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Microbiological study of role of fungi in primary atrophic rhinitis

Published online by Cambridge University Press:  17 October 2008

K G Effat*
Affiliation:
Ear, Nose and Throat Department, El-Sahel Teaching Hospital, Cairo, Egypt
N M Madany
Affiliation:
Department of Medical Microbiology and Immunology, Faculty of Medicine, Cairo University, Egypt
*
Address for correspondence: Dr Kamal G Effat, 51A El-Madina El-Monawara St, Madinat El-Mohandeseen, Giza, Egypt. E-mail: kamaleffat@hotmail.com
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Abstract

Background:

Fungal rhinosinusitis has gained much attention in recent years. To our knowledge, no previous studies have addressed the role of fungus in primary atrophic rhinitis.

Study design:

Prospective case study.

Patients and methods:

All cases of primary atrophic rhinitis presenting to the out-patient department at El-Sahel Teaching Hospital over a five-month period were included in the study. Crusts and purulent secretions removed from patients' nasal cavities underwent microbiological analysis at the Medical Microbiology and Immunology department of the Cairo University Faculty of Medicine. Special emphasis was placed on fungal isolation.

Results:

Fourteen consecutive cases of primary atrophic rhinitis were studied in the five-month period starting 26 November 2007. Patients comprised eight females and six males, with an age range of 12 to 65 years (mean 37 years). Microscopy of the crusts and purulent secretions showed pus cells in most of the samples. Klebsiella species were isolated from nine patients (65 per cent), and other bacterial species were isolated in most of the remainder. Fungal elements, most commonly aspergillus species, were isolated in 13 patients (93 per cent).

Conclusion:

It is proposed that the initial trigger for primary atrophic rhinitis is a virulent bacterial infection of the nasal lining, which leads to damage of the ciliated epithelium. This initiates the cascade of events leading to inflammation of the mucosa and submucosa, with secondary pyogenic osteomyelitis of the turbinate bone. The persistence of purulent secretion, within the setting of impaired mucociliary clearance, leads to saprophytic fungal colonisation which contributes greatly to the clinical picture.

Type
Main Articles
Copyright
Copyright © JLO (1984) Limited 2008

Introduction

Primary atrophic rhinitis is a chronic nasal disease characterised by progressive nasal mucosal atrophy, progressive atrophy of the underlying turbinate bones, abnormal widening of the nasal cavities, and formation of viscid secretions and dried crusts leading to a characteristic fetor (ozaena).Reference Dutt and Kameswaran1 Numerous theories have been proposed to account for the pathogenesis of this condition.Reference Dutt and Kameswaran1, Reference Sayed, Abou-Elhamd, Abdel-Kader and Saleem2

Although fungal rhinosinusitis has gained much attention in recent years, the role of fungi in the pathogenesis of primary atrophic rhinitis is scarcely documented in the literature. A search of the PubMed/Medline database failed to identify fungal studies in this condition in humans. In humans, Klebsiella ozaenae has been isolated with relative frequency from patients with primary atrophic rhinitis.Reference Ferguson, McCaffrey, Kern and Martin3 However, as far as the authors are aware, no specific fungal studies have been performed on the crusts and secretions associated with this condition in humans.

The aim of this study was to microbiologically examine the organisms involved in primary atrophic rhinitis, with special emphasis on fungal elements. For this purpose, we recruited all cases presenting to a single institution over a five-month period.

Patients and methods

The subjects comprised patients with primary atrophic rhinitis who presented consecutively to the out-patient department at El-Sahel Teaching Hospital over a five-month period, commencing on 26 November 2007. The criteria for diagnosis and inclusion in the study included nasal crusting, enlarged nasal cavities, resorption of the turbinates, mucosal atrophy and paradoxical nasal congestion, in the absence of previous surgery or presence of a specific granulomatous disease.Reference Moore and Kern4

Crusts were removed from the nasal cavity by sterile forceps and placed in a sterile container for prompt microbiological analysis at the Medical Microbiology and Immunology Department, Faculty of medicine, Cairo University. Initially, microscopic examination of the sample was performed after Gramstaining. Bacterial culture was performed on blood agar, chocolate agar and MacConkey medium. Fungal culture was performed on Sabouraud's dextrose agar. The stains used for microscopic examination of isolates were Gram stain for bacteria and lactophenol cotton blue stain for fungi.

Approval for the study was obtained from the ethical committee at the General Organisation for Teaching Hospitals and Institutes, Cairo.

