|Year : 1999 | Volume
| Issue : 2 | Page : 72-74
Diagnosis of superficial mycoses by direct microscopy - A statistical evaluation
JC Mohanty, SK Mohanty, RC Sahoo, A Sahoo, Prahara
J C Mohanty
Source of Support: None, Conflict of Interest: None
A mycological study was undertaken in 250 cases of superficial mycotic infections, which included 210 cases of dermatophytosis, 18 cases of cutaneous candidiasis and 22 cases of tinea versicolor. The scrapings from all the cases were subjected to direct microscopic examination in 10% KOH solution and culture was done in case of candidiasis and dermatophytosis. Out of 250 cases direct microscopy was positive (KOH +ve) in 88 cases of dermatophytosis, 11 cases of candidiasis and all cases of tinea versicolor. Culture for dermatophytes and candida species in SDA medium were positive in 76 and 9 cases respectively. The diagnostic sensitivity, specificity, positive predictive value, negative predictive value and the overall efficiency of the direct microscopy in the diagnosis of superficial mycotic infections were calculated to be 89.41%, 83.90%, 76.76%, 93.02% and 85.96% respectively.
Keywords: Superficial mycoses, Positive predictive value, Negative predictive value
|How to cite this article:|
Mohanty J C, Mohanty S K, Sahoo R C, Sahoo A, Prahara. Diagnosis of superficial mycoses by direct microscopy - A statistical evaluation. Indian J Dermatol Venereol Leprol 1999;65:72-4
|How to cite this URL:|
Mohanty J C, Mohanty S K, Sahoo R C, Sahoo A, Prahara. Diagnosis of superficial mycoses by direct microscopy - A statistical evaluation. Indian J Dermatol Venereol Leprol [serial online] 1999 [cited 2020 Jan 28];65:72-4. Available from: http://www.ijdvl.com/text.asp?1999/65/2/72/4764
| Introduction|| |
Superficial mycotic infections constitute the main bulk of mycotic diseases in India. The three main superficial fungal infections are dermatophytosis, candidiasis and tinea versicolor. Studies on superficial mycoses in India have received increasing attention in recent years and a number of reports are available from different parts of the country by eminent workers.[2-4] Although the diagnosis of superficial fungal infections may be strongly suspected on clinical grounds, it is usually prudent and sometimes essential to seek laboratory aid. The laboratory diagnosis includes the direct microscopic examination of the specimen in 10% KOH solution and culture in Sabouraud's dextrose agar (SDA) medium. In experienced hands the direct microscopic examination in 10% KOH solution is one of the most useful procedure in medical mycology and it has been adjudged more reliable than culture for demonstrating dermatophytes. However it is best not to rely routiney solely on cultures. Keeping this in view the present study was undertaken to find out the sensitivity, specificity, positive predictive value, negative predictive value and overall efficiency of direct microscopy in the diagnosis of superficial mycoses, especially in the out patient department.
| Materials and Methods|| |
The present study was carried out in 250 clinically diagnosed cases of superficial mycoses from Skin and VD OPD of M.K.C.G. Medical College Hospital, Berhampur. The sites of lesion were thouroughly cleaned with 70% alchohol. The samples were collected in a sterile paper packet by scraping across the inflamed margin of the lesions by the help of a disposable scalpel blade. In onychomycosis the subungual friable debris was collected. Infected hairs were collected by plucking with epilating forceps so that the hair roots are preserved intact. The samples obtained were subjected for a thorough mycological study.
A small quantity of the material (skin, nail, hair) was placed in a drop of 10% KOH solution on a microscope slide and a coverslip was placed over it. Then the slide was gently warmed over the flame to bring about clearing and the preparation was left inside a Petri dish More Details for 20 minutes or more if the specimen was very thick. Then the slide was examined under the microscope for the presence of fungal elements. It was sometimes necessary for nails to be kept in 10% KOH solution overnight to dissolve completely for microscopic examination.
The specimens were cultured in SDA medium with chloramphenicol (0.05mg.ml.) and cyclohexamide (0.5mg.ml.). Fungal species were identified on the basis of cultural characteristics, pigment production, microscopic examination in lactophenol cotton blue preparation and slide culture whenever necessary.
