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*Corresponding Author Address: Ziad Salim Abdul Majid BDS, Department of Oral Medicine, Surgery, and Diagnosis, Faculty
of Dentistry, Libyan International Medical University, Benghazi - Libya. Email: Ziaddental@gmail.com.
International Journal of Dental and Health Sciences
Volume 02, Issue 02Case Report
A CASE REPORT OF: PSEUDOMEMBRANOUS
CANDIDIASIS INDUCED BY LONG TERM SYSTEMIC
CORTICOSTEROIDS THERAPY
Ziad Salim Abdul Majid1, Elsanousi M.Taher2.
1. BDS, Department of Oral Medicine, Surgery, and Diagnosis.Faculty of Dentistry, Libyan
International Medical University.
2.BDS, MSc Ireland, FFDRCSI, Head Of the Department of Oral Medicine, Surgery, and Diagnosis,
Dean of the Faculty of Dentistry/ Libyan International Medical University.
ABSTRACT:
Oral candidiasis is a common opportunistic infection of the oral cavity caused by an
overgrowth of Candida species, the commonest being the Candida albicans. It is one of the
common side effect associated with long term use of systemic corticosteroids. The purpose
of this case report is to discuss the Acute Pseudomembranous Candidiasis in 24 Negroid
Female Libyan patient on long term use of systemic corticosteroids therapy who came to
the department of Oral Medicine, Surgery, and Diagnosis at the Faculty of Dentistry, Libyan
International Medical University with the clinical appearance of Acute Pseudomembranous
Candidiasis.
Proper patient management with successful treatment protocol, and follow up were
performed to overcome the patient presenting symptoms, and to eliminate the
corticosteroids therapy related problems.
Key words: Acute Pseudomembranous Candidiasis, Candida albicans, Systemic
Corticosteroids, Ketoconazole, Chlorhexidine gluconate.
INTRODUCTION:
Oropharyngeal candidiasis is a common
opportunistic infection of the oral cavity
caused by commensal Candida species.
the Candida genus is comprised of over
150 species of asporogenous ‘yeast-like’
fungi [1]. Since the majority of healthy
individuals have an intraoral candida
species, it is shown that some individuals
exposed to oral candidial lesions. The
most commonly implicated species is
Candida albicans which is isolated in over
80% of lesions [2].
A change from the harmless commensal
existence of Candida to a pathogenic state
can occur following alteration of the oral
cavity environment to one that favors the
growth of Candida. The causes of such
changes most often related to a
weakening of host immune defenses [1].
The implicated predisposing factors are
classified into local factors which includes:
Impaired salivary gland function, inhaled
steroids, dentures, oral
cancer/leukoplakia, and high
carbohydrate diet. The systemic factors
includes: Drugs such as long term use of
broad spectrum antibiotics,
Abdul Majid. et al., Int J Dent Health Sci 2015; 2(2): 454-458
455
Immunosuppressives , corticosteroids,
diabetes, Cushing’s syndrome, HIV
infection, malignancies as leukemia,
nutritional deficiencies as vitamin B12,
smoking, and stress [3].
Candidiasis is categorized into primary
oral candidiasis in which the condition is
only confined to the mouth where as in
secondary oral candidiasis the condition is
confined to other body parts in addition
to the mouth [4]. Primary oral candidiasis
has generally four forms are described
based on clinical presentation : Acute
Pseudomembranous Candidiasis, Acute
Erythematous Candidiasis, Chronic
Erythematous Candidiasis, and Chronic
Hyperplastic Candidiasis [1].
Pseudomembranous candidiasis (oral
thrush) presents as creamy white lesions
on the oral mucosa and a diagnostic
feature of this infection is that these
plaques can be removed by gentle
scraping leaving behind an underlying
erythematous mucosal surface.
Histological examination of recovered
pseudomembranous reveals
desquamated epithelial cells together
with yeast and filamentous forms of
Candida [1]. The infection has been
demonstrated as an acute condition often
affecting newborns where the immune
system is immature, in older individuals,
Acute Pseudomembranous Candidiasis
often occurs when there is a nutritional
limitation, immune suppression, or by an
underlying disease most notably HIV
infection [5].
CASE DETAIL:
A 24 years old negroid female Libyan
patient, came to the department of Oral
Medicine, Surgery, and Diagnosis, at the
Libyan International Medical University,
with a complaint of roughness, peeling of
oral tissue, burning sensation on the
tongue and sore mouth since one and half
month ago. The patient medical, and drug
history revealed that she had surgical
removal of intracranial cystic lesion since
three months ago, and since then she was
on systemic corticosteroids therapy
(dexamethasone 10mg/day) till a week
before her visit to the department.
