez Microbiol 2001;21:46-53.        [ Links ]

29. Kamp AA. Neoplastic diseases in a pediatric population: a survey of the incidence of oral complications. Pediatr Dent. 1988 Mar;10(1):25-9.        [ Links ]

30. Scully C, MacFarlane TW. Orofacial manifestations of childhood malignancy: clinical and microbiological findings during remission. ASDC J Dent Child. 1983 Mar-Apr;50(2):121-5.        [ Links ]

31. Lockhart PB, Sonis ST. Relationship of oral complications to peripheral blood leukocyte and platelet counts in patients receiving cancer chemotherapy. Oral Surg Oral Med Oral Pathol. 1979 Jul;48(1):21-8.        [ Links ]

 

 

Correspondence:
Dra Luz Mesa
Faculty of Dentistry University of Zulia, Maracaibo
Venezuela
E-mail: lmilamesac@cantv.net

Received: 15-04-2006
Accepted: 3-06-2007

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons