Indian Journal of Dermatology
  Publication of IADVL, WB
  Official organ of AADV
Indexed with Science Citation Index (E) , Web of Science and PubMed
 
Users online: 1736  
Home About  Editorial Board  Current Issue Archives Online Early Coming Soon Guidelines Subscriptions  e-Alerts    Login  
    Small font sizeDefault font sizeIncrease font size Print this page Email this page


 
Table of Contents 
ORIGINAL ARTICLE
Year : 2018  |  Volume : 63  |  Issue : 2  |  Page : 141-146
A study of onychomycosis at a tertiary care hospital in Eastern Bihar


1 Department of Microbiology, MGM Medical College, Kishanganj, Bihar, India
2 Department of Dermatology, MGM Medical College, Kishanganj, Bihar, India

Date of Web Publication6-Apr-2018

Correspondence Address:
Dr. Anindita Sen
AB 51/1 Saltlake, Kolkata - 700 064, West Bengal
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijd.IJD_630_16

Rights and Permissions

   Abstract 


Background: Onychomycosis (OM) is a major public health problem which is increasing worldwide. It is associated with high morbidity and causes physical, psychological, and occupational problems in patients. Aims: This study aims to study the pattern of etiological agents, clinical features, and severity assessment of OM in this part of India. Materials and Methods: Sixty eight clinically suspected patients with positive potassium hydroxide and fungal culture were studied. Results: Males were infected more often than females (1.61:1). The most common age group affected was 21–40 years. Finger nails were affected more frequently than toe nails. Distal and lateral subungual OM was the most common (48 cases, 70.59%) clinical pattern. For most of the patients (66.18%), nail involvement was severe. Discoloration was the most common (67 cases, 98.53%) change, followed by subungual hyperkeratosis (51 cases, 75%). Principal causative agents were dermatophytes (55 cases, 80.88%) with Trichophyton rubrum being the most common one (35 cases, 51.47%). In 9 (13.23%) cases, Candida albicans, in 6 (8.82%) Aspergillus niger and in 1 (1.47%) case Acremonium sp. (AC) have been isolated as the sole causative agent. In 2 (2.94%) cases, mixed infection with dermatophyte and Aspergillus and in 1 (1.47%) case dermatophyte and Candida were noted. Conclusion: Although dermatophytes were the most common causative agent of OM, nondermatophytic molds, and yeasts were also encountered. The genus and species identification helps in the proper diagnosis and management. Morphological changes in nail may help in presumptive diagnosis of OM.


Keywords: Fungal culture, onychomycosis, potassium hydroxide, Trichophyton rubrum


How to cite this article:
Sen A, Bhunia D, Datta PK, Ray A, Banerjee P. A study of onychomycosis at a tertiary care hospital in Eastern Bihar. Indian J Dermatol 2018;63:141-6

How to cite this URL:
Sen A, Bhunia D, Datta PK, Ray A, Banerjee P. A study of onychomycosis at a tertiary care hospital in Eastern Bihar. Indian J Dermatol [serial online] 2018 [cited 2023 Sep 26];63:141-6. Available from: https://www.e-ijd.org/text.asp?2018/63/2/141/229457

What was known?
Yeasts and nondermatophytic molds are important causes of onychomycosis apart from dermatophytes.



   Introduction Top


The term onychomycosis (OM) is derived from the Greek word onyx meaning nail and mykes meaning fungus.[1] It describes fungal infection of the nail caused by dermatophytes, yeasts, or nondermatophytic molds.[2] It constitutes 50% of all nail-related diseases.[3] Till the late 1990, OM was not in the limelight as an important health problem and is getting focussed only in the last decade.[4] At present, the worldwide incidence of OM is increasing and the prevalence rate ranges from 2% to 50%.[5] A number of factors contribute to the occurrence of this disease, namely, the age, sex, occupation, chronic health problem, immunity of the patient, type of footwear used, bathing in communal swimming pool, procedure of trimming nail, climatic condition, frequency of travel, etc.[6],[7] OM can be caused by dermatophytes, yeasts (Candida albicans [CA]) and nondermatophytic molds (Aspergillus [AC], Fusarium, Onychocola canadensis, Scopulariopsis brevicaulis, Scytalidium dimidiatum). Dermatophytes are the most common agent and among them Trichophyton rubrum (TR) and Trichophyton mentagrophytes (TM) constitute 90% of toenail and 50% of finger nail infections.[8] Clinically, OM can be classified into distal and lateral subungual OM (DLSO), proximal subungual OM (PSO), white superficial OM (WSO), and total dystrophic OM (TDO).[1] Endonyx and mixed patterns of OM have also been described.[9] Nail changes associated with OM are onychodystrophy, onycholysis, subungual hyperkeratosis, discoloration, thickening of nail plate, etc. However, these changes are not specific of fungal infection. Similar changes are also observed in psoriasis, lichen planus, and following trauma.[10] Therefore, mycological examinations (direct microscopy using potassium hydroxide [KOH] preparation along with culture, the gold standard techniques) are essential, considering the cost of prolonged antifungal drug therapy, and the inconvenience caused to the patient.[11]


