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Li 2016
Li 2016
Tinea Versicolor
Jennifer C. Li and Roopal V. Kundu
History
A 15-year old African American male presents with 3 months
of hypopigmented spots localized to his chest and back. The
discoloration became more noticeable at the end of summer.
He is asymptomatic.
Physical Examination
On examination, multiple well-marginated hypopigmented
round to oval macules, with fine dust-like scaling, on the chest
and back were noted. Few isolated macules are noted on the
proximal arms, and abdomen. The macules on the back have
coalesced to larger patches (Figs. 11.1 and 11.2).
P.B. Love, R.V. Kundu (eds.), Clinical Cases in Skin of Color: 105
Adnexal, Inflammation, Infections, and Pigmentary Disorders,
Clinical Cases in Dermatology, DOI 10.1007/978-3-319-22392-6_11,
© Springer International Publishing Switzerland 2016
106 J.C. Li and R.V. Kundu
Histopathology
Although biopsy is not usually performed, histologic findings
of the hypopigmented macules would show slight hyperkera-
tosis and acanthosis, minimal inflammatory infiltrate, and
most notably positive Periodic acid-Schiff (PAS) stain
revealing hyphae or yeast forms in the straum corneum.
Diagnosis
Tinea versicolor
Case Treatment
The diagnosis of tinea versicolor was discussed with the
patient. Even though the patient was asymptomatic, the
presence of the rash caused emotional distress due to the
clinical appearance and the patient opted for treatment.
108 J.C. Li and R.V. Kundu
Discussion
Diagnosing tinea versicolor in patients with skin of color may
pose challenges, including unique cultural implications and
differing clinical presentations. Tinea versicolor has been
shown to be especially common in dark-skinned individuals.
If untreated, tinea versicolor could last for years.
In the United States from 1990 to 1999, tinea versicolor
was diagnosed in 110 office visits per 100,000 population per
year on average. However, people with skin of color accounted
for higher frequencies than average, with 140 visits for black
patients, 150 visits for Native Americans/Eskimos, and 40
visits for Asians/Pacific Islanders, respectively; while
Caucasians accounted for 110 visits per 100,000 per year
(Mellen et al. 2004). Similarly, a study conducted in
southeastern London demonstrated that tinea veriscolor was
statistically more common in those of darker skin, with 48 %
of tinea versicolor diagnoses in the study in blacks versus
35 % in whites and 17 % in other races, including those of
Asian and Arabic origin (Child et al. 1999). The reasons for
these frequencies may vary; dark-skinned individuals may be
more prone to infection by tinea versicolor or have greater
health care utilization due to more concern about the
dyspigmentation.
No differences in the causative species of tinea versicolor
between dark-skinned or light-skinned patients have been
identified. Tinea versicolor is caused by the dimorphic,
Chapter 11. Tinea Versicolor 109
Treatment
Since tinea versicolor is caused by a fungus normally present
on the skin surface, it is not contagious. There is no permanent
scarring or pigmentary changes. However, dyspigmentation
can take 3–4 months or more to improve. Treatment of tinea
versicolor for people with skin of color involves selecting from
a variety of antifungal topical and systemic agents, with careful
consideration that recurrence is common despite clearance of
Chapter 11. Tinea Versicolor 111
Key Points
• Tinea versicolor is a common infection among
people with skin of color.
• Dark-skinned individuals may be more likely to
present with hypopigmentation, though presenting
with hyperpigmentation or a combination of both is
not uncommon.
• Alternate variants of tinea versicolor, such as inverse
tinea versicolor and tinea versicolor alba, have been
seen in patients of color.
• “Acid skin” is a black American cultural term used
to typically describe macules characteristic of tinea
versicolor, and arise from the mistaken belief that
these macules arise from an overly acidic diet.
• Patients with skin of color should be considered to
be treated more aggressively than standard treat-
ment recommendations, since they are more likely to
experience postinflammatory pigmentary changes.
References
Aljabre SH, Alzayir AA, Abdulghani M, Osman O. Pigmentary
changes of tinea versicolor in dark-skinned patients. Int J
Dermatol. 2001;40(4):273–5.
Bélec L, Testa J, Bouree P. Pityriasis versicolor in the Central African
Republic: a randomized study of 144 cases. J Med Vet Mycol.
1991;29(5):323–9.
Child FJ, Fuller LC, Higgins EM, Du Vivier AW. A study of the spec-
trum of skin disease occurring in a black population in south-east
London. Br J Dermatol. 1999;141(3):512–7.
Ghosh SK, Dey SK, Saha I, Barbhuiya JN, Ghosh A, Roy AK.
Pityriasis versicolor: a clinicomycological and epidemiological
study from a tertiary care hospital. Indian J Dermatol.
2008;53(4):182–5.
Gupta AK, Lane D, Paquet M. Systematic review of systemic treat-
ments for tinea versicolor and evidence-based dosing regimen
recommendations. J Cutan Med Surg. 2014;18(2):79–90.
Chapter 11. Tinea Versicolor 113