AUTHOR INFORMATION

Section 1 of 12

Authored by Alexandra Y Zhang, MD, Staff Physician, Department of Dermatology, University of Alabama at Birmingham

Coauthored by Craig A Elmets, MD, Director of Dermatology, Departments of Dermatology, Professor, Pathology, Environmental Health Sciences, The Kirklin Clinic, University of Alabama at Birmingham

Alexandra Y Zhang, MD, is a member of the following medical societies: American Academy of Dermatology, American Association of Immunologists, and Society for Investigative Dermatology

Edited by Abdul-Ghani Kibbi, MD, Chairman, Professor, Department of Dermatology, American University of Beirut Medical Center, Lebanon; David F Butler, MD, Professor, Texas A&M University College of Medicine; Director, Division of Dermatology, Scott and White Clinic; Jeffrey P Callen, MD, Chief, Division of Dermatology, Professor of Medicine (Dermatology), Department of Internal Medicine, University of Louisville School of Medicine; Catherine Quirk, MD, Clinical Assistant Professor, Department of Dermatology, Brown University; and Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center

Author's Email:	Alexandra Y Zhang, MD
Editor's Email:	Abdul-Ghani Kibbi, MD

eMedicine Journal, March 19 2007, VOLUME 8, Number 3

INTRODUCTION

Section 2 of 12

Background: Drug-induced photosensitivity refers to the development of cutaneous disease as a result of the combined effects of a chemical and light. Exposure to either the chemical or the light alone is not sufficient to induce the disease; however, when photoactivation of the chemical occurs, one or more cutaneous manifestations may arise. These include phototoxic and photoallergic reactions, a planus lichenoides reaction, pseudoporphyria, and subacute cutaneous lupus erythematosus. Photosensitivity reactions may result from systemic medications and topically applied compounds (Table 1).

Wavelengths within the UV-A (320-400 nm) range and, for certain compounds, within the visible range, are more likely to cause drug-induced photosensitivity reactions, although occasionally UV-B (290-320 nm) can also be responsible for such effects. UV-B wavelengths are most efficient at causing sunburn and nonmelanoma skin cancer. In patients who present with photosensitivity, it is often difficult to differentiate phototoxic from photoallergic reactions. However, they have a number of distinguishing characteristics (Table 2).

Table 1. Common Photosensitizing Medications

Class	Medication	Phototoxic Reaction	Photoallergic Reaction	Planus Lichenoides Reaction	Pseudoporphyria	Subacute Cutaneous Lupus Erythematosus (SCLE)
Antibiotics	Tetracyclines (doxycycline, tetracycline)	Yes	No	Yes	Yes	No
	Fluoroquinolones (ciprofloxacin, ofloxacin, levofloxacin)	Yes	No	No	No	No
	Sulfonamides	Yes	No	No	No	No
Nonsteroidal anti- inflammatory drugs (NSAIDs)	Ibuprofen	Yes	No	Yes	No	No
	Ketoprofen	Yes	Yes	No	No	No
	Naproxen	Yes	No	Yes	Yes	No
	Celecoxib	No	Yes	No	Yes	No
Diuretics	Furosemide	Yes	No	No	Yes	No
	Bumetanide	No	No	No	Yes	No
	Hydrochlorothiazide	Yes	Yes	Yes	No	Yes
Retinoid	Isotretinoin	Yes	No	No	No	No
	Acitretin	Yes	No	No	No	No
Hypoglycemics	Sulfonylureas (glipizide, glyburide)	No	Yes	Yes	Yes	No
PDT Pro- photosensitizers	5-aminolevulinic acid	Yes	No	No	No	No
	Methyl-5-aminolevulinic acid	Yes	No	No	No	No
	Verteporfin	Yes	No	No	No	No
	Photofrin	Yes	No	No	No	No
Neuroleptic drugs	Phenothiazines (chlorpromazine, fluphenazine, perazine, perphenazine, thioridazine)	Yes	Yes	Yes	No	No
	Thioxanthenes (chlorprothixene, thiothixene)	Yes	No	No	No	No
Anti-Fungals	Terbinafine	No	No	No	No	Yes
	Itraconazole	Yes	Yes	No	No	No
	Voriconazole	Yes	No	No	Yes	No
Other drugs	Para-aminobenzoic acid (PABA)	Yes	Yes	No	No	No
	5-FU	Yes	Yes	Yes	Yes	No
	Amiodarone	Yes	No	No	Yes	No
	Diltiazem	Yes	No	No	No	Yes
	Quinidine	Yes	Yes	Yes	No	No
	Hydroxychloroquine	No	No	Yes	No	No
	Coal tar	Yes	No	No	No	No
	Enalapril	No	No	No	No	Yes
	Dapsone	No	Yes	Yes	Yes	No
	Oral Contraceptives	No	Yes	No	Yes	No
Sunscreens	Para-aminobenzoic acid (PABA)	No	Yes	No	No	No
	Cinnamates	No	Yes	No	No	No
	Benzophenones	No	Yes	No	No	No
	Salicylates	No	Yes	No	No	No
Fragrances	Musk ambrette	No	Yes	No	No	No
	6-Methylcoumarin	No	Yes	No	No	No