Results

The study group comprised 14 patients, eight females and six males, aged from 12 to 65 years (mean 37 years). The patients presented with fetor and nasal obstruction. Two patients reported significant epistaxis associated with removal of crusts. The cases reported had not received antibiotic treatment over the two months prior to presentation.

The results of the microbiological study are shown in Table I. Pus cells were commonly seen on direct microscopic examination. The bacteria isolated from cultures comprised klebsiella species (in nine patients, 65 per cent) and others (including Pseudomonas aeruginosa, Escherichia coli and Streptococcus pneumoniae). Fungal cultures were positive in 13 patients (93 per cent), with the predominant fungi isolated being aspergillus species; candida, rhizomucor and alternaria species were also isolated.

Table I Microbiological data from the study group

Pt no = patient number; yr = years; F = female; M = male; G −ve = Gram-negative; G + ve = Gram-positive; spp = species; R = right

Discussion

This study isolated fungal elements from the majority of specimens (93 per cent) obtained from patients with primary atrophic rhinitis. As far as we are aware, no previous study has focussed on the presence of fungi in the crusts and secretions of such patients. Generous biopsies were taken from the inferior turbinates of three patients under general anaesthesia, during surgery for unilateral closure of the nasal vestibule (Young's procedure). Histopathological examination did not reveal fungal invasion of the nasal tissues (Figure 1). Non-invasive fungal sinusitis affects immunocompetent hosts and is broadly classified into allergic fungal sinusitis and saprophytic fungal colonisation.Reference Ferguson5 The elements necessary for diagnosis of allergic fungal sinusitis, such as nasal polyps and eosinophilic mucin, were absent in our patients; therefore, it may be concluded that the fungal elements detected in this study represented saprophytic fungal colonisation.Reference Daudia and Jones6

Fig. 1 Photomicrograph of lateral nasal wall biopsy from patient with primary atrophic rhinitis, showing squamous metaplasia of epithelium, chronic inflammatory cells, hyper vascularity, submucosal fibrosis and necrosis of underlying bone (H&E; ×150).

The predominant bacterial species previously isolated from cases of primary atrophic rhinitis has been Klebsiella ozaenae.Reference Ferguson, McCaffrey, Kern and Martin3 Klebsiella species are capsulated, enteric, Gram-negative, rod-form bacilli.Reference Strohl, Rouse, Fisher, Strohl, Rouse and Fisher7 These were isolated in 65 per cent of our patients (Table I). Other cultured bacteria were predominantly Gram-negative rods. It has been found that the bacterial lipopolysaccharide of Gram-negative organisms causes ciliostasis of the mucosal epithelium,Reference Nell and Grote8Reference Yeh, Hsu, Chen, Hsu and Lee10 thus accounting for the persistence of infection. Bacterial colonisation takes the form of a bacterial biofilm, making the organisms resistant to host defences and antibiotics.Reference Galli, Ardito, Calo, Mancinelli, Imperiali and Parrilla11 The presence of pus cells was a common finding in microscopic examination of the discharge obtained from our patients (Table I). Histopathological examination of biopsy material revealed inflammatory cells in the submucosa and necrotic inferior turbinate bone, consistent with chronic pyogenic osteomyelitis (Figure 1).Reference Burns, Kumar, Kumar, Cotran and Robbins12 Chronic osteomyelitis accounts for the bone loss seen in primary atrophic rhinitis; furthermore, it contributes to the persistence of the neighbouring mucosal disease.Reference Perloff, Gannon, Bolger, Montone, Orlandi and Kennedy13, Reference Khalid, Hunt, Perloff and Kennedy14

  • This study undertook microbiological analysis of crusts and secretions obtained from 14 patients with primary atrophic rhinitis

  • Pyogenic bacteria were isolated from the majority of specimens; klebsiella species were encountered in 65 per cent and other pyogenic bacteria were also isolated (mostly Gram-negative rods)

  • Fungal elements were isolated from 93 per cent of specimens, the most common being aspergillus species; the fungal infestation represented saprophytic fungal colonisation

The predominant fungi isolated from our patients were aspergillus species (Table I). The persistence of purulent discharge and impaired mucociliary clearance facilitates saprophytic fungal infestation, associated with germination of inhaled fungal spores. This fungal colonisation contributes to the offensive odour and the characteristic friable, cheesy material associated with crusts encountered in cases of primary atrophic rhinitis.Reference Grosjean and Weber15 Moreover, pressure by the fungal mass may contribute to pressure atrophy of the turbinate bone.Reference Chole, McGinn and Tinling16, Reference Moriyama, Huang, Kato and Abramson17

Conclusion

The pathogenesis of primary atrophic rhinitis probably involves virulent bacterial infection of the mucosa, with secondary inflammatory effects on the submucosa and bone. Saprophytic fungal colonisation of the purulent discharge contributes to the clinical picture of the disease.

