|Year : 2012 | Volume
| Issue : 2 | Page : 229-232
Trichosporon inkin, an unusual agent of fungal sinusitis: A report from south India
Anand Janagond1, K Mohana Krishnan1, AJ Kindo2, G Sumathi1
1 Department of Microbiology, Sri Muthukumaran Medical College, Chikkarayapuram, Near Mangadu, Chennai - 600 069, India
2 Department of Microbiology, Sri Ramachandra University, Chennai, India
|Date of Submission||10-Oct-2011|
|Date of Acceptance||23-Feb-2012|
|Date of Web Publication||28-May-2012|
Department of Microbiology, Sri Muthukumaran Medical College, Chikkarayapuram, Near Mangadu, Chennai - 600 069
Source of Support: None, Conflict of Interest: None
The aetiology of fungal sinusitis is diverse and changing. Aspergillus species has been the most common cause for fungal sinusitis, especially in dry and hot regions like India. Trichosporon species as a cause for fungal sinusitis has been very rarely reported the world over. Here, we report a rare case of allergic fungal sinusitis caused by Trichosporon inkin in a 28-year-old immunocompetent woman. Bilateral nasal obstruction, nasal discharge and loss of smell were her presenting complaints. Diagnostic nasal endoscopy showed bilateral multiple polyps. Functional endoscopic sinus surgery was performed and many polyps were removed. Based on mycological and histopathological studies, the pathogen was identified as T. inkin.
Keywords: Fungal sinusitis, polyps, Trichosporon
|How to cite this article:|
Janagond A, Krishnan K M, Kindo A J, Sumathi G. Trichosporon inkin, an unusual agent of fungal sinusitis: A report from south India. Indian J Med Microbiol 2012;30:229-32
|How to cite this URL:|
Janagond A, Krishnan K M, Kindo A J, Sumathi G. Trichosporon inkin, an unusual agent of fungal sinusitis: A report from south India. Indian J Med Microbiol [serial online] 2012 [cited 2019 Sep 19];30:229-32. Available from: http://www.ijmm.org/text.asp?2012/30/2/229/96704
| ~ Introduction|| |
Fungi are being increasingly implicated in the aetiopathology of rhinosinusitis. Though fungal sinusitis is frequently seen in diabetic or immunocompromised patients, it has also been reported in immunocompetent individuals. Many fungi have been implicated with fungal sinusitis, including the Aspergillus species, several of the dematiaceous fungi including Curvularia, Bipolaris, Exserohilum and also zygomycetes. Aspergillus spp are more commonly isolated from the Indian subcontinent.  The diversity of fungal pathogens causing sinusitis is on the rise. , To the best of our knowledge, this is the first report of allergic fungal sinusitis with polyposis caused by Trichosporon inkin from India.
| ~ Case Report|| |
A 28-year-old woman from Chennai, South India, presented with bilateral nasal obstruction, nasal discharge and loss of smell for a period of 6 months. She was not a known diabetic and was not on steroid treatment. She was HIV seronegative. Routine ENT examination and diagnostic nasal endoscopy revealed multiple pale polyps over the middle turbinate in both the nasal cavities. It was possible to probe all around the polyps and they did not bleed to touch. Mucopurulent discharge was noted from both nasal cavities. Nasal septum was central, and middle as well as inferior turbinates appeared normal.
Functional endoscopic sinus surgery (FESS) was performed. Uncinectomy, middle meatal antrostomy and sphenoidectomy were done on the left nasal cavity. The polyps were removed from anterior and posterior ethmoidal sinuses as well as sphenoid sinus. The same procedure was performed on the right side as well. The material was sent for microbiological and histopathological study.
Direct microscopic examination of the specimen by 10% potassium hydroxide (KOH) mount [Figure 1] and lactophenol cotton blue (LPCB) mount showed multiple hyaline septate branching hyphae. Histopathological examination of the specimen showed hyaline septate acutely branching hyphae and allergic mucin [Figure 2].
|Figure 1: KOH (10%) preparation of the specimen showing hyaline septate branching hyphae (×400)|
Click here to view
|Figure 2: Histopathological sections of polyp in Periodic Acid Schiff (PAS) stain (×400) showing septate, acutely branching hyphae and allergic mucin (inset)|
Click here to view
The specimen was inoculated onto two sets of Sabouraud's Dextrose Agar (SDA) slopes and incubated at 25°C and 37°C. White pasty colonies appeared on all the media (at 25°C and 37°C) on the second day of incubation, and over the next 3-4 days white to tan, soft pasty colonies with fine cerebriform folds were formed [Figure 3]. Cracking of the media was observed around the colonies. Microscopic examination of the isolate by 10% KOH, LPCB and Gram stain [Figure 4] preparations revealed yeast-like cells with blastoconidia, hyaline septate hyphae and numerous arthroconidia. The arthroconidia were rectangular initially and later became more spherical. The isolate was urease positive. Sarcinae (swollen, meristematic clump of cells),  which are characteristic morphological features of Trichosporon inkin, were demonstrated in Gram-stained smears [Figure 4]. Based on the macroscopic and microscopic findings, the organism was identified as a T. inkin.
|Figure 3: Colony morphology on SDA showing white pasty colony with fi ne cerebriform folds. Cracking of the agar is also seen|
Click here to view
|Figure 4: Gram staining morphology of the isolate (×1000) showing yeast-like cells with blastoconidia (red arrow), many arthroconidia (green arrow), hyphae and sarcinae (black arrow) that are characteristic|
of T. inkin
Click here to view
Correlating all the clinical, microbiological and histopathological information, the final diagnosis was made as allergic fungal sinusitis with multiple polyposis caused by T. inkin. The patient was started on treatment with a tapering course for 20 days of oral prednisolone with a starting dose of 10 mg thrice a day. Unfortunately, the patient was lost to follow-up.
| ~ Discussion|| |
Trichosporon species are yeast-like fungi, widely distributed in nature and commonly isolated from soil and other environmental sources, which have been involved in a variety of opportunistic infections and have been recognised as emerging fungal pathogens in immunocompromised hosts. Therefore, recovery of Trichosporon species capable of growing at 37°C, especially from immunocompromised patients, should be regarded as significant.  Currently, the genus Trichosporon includes the following species as potential human pathogens: Trichosporon cutaneum, Trichosporon asahii, Trichosporon asteroides, Trichosporon mucoides, T. inkin, etc. There is a consensus that molecular methods are required for accurate identification of this genus, but they are still costly and not suitable for most laboratories. 