   Materials and Methods Top


This study was carried out over a 13 months period from February 2015 to February 2016 in a tertiary care hospital in eastern Bihar, after obtaining institutional ethical committee clearance. One hundred and fifty-two patients with clinical suspicion of fungal nail infection, attending the dermatology outpatient department were subjected to mycological investigations in the Department of Microbiology of this hospital after obtaining written informed consent from them. Out of them, 68 (44.73%) patients showing positive results with both KOH and fungal culture were included in the present study. Detailed histories were taken from the patients regarding age, sex, occupation, education, associated comorbidities, method of trimming nail, and history of trauma. Elaborate clinical examinations were made regarding the site of nail involvement, the number of involved nails, the type of involvement, morphological changes, and also any associated dermatological disorder. The severity of nail involvement was assessed by OM severity index (OSI).[12] The OSI score is obtained by multiplying the score for the area of involvement (range 0–5) by the score for the proximity of disease to the matrix (range 1–5). Ten points are added for the presence of a longitudinal streaking or a patch (dermatophytoma) or for >2 mm of subungual hyperkeratosis. Patients who gave a history of intake of systemic antifungal or use of topical antifungal within the last 6 months were not included in the study. For sample collection, the affected nail was first cleaned with 70% alcohol to remove contamination and then nail clipping was done, and scrapings were collected from the distal portion of the nail plate, the nail bed and undersurface of the nail with the help of sterile scalpel blade. In case of multiple nail involvement, the nail that was most severely affected was selected for sample collection. A portion of each sample was subjected to direct microscopic examination using 20% KOH and the remaining portion was put to culture in both Sabouraud Dextrose Agar (SDA) and SDA with chloramphenicol and cycloheximide. The culture tubes were put to incubation at 25°C in biological oxygen demand and were observed for 6 weeks period for the presence of growth before being discarded as negative. The growth on primary culture tubes was subjected to slide cultures on Corn Meal Agar for detailed morphological identification to species level. The colony character, surface color, color on reverse, and presence of any diffusible pigment were also noted from the primary culture tubes. Urease test and hair perforation test were also done for the identification of dermatophytes. For confirmation of yeast to species level germ tube test and color production on Chromagar candida media were also used. To report a nondermatophytic fungus as the causative agent, a combination of a positive direct microscopic finding was correlated with isolation of same fungus in a second sample that was collected from the patient some days later.


   Results Top


Among 152 clinically suspected cases of OM, 92 (60.52%) patients showed positive results with KOH. Out of them, 68 showed positivity in culture and were included in this study. Male outnumbered female, the number is 42 (61.76%) and 26 (38.23%), respectively. Age of the patients in this study ranged from 12 to 75 years with a mean (±SD) of 38.85 (±15.22) years. Majority of the patients belonged to 21–40 year age group (54, 79.4%). Only 17 (25%) patients were literate. Majority of our patients (85.29%) were from rural background. Regarding the occupation, 22 (32.35%) patients were farmer, 19 (27.94%) housewife, 18 (26.47%) laborer, and 9 (13.23%) were student. All the patients belonged to the below poverty line income group. Family history of fungal infection was there in 2 patients. There was history of trauma over the involved nail in five patients. Ten patients gave a history of repeated contact with detergents. Majority (75%) of the patients were used to wearing chappal. Sixteen patients gave a history of trimming nail with barber and the rest used to do self-trimming. Associated comorbidities were as follows –12 patients had diabetes, two had hypertension. Paronychia was the most common (20 cases, 29.41%) associated cutaneous finding, followed by dermatophytic infections of palms, soles or other areas (16 cases, 23.53%). Other associated skin disorders were dermatitis (5 cases, 7.35%), psoriasis (2 cases, 2.94%) and leprosy (1 case, 1.47%).

