Linear IgA bullous dermatosis (LABD), also known as linear IgA dermatosis, is a rare immune-mediated disease that results in blistering of the skin, in the subepidermal layers. It is commonly ...

Here, we describe a patient with non-Hodgkin's lymphoma who developed LABD after autologous HSCT and was successfully treated with glucocorticoid, dapsone and high-dose i.v. Ig, but the lymphoma ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. A 26-month-old boy presented for evaluation of acute ...

A five-month-old girl was referred to our department for an erythematous papular nonpruritic eruption that evolved into the formation of blisters on the trunk, hands and feet over a two-week period.

The morphology, distribution, and history of recent exposure to vancomycin is consistent with linear IgA bullous dermatosis (LABD). LABD is a rare autoimmune mucocutaneous disorder that may be ...

We describe a novel autoimmune disease characterized by severe subepidermal bullous eruption and crescentic glomerulonephritis with autoantibodies directed against the noncollagenous domain of the α5 ...

The autoantibodies are directed against a 97-kd basement membrane zone protein, as in linear IgA bullous dermatosis. The similarity between chronic bullous disease of childhood and IgA bullous ...

Direct immunofluorescence (DIF) microscopy showed a 15.5% positivity rate in pediatric patients and changed the clinical diagnosis in 16.7% of those cases. Researchers conducted a retrospective review ...

For centuries, bullous pemphigoid (BP) was grouped with and considered a condition similar to pemphigus vulgaris (PV). In 1953, however, Lever recognized BP as a disorder distinct from PV. 9 BP, the ...