Pathophysiology: The pathophysiology of infantile acropustulosis is unknown. Many cases are preceded by well-documented or suspected scabies infestation, and a scabies id reaction has been suggested. More often, cases occur despite scabies having been thoroughly ruled out. Bacterial and viral culture results are consistently negative, and negative immunofluorescence results suggest that infantile acropustulosis is not an antibody-mediated autoimmune process.
Frequency:
- In the US: The exact incidence is unknown.
- Internationally: The exact incidence is unknown. One study from Israel reported 25 cases in a 9-year period, suggesting that this is not as uncommon as once thought.
Mortality/Morbidity: All cases spontaneously resolve in a few months to 3 years.
Race: Early reports suggested a predominance of African Americans. Now, acropustulosis is believed to affect all races equally.
Sex: Early reports suggested a male predominance. Larger series have since shown an equal distribution between males and females.
Treatment
Medical Care: Treatment is often unnecessary because of the self-limited nature of this condition.
- Topical steroids and oral dapsone have been used successfully, if justified in more difficult cases.
- Topical pramoxine preparations are available without prescription for the treatment of pruritus.
- Oral antihistamines may be useful.
Consultations: Consult a dermatologist or a pediatric dermatologist.
Medication
High-potency topical steroids (classes 1 and 2) have been used successfully for control of pruritus. Children who are extremely symptomatic may be treated with dapsone.
Drug Category: Topical steroids -- These agents provide symptomatic relief of pruritus.
Drug Name | Betamethasone (Diprolene, Betatrex) -- For inflammatory dermatoses responsive to steroids. Decreases inflammation by suppressing migration of polymorphonuclear leukocytes and reversing capillary permeability. Use fluorinated topical steroids with caution in children. |
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Pediatric Dose | Apply thin film to affected areas bid; occlusion increases effectiveness; avoid wraps that may present choking hazard |
Contraindications | Documented hypersensitivity; paronychia; cellulitis; impetigo; angular cheilitis; erythrasma; erysipelas; rosacea; perioral dermatitis; acne |
Interactions | None reported |
Pregnancy | C - Safety for use during pregnancy has not been established. |
Precautions | Application over large surface areas may cause systemic absorption and adrenal suppression; 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 |
Drug Name | Dapsone (Avlosulfon) -- Bactericidal and bacteriostatic against mycobacteria; mechanism of action is similar to that of sulfonamides where competitive antagonists of PABA prevent formation of folic acid, inhibiting bacterial growth. Used mainly to treat leprosy and dermatitis herpetiformis. Has antineutrophil and anti-inflammatory properties. |
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Pediatric Dose | 1-2 mg/kg/d PO; not to exceed 100 mg |
Contraindications | Documented hypersensitivity; known G-6-PD deficiency (assay for G-6-PD activity prior to initiation of therapy) |
Interactions | May inhibit anti-inflammatory effects of clofazimine; hematologic reactions may increase with folic acid antagonists, eg, pyrimethamine (monitor for agranulocytosis during second and third months of therapy); probenecid increases toxicity; trimethoprim with dapsone may increase toxicity of both drugs; because of increased renal clearance, levels may significantly decrease when administered concurrently with rifampin |
Pregnancy | C - Safety for use during pregnancy has not been established. |
Precautions | Associated with a variety of systemic toxicities, including agranulocytosis, anemia, methemoglobinemia, hepatitis, and neuropathy; patients may experience headache and/or GI distress on initiation of therapy; perform weekly blood counts (first mo), then monthly WBC counts (6 mo), then semiannual WBC counts; discontinue if a significant reduction in platelets, leukocytes, or hematopoiesis occurs; caution in methemoglobin reductase deficiency, G-6-PD deficiency, or hemoglobin M because of high risk for hemolysis and Heinz body formation Caution in patients exposed to other agents or conditions (eg, infection, diabetic ketosis) capable of producing hemolysis; peripheral neuropathy can occur (rare); phototoxicity may occur when exposed to UV light; pancreatitis may occur; various forms of renal complications including acute renal failure, acute tubular necrosis, and oliguria have occurred with dapsone use |
Drug Name | Pramoxine (Tronothane, Prax) -- Blocks nerve conduction and impulses by inhibiting depolarization of neurons. Use 1% lotion or cream. |
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Pediatric Dose | Apply to affected area prn; not to exceed 200 mg |
Contraindications | Documented hypersensitivity; do not apply over large areas; avoid contact with eyes and nose |
Interactions | None reported |
Pregnancy | C - Safety for use during pregnancy has not been established. |
Precautions | Caution in patients with trauma in area to be treated |