Phototoxic reactions occur because of the damaging effects of light-activated compounds on cell membranes and, in some instances, DNA. By contrast, photoallergic reactions are cell-mediated immune responses to a light-activated compound. Phototoxic reactions develop in most individuals if they are exposed to sufficient amounts of light and drug. Typically, they appear as an exaggerated sunburn response. Photoallergic reactions resemble allergic contact dermatitis, with a distribution limited to sun-exposed areas of the body. However, when the reactions are severe or prolonged, they may extend into covered areas of skin.

Table 2. Distinguishing Characteristics of Phototoxic and Photoallergic Reactions

Feature	Phototoxic Reaction	Photoallergic Reaction
Incidence	High	Low
Amount of agent required for photosensitivity	Large	Small
Onset of reaction after exposure to agent and light	Minutes to hours	24-72 hours
More than one exposure to agent required	No	Yes
Distribution	Sun-exposed skin only	Sun-exposed skin, may spread to unexposed areas
Clinical characteristics	Exaggerated sunburn	Dermatitis
Immunologically mediated	No	Yes; Type IV

Photoallergic reactions develop in only a minority of individuals exposed to the compound and light; they are less prevalent than phototoxic skin reactions. The amount of drug required to elicit photoallergic reactions is considerably smaller than that required for phototoxic reactions. Moreover, photoallergic reactions are a form of cell-mediated immunity; their onset often is delayed by as long as 24-72 hours after exposure to the drug and light. By contrast, phototoxic responses often occur within minutes or hours of light exposure.

Pathophysiology:

Phototoxicity

Phototoxic reactions result from direct damage to tissue caused by a photoactivated compound. Many compounds have the potential to cause phototoxicity. Most have at least one resonating double bond or an aromatic ring that can absorb radiant energy. Most compounds are activated by wavelengths within the UV-A (320-400 nm) range, although some compounds have a peak absorption within the UV-B or visible range.

In most instances, photoactivation of a compound results in the excitation of electrons from the stable singlet state to an excited triplet state. As excited-state electrons return to a more stable configuration, they transfer their energy to oxygen, leading to the formation of reactive oxygen intermediates. Reactive oxygen intermediates such as an oxygen singlet, superoxide anion, and hydrogen peroxide damage cell membranes and DNA. Signal transduction pathways that lead to the production of proinflammatory cytokines and arachidonic acid metabolites are also activated. The result is an inflammatory response that has the clinical appearance of an exaggerated sunburn reaction.

The exception to this mechanism of drug-induced phototoxicity is psoralen-induced phototoxicity. Psoralens intercalate within DNA, forming monofunctional adducts. Exposure to UV-A radiation produces bifunctional adducts within DNA. Exactly how bifunctional adducts cause photosensitivity is unknown.