Fingernails were more commonly affected than toe nails. The sites of involvement are shown in [Table 1]. Majority of our patients (48 cases, 70.59%) had DLSO [Figure 1] and eight (11.76%) had TDO [Figure 2] as sole clinical pattern. Twelve patients (17.65%) had mixed types. Among them, ten patients (14.71%) had both DLSO and TDO types in their nails, one patient (1.47%) had both DLSO and WSO [Figure 3], and one (1.47%) had both TDO and WSO patterns. We did not find any cases of PSO or endonyx type. The distributions of the types are shown [Table 2].
Table 1: Distribution of nail involvement

Click here to view
Figure 1: Distal and lateral subungual onychomycosis with brownish discoloration, subungual hyperkeratosis, distal onycholysis, and longitudinal ridges

Click here to view
Figure 2: Total dystrophic onychomycosis with brownish-black discoloration, total nail dystrophy, and paronychia

Click here to view
Figure 3: Distal and lateral subungual onychomycosis and white superficial onychomycosis mixed pattern with white discoloration, subungual hyperkeratosis, distal onycholysis, and partial nail plate dystrophy

Click here to view
Table 2: Distribution of the types of onychomycosis

Click here to view


We selected the most severely involved nail for the assessment of grading by OSI. According to this scoring, 45 patients (66.18%) had severe OM (score 16–35). Moderately (score 6–15) affected nails were seen in 19 patients (27.94%) and the remaining four patients (5.88%) had mild (score 1–5) nail involvement.

Color change of nail plate or nail bed, the most common change, was seen in all but one patient (98.53%). Single or mixed discoloration was seen in different nails of them. Brownish pigmentation (40 cases, 58.82%) was the most common among these. Apart from the color change, subungual hyperkeratosis was the most common structural change (75%) followed by distal onycholysis (52.94%), total nail plate dystrophy (27.94%), partial nail plate dystrophy (23.53%), nail plate thickening (19.12%), transverse ridges (16.18%), nail plate thinning (11.76%), and longitudinal ridges (8.82%) [Table 3].
Table 3: Distribution of nail changes (n=68)

Click here to view


Of the causative agents, sole infection by dermatophytes [Figure 4] was identified in 52 (76.47%) patients, yeast (CA) in 8 (11.76%) [Figure 5], nondermatophytic molds including Aspergillus niger (AN) in 4 (5.88%) patients and AC in 1 (1.47%) patient [Figure 6]. Among the dermatophytes, 35 (63.63%) patients had TR infection, and 20 (36.36%) had TM infection. Mixed infections were found in 3 (4.41%) patients – one had yeast (CA) and dermatophyte (TR) infection and the other two had dermatophyte and nondermatophyte mould infection (AN and TR, AN and TM). The various types of isolates are shown [Table 4].
Figure 4: Primary culture tubes and slide culture microscopy (x400) of dermatophytes (a and b-Trichophyton rubrum, c and d-Trichophyton mentagrophytes), (b) Showing septate hyphae, tear-shaped microconidia and pencil-like macroconidia. (d) Septate hyphae and coiled spiral hyphae seen

Click here to view
Figure 5: (a) Candida albicans in Chrome Candida Differential Agar (M1297A-100G) showing light green color of the colony of Candida albicans. and (b) Slide culture microscopy (x400) showing budding yeast cells and pseudohyphae

Click here to view
Figure 6: Primary culture tubes and slide culture microscopy (x400) of nondermatophyte molds (a and b-Aspergillus niger, c and d-Acremonium). (b) Showing septate hyphae with biseriate arrangement of phialides covering the entire vesicle. (d) Showing one-celled oblong conidia

Click here to view
Table 4: Mycological types of isolates

Click here to view


Among the sole isolates (65 cases), 44 patients had severe nail involvement, and the rest (21) had mild-to-moderate involvement. Dermatophytes were isolated in 36 patients with severe disease and in 16 cases with mild-to-moderate involvement. Remaining cases in these groups had nondermatophyte isolates. Statistical analysis failed to show any significant correlation between the severity of the disease and the type of mycological isolates.