References

1 Dutt, SN, Kameswaran, M. The aetiology and management of atrophic rhinitis. J Laryngol Otol 2005;119:843–52CrossRefGoogle ScholarPubMed
2 Sayed, RH, Abou-Elhamd, KA, Abdel-Kader, M, Saleem, TH. Study of surfactant level in cases of primary atrophic rhinitis. J Laryngol Otol 2000;114:254–9CrossRefGoogle ScholarPubMed
3 Ferguson, JL, McCaffrey, TV, Kern, EB, Martin, WJ 2nd. Effects of Klebsiella ozaenae on ciliary activity in vitro: implications in the pathogenesis of atrophic rhinitis. Otolaryngol Head Neck Surg 1990;102:207–11CrossRefGoogle ScholarPubMed
4 Moore, EJ, Kern, EB. Atrophic rhinitis: a review of 242 cases. Am J Rhinol 2001;15:355–61CrossRefGoogle ScholarPubMed
5 Ferguson, BJ. Fungus balls of the paranasal sinuses. Otolaryngol Clin North Am 2000;33:389–98CrossRefGoogle ScholarPubMed
6 Daudia, A, Jones, NS. Advances in management of paranasal sinus aspergillosis. J Laryngol Otol 2008;122:331–5CrossRefGoogle ScholarPubMed
7 Strohl, WA, Rouse, H, Fisher, BD. Enteric Gram-negative rods. In: Strohl, WA, Rouse, H, Fisher, BD, eds. Microbiology. Philadelphia: Lippincott Williams & Wilkins, 2001;175–90Google Scholar
8 Nell, MJ, Grote, JJ. Effects of bacterial toxins on air-exposed cultured human respiratory sinus epithelium. Ann Otol Rhinol Laryngol 2003;112:461–8CrossRefGoogle ScholarPubMed
9 Mewe, M, Tielker, D, Schonberg, R, Schachner, M, Jaeger, K, Schumacher, U. Pseudomonas aeruginosa lectins I and II and their interaction with human airway cilia. J Laryngol Otol 2005;119:595–9CrossRefGoogle ScholarPubMed
10 Yeh, T-H, Hsu, W-C, Chen, Y-S, Hsu, C-J, Lee, S-Y. Lipopolysaccharide decreases connexin 43 expression on nasal epithelial cells in vitro. Acta Otolaryngol 2005;125:1091–6CrossRefGoogle ScholarPubMed
11 Galli, J, Ardito, F, Calo, L, Mancinelli, L, Imperiali, M, Parrilla, C et al. Recurrent upper airway infections and bacterial biofilms. J Laryngol Otol 2007;121:341–4CrossRefGoogle ScholarPubMed
12 Burns, DK, Kumar, V. The musculoskeletal system. In: Kumar, V, Cotran, RS, Robbins, SL, eds. Basic Pathology, 7th edn. Philadelphia: WB Saunders, 2003;755–88Google Scholar
13 Perloff, JR, Gannon, FH, Bolger, WE, Montone, KT, Orlandi, R, Kennedy, DW. Bone involvement in sinusitis: an apparent pathway for the spread of disease. Laryngoscope 2000;110:2095–9CrossRefGoogle ScholarPubMed
14 Khalid, AN, Hunt, J, Perloff, JR, Kennedy, DW. The role of bone in chronic rhinosinusitis. Laryngoscope 2002;112:1951–7CrossRefGoogle ScholarPubMed
15 Grosjean, P, Weber, R. Fungus balls of the paranasal sinuses: a review. Eur Arch Otorhinolaryngol 2007;264:461–70CrossRefGoogle ScholarPubMed
16 Chole, RA, McGinn, MD, Tinling, SP. Pressure-induced bone resorption in the middle ear. Ann Otol Rhinol Laryngol 1985;94:165–70CrossRefGoogle ScholarPubMed
17 Moriyama, H, Huang, CC, Kato, M, Abramson, M. Effects of pressure on bone resorption in the middle ear of rats. Ann Otol Rhinol Laryngol 1985;94:60–4CrossRefGoogle Scholar
Figure 0

Table I Microbiological data from the study group

Figure 1

Fig. 1 Photomicrograph of lateral nasal wall biopsy from patient with primary atrophic rhinitis, showing squamous metaplasia of epithelium, chronic inflammatory cells, hyper vascularity, submucosal fibrosis and necrosis of underlying bone (H&E; ×150).