Photoallergic reactions

Photoallergic reactions are cell-mediated immune responses in which the antigen is a light-activated drug. Photoactivation results in the development of a metabolite that can bind to protein carriers in the skin to form a complete antigen. The reaction then proceeds exactly as other cell-mediated immune responses do. Specifically, Langerhans cells and other antigen-presenting cells take up the antigen and then migrate to regional lymph nodes. In those locations, the Langerhans cells present the photoallergen to T lymphocytes that express antigen-specific receptors. The T cells become activated and proliferate, and they return to the site of photoallergen deposition. In the skin, the T cells orchestrate an inflammatory response that usually has an eczematous morphology if the photoallergen is applied topically or the characteristics of a drug eruption if the photoallergen is administered systemically.

Frequency:

• In the US: Although the incidence of drug-induced photosensitivity in the United States is uncertain. Phototoxic reactions are considerably more common than photoallergic reactions.

• Internationally: The incidence is unknown.

Mortality/Morbidity: Drug-induced photosensitivity is associated with death only in rare individuals who are exposed to large amounts of sunlight after taking large doses of psoralens. Although mortality is rare, drug-induced photosensitivity can cause significant morbidity in some individuals, who must severely limit their exposure to natural or artificial light. The carcinogenic potential due to prolonged exposure to these photosensitizing drugs has been suggested; its clinical relevance remains to be determined.

Race: The racial incidence of drug-induced photosensitivity reactions is unknown. Photosensitivity reactions can occur in races with heavily pigmented skin.

Sex: Men are more likely to have photoallergic reactions than women.

Age: Drug-induced photosensitivity reactions can occur in persons of any age.

CLINICAL

Section 3 of 12

History:

• Patients with drug-induced photosensitivity often, but not always, note intolerance to sunlight.


• • While most individuals can tolerate minutes or hours of sun exposure, patients with drug-induced photosensitivity exhibit skin lesions of one type or another. In most cases, a sunburn response or dermatitis occurs.
  
  
  
  • Drug-induced photosensitivity reactions may result in phototoxicity, photoallergy, lichenoid reactions, subacute cutaneous lupus, or pseudoporphyria.
  
  
  
• Pseudoporphyria may occur with some medications, the most common of which is naproxen.


• • Pseudoporphyria is characterized by a bullous reaction that clinically and histologically resembles porphyria cutanea tarda.
  
  
  
  • The hypertrichosis and sclerodermoid changes typically seen in porphyria cutanea tarda are not seen in pseudoporphyria.
  
  
  
  • The results of porphyrin studies are normal.
  
  
  
• Lichenoid reactions that occur in a photodistribution are often difficult to distinguish from idiopathic lichen planus.


• • These reactions are characterized by violaceous or erythematous papules and plaques that sometimes have Wickham striae.
  
  
  
  • Hydrochlorothiazide, hydroxychloroquine, and captopril are known causes of drug-induced lichenoid reactions.
  
  
  
• Drug-induced photosensitivity reactions also may include lupuslike reactions.


• • Drug-induced reactions usually resemble SCLE because of their scaling, annular, and psoriasiform characteristics.
  
  
  
  • Hydrochlorothiazide is the drug most frequently associated with this reaction, but calcium channel blockers, ACE inhibitors, griseofulvin, and terbinafine are other agents that have been implicated. The rate of reaction is low for any of these agents. Hydrochlorothiazide is commonly used in many combined antihypertensive agents.

  • Patients with drug-induced reactions commonly have anti-Ro (SS-A) antibodies.
  
  
  
• As photodynamic therapy (PDT) becomes a more popular treatment modality for actinic keratoses and nonmelanoma skin cancer, recognition of PDT photosensitizer–induced phototoxicity is important.


• • 5-Aminolevulinic acid or methyl 5-aminolevulinic acid is applied topically, followed by the use of a blue (410-420 nm) or red light (570-670 nm) PDT illuminator.