   Discussion Top


OM is a major public health problem. Because of the existence of many diseases with high mortality and morbidity, people especially of developing countries are unaware of OM which is not life-threatening. However, it has a significant impact on the social, emotional, and occupational life of the patient.

In our study, 44.73% of the clinically suspected patients showed positive results both in KOH and culture. This is at par with findings from many places, for example, 43.7% in Poland,[13] 50.6% in Turkey,[14] and 45.53% in some other parts of India.[15] The male preponderance seen in our study was also noted in other studies from India.[15],[16] In our study, young adults, and middle-aged people were mostly affected (mean age 38.85 years) similar to that mentioned in other studies.[4],[15],[16]

Majority of our patients (70.59%) had DLSO type of OM as also described in other studies from India.[4],[5],[16] A considerable number (17.65%) of our patients had multiple nail involvement with different types or overlapping features, we also looked for the color and structural changes of the affected nails. Color change was the most common (98.53%) nail change. Subungual hyperkeratosis (75%), distal onycholysis (52.94%), and nail plate dystrophy (51.47%) were common structural changes. These features, as well as nail plate thickening were also previously described in an Indian literature.[17] In addition, nail plate thinning and transverse or longitudinal ridges were also found in our study. Although these morphological changes are not specific for OM, they can be helpful to suspect those cases. We assessed the severity of nail involvement and found that most of our patients (66.18%) had severely affected nails which definitely needed long-term antifungal therapy. Dermatophytes have been identified as the major cause of OM constituting 80.88% of the cases in which TR has been identified in 51.47%. Similar result has been obtained worldwide [18],[19],[20],[21] and also from India.[16],[22],[23]Candida sp.[14],[24] and AN [25] have been found as the main causative agents in some studies. However, in our study, 13.23% patients had CA only as causative fungus, and 8.82% had AN as the only causative agent.

Severity of nail involvement failed to show any significant correlation with the etiological agent.


   Conclusion Top


Morphological changes of nails, though many are nonspecific, may be helpful to suspect a case of OM. However, mycological identification of clinically suspected cases of OM should be done for genus and species level identification for confirmation of diagnosis and also to provide appropriate treatment to the patient. A continuous monitoring for the change in etiological agent should be carried out. The severity of each case should also be assessed for the therapeutic purpose.

In this study, due to absence of control group, we could not establish the significance of morphological nail changes with mycological findings.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Chander J. Textbook of Medical Mycology. 3rd ed. New Delhi: Mehta Offset Pvt. Ltd.; 2009. p. 122-46.  Back to cited text no. 1
    
2.
Weitzman I, Summerbell RC. The dermatophytes. Clin Microbiol Rev 1995;8:240-59.  Back to cited text no. 2
    
3.
Scher RK. Onychomycosis: A significant medical disorder. J Am Acad Dermatol 1996;35:S2-5.  Back to cited text no. 3
    
4.
Satpathi P, Achar A, Banerjee D, Maiti A, Sengupta M, Mohata A. Onychomycosis in Eastern India – Study in a peripheral tertiary care centre. J Pak Assoc Dermatol 2013;23:14-9.  Back to cited text no. 4
    
5.
Sarma S, Capoor MR, Deb M, Ramesh V, Aggarwal P. Epidemiologic and clinicomycologic profile of onychomycosis from North India. Int J Dermatol 2008;47:584-7.  Back to cited text no. 5
    
6.
Proceedings of the international summit on cutaneous antifungal therapy and mycology workshop. San Francisco, California, October 21-24, 1993. J Am Acad Dermatol 1994;31:S1-116.  Back to cited text no. 6
    
7.
Williams HC. The epidemiology of onychomycosis in Britain. Br J Dermatol 1993;129:101-9.  Back to cited text no. 7
    
8.
Elewski BE. Onychomycosis: Pathogenesis, diagnosis, and management. Clin Microbiol Rev 1998;11:415-29.  Back to cited text no. 8
    
9.
Hay RJ, Baran R. Onychomycosis: A proposed revision of the clinical classification. J Am Acad Dermatol 2011;65:1219-27.  Back to cited text no. 9
    
10.
Gupta AK, Ricci MJ. Diagnosing onychomycosis. Dermatol Clin 2006;24:365-9.  Back to cited text no. 10
    
11.
Feuilhade de Chauvin M. New diagnostic techniques. J Eur Acad Dermatol Venereol 2005;19 Suppl 1:20-4.  Back to cited text no. 11
    
