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2.
Indian J Dermatol Venereol Leprol ; 2008 May-Jun; 74(3): 226-9
Article in English | IMSEAR | ID: sea-52383

ABSTRACT

BACKGROUND: Onychomycosis is a common problem noticed in clinical practice. Currently available standard laboratory methods show inconsistent sensitivity; hence there is a need for newer methods of detection. AIMS: This study involves comparison of standard laboratory tests in the diagnosis of onychomycosis, namely, potassium hydroxide mount (KOH mount) and mycological culture, with histopathologic examination using periodic acid-Schiff (PAS) staining of the nail clippings. METHODS: A total of 101 patients with clinically suspected onychomycosis were selected. Nail scrapings and clippings were subjected to KOH mount for direct microscopic examination, culture using Sabouraud's dextrose agar (with and without antibiotics) and histopathologic examination with PAS staining (HP/PAS). Statistical analysis was done by McNemar's test. RESULTS: Direct microscopy with KOH mount, mycological culture, and HP/PAS showed positive results in 54 (53%), 35 (35%), and 76 (75%) patients respectively. Laboratory evidence of fungal infection was obtained in 84 samples by at least one of these three methods. Using this as the denominator, HP/PAS had a sensitivity of 90%, which was significantly higher compared to that of KOH mount (64%) or mycological culture (42%). CONCLUSIONS: Histopathologic diagnosis with PAS staining of nail clippings was the most sensitive among the tests. It was easy to perform, rapid, and gave significantly higher rates of detection of onychomycosis compared to the standard methods, namely KOH mount and mycological culture.


Subject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Arthrodermataceae/isolation & purification , Culture Media , Female , Humans , Hydroxides , Male , Middle Aged , Mitosporic Fungi/isolation & purification , Mycology/methods , Nails/microbiology , Onychomycosis/diagnosis , Periodic Acid-Schiff Reaction , Potassium Compounds/diagnosis , Sensitivity and Specificity
3.
Indian J Dermatol Venereol Leprol ; 2006 Mar-Apr; 72(2): 179-81
Article in English | IMSEAR | ID: sea-52501
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