On intraoral examination, almost all over
her oral mucosa ( buccal, labial, palatal
mucosa) covered by elevated white
patches, diffuse erythema over the soft
palate, uvula, and oropharynx (Fig.1
A,B,C), with scrapable white patches. On
gently rubbing these white patches , a
visible erythematous areas were seen.
The complete blood examination report
showed normal figures, a smear was
made from scrapings of these lesions For
cytological evaluation, and the results
indicated candidiasis, Culture Candida
using a Sabouraud's dextrose agar was
also done to aid the definitive
identification of the fungal organism.
Based on both clinical examination , and
investigations; the diagnosis indicate
Acute Pseudomembranous Candidiasis
due to prolonged use of systemic
corticosteroids. Following to that the
patient was treated with ketoconazole
Abdul Majid. et al., Int J Dent Health Sci 2015; 2(2): 454-458
456
tablet 200 mg once daily, chlorhexidine
gluconate 0.12% mouthwash 2 times/day
for 2 weeks. On the follow up visit, a one
week after an improvement of the
presenting complaints was noticed , and
the oral lesions was completely
disappeared (Fig.2 A,B,C).
DISCUSSION:
Although, Candida albicans is the most
frequently involved species in oral
candidiasis, other species are increasingly
being encountered. The unique virulence
factors of Candida albicans includes the
ability to adhere to host tissue surfaces,
produce filamentous fungal growth, and
release hydrolytic enzymes that cause
damage to the host tissue.
Pseudomembranous candidiasis can be
develop as a result of long term use of
systemic corticosteroids, or the case
where the individual being
immunocompromised for long term.
Concurrent with their therapeutic
properties subsist a plethora of adverse
effects, including the susceptibility to
infection [2]. They produce a multiple
effects on different immunocytes, as
suppressing the dendritic cell activation,
reducing the release of macrophage
cytokines, B lymphocytes and
immunoglobulin/antibody production,
increasing in the number of circulating
neutrophils, but delaying their apoptosis,
and alter T-lymphocyte cytokine
production [6] .
Systemic antifungals are usually indicated
in cases of disseminated disease and/or in
immunocompromised patients [3]. In
addition the use of Chlohexidine
gluconate mouthwash shows a significant
improvement in the reduction, and
prevention of the candidal infections [1].
"Chlorhexidine binds to negatively
charged microbial cell surfaces leading to
a disruption of the cell membrane of the
microorganisms (W Nittayananta et al,
2008)" [7]. Thus, antifungal activity of
chlorhexidine due to both its fungicidal
activity and its mechanical effect inhibits
the fungal adhesion to mucosal epithelial
cells [7].
CONCLUSION:
Candida species are normal oral
commensals found in 17-75% of healthy
individuals and most debilitated people.
The transition of this innocuous
commensal to the disease-causing
associated with the virulence attributes of
the microorganism.
Long term use of systemic corticosteroids
results in development of Acute
Pseudomembranous Candidiasis due to
the fungal overgrowth in
immunosuppression status. Effective
management of oral candidiasis demands
the elimination of any identified
predisposing factors together with the
administration of appropriate antifungal
agents.
Abdul Majid. et al., Int J Dent Health Sci 2015; 2(2): 454-458
457
REFERENCES:
1. Williams D, Lewis M.
Pathogenesis and
treatment of oral
candidosis. Journal of Oral
Microbiology 2011;3:10.
3402 /jom.v3i0.5771.
2. Farah C., Lynch N., and
McCullough M. Oral fungal
infections: An update for
the general practitioner.
Australian Dental Journal,
2010;55: 48–54.
3. Singh A, Verma R, Murari A,
Agrawal A. Oral candidiasis:
An overview. Journal of
Oral and Maxillofacial
Pathology 2014;18:81-5.
4. Scully C. Oral and
Maxillofacial Medicine: The
Basis of Diagnosis and
Treatment. 2nd ed.
Edinburgh: Churchill
Livingstone. 2008.pp.191-9.
5. Thompson GR, Patel PK,
Kirkpatrick WR, et al.
Oropharyngeal Candidiasis
in the Era of Antiretroviral
Therapy. Oral surgery, oral
medicine, oral pathology,
oral radiology, and
endodontics.2010;109(4):4
88-495.
6. Georgakopoulou EA, Scully
C. Systemic use of non-
biologic corticosteroids in
orofacial diseases. Oral
Diseases 2014; 20: 127-135.
7. Nittayananta W, DeRouen
T, Arirachakaran P, et al. A
randomized clinical trial of
chlorhexidine in the
maintenance of oral
candidiasis-free period in
HIV infection. Oral
Diseases. 2008;14(7):665-
670.
