keratin.com, hair loss, baldness, alopecia, disease, and treatment information

hair and scalp fungal infection tests

Hair Biology
Diagnosis / Decisions
Androgenetic Alopecia Biology
Androgenetic Alopecia Clinical Patterns
Androgenetic Alopecia Treatments
Hair Restoration
Alopecia Areata
Effluviums
Scarring Alopecias
Inflammatory Alopecias
Other Alopecias
Hair Shaft Defects
Infectious Hair Disease
Hirsutism / Hypertrichosis
Hair Color
Hair Cosmetics
Bits and Pieces
Immunology


The Woods lamp for fungal infections

Once upon a time and not so long ago the Wood's lamp was an important part of any dermatology clinic. The Wood's lamp produces invisible long-wave ultraviolet light (340-450 nm wavelength). This UV light can help to detect medications that are taken systemically (tetracycline) or that are applied to the skin as well as help diagnose skin disease inducing infectious agents that have a characteristic fluorescence. The test is simple, the UV light from the Wood's lamp is directed over the area of the suspected infection and the dermatologist looks to see if there is any fluorescence/visible light reflected back.

However, in recent times the Wood's lamp has become less helpful as a diagnostic tool for fungal infections. Up until the 1960s the typical fungal species encountered by a dermatologist readily fluoresced under UV light. But today in the USA, and to a somewhat lesser extent in Europe, the type of fungal species encountered in the dermatology clinic have changed. The species that were common prior to 1970 and were fluorescent under UV light are now in the minority today. The common fungal species that cause skin disease in the Western hemisphere of the twenty first century are predominantly non-fluroescent.

Today the Wood's lamp is used for diagnosing a brown, scaly rash in the scrotum or axilla: erythrasma, caused by the bacterium Corynebacterium minutissimum, fluoresces a brilliant coral red, whereas tinea cruris or cutaneous candidal infections do not fluoresce. UV light can be used for diagnosing tinea (pityriasis) versicolor, which fluoresces pale yellow to white. A minor percentage of tinea capitis cases in North America and Europe caused by two zoophilic Microsporum species that fluoresce blue-green can be identified with a Wood's lamp. The Wood's lamp can also help diagnose Pseudomonas infections, porphyrians, and pigmentary alterations.


The potassium hydroxide test

The potassium hydroxide (KOH) test is used primarily as a method to determine if there is a fungal infection of the skin, nails and/or hair. If a person has flakes of dead skin (dandruff-like scaling) on the hair; broken, crusted, or matted hair; redness, irritation of the scalp or beard; swollen areas and blister-like bumps with pus (kerions); or a patchy hair loss the KOH test may be done. It does not define the specific fungal species involved in any infection, but the process is quick and easy to perform so as a simple diagnostic tool it is very useful.

The KOH test involves taking a sample of skin where the suspected infection is. This can be done with a scalpel if the skin is particularly crusty, but more usually a wet gauze or maybe a tooth brush is used to collect some dead skin scales. With hair fiber infections collecting a sample can be more difficult because hair infections weaken the hair and cause it to break off at the root leaving very little of the infectious agent behind. Normal length hair is probably not infected. However, some damaged hair around the periphery of an infected area is usually present and the dermatologist will take around 10 broken, infected-looking hairs. With nails a sample of the dead skin under the nail plate is used.

The hair or skin sample is placed on a slide with a little of a 10% to 20% concentration potassium hydroxide solution and gently heated. This solution slowly dissolves the hair and skin cells but not the fungus cells. The fungus cells can then be seen with a microscope. Color stains may be used so that the fungus is easier to see. This technique aids the visualization of the fungal hyphae (branching, rod-shaped filaments of uniform width with lines of separation called septa). In tinea capitis, the hair shaft may be uniformly coated with minute dermatophyte spores.

Unfortunately the KOH test is not fool proof. It is possible to get a negative KOH test result when a fungal agent is actually present. In particular, a common fungal agent that causes ringworm called Trichophyton tonsurans does not show up well in a KOH test. Thus, even when a KOH test is negative, a fungal infection may still be suspected. If so, a fungal culture must be done to confimr that a fungal agent is involved.


The fungal culture test

A more advanced and more sensitive test that can be used to determine the particular nature of the fungal species involved in a skin, nail, or hair infection is a fungal culture. Fungal cultures are slow and expensive to perform. They require incubators, culture mediums, and some expertise on the part of the technician looking after the cultures. For this reason fungal culture tests are rarely done in the average dermatology clinic. More usually, a sample is sent away to a laboratory for testing.

