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Clinical and Experimental Dermatology 05/2013; · 1.20 Impact Factor
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Clinical and Experimental Dermatology 06/2011; 36(4):424-6. · 1.20 Impact Factor
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ABSTRACT: Toxic epidermal necrolysis (TEN) is a life-threatening, immune-mediated reaction, characterized by severe cutaneous and mucosal blisters and erosions. It often presents with flu-like symptoms, followed by a maculopapular, urticarial, purpuric or erythema multiforme-like eruption, which then evolves into blisters and sheet-like erosions. Presentation with pustules, however, is not well described in the English literature, and may lead to delayed diagnosis. We present two unusual cases of TEN that initially presented with pustular lesions.
Clinical and Experimental Dermatology 05/2010; 36(1):42-5. · 1.20 Impact Factor
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Clinical and Experimental Dermatology 04/2009; 34(2):273-4. · 1.20 Impact Factor
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ABSTRACT: Juvenile xanthogranuloma (JXG) is a benign, self-healing non-Langerhans cell histiocytosis of unknown aetiology, most commonly occurring in infants and children. JXG is characterized by solitary or multiple yellowish cutaneous nodules, the two common clinical variants being a small nodular form and large nodular form, which frequently coexist. Unusual morphological presentations include keratotic, lichenoid, pedunculated, subcutaneous, clustered, plaque-like and giant lesions. We describe the first reported case of 'disseminated' clustered juvenile xanthogranuloma presenting in an infant.
Clinical and Experimental Dermatology 06/2008; 33(5):575-7. · 1.20 Impact Factor
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Clinical and Experimental Dermatology 12/2007; 32(6):784-5. · 1.20 Impact Factor
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ABSTRACT: Desmoplastic trichoepithelioma (DT) is a rare benign adnexal neoplasm considered to have follicular differentiation. It usually presents as an asymptomatic, firm, annular plaque with a raised border. The most common site of occurrence is the face, usually on the cheek. Females are more often affected than males and the age range of patients previously reported is 8-79 years. We present a case of congenital desmoplastic trichoepithelioma. A girl was born at term to a healthy mother after an uneventful pregnancy and was noted to have widespread erythematous plaques with milia-like lesions over the right scalp, face and neck, with some areas of atrophic scarring. Histology and immunohistochemistry of incisional biopsies of the lesions were consistent with a diagnosis of DT. To our knowledge, this is the first reported case of congenital DT.
Clinical and Experimental Dermatology 10/2007; 32(5):522-4. · 1.20 Impact Factor
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Clinical and Experimental Dermatology 04/2007; 32(2):237-8. · 1.20 Impact Factor
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British Journal of Dermatology 12/2006; 155(5):1089-90. · 3.67 Impact Factor
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Journal of the European Academy of Dermatology and Venereology 05/2006; 20(4):466-7. · 2.98 Impact Factor
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British Journal of Dermatology 10/2005; 153(3):689-91. · 3.67 Impact Factor