Polymorphous light eruption

Polymorphous light eruption (PLE), sometimes also called polymorphic light eruption (PMLE), is a non-life-threatening and potentially distressing[2] skin condition that is triggered by sunlight and artificial UV exposure[3] in a genetically susceptible person,[4] particularly in temperate climates during the spring and early summer.[1] Due to its many clinical appearances, it is named polymorphic or polymorphous and the terms are used interchangeably.[5] The resulting itch can cause significant suffering.[2][6]

Polymorphous light eruption
Other namesPolymorphic light eruption
PLE at V-neck/front of chest[1]
SpecialtyDermatology 
DurationSeveral days with annual recurrence
CausesIncompletely understood
Prevention
  • Sun protection (SPF 50+)
  • Cover up with densely woven clothing[1]
Treatment
  • Gradual sun exposure (hardening)[1]
Medication
  • Topical corticosteroids[1]
FrequencyYearly (spring/summer)

PLE is also defined as an idiopathic primary photodermatosis,[7] in which the photosensitizer is unknown.[2]

Treatments include prevention with sun avoidance and supervised light therapy, and symptom control with topical steroids.[2]

Signs and symptoms

Typically, the first episode develops in the spring following the first exposure to intense sun.[8] Further episodes of the irritable rash occur several hours to days following subsequent sun exposure.[9]

PLE appears on areas of the skin newly exposed to sunlight such as the visible part of the neckline, backs of hands, arms and legs, and feet, but less commonly the face.[1][4] At these areas, there may be feelings of burning[7] and severe itching. Smooth red-topped small papules which merge into plaques, small fluid-filled blisters (papulovesicles)[1] and less commonly target-shaped lesions which look like erythema multiforme may be visible.[3] In addition, it may occur in other parts of the body in some people treated for inflammatory skin diseases with phototherapy.[1]

The rash is usually quite symmetrical and characteristic for each individual, appearing similar with each recurrence, but can look dissimilar in different people.[8]

Fever, fatigue and headaches have been previously associated with the eruption, but are rare.[1]

The rash may persist for many days to a couple of weeks,[3] resolving spontaneously without scarring as long as further sunlight exposure is avoided.[1]

Recurring yearly, the eruption can sometimes last longer than a few days if persistent and repeated sun exposure occurs.[1] However, the "hardening" effect, with respite during the later summer, frequently occurs with gradual exposure of sunlight,[3] eventually leading to significant improvement.[1]

Causes

The cause of PLE is not yet understood, but several factors may be involved.[4] It is thought to be due to a type IV delayed-type hypersensitivity to an allergen produced in the body following sunlight exposure,[10] in a genetically susceptible person.[8] It is also thought that skin microbiome or microbial elements could be involved in pathogenesis of the disease [11][12]

UV exposure

PLE can be provoked by UVA or UVB (chief cause of sunburn) rays, meaning it can be triggered even by sunlight through glass. UV-A is a major constituent of sunlight, can pass through glass, is relatively resistant to sunscreen and can cause light eruption without sunburn.[1]

Artificial UV light sources from tanning units and phototherapy treatment units can also trigger PLE. About three-quarters of sufferers acquire PLE after UV-A exposure only, one-tenth after UV-B exposure only, and the rest after a combination of UV-A and UV-B exposure.[4]

People vary in the amount of sun exposure needed to trigger the rash.[13]

Oxidative stress

Oxidative stress and the modification of the redox status of the skin has been implicated in the expression of PLE.[4]

Photosensitizer

It has been suggested that an undefined endogenous or exogenous photo-allergen may trigger a delayed immune reaction resulting in PLE.[4]

Genetics

Half of sufferers have a family history of PLE,[4] demonstrating a clear genetic influence.[14]

Oestrogen effect

The preponderance in women with a decline in severity following menopause has been thought to be associated with oestrogen effects,[4] the resulting belief being that estrogen prevents the hypersensitivity response.[7]

Diagnosis

The diagnosis of PLE is typically made by assessing the history and clinical observations. Any investigations are usually to exclude other conditions, particularly lupus and porphyria.[7]

Blood tests are usually normal. However, positive antinuclear antibody and extractable nuclear antigen (anti-Ro/La) in low titre may be found, even in the absence of other criteria to suggest a diagnosis of lupus erythematosus. If clinical findings suggest a possibility of porphyria, urinary and red cell porphyrin screening may be performed and are negative in PLE.[1]

Photoprovocation tests are usually not required but may be undertaken by specialised centres in winter.[1] When a decision to undertake this is made, a small area of the frequently affected skin is exposed to varying doses of UVA and minimal erythema dose (MED) (amount of UV radiation that will produce minimal redness of skin within a few hours following exposure)[1][15] of broadband UVB for three consecutive days. An examination of the skin to detect the rash is made, however, up to 40% have false negative responses.[1]

Biopsy findings

Depending on the clinical signs, histology of a skin biopsy may vary. There may be oedema in the epidermis with a dense superficial and deep lymphocytic infiltrate[8] without vasculitis. Recently appearing lesions may show neutrophils. Spongiosis and vesicle formation may also be present. Direct immunofluorescence testing is negative.[1]