From the results obtained by direct microscopy (KOH +ve, KOH -ve) and culture (Cul +ve, Cul -ve) different statistical data like diagnostic sensitivity and specificity, positive predictive value, negative predictive value and overall efficiency of the direct microscopy were calculated.
| Results|| |
In the direct microscopic examination, the fungal elements seen in superficial mycoses were the septate branching hyphae of dermatophytes, the short mycelial elements and clumps of round spores (spaghetti and meat ball) of Malassezia furfur and the pseudohyphae and blastospores of Candida. The samples showing fungal elements in direct microscopy were called KOH +ve and those didn't, were called KOH -ve.
| Discussion|| |
Out of 250 clinically diagnosed cases of superficial mycotic infections fungal elements were found by direct microscopy in 48.40% of cases. Direct microscopy was positive in all cases of tinea versicolor showing 100% diagnostic efficacy in diagnosing these cases. Out of 228 specimens subjected for culture, dermatophytes were isolated in 85 cases and Candida species in 9 cases. The sensitivity, specificity, positive predictive value, negative predictive value and the overall efficiency of the direct microscopy were calculated to be 89.41%, 83.90%, 76.75%, 93.02% and 85.96% respectively. As the sum of the sensitivity and specificity is far more than 100%, the direct microscopy was proved to be a very good and reliable method in diagnosing the cases of superficial mycoses. Had it been 100%, the test would be no better than loss of a coin. The above statistical data in our series were also compared with that of different workers from different parts of our country [Table - 4].
Malassezia furfur was easiest to be identified and direct microscopy is usually enough to confirm diagnosis. Regarding dermatophytes, the mycelium of E. floccosum was usually easily seen with its prominent beaded hyphae. The long delicate hypae of T. mentagfophytes and broad, more regular hyphae of T. rubrum were also found fairly easily. The pseudohyphae and blastospores of Candida, though difficult, were rarely missed in expert hands.
So the direct microscopy is as good as culture in the diagnosis of superficial mycoses and a clinician with experience in this method, can frequently diagnose the type of superficial fungal infection by this simple time saving method in his consulting chamber. Again, this method can be adopted in the OPD as a routine diagnostic test, where in the hand of skilled personnel it can give instantaneous diagnosis.
| Acknowledgement|| |
We are highly grateful to Dr. S.S. Mishra, Assistant Professor, Dept. of Pharmacology M.K.C.G. Medical College, Berhampur for his valuable help in the statistical analysis of the data.
| References|| |
|1.||Oberai C, Miskeen AK. Superficial fungal infections, In: IADVL Textbook and Atlas of Dermatology, Edited by Valia RG, Valia AR, Siddappa K, Bhalani Publishing House Bombay, 1994;173-212. |
|2.||Kalra SL., Mohapatra LN. Etiology of dermatophytosis in Delhi, lnd J Med Res 1964:52:553-558. |
|3.||Verma BS. Vaishnav VP, Bhatt R.PA study of dermatomycosis. Indian J Dermatol Venereol. 1970;36:182-184. |
|4.||Pankajalakshmi VV. Subramanian S. Mycoses in Madras (superficial), Indian J Dermatol Venereol. 1974;40:228-235. |
|5.||Roberts SOB, Mackenzie DWR. Mycology. In: Textbook of Dermatology, Edited by Rook A, Wilkinson DS, Ebling FJG, Oxford University Press Bombayl987;885-986. |
|6.||Stoughton RB. Dermatophytosis. In: Medical Microbiology and Infectious Diseases, Edited by Braude AI, WB Saunders, Philadelphia 1981;1566-1573. |
|7.||Cembrowski GS, Sullivan AM. Quality control and statistics. In; Clinical Chemistry: Principles, Procedures, Correlations. Edited by Bishop ML, Duben-Engelkirk JL, Fody EP: J.B Lippincott Company, Philadelphia 1992;63-101. |
|8.||Robles WS. Laboratory diagnosis of tropical fungal infections, Tropical Doctor 1992;(Suppl I):91-96. |
[Table - 1], [Table - 2], [Table - 3], [Table - 4]