  • 5-Aminolevulinic acid is a prodrug that enters the heme biosynthetic pathway and is metabolized intracellularly to form the photosensitizing molecule protoporphyrin IX (PpIX).

  • Light activates PpIX to generate free radicals and cytotoxic reactive oxygen species that may cause destruction of malignant and nonmalignant hyperproliferative tissue.

  • Common adverse effects include mild-to-moderate local phototoxic reactions that usually resolve in several days.
  
  
  
• Discriminating between photosensitivity diseases and heat-related exacerbation of skin diseases may be difficult for the patient.


• • Clarify this issue in the history.

  • Assess symptoms of other diseases that are known to cause photosensitivity and determine if a family history of photosensitivity exists.
  
  
  
• Establishing whether the photosensitivity can be elicited with exposure to sunlight through window glass may provide information about the wavelengths of light that cause the response. UV-B light does not penetrate window glass, whereas UV-A light and visible light do.



• In most patients, the findings of the physical examination suggest a photosensitivity reaction.


• • Specifically, inquire about intolerance to the sun.

  • Ask patients who report photosensitivity about the medications they are taking and the products they are applying to the skin (see Table 1). Sunscreens; fragrances; and, occasionally, antibacterial soaps may cause photoallergic reactions when applied to the skin.
  
  
  

Physical: Both phototoxic and photoallergic reactions occur in sun-exposed areas of skin, including the face, V of the neck, and dorsa of the hands and forearms. The hair-bearing scalp, postauricular and periorbital areas, and submental portion of the chin are usually spared. A widespread eruption suggests exposure to a systemic photosensitizer, whereas a localized eruption indicates a reaction to a locally applied topical photosensitizer.

• Phototoxic reactions in skin


• • Acute phototoxicity often begins as an exaggerated sunburn reaction with erythema and edema that occurs within minutes to hours of light exposure. Vesicles and bullae may develop with severe reactions. The lesions often heal with hyperpigmentation, which resolves in a matter of weeks to months. Chronic phototoxicity may also appear as an exaggerated sunburn reaction. However, lichenification often develops because of repeated rubbing and scratching of the photosensitive area. Thus, distinguishing phototoxic reactions from photoallergic reactions strictly based on physical appearance of the lesions may be difficult.
  
  
  
  • Other less common skin manifestations of phototoxicity include pigmentary changes. A blue-gray pigmentation is associated with several agents, including amiodarone, chlorpromazine, and some tricyclic antidepressants. Reactions to psoralen-containing botanicals (phytophotodermatitis) and drugs may resolve, with a brownish discoloration. Frequently, the pigmentary change is preceded by a typical sunburn reaction. If the reaction is not severe, some patients may not notice the erythema.
  
  
  
  • Photosensitizing drugs may also cause a lichen planus–like eruption in sun-exposed areas. Drugs likely to cause this type of reaction include demeclocycline, hydrochlorothiazide, enalapril, quinine, quinidine, chloroquine, and hydroxychloroquine.
  
  
  
  • Pseudoporphyria, which involves porphyria cutanea tarda–like changes of skin fragility and subepidermal blisters on the dorsa of hands, may occur after exposure to naproxen, nalidixic acid, tetracycline, sulfonylureas, furosemide, dapsone, amiodarone, bumetanide, and pyridoxine. Frequent use of sun-tanning beds and chronic renal failure are other predisposing factors.
  
  
  
• Phototoxic reactions in nails


• • Photo-onycholysis, or separation of the distal nail plate from the nail bed, is another manifestation of phototoxicity. Photo-onycholysis has been reported with the use of many systemic medications, including tetracycline, psoralen, chloramphenicol, fluoroquinolones, oral contraceptives, quinine, and mercaptopurine.
  
  
  
  • Photo-onycholysis may be the only manifestation of phototoxicity in individuals with heavily pigmented skin.
  
  
  
• Photoallergic reactions in skin


• • Photoallergic reactions typically develop in sensitized individuals 24-48 hours after exposure. The reaction usually manifests as a pruritic eczematous eruption. Erythema and vesiculation are present in the acute phase.
  