Abdul Majid. et al., Int J Dent Health Sci 2015; 2(2): 454-458
458
FIGURES:
Fig. 1 A,B,C
Fig. 2 A,B,C
A B
B
C
C
A
A
C
C
B
B

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A Case Report Of Pseudomembranous Candidiasis Induced By Long Term Systemic Corticosteroids Therapy

  • 1. *Corresponding Author Address: Ziad Salim Abdul Majid BDS, Department of Oral Medicine, Surgery, and Diagnosis, Faculty of Dentistry, Libyan International Medical University, Benghazi - Libya. Email: Ziaddental@gmail.com. International Journal of Dental and Health Sciences Volume 02, Issue 02Case Report A CASE REPORT OF: PSEUDOMEMBRANOUS CANDIDIASIS INDUCED BY LONG TERM SYSTEMIC CORTICOSTEROIDS THERAPY Ziad Salim Abdul Majid1, Elsanousi M.Taher2. 1. BDS, Department of Oral Medicine, Surgery, and Diagnosis.Faculty of Dentistry, Libyan International Medical University. 2.BDS, MSc Ireland, FFDRCSI, Head Of the Department of Oral Medicine, Surgery, and Diagnosis, Dean of the Faculty of Dentistry/ Libyan International Medical University. ABSTRACT: Oral candidiasis is a common opportunistic infection of the oral cavity caused by an overgrowth of Candida species, the commonest being the Candida albicans. It is one of the common side effect associated with long term use of systemic corticosteroids. The purpose of this case report is to discuss the Acute Pseudomembranous Candidiasis in 24 Negroid Female Libyan patient on long term use of systemic corticosteroids therapy who came to the department of Oral Medicine, Surgery, and Diagnosis at the Faculty of Dentistry, Libyan International Medical University with the clinical appearance of Acute Pseudomembranous Candidiasis. Proper patient management with successful treatment protocol, and follow up were performed to overcome the patient presenting symptoms, and to eliminate the corticosteroids therapy related problems. Key words: Acute Pseudomembranous Candidiasis, Candida albicans, Systemic Corticosteroids, Ketoconazole, Chlorhexidine gluconate. INTRODUCTION: Oropharyngeal candidiasis is a common opportunistic infection of the oral cavity caused by commensal Candida species. the Candida genus is comprised of over 150 species of asporogenous ‘yeast-like’ fungi [1]. Since the majority of healthy individuals have an intraoral candida species, it is shown that some individuals exposed to oral candidial lesions. The most commonly implicated species is Candida albicans which is isolated in over 80% of lesions [2]. A change from the harmless commensal existence of Candida to a pathogenic state can occur following alteration of the oral cavity environment to one that favors the growth of Candida. The causes of such changes most often related to a weakening of host immune defenses [1]. The implicated predisposing factors are classified into local factors which includes: Impaired salivary gland function, inhaled steroids, dentures, oral cancer/leukoplakia, and high carbohydrate diet. The systemic factors includes: Drugs such as long term use of broad spectrum antibiotics,
  • 2. Abdul Majid. et al., Int J Dent Health Sci 2015; 2(2): 454-458 455 Immunosuppressives , corticosteroids, diabetes, Cushing’s syndrome, HIV infection, malignancies as leukemia, nutritional deficiencies as vitamin B12, smoking, and stress [3]. Candidiasis is categorized into primary oral candidiasis in which the condition is only confined to the mouth where as in secondary oral candidiasis the condition is confined to other body parts in addition to the mouth [4]. Primary oral candidiasis has generally four forms are described based on clinical presentation : Acute Pseudomembranous Candidiasis, Acute Erythematous Candidiasis, Chronic Erythematous Candidiasis, and Chronic Hyperplastic Candidiasis [1]. Pseudomembranous candidiasis (oral thrush) presents as creamy white lesions on the oral mucosa and a diagnostic feature of this infection is that these plaques can be removed by gentle scraping leaving behind an underlying erythematous mucosal surface. Histological examination of recovered pseudomembranous reveals desquamated epithelial cells together with yeast and filamentous forms of Candida [1]. The infection has been demonstrated as an acute condition often affecting newborns where the immune system is immature, in older individuals, Acute Pseudomembranous Candidiasis often occurs when there is a nutritional limitation, immune suppression, or by an underlying disease most notably HIV infection [5]. CASE DETAIL: A 24 years old negroid female Libyan patient, came to the department of Oral Medicine, Surgery, and Diagnosis, at the Libyan International Medical University, with a complaint of roughness, peeling of oral tissue, burning sensation on the tongue and sore mouth since one and half month ago. The patient medical, and drug history revealed that she had surgical removal