ointment 0.05% to the affected areas of the face for 1-2 weeks,
and patient was advised to begin using broad spectrum facial
sunscreen with an SPF of at least 30.
Patient returned to the clinic for a 2-week follow-up where he
reported mild improvement and minimal pruritus of his facial
rash. On examination of his face revealed multiple flesh colored
1-2mm papules on the cheeks and malar prominences. Patient
was offered a biopsy during this visit, but declined due to concern
of developing a scar. The use of fluocinonide ointment was
discontinued, and patient was told to continue using sunscreen.
Patient’s facial papular lesions resolved with subsequent visits.
DISCUSSION
PMLE is the most common chronic idiopathic photosensitivity
disorder. Lesions manifest as a wide range of morphological
variants with the pinpoint papular variant presenting most
commonly in patients with skin of color, for example, African
Americans and Asians,4 which was reported in this case series.
Although PMLE has often been described as sparing the face,
we report two cases where facial involvement is the dominant
feature of the disorder. Recognition of this variant of PMLE
along with the distribution is important for diagnosing and
managing these patients.
Diagnosis of PMLE is frequently made by obtaining a thorough
history and physical examination, with specific attention to the morphology, location, seasonal variation, and time course to
the evolution of the lesions following UV radiation exposure.4
In the treatment of PMLE, prevention is important with sun
avoidance and photoprotection. Additionally, hardening can be
achieved with the use of narrowband UVB (as demonstrated in
case 1), or photochemotherapy with psoralen and UVA (PUVA)
before the beginning of sunny period.2 Other treatment modalities
include topical corticosteroids, antimalarials; although
rare, systemic corticosteroids may be required.2
disclosures
Dr. Lim serves as a consultant for Clinuvel Pharmaceuticals
Limited, Estee Lauder Companies, Ferndale, La Roche-Posay,
Pierre Fabre, Palatin and Uriage and has received clinical research
grants from Clinuvel and Estee Lauder. Dr. Isedeh does
not have any relevant conflicts to disclose.
References
- Honigsmann H, Hojyo-Tomoka MT. Polymorphous Light Eruption, Hydroa Vacciniforme, and Actinic Prurigo. In Lim, HW, Honigsmann H, Hawk JLM eds. Photodermatology. New York: Informa Healthcare. 2007; 149-165.
- Bansal I, Kerr H, Janiga JJ, Qureshi HS, Chaffins M, Lim HW, Ormsby A. Pinpoint papular variant of polymorphous light eruption: clinical and pathological correlation. J Eur Acad Dermatol and Venereol. 2006; 20:406-410.
- Chiam, LYT and Chong W. Pinpoint popular polymorphous light eruption in Asian skin: a variant in darker-skinned individuals. Photodermatol, Photoimmunol and Photomed. 2009; 25:71-74.
- Kontos, AP, Cuscak CA, Chaffins M, Lim HW. Polymorphous light eruption in African Americans: pinpoint papular variant. Photodermatol Photoimmunol Photomed. 2002; 18: 303-306.
- Kerr HA and Lim HW. Photodermatoses in African Americans: A retrospective analysis of 135 patients over a 7-year period. J Am Acad Dermatol. 2007; 57: 638-43.
AUTHOR CORRESPONDENCE
Henry W. Lim MDhlim1@hfhs.org