  
  
  • More chronic exposure results in erythema, lichenification, and scaling.
  
  
  
  • Hyperpigmentation does not occur in photoallergic reactions.
  
  
  

Causes:

• Most phototoxic reactions result from the systemic administration of drugs.



• Photoallergic reactions can be caused by either topical or systemic administration of the chemical.



• Compounds that commonly cause phototoxic and/or photoallergic reactions are listed in Table 1.

DIFFERENTIALS

Section 4 of 12

Contact Dermatitis, Allergic
Contact Dermatitis, Irritant
Drug Eruptions
Epidermolysis Bullosa
Epidermolysis Bullosa Acquisita
Lichen Planus
Lupus Erythematosus, Subacute Cutaneous
Urticaria, Solar

Other Problems to be Considered:

Chronic actinic dermatitis

WORKUP

Section 5 of 12

Lab Studies:

• To exclude porphyria cutanea tarda, assess urine porphyrin levels, which are elevated in porphyria cutanea tarda and within the normal range in pseudoporphyria and drug-induced photosensitivity.



• Determine antinuclear antibody (ANA) and anti-Ro (SS-A) antibody levels.

Other Tests:

• Photopatch testing is an important tool in the diagnosis of photoallergic contact dermatitis.


• • Suspected photoallergens are applied to the back in 2 sets.
  
  
  
  • One set is removed after 24 hours and irradiated with 5-10 J/cm² UV-A.
  
  
  
  • Both sets of patch tests are evaluated for a positive reaction after 48 hours.
  
  
  
  • Erythema, edema, and/or vesiculation at an irradiated site indicate a positive reaction.
  
  
  
  • A positive reaction at both sites is interpreted as an allergic contact dermatitis.
  
  
  
  • A positive reaction at the unirradiated site with a stronger one at the irradiated site should be interpreted as both allergic dermatitis and photoallergic contact dermatitis reaction to the same compound.
  
  
  
• Phototesting with UV-A; UV-B; and, sometimes, visible light is helpful in diagnosing photosensitivity disorders.


• • This test is performed by treating small areas of skin on the back or inner aspect of the forearms with gradually increasing doses of light.
  
  
  
  • The minimum dose of light required to produce uniform erythema over the entire irradiated site after 24 hours is called the minimum erythema dose (MED).
  
  
  
  • Patients with phototoxic reactions have a reduced MED to UV-A or, in some instances UV-B.
  
  
  

The histologic features of a lichen planus–like phototoxic reaction are essentially indistinguishable from idiopathic lichen planus. However, increased amounts of spongiosis and necrotic keratinocytes may be present.

The histologic features of a SCLE-like reaction reveal an interface dermatitis that is indistinguishable from non–drug-induced SCLE. Like porphyria cutanea tarda, pseudoporphyria causes a subepidermal blister at the level of the lamina lucida. A characteristic feature of both pseudoporphyria and porphyria cutanea tarda is festooning, which refers to the irregular configuration of the dermal papillae in the floor of the bulla.

Photoallergic reactions are histologically similar to contact dermatitis. Epidermal spongiosis with a dermal lymphocytic infiltrate is a prominent feature. However, the presence of necrotic keratinocytes is suggestive of photoallergy rather than allergic contact dermatitis.

TREATMENT

Section 6 of 12

Medical Care: The mainstays of treatment are identification and avoidance of the causative agent, the use of sun protection, and the institution of measures for symptomatic relief.

• Topical corticosteroids and cool compresses may alleviate the condition.



• The use of systemic corticosteroids should be reserved for the most severe cases.



• If sunscreens are not the cause of the photosensitivity, they should be used liberally.


• • The sun protection factor (SPF) may not be a reliable indicator of protection against drug-induced photosensitivity. The SPF refers to the degree of protection against sunlight-induced sunburn, primarily that caused by UV-B. Most drug-induced photosensitivity reactions are caused by wavelengths within the UV-A range. Therefore, sunscreens that absorb UV-A should be prescribed.
  