The dermatologist will take skin or nail scrapings, or a hair sample. The sample is put into a sterile container and sent to the laboratory. At the laboratory, the container is opened in a sterile chamber and the sample is inoculated on test medium - usually Sabouraud's dextrose agar or something similar. If there are fungal spores present, they will grow on the agar. The culture usually takes 7 to 14 days to be declared positive. It must be held for 21 days without development of fungal growth to be declared negative. If the culture is positive the laboratory can take a sample of the fungal growth and examine it to see which particular species is involved.

A dermatology clinic may conduct a simplified fungal culture test that does not define the fungal species involved, but does provide a more sensitive test than the KOH test. "Dermatophyte test medium" is a commercially available, nutrient-rich culture solution supplied in a form that is ready for direct inoculation in the office. The dermatologist takes a sample of dead skin or a hair sample and puts it in a small tube containing the culture medium. The yellow medium has a phenol red indicator that turns pink in the presence of the alkaline metabolic products produced by fungal agents. It takes up to 7 days of culturing before a conclusion can be made as to whether the test is positive or negative. The medium must be discarded 14 days after opening the culture tube because saprophytes will slowly produce a similar change in the culture medium color. This is a false positive result.

This simplified fungal culture test is more complex to conduct than the KOH test, but easier to conduct than a full scale laboratory fungal culture. These basic fungal culture tests are most likely to be done in mid sized, private dermatology clinics. Large hospital based clinics will most likely have the facilities to do full scale culture testing while small practices will probably run a KOH test first and then if there is still some doubt they may collect a sample and send it to a central test laboratory for culturing.


Hair and scalp fungal infection test references

  • Hainer BL. Dermatophyte infections. Am Fam Physician. 2003 Jan 1;67(1):101-8.
  • Rezabek GH, Friedman AD. Superficial fungal infections of the skin. Diagnosis and current treatment recommendations. Drugs. 1992 May;43(5):674-82.
  • Prevost E. The rise and fall of fluorescent tinea capitis. Pediatr Dermatol. 1983 Oct;1(2):127-33.
  • Liu D, Coloe S, Baird R, Pedersen J. Application of PCR to the identification of dermatophyte fungi. J Med Microbiol. 2000 Jun;49(6):493-7.
  • Caddell JR. Differentiating the dermatophytes. Clin Lab Sci. 2002 Winter;15(1):13-5.
  • Moriello KA. Diagnostic techniques for dermatophytosis. Clin Tech Small Anim Pract. 2001 Nov;16(4):219-24.
  • Gupta AK, Einarson TR, Summerbell RC, Shear NH. An overview of topical antifungal therapy in dermatomycoses. A North American perspective. Drugs. 1998 May;55(5):645-74.
  • Rosen T. Dermatophytosis: diagnostic pointers and therapeutic pitfalls. Consultant 1997;37:1545-57.
  • Brodell RT, Elewski B. Superficial fungal infections. Errors to avoid in diagnosis and treatment. Postgrad Med. 1997 Apr;101(4):279-87.
  • Wigger-Alberti W, Elsner P. [Fluorescence with Wood's light. Current applications in dermatologic diagnosis, therapy follow-up and prevention] Hautarzt. 1997 Aug;48(8):523-7.
  • Honig PJ, Sullivan K, McGowan KL. The rapid diagnosis of tinea capitis using calcofluor white. Pediatr Emerg Care. 1996 Oct;12(5):333-5.
  • Amichai B, Finkelstein E, Halevy S. Early detection of Pseudomonas infection using a Wood's lamp. Clin Exp Dermatol. 1994 Sep;19(5):449.
  • Goldgeier MH. Fungal infections of the skin, hair, and nails. Pediatr Ann. 1993 Apr;22(4):253-9.
  • Hubbard TW, de Triquet JM. Brush-culture method for diagnosing tinea capitis. Pediatrics. 1992 Sep;90(3):416-8.
  • Cowen P. Microscopy of skin scrapings for dermatophyte diagnosis. Aust Fam Physician. 1990 May;19(5):685-90.
  • Katz HI, Prawer SE, Hien NT, Mooney JJ. Skin-surface touch print for diagnosing fungal infections. Am Fam Physician. 1985 Apr;31(4):189-94.
  • Sinski JT, Van Avermaete D, Kelley LM. Analysis of tests used to differentiate Trichophyton rubrum from Trichophyton mentagrophytes. J Clin Microbiol. 1981 Jan;13(1):62-5.
  • Lefler E, Haim S, Merzbach D. Evaluation of direct microscopic examination versus culture in the diagnosis of superficial fungal infections. Mykosen. 1981 Feb;24(2):102-6.
  • Kane J, Smitka C. Early detection and identification of Trichophyton verrucosum. J Clin Microbiol. 1978 Dec;8(6):740-7.
 Disclaimer   Copyright   Privacy   Contact Us 
  Copyright . All Rights Reserved www.keratin.com