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1.
JAMA Dermatol ; 149(6): 727-31, 2013 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-23616197

RESUMO

IMPORTANCE: Epidermolysis bullosa (EB) pruriginosa is a rare variant of dystrophic EB. It may manifest late in life and is characterized by intense pruritus, resulting in a phenotype resembling acquired inflammatory dermatoses. Dermatopathology textbooks include hereditary forms of EB among the "cell-poor" list of subepidermal blistering disorders. OBSERVATIONS: We report a case of dominant dystrophic EB pruriginosa with late-onset cutaneous manifestations. A biopsy specimen showed subepidermal blistering with prominent inflammatory cells, including numerous eosinophils. Unfamiliarity with the distinctive clinicopathologic features of EB pruriginosa led to an initial erroneous histopathologic diagnosis of an acquired autoimmune blistering disorder. Direct immunofluorescence study results were negative for immune reactants. A strong clinical suspicion of hereditary EB pruriginosa led to mutation analysis of COL7A1, which confirmed a novel, heterozygous nonglycine missense mutation. Subsequently, 2 other family members who had nail dystrophy were also correctly diagnosed as having dominant dystrophic EB, highlighting the clinical spectrum of the disorder and the intrafamilial variability in disease presentation. CONCLUSIONS AND RELEVANCE: The clinical features of EB pruriginosa are becoming more widely recognized, but dermatologists, dermatopathologists, and histopathologists should be aware that inflammatory infiltrates and late presentation are potential pitfalls in correctly diagnosing this subtype of hereditary EB.


Assuntos
Colágeno Tipo VII/genética , Epidermólise Bolhosa/patologia , Inflamação/patologia , Adulto , Erros de Diagnóstico , Epidermólise Bolhosa/diagnóstico , Epidermólise Bolhosa/genética , Epidermólise Bolhosa Distrófica , Feminino , Técnica Direta de Fluorescência para Anticorpo , Humanos , Inflamação/diagnóstico , Mutação
2.
Pediatr Dermatol ; 27(3): 294-7, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20609149

RESUMO

Cutaneous lymphoid hyperplasia or pseudolymphoma is a usually benign inflammatory response that mimics lymphoma. Stimulation from foreign antigens introduced into the skin can induce this response. Scratches from pets are an effective mode of transmitting infections and inoculating foreign antigens into the skin. We report an unusual case of a child where cutaneous lymphoid hyperplasia presented as subcutaneous nodules at sites scratched by a pet cat.


Assuntos
Gatos , Pseudolinfoma/etiologia , Dermatopatias/etiologia , Combinação Amoxicilina e Clavulanato de Potássio/uso terapêutico , Animais , Antígenos/efeitos adversos , Azitromicina/uso terapêutico , Criança , Fármacos Dermatológicos/uso terapêutico , Feminino , Humanos , Itraconazol/uso terapêutico , Naftalenos/uso terapêutico , Pseudolinfoma/diagnóstico , Pseudolinfoma/tratamento farmacológico , Pseudolinfoma/patologia , Radiografia Torácica , Dermatopatias/diagnóstico , Dermatopatias/tratamento farmacológico , Dermatopatias/patologia , Terbinafina
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