  
  
  • Sunscreens that contain avobenzone (Parsol 1789), titanium dioxide, and zinc oxide are more effective in blocking out UV-A radiation than sunscreens that contain other ingredients.
  
  
  

MEDICATION

Section 7 of 12

The goal of pharmacotherapy is to reduce morbidity and to prevent complications. Broad-spectrum sunscreens with coverage in the UV-A and UV-B ranges are recommended. Sunscreens containing avobenzone (Parsol 1789) absorb light in the UV-A range. Physical sunscreen agents, such as titanium dioxide and zinc oxide, have full UV spectrum protection. Note that some individuals are allergic to some chemical sunscreens that are sensitizers and may induce contact dermatitis and/or photoallergy.

Drug Category: Corticosteroids -- These agents have anti-inflammatory properties and cause profound and varied metabolic effects. Corticosteroids modify the body's immune response to diverse stimuli. Potent class I and II topical steroids may be used. Less potent topical steroids such as hydrocortisone valerate, desonide, or fluticasone may be used twice a day in children to decrease risk of systemic absorption.

Drug Name	Clobetasol (Cormax, Temovate) -- Suppresses mitosis and increases synthesis of proteins that decrease inflammation and cause vasoconstriction.
Adult Dose	Apply to affected areas qd
Pediatric Dose	Not established
Contraindications	Documented hypersensitivity; viral or fungal skin infections
Interactions	None reported
Pregnancy	C - Safety for use during pregnancy has not been established.
Precautions	May suppress adrenal function in prolonged therapy; to prevent systemic absorption, avoid areas with thin skin such as the axilla, groin, and face; atrophy of skin, striae, or telangiectasias may occur

Drug Name	Betamethasone (Diprolene, Betatrex, Diprosone) -- For treatment of inflammatory dermatoses responsive to steroids. Decreases inflammation by suppressing migration of polymorphonuclear leukocytes and reversing capillary permeability.
Adult Dose	Apply thin film to affected areas bid
Pediatric Dose	Apply as in adults
Contraindications	Documented hypersensitivity; paronychia; cellulitis; impetigo; angular cheilitis; erythrasma; erysipelas; rosacea; perioral dermatitis; acne
Interactions	Effects decrease with coadministration of barbiturates, phenytoin, and rifampin; dexamethasone decreases effect of salicylates and vaccines used for immunization
Pregnancy	C - Safety for use during pregnancy has not been established.
Precautions	Do not use on skin with decreased circulation; can cause atrophy of groin, face, and axillae; if infection develops and is not responsive to antibiotic treatment, discontinue until infection is under control; do not use monotherapy to treat widespread plaque psoriasis

Drug Name	Hydrocortisone valerate (Westcort) -- Adrenocorticosteroid derivative suitable for application to skin or external mucous membranes. Has mineralocorticoid and glucocorticoid effects that result in anti-inflammatory activity.
Adult Dose	More potent corticosteroids recommended in adults
Pediatric Dose	Apply sparingly to affected areas bid
Contraindications	Documented hypersensitivity; viral, fungal, and bacterial skin infections
Interactions	None reported
Pregnancy	C - Safety for use during pregnancy has not been established.
Precautions	Prolonged use, applying over large surface areas, application of potent steroids, and use of occlusive dressings may increase systemic absorption of corticosteroids and cause Cushing syndrome, reversible HPA axis suppression, hyperglycemia, or glycosuria

Drug Name	Desonide (DesOwen, Tridesilon) -- Stimulates synthesis of enzymes that decrease inflammation. Suppresses mitotic activity and causes vasoconstriction.
Adult Dose	More potent corticosteroids recommended in adults
Pediatric Dose	Apply sparingly to affected areas bid
Contraindications	Documented hypersensitivity; viral, fungal, and bacterial skin infections
Interactions	None reported
Pregnancy	C - Safety for use during pregnancy has not been established.
Precautions	Prolonged use, applying over large surface areas, application of potent steroids, and use of occlusive dressings may increase systemic absorption of corticosteroids and cause Cushing syndrome, reversible HPA axis suppression, hyperglycemia, or glycosuria