Differential diagnosis

The photosensitivity connected with lupus erythematosus is the main condition that may appear like PLE. However, the rash of lupus is inclined to be more persistent.[1] PLE does not increase the risk of lupus.[13]

Other similar appearing conditions are solar urticaria, which has a shorter duration, the eczema-like condition, photosensitive dermatitis,[1] and photosensitivity drug reaction.[7]

Prickly heat, which is caused by warm weather or heat is not the same as PLE.[3]

Photosensitivity is also found in some of the porphyrias. Nearly all cases of porphyria cutanea tarda[16] exhibit blister formation on the skin within 2–4 days of light exposure. Variegate porphyria[17] and hereditary coproporphyria[18] can also exhibit symptoms of light-induced blisters.[16]

Classification

Sunlight has been documented to trigger numerous skin conditions and the confusing terminology and categorisation previously has made the correct diagnosis and subsequent treatment difficult.[2]

Variants of PLE have been described:[19][10]

  • Juvenile spring eruption is a cutaneous condition that affects the helices of the ears, particularly in boys, because their ears are relatively more exposed to sunlight.[19][8]
  • Benign summer light eruption is a cutaneous condition, and a name used in continental Europe, particularly France, to describe a clinically short-lived, itchy, papular eruption particularly affecting young women after several hours of sunbathing at the beginning of summer or on sunny vacations.[19]
  • Actinic Prurigo is a hereditary form of PLE occurring typically in native Americans.[10]

Treatment

Management entails regulating triggers whilst simultaneously inducing “hardening”; that is, steadily increasing exposure to sunlight,[1] as light sensitivity is reduced with repeated sun exposure[13]

Covering up with densely woven clothing has also been shown to help, in addition to applying a broad-spectrum, water-resistant semi-opaque sun protection factor (SPF) 50+ sunblock cream before sun exposure and then every two hours thereafter confers some protection.[1]

The application of topical corticosteroids may lessen the redness and itch,[1] and for preventing predictable holiday flare-ups, short courses of oral corticosteroids are sometimes considered.[1]

Another treatment option is a supervised course of low dose phototherapy, usually undertaken in winter.[1] If resistant, the administration of hydroxychloroquine in early spring is sometimes considered.[8]

As sun exposure is avoided, vitamin D levels may fall and hence supplements are sometimes advised.[20]

Prognosis

Generally, PLE resolves without treatment; also, PLE irritations generally leave no scar.[13]

There may be a possible of link with autoimmune thyroid disease.[7] Some progression to autoimmune disease has been observed.[21] However, another study of people with elevated titres of antinuclear antibodies with PLE found no progression to lupus erythematosus after an 8 year follow-up.[14]

Epidemiology

In the United States, whilst one-quarter of people being investigated for a photosensitivity disorder were diagnosed with PLE, the prevalence in the general population is 10 to 15% and may even be as high as 40% as suggested in one study of more than 2000 people.[3][4] It is also particularly more prevalent in Central Europe and Scandinavia.[2]

PLE is more common in young adults and has a female preponderance[3] with a ratio of 2:1 female-to-male. In Germany the female to male ratio has been cited as 9:1.[2] It can, however, occur in all age groups and all skin types.[4]

Those experiencing sun exposure all year round seldom acquire PLE eruption.[13] Hence, it is less common near the equator.[14]

The cases of this condition are most common between the spring and autumn months in the northern hemisphere and at higher altitudes.[10]

Society and culture

Reports of psychological distress have been made in more than 40% of peoples with PLE.[14] This includes emotional distress, anxiety and depression[10]

History

Thomas Bateman, following on from findings of his predecessor, Robert Willan,[22] first recorded a description of PLE in the nineteenth century, defining it as eczema solare with recurrent non scarring eczematous lesions triggered by sun exposure.[23][24]

Danish physician Carl Rasch first described the eczema-like polymorphic light eruption in 1900, following his interest in the effect of sunlight on the skin. He has since been credited with coining the term "polymorphic light eruption".[25][26]