of intracranial cystic lesion since three months ago, and since then she was on systemic corticosteroids therapy (dexamethasone 10mg/day) till a week before her visit to the department. On intraoral examination, almost all over her oral mucosa ( buccal, labial, palatal mucosa) covered by elevated white patches, diffuse erythema over the soft palate, uvula, and oropharynx (Fig.1 A,B,C), with scrapable white patches. On gently rubbing these white patches , a visible erythematous areas were seen. The complete blood examination report showed normal figures, a smear was made from scrapings of these lesions For cytological evaluation, and the results indicated candidiasis, Culture Candida using a Sabouraud's dextrose agar was also done to aid the definitive identification of the fungal organism. Based on both clinical examination , and investigations; the diagnosis indicate Acute Pseudomembranous Candidiasis due to prolonged use of systemic corticosteroids. Following to that the patient was treated with ketoconazole
  • 3. Abdul Majid. et al., Int J Dent Health Sci 2015; 2(2): 454-458 456 tablet 200 mg once daily, chlorhexidine gluconate 0.12% mouthwash 2 times/day for 2 weeks. On the follow up visit, a one week after an improvement of the presenting complaints was noticed , and the oral lesions was completely disappeared (Fig.2 A,B,C). DISCUSSION: Although, Candida albicans is the most frequently involved species in oral candidiasis, other species are increasingly being encountered. The unique virulence factors of Candida albicans includes the ability to adhere to host tissue surfaces, produce filamentous fungal growth, and release hydrolytic enzymes that cause damage to the host tissue. Pseudomembranous candidiasis can be develop as a result of long term use of systemic corticosteroids, or the case where the individual being immunocompromised for long term. Concurrent with their therapeutic properties subsist a plethora of adverse effects, including the susceptibility to infection [2]. They produce a multiple effects on different immunocytes, as suppressing the dendritic cell activation, reducing the release of macrophage cytokines, B lymphocytes and immunoglobulin/antibody production, increasing in the number of circulating neutrophils, but delaying their apoptosis, and alter T-lymphocyte cytokine production [6] . Systemic antifungals are usually indicated in cases of disseminated disease and/or in immunocompromised patients [3]. In addition the use of Chlohexidine gluconate mouthwash shows a significant improvement in the reduction, and prevention of the candidal infections [1]. "Chlorhexidine binds to negatively charged microbial cell surfaces leading to a disruption of the cell membrane of the microorganisms (W Nittayananta et al, 2008)" [7]. Thus, antifungal activity of chlorhexidine due to both its fungicidal activity and its mechanical effect inhibits the fungal adhesion to mucosal epithelial cells [7]. CONCLUSION: Candida species are normal oral commensals found in 17-75% of healthy individuals and most debilitated people. The transition of this innocuous commensal to the disease-causing associated with the virulence attributes of the microorganism. Long term use of systemic corticosteroids results in development of Acute Pseudomembranous Candidiasis due to the fungal overgrowth in immunosuppression status. Effective management of oral candidiasis demands the elimination of any identified predisposing factors together with the administration of appropriate antifungal agents.
  • 4. Abdul Majid. et al., Int J Dent Health Sci 2015; 2(2): 454-458 457 REFERENCES: 1. Williams D, Lewis M. Pathogenesis and treatment of oral candidosis. Journal of Oral Microbiology 2011;3:10. 3402 /jom.v3i0.5771. 2. Farah C., Lynch N., and McCullough M. Oral fungal infections: An update for the general practitioner. Australian Dental Journal, 2010;55: 48–54. 3. Singh A, Verma R, Murari A, Agrawal A. Oral candidiasis: An overview. Journal of Oral and Maxillofacial Pathology 2014;18:81-5. 4. Scully C. Oral and Maxillofacial Medicine: The Basis of Diagnosis and Treatment. 2nd ed. Edinburgh: Churchill Livingstone. 2008.pp.191-9. 5. Thompson GR, Patel PK, Kirkpatrick WR, et al. Oropharyngeal Candidiasis in the Era of Antiretroviral Therapy. Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics.2010;109(4):4 88-495. 6. Georgakopoulou EA, Scully C. Systemic use of non- biologic corticosteroids in orofacial diseases. Oral Diseases 2014; 20: 127-135. 7. Nittayananta W, DeRouen T, Arirachakaran P, et al. A randomized clinical trial of chlorhexidine in the maintenance of oral candidiasis-free period in HIV infection. Oral Diseases. 2008;14(7):665- 670.
  • 5. Abdul Majid. et al., Int J Dent Health Sci 2015; 2(2): 454-458 458 FIGURES: Fig. 1 A,B,C Fig. 2 A,B,C A B B C C A A C C B B