Drug Name	Fluticasone (Cutivate) -- Has extremely potent vasoconstrictive and anti-inflammatory activity. Has a weak hypothalamic-pituitary adrenocortical axis inhibitory potency when applied topically.
Adult Dose	More potent corticosteroids recommended in adults
Pediatric Dose	Apply sparingly to affected area bid
Contraindications	Documented hypersensitivity; viral, fungal, and bacterial skin infections
Interactions	None reported
Pregnancy	C - Safety for use during pregnancy has not been established.
Precautions	Prolonged use, applying over large surface areas, application of potent steroids, and use of occlusive dressings may increase systemic absorption of corticosteroids and cause Cushing syndrome, hyperglycemia, or glycosuria

FOLLOW-UP

Section 8 of 12

Deterrence/Prevention:

• Patients should identify and avoid the causative agent.



• Patients should use a sunscreen if it is not the offending agent. Sun protection often prevents photosensitivity reactions.

Complications:

• Chronic effects


• • Chronic cutaneous effects of repeated phototoxic injury have been evaluated only with psoralen-containing compounds.
  
  
  
  • Premature aging of the skin, lentigines, and skin cancer are common. With respect to skin cancer, increases in the incidence of squamous cell carcinoma are greater than those of basal cell carcinoma. The incidence of melanoma may also increase over time.
  
  
  
  • The effects of chronic exposure to virtually all other photosensitizing compounds are unknown.
  
  
  
• Persistent light reactivity is a form of chronic actinic dermatitis that occurs in patients with photoallergic contact dermatitis.


• • In patients with persistent light reactivity, photosensitivity persists for months or years after the offending agent is eliminated.

  • The disease may involve all sun-exposed areas and spread to covered areas of skin.

  • Initially, persistent light reactivity is misdiagnosed as atopic dermatitis or a lichenoid drug reaction. The photosensitivity can be incapacitating because the patients are sensitive to light not only in the UV-A range but also in both the UV-B and visible ranges.

  • Some patients confine themselves to darkened rooms because of their severe photosensitivity.

  • Although systemic drugs (eg, thiazides, quinidine) have been implicated as causes of persistent light reactivity, sunscreens, halogenated salicylanilides and musk ambrette are the most frequent causes.
  
  
  
  • The treatment of persistent light reactivity involves the avoidance of contact with exacerbating agents and photoallergens.
  
  
  
  • Emollients, topical steroids, systemic steroids, and (at times) hydroxychloroquine.
  
  
  
  • Paradoxically, psoralen UV-A (PUVA) and narrow band UV-B have been used, although relapse is common.
  
  
  
  • Patients who show no signs of improvement may require the use of immunosuppressive agents (eg, azathioprine, cyclosporine).
  
  
  

Prognosis:

• In most patients, the prognosis is excellent once the offending agent is removed. However, complete resolution of the photosensitivity may take several weeks to months with some compounds.



• Occasionally, patients have persistent light reactivity for which the prospects for resolution are poor.

Patient Education:

• Patients need to be counseled regarding the possible photosensitizing properties of both prescription and nonprescription medications.



• Most often, appropriate sun protection measures prevent drug-induced photosensitivity reactions.



• For excellent patient education resources, visit eMedicine’s Burns Center. Also, see eMedicine’s patient education article Sunburn.

MISCELLANEOUS

Section 9 of 12

Medical/Legal Pitfalls:

• Failure to diagnose drug-induced photosensitivity may result in severe sunburn reactions, especially if the offending drug is not discontinued. Repeated phototoxic injury results in premature photoaging and an increased risk of cutaneous malignancies.



