Linear IgA bullous dermatosis of childhood in Child
Childhood LABD usually presents around age 5 years, but it has been seen in neonates up to children aged 10 years. There is a 3:2 female-to-male predominance. This condition is usually self-limited over several months, up to 2-4 years, following a less chronic course than childhood pemphigoid, , or . While the majority of cases resolve before puberty, a small proportion of patients will have recurrences into adulthood.
Classically, the lesions appear as clusters or rings of tense bullae in the perioral and perineal regions. Lesions tend to burn or itch, with the blistering becoming less severe with time. The bullae heal with pigmentary changes and infrequently with scarring. Mucosal involvement is rarer in children than in adults.
Drug-induced LABD may be seen in childhood. Clinical presentation is typically indistinguishable from the classic idiopathic form with the exception that large erosions may be more commonly seen in the drug-induced compared with the idiopathic form. Localized or widespread macular erythema may be seen in association. A number of drugs have been associated with LABD, most commonly a variety of antibiotics (eg, trimethoprim-sulfamethoxazole, amoxicillin-clavulanate, and amoxicillin alone), NSAIDs, and cephalosporins.
Most patients with childhood LABD have IgA1 antibodies to a 97-kDa and a 120-kDa fragment of the extracellular portion of bullous pemphigoid antigen 2 (BP180 / type XVII collagen), typically the 15 collagenous domain and less frequently the NC16A epitope. Reactivity to collagen VII, laminin-332, and laminin gamma-1 have also been described.
L13.8 – Other specified bullous disorders
109250009 – Chronic bullous dermatosis of childhood
- Childhood bullous pemphigoid – immunofluorescence will help distinguish
- Dermatitis herpetiformis – associated diarrhea or failure to thrive
- Impetigo – classic yellow crusting and positive bacterial cultures
- Herpes simplex virus (HSV) infection – positive HSV polymerase chain reaction (PCR)
- Epidermolysis bullosa acquisita – direct immunofluorescence on salt-split skin can distinguish
- Bullous fixed drug eruption – history of drug exposure
- Stevens-Johnson syndrome – histology will distinguish
- Contact dermatitis – linear or geometric shapes of eruption
- Poison ivy dermatitis – history or exposure
- Urticaria pigmentosa – may have positive Darier sign
- Acute febrile neutrophilic dermatosis (Sweet syndrome) – presence of fever
- IgA vasculitis (formerly Henoch-Schönlein purpura) – may have joint pains or abdominal pain
- Bullous drug eruption – history of drug exposure