Although uncommon, pathogenic species of this genus are being increasingly reported, in patients with malignant diseases, bone marrow transplant recipient, solid organ transplant recipient and patients with HIV infection  Trichosporon species have been reported to be the most common cause of non-Candida yeast infections in patients with haematological malignancies, and the infections were associated with high mortality rates despite antifungal therapy.  No such risk factors were seen in the present case.
T. inkin is frequently isolated from clinical specimens, such as white piedra, and also from patients with peritonitis, endocarditis, lung abscesses, subcutaneous nodules (rheumatoid arthritis patients receiving corticosteroid therapy), sternal surgical wound infections, balanitis, urethral discharge and invasive infections.  Three cases of fungal sinusitis caused by Trichosporon have been reported from Iran by Hedayati et al. 
The incidence of fungal sinusitis varies widely, with higher frequency in geographical areas which have hot and dry climate, as in India. The disease has been described as having four types: Allergic, non-invasive, invasive and fulminate.  Allergic type has been described as the most common type of fungal sinusitis in many studies. , Except for the fulminant variety, the disease is commonly found in the young immunocompetent population of rural areas. Aspergillus species are the commonest aetiological agents, with Aspergillus flavus being the commonest species isolated. ,, Allergic fungal sinusitis needs comprehensive treatment with endoscopic sinus surgery, steroids and antifungal therapy. Allergic fungal sinusitis is readily recurrent. Long-term follow-up is important.  For effective management, non-invasive disease requires surgical debridement and sinus ventilation only. But for the invasive type, adjuvant medical therapy (antifungals) is recommended to prevent recurrence and further extension.  Since there were no signs of invasion in this case, antifungals were not given. This case emphasises the need to have a high index of suspicion and careful microbiological evaluation for fungal pathogens even in immunocompetent individuals with no specific risk factors.
| ~ References|| |
|1.||Michael RC, Michael JS, Ashbee RH, Mathews MS. Mycological profile of fungal sinusitis: An audit of specimens over a 7-year period in a tertiary care hospital in Tamil Nadu. Indian J Pathol Microbiol 2008;51:493-6. |
|2.||Kindo AJ, Pramod C, Anita S, Mohanty S. Maxillary sinusitis caused by Lasiodiplodia theobromae. Indian J Med Microbiol 2010;28:167-9. |
|3.||Swain B, Panigrahy R, Panigrahi D. Schizophyllum commune sinusitis in an immunocompetent host. Indian J Med Microbiol 2011;29:439-42. |
|4.||De Hoog CS, Guarro J, Gené J, Figueras MJ. Atlas of Clinical Fungi: 2 nd ed. Utrecht, The Netherlands: Centraalbureau voor Schimmelcultures; 2000. p. 171-2. |
|5.||Taj-Aldeen SJ, Al-Ansari N, El Shafei S, Meis JF, Curfs-Breuker I, Theelen B, et al. Molecular identification and susceptibility of Trichosporon species isolated from clinical specimens in Qatar: Isolation of Trichosporon dohaense Taj-Aldeen, Meis and Boekhout sp. nov. J Clin Microbiol 2009;47:1791-9. |
|6.||Chagas-Neto TC, Chaves GM, Melo AS, Colombo AL. Bloodstream infections due to Trichosporon spp.: Species distribution, Trichosporon asahii genotypes determined on the basis of ribosomal DNA intergenic spacer 1 sequencing, and antifungal susceptibility testing. J Clin Microbiol 2009;47:1074-81. |
|7.||Hedayati MT, Bahoosh M, Kasiri A, Ghasemi M, Motahhari SJ, Poormosa R. Prevalence of fungal rhinosinusitis among patients with chronic rhinosinusitis from Iran. J Med Mycol 2010;20:298-303. |
|8.||Chakrabarti A, Sharma SC. Paranasal sinus mycoses. Indian J Chest Dis Allied Sci 2000;42:293-304. |
|9.||Das A, Bal A, Chakrabarti A, Panda N, Joshi K. Spectrum Histopathology 2009;54:854-9. |
|10.||Rupa V, Jacob M, Mathews MS, Job A, Kurien M, Chandi SM. Clinicopathological and mycological spectrum of allergic fungal sinusitis in South India. Mycoses 2002;45:364-7. |
|11.||Singh N, Bhalodiya NH. Allergic fungal sinusitis (AFS)-earlier diagnosis and management. J Laryngol Otol 2005;119:875-81. |
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
|This article has been cited by|
||Unusual causes of fungal rhinosinusitis: A study from a tertiary care centre in South India
| ||Giri, S., Kindo, A.J., Rao, S., Kumar, A.R. |
| ||Indian Journal of Medical Microbiology. 2013; 31(4): 379-384 |
||The clinical importance of fungal biofilms
| ||Ramage, G., Williams, C. |
| ||Advances in Applied Microbiology. 2013; 84(27): 83 |