• Patients with drug-induced photosensitivity reactions should be warned against the use of tanning beds and about potential cross-reactions of the offending drug. The risks of severe sunburn reactions including the potential for and complications from widespread blistering reactions, should be discussed with the patient.

TEST QUESTIONS

Section 10 of 12

CME Question 1: Which of the following characterizes photoallergic reactions?

A: An exaggerated sunburn reaction
B: Reaction upon first exposure to photosensitizer
C: Interface reaction on histologic evaluation
D: An eczematous dermatitis
E: Significant hyperpigmentation upon resolution

The correct answer is D: Photoallergic reactions usually manifest as eczematous reactions. Photoallergic reactions resemble allergic contact dermatitis, with a distribution limited to sun-exposed areas of the body. However, when the reactions are severe or prolonged, they may extend into covered areas of skin. These reactions are cell-mediated immune responses to a light-activated compound. Photoactivation results in the development of a metabolite that can bind to protein carriers in the skin to form a complete antigen. The reaction proceeds exactly as other cell-mediated immune responses do. Specifically, Langerhans cells and other antigen-presenting cells take up the antigen and then migrate to regional lymph nodes. There the Langerhans cells present the photoallergen to T lymphocytes that express antigen-specific receptors. The T cells become activated and proliferate, and they return to the site of photoallergen deposition.

CME Question 2: Which of the following is not a possible clinical manifestation of drug-induced phototoxic reactions?

A: Blue-gray hyperpigmentation
B: Photo-onycholysis
C: Lichen planus–like reaction
D: Pseudoporphyria
E: Gyrate erythema

The correct answer is E: Phototoxic reactions may present with blue-gray hyperpigmentation, photo-onycholysis, pseudoporphyria, or a lichen planus–like eruption. Gyrate erythema is not associated with a phototoxic reaction. Acute phototoxicity often begins as an exaggerated sunburn reaction with erythema and edema within minutes to hours of light exposure. Vesicles and bullae may develop with severe reactions. The lesions often heal; hyperpigmentation resolves in a matter of weeks to months. Often, lichenification occurs because of repeated rubbing and scratching of the photosensitive area.

Pearl Question 1 (T/F): Sunscreens are a common cause of photoallergic reactions.

The correct answer is True: Sunscreens, fragrances, topical antimicrobials, sulfonylureas, and hydrochlorothiazide are common causes of photoallergic reactions.

Pearl Question 2 (T/F): Narcotics commonly cause phototoxic reactions.

The correct answer is False: Phototoxic reactions commonly are associated with tetracyclines, psoralen, hydrochlorothiazide, nonsteroidal anti-inflammatory drugs, furosemide, and fluoroquinolones.

Pearl Question 3 (T/F): Drug-induced photosensitivity reactions usually occur within minutes but no longer than a few hours after exposure.

The correct answer is False: Phototoxic reactions develop within minutes or hours, whereas photoallergic reactions develop within 24-72 hours. The time course of photoallergic reactions is delayed because it is a cell-mediated immune response.

Pearl Question 4 (T/F): A common test is available to help in diagnosing photoallergic dermatitis.

The correct answer is True: Photopatch testing can be helpful in diagnosing photoallergic dermatitis. This test is performed by treating small areas of skin on the back or inner aspect of the forearms with gradually increasing doses of light. The minimum dose of light required to produce uniform erythema over the entire irradiated site after 24 hours is called the minimum erythema dose (MED). If no photoallergens were applied to the skin and no phototoxic agents are still present after systemic administration, the MED for both UV-A and UV-B should be normal in drug-induced photosensitivity disorders. It should be reduced in several other photosensitivity disorders.

PICTURES

Section 11 of 12

Caption: Picture 1. Phototoxic reaction.
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Caption: Picture 2. Photoallergic reaction.
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Caption: Picture 3. Pseudoporphyria.
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Caption: Picture 4. Subacute cutaneous lupus erythematosus exacerbated by terbinafine. Courtesy of Jeffrey P. Callen.
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BIBLIOGRAPHY

Section 12 of 12

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