We present 3 new patients with transient bullous dermolysis of the newborn
(TBDN), which is a form of dystrophic epidermolysis bullosa. TBDN may be di
agnosed by electron microscopy showing a sublamina densa cleavage; immunofl
uorescence antigenic mapping demonstrating bullous pemphigoid antigen, lami
nin-l, and type IV collagen along the epidermal roof of subepidermal clefts
; and indirect immunofluorescence with monoclonal antibodies revealing intr
aepidermal type VII collagen. Although intraepidermal type VII collagen has
been reported in other forms of dystrophic epidermolysis bullosa, we belie
ve that the presence of type VII collagen in a striking intraepidermal gran
ular array is a finding unique to TBDN. Our cases demonstrate the importanc
e of immunodermatologic studies in the diagnosis of bullous disorders that
are seen at birth because accurate diagnosis carries prognostic implication
s. This variant of epidermolysis bullosa, in contrast to other forms of dys
trophic epidermolysis bullosa, is a benign, self-limited disease.