12.
Carney C, Tosti A, Daniel R, Scher R, Rich P, DeCoster J, et al. A new classification system for grading the severity of onychomycosis: Onychomycosis severity index. Arch Dermatol 2011;147:1277-82.  Back to cited text no. 12
    
13.
Maleszka R, Ratajczak-Stefańska V, Mikulska D. The importance of mycological investigations in diagnostics of nail changes. Rocz Akad Med Bialymst 2005;50 Suppl 1:36-8.  Back to cited text no. 13
    
14.
Meriç M, Yuluǧkural Z, Keçeli S, Willke A. Dermatophyte species isolated from patients prediagnosed as onychomycosis and the value of fungal culture. Mikrobiyol Bul 2004;38:435-9.  Back to cited text no. 14
    
15.
Jesudanam TM, Rao GR, Lakshmi DJ, Kumari GR. Onychomycosis: A significant medical problem. Indian J Dermatol Venereol Leprol 2002;68:326-9.  Back to cited text no. 15
[PUBMED]  [Full text]  
16.
Garg A, Venkatesh V, Singh M, Pathak KP, Kaushal GP, Agrawal SK, et al. Onychomycosis in central India: A clinicoetiologic correlation. Int J Dermatol 2004;43:498-502.  Back to cited text no. 16
    
17.
Das NK, Ghosh P, Das S, Bhattacharya S, Dutta RN, Sengupta SR, et al. A study on the etiological agent and clinico-mycological correlation of fingernail onychomycosis in Eastern India. Indian J Dermatol 2008;53:75-9.  Back to cited text no. 17
[PUBMED]  [Full text]  
18.
Boukachabine K, Agoumi A. Onychomycosis in Morocco: Experience of the parasitology and medical mycology laboratory from rabat children hospital (1982-2003). Ann Biol Clin (Paris) 2005;63:639-42.  Back to cited text no. 18
    
19.
Wang SH, Chi CC. Onychomycosis in Taiwan. Int J Clin Pract 2005;59:906-11.  Back to cited text no. 19
    
20.
Araj GF, Racoubian ES, Daher NK. Etiologic agents of dermatophyte infection in Lebanon. J Med Liban 2004;52:59-63.  Back to cited text no. 20
    
21.
Perea S, Ramos MJ, Garau M, Gonzalez A, Noriega AR, del Palacio A, et al. Prevalence and risk factors of tinea unguium and tinea pedis in the general population in Spain. J Clin Microbiol 2000;38:3226-30.  Back to cited text no. 21
    
22.
Banerjee U, Sethi M, Pasricha JS. Study of onychomycosis in India. Mycoses 1990;33:411-5.  Back to cited text no. 22
    
23.
Grover S. Clinico-mycological evaluation of onychomycosis at Bangalore and Jorhat. Indian J Dermatol Venereol Leprol 2003;69:284-6.  Back to cited text no. 23
[PUBMED]  [Full text]  
24.
Vijaya D, Anandkumar BH, Geetha SH. Study of onychomycosis. Indian J Dermatol Venereol Leprol 2004;70:185-6.  Back to cited text no. 24
[PUBMED]  [Full text]  
25.
Brilhante RS, Cordeiro RA, Medrano DJ, Rocha MF, Monteiro AJ, Cavalcante CS, et al. Onychomycosis in Ceará (Northeast Brazil): Epidemiological and laboratory aspects. Mem Inst Oswaldo Cruz 2005;100:131-5.  Back to cited text no. 25
    

What is new?

  • Dermatophytes, particularly TR, still remain the most common etiological agent causing onychomycosis in Bihar.
  • Morphological changes of nail may aid in presumptive diagnosis of onychomycosis.
  • Severity of nail involvement is not dependent on etiological agents.


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]
 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4]



 

Top
Print this article  Email this article
 
 
  Search
 
  
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Article in PDF (2,445 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  


    Abstract
   Introduction
    Materials and Me...
   Results
   Discussion
   Conclusion
    References
    Article Figures
    Article Tables

 Article Access Statistics
    Viewed4244    
    Printed95    
    Emailed0    
    PDF Downloaded106    
    Comments [Add]    

Recommend this journal