Coexistence of granuloma annulare and chronic spontaneous urticaria
An. bras. dermatol; 91 (4), 2016
Results: 196
Eosinophilic annular erythema in childhood - Case report
An. bras. dermatol; 91 (4), 2016
Abstract: Eosinophilic annular erythema is a rare, benign, recurrent disease, clinically characterized by persistent, annular, erythematous lesions, revealing histopathologically perivascular infiltrates with abundant eosinophils. This report describes an unusual case of eosinophilic annular erythema in ...
Primary cutaneous plasmablastic lymphoma revealing clinically unsuspected HIV infection
An. bras. dermatol; 91 (4), 2016
Abstract: Plasmablastic lymphoma is a rare subtype of diffuse large B-cell lymphoma more frequently diagnosed in immunosuppressed patients, mainly HIV-infected. Primary cutaneous plasmablastic lymphoma is extremely rare, and in this patient it was the first clinical manifestation of unsuspected HIV-infec...
Case for diagnosis. Metastatic Crohn's disease
An. bras. dermatol; 91 (4), 2016
Abstract: Metastatic Crohn's disease is a rare skin manifestation, defined by granulomatous skin lesions that are discontinuous to the affected gastrointestinal tract and histopathologically resembling inflammatory bowel lesions. Up to 44% of patients with Crohn's disease have cutaneous manifestations, o...
Lichen sclerosus associated with localized scleroderma: dermoscopy contribution
An. bras. dermatol; 91 (4), 2016
Abstract: Lichen sclerosus is an uncommon inflammatory dermatosis with preferential involvement of the urogenital region. The extragenital involvement is uncommon and is characterized by small rounded macules or papules, pearly white in color. The coexistence of lichen sclerosus and scleroderma plaques i...
Dermoscopía/métodos, Liquen Escleroso y Atrófico/diagnóstico por imagen, Liquen Escleroso y Atrófico/patología, Esclerodermia Localizada/diagnóstico por imagen, Esclerodermia Localizada/patología, Eritema/diagnóstico por imagen, Eritema/patología, Liquen Escleroso y Atrófico/complicaciones, Esclerodermia Localizada/complicaciones, Piel/diagnóstico por imagen, Piel/patología
Porphyria cutanea tarda in a HIV- positive patient
An. bras. dermatol; 91 (4), 2016
Abstract: This is a case report about Porphyria cutanea tarda (PCT) and its relationship with the infection caused by the human immunodeficiency virus (HIV). Cutaneous porphyria is an illness caused by enzymatic modification that results in partial deficiency of uroporphyrinogen decarboxylase (Urod), whi...
Infecciones por VIH/complicaciones, Porfiria Cutánea Tardía/patología, Porfiria Cutánea Tardía/virología, Terapia Antirretroviral Altamente Activa, Infecciones por VIH/tratamiento farmacológico, Porfiria Cutánea Tardía/tratamiento farmacológico, Factores de Riesgo, Piel/patología, Uroporfirinógeno Descarboxilasa/orina
Rheumatoid arthritis and pseudo-vesicular skin plaques: rheumatoid neutrophilic dermatosis
An. bras. dermatol; 91 (4), 2016
Abstract: A 54 year-old woman with a 3-year history of rheumatoid arthritis (RA) consulted us because of weight loss, fever and skin eruption. On physical examination, erythematous plaques with a pseudo-vesicular appearance were seen on the back of both shoulders. Histological examination was consistent ...
Mosaic trisomy 8 detected by fibroblasts cultured of skin
Colomb. med; 47 (2), 2016
Introduction: Mosaic trisomy 8 or "Warkany's Syndrome" is a chromosomopathy with an estimated prevalance of 1:25,000 to 1:50,000, whose clinical presentation has a wide phenotypic variability. Case Description: Patient aged 14 years old with antecedents of global retardation of development, moderate cogn...
DRESS syndrome in ophthalmic patients
Arq. bras. oftalmol; 79 (3), 2016
ABSTRACT Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a rare and potentially fatal adverse drug reaction associated with skin rash, fever, eosinophilia, and multiple organ injury. A number of pharmacological agents are known to cause DRESS syndrome such as allopurinol, antico...
Antibacterianos/efectos adversos, Antiprotozoarios/efectos adversos, Biopsia, Síndrome de Hipersensibilidad a Medicamentos/etiología, Síndrome de Hipersensibilidad a Medicamentos/patología, Endoftalmitis/tratamiento farmacológico, Fiebre/patología, Inyecciones Intravítreas/efectos adversos, Piel/patología, Toxoplasmosis Ocular/tratamiento farmacológico
Hyaline fibromatosis syndrome: cutaneous manifestations
An. bras. dermatol; 91 (2), 2016
Abstract Hyaline fibromatosis syndrome is the current name for clinical manifestations of diseases previously known as “infantile systemic hyalinosis” and “juvenile hyaline fibromatosis”. The authors report representative clinical cases of each one of the above subtypes with empha...