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See also

References

  1. Oakley AM, Ramsey ML (1 October 2017). "Polymorphic Light Eruption". StatPearls. Treasure Island (FL): StatPearls Publishing. PMID 28613636.
  2. Lehmann P, Schwarz T (March 2011). "Photodermatoses: diagnosis and treatment". Deutsches Ärzteblatt International. 108 (9): 135–41. doi:10.3238/arztebl.2011.0135. PMC 3063367. PMID 21442060.
  3. George A (2017). "Chapter 37: Polymorphic Light Eruption". In Vasudevan B (ed.). Clinical Correlation with Diagnostic Implications in Dermatology. Jaypee Brothers Medical Publishers Ltd. p. 172. ISBN 978-93-86322-66-1.
  4. Hogan S, Zahiri S, Hardman K. "Polymorphous light eruption - Symptoms, diagnosis and treatment | BMJ Best Practice". bestpractice.bmj.com. ISSN 2515-9615. Retrieved 4 June 2018.(subscription required)
  5. "Polymorphic light eruption | DermNet New Zealand". www.dermnetnz.org. Retrieved 4 June 2018.
  6. Patra, V.; Strobl, J.; Gruber‐Wackernagel, A.; Vieyra‐Garcia, P.; Stary, G.; Wolf, P. (2019). "CD 11b + cells markedly express the itch cytokine interleukin‐31 in polymorphic light eruption". British Journal of Dermatology. 181: 1079–1081. doi:10.1111/bjd.18092. PMC 6899657. PMID 31049931.
  7. "Polymorphic Light Eruption. PMLE skin rash; information". patient.info. Retrieved 8 June 2018.
  8. Kliegman R, Stanton B, Behrman RE, St Geme JW, Schor NF, Nelson WE (2016). "656". Nelson textbook of pediatrics (Edition 20 ed.). Phialdelphia, PA. ISBN 9781455775668. OCLC 893451530.
  9. Schornagel IJ, Sigurdsson V, Nijhuis EH, Bruijnzeel-Koomen CA, Knol EF (July 2004). "Decreased neutrophil skin infiltration after UVB exposure in patients with polymorphous light eruption". The Journal of Investigative Dermatology. 123 (1): 202–6. doi:10.1111/j.0022-202X.2004.22734.x. PMID 15191561.
  10. Oakley A (2017). Dermatology Made Easy. UK: Scion Publishing Ltd. p. 239. ISBN 978-1-907904-82-0.
  11. Patra V, Wolf P (December 2016). "Microbial elements as the initial triggers in the pathogenesis of polymorphic light eruption?". Experimental Dermatology. 25 (12): 999–1001. doi:10.1111/exd.13162. PMC 5396279. PMID 27514020.
  12. Patra V, Mayer G, Gruber-Wackernagel A, Horn M, Lembo S, Wolf P (March 2018). "Unique profile of antimicrobial peptide expression in polymorphic light eruption lesions compared to healthy skin, atopic dermatitis, and psoriasis". Photodermatology, Photoimmunology & Photomedicine. 34 (2): 137–144. doi:10.1111/phpp.12355. PMC 5888155. PMID 29044786.
  13. Habif TP (2015-04-23). "19. Light-related diseases and disorders of pigmentation". Clinical dermatology : a color guide to diagnosis and therapy (Sixth ed.). [St. Louis, Mo.]: Mosby. pp. 746–783. ISBN 9780323266079. OCLC 911266496.
  14. Patterson JW (2016). Weedon's skin pathology. Hosler, Gregory A. (Fourth ed.). [Edinburgh]: Churchill Livingstone Elsevier. ISBN 9780702062001. OCLC 900724639.
  15. Heckman CJ, Chandler R, Kloss JD, Benson A, Rooney D, Munshi T, Darlow SD, Perlis C, Manne SL, Oslin DW (May 2013). "Minimal Erythema Dose (MED) testing". Journal of Visualized Experiments (75): e50175. doi:10.3791/50175. PMC 3734971. PMID 23748556.
  16. "Porphyria Cutanea Tarda (PCT)". American Porphyria Foundation. 2009-02-18. Retrieved 4 June 2018.
  17. "Variegate Porphyria (VP)". Porphyriafoundation.com. 18 February 2009. Retrieved 4 June 2018.
  18. "Hereditary Coproporphyria (HCP)". American Porphyria Foundation. 18 February 2009. Retrieved 4 June 2018.
  19. Rapini RP, Bolognia JL, Jorizzo JL (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
  20. "Polymorphic Light Eruption". www.bad.org.uk. 9 June 2018.
  21. Hasan T, Ranki A, Jansen CT, Karvonen J (September 1998). "Disease associations in polymorphous light eruption. A long-term follow-up study of 94 patients". Archives of Dermatology. 134 (9): 1081–5. doi:10.1001/archderm.134.9.1081. PMID 9762018. Archived from the original on 2009-05-11.
  22. Bergmann, K.-C.; Ring, J. (2014). History of Allergy. Karger. p. 84. ISBN 978-3-318-02194-3.
  23. Guarrera M (2017). Ahmad SI (ed.). Ultraviolet Light in Human Health, Diseases and Environment. Springer International Publishing. pp. 61–68. ISBN 978-3-319-56017-5.
  24. Bolognia J, Schaffer JV, Cerroni L (1814). A Practical Synopsis of Cutaneous Diseases According to the Arrangement of Dr. Willan, Exhibiting a Concise View of the Diagnostic Symptoms and the Method of Treatment. Longman, Hurst, Rees, Orme, and Brown. p. 251.
  25. Braun-Falco O, Plewig G, Wolff HH, Winkelmann RK (1991). "13. Skin diseases due to physical and chemical causes". Dermatology. New York: Springer-Verlag Berlin Heidelberg GmbH. p. 397. ISBN 978-3-662-00183-7.
  26. Lim HW, Hawk JL, Rosen CF. "87. Photodermatologic Disorders". Dermatology (Fourth ed.). [Philadelphia, Pa.] pp. 1548–1568. ISBN 9780702063428. OCLC 1011508489.
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