RESUMEN
Abstract Gianotti-Crosti syndrome is a rare disease characterized by acral papular eruption with symmetrical distribution. It is a benign and self-limited disease; the symptoms disappear after two to eight weeks, without recurrences or scars. Skin lesions are usually asymptomatic. Prodrome might occur, suggesting upper respiratory infection, or constitutional symptoms. Diagnosis is eminently clinical, and this disease is associated with viral infections. Due to its rarity and low occurrence in adolescents and adults, we report a case of Gianotti-Crosti syndrome of a teenager.
Asunto(s)
Humanos , Femenino , Adolescente , Piel/patología , Acrodermatitis/patología , Diagnóstico Diferencial , Exantema/patologíaRESUMEN
Abstract The occurrence of multiple primary melanomas in a single individual is rare. Most commonly, malignant melanocytic lesions subsequent to the initial diagnosis of melanoma are secondary cutaneous metastases. We report a patient with gastrointestinal bleeding from gastric metastasis of cutaneous melanoma. During clinical evaluation and staging, we discovered a brain metastasis associated with 3 synchronous primary cutaneous melanomas. We suggest the research on the mutation in the cyclin-dependent kinase inhibitor 2A (CDKN2A) (INK4a) in such cases. We also emphasize the importance of clinical examination and dermoscopy of the entire tegument, even after a malignant melanocytic lesion is identified.
Asunto(s)
Humanos , Anciano , Neoplasias Cutáneas/patología , Neoplasias Gástricas/secundario , Neoplasias Encefálicas/secundario , Melanoma/secundario , Neoplasias Primarias Múltiples/patología , Neoplasias Cutáneas/genética , Neoplasias Gástricas/genética , Biopsia , Neoplasias Encefálicas/genética , Dermoscopía , Inhibidor p18 de las Quinasas Dependientes de la Ciclina/genética , Melanoma/genética , Mutación , Neoplasias Primarias Múltiples/genéticaRESUMEN
Abstract Steatocystoma multiplex is a rare genetic disorder characterized by the presence of hamartomatous malformations at the junction of the pilosebaceous duct. It consists of encapsulated cystic lesions in the dermis, with adjacent sebaceous gland. When associated with inflammation, resembling hidradenitis, it is called steatocystoma multiplex suppurativa, a condition rarely reported. This is the first case of steatocystoma multiplex suppurativa reported in the Brazilian literature. Female patient, 23 years old, with papular and nodular cystic lesions that started in the armpits and groin, later spreading to the trunk, lower limbs, anticubital fossa, face and scalp. The presence of papular-nodular lesions associated with disseminated hidradenitis-like lesions in flexural areas and the histopathological diagnosis of steatocystoma defined the diagnosis of steatocystoma multiplex suppurativa.
Asunto(s)
Humanos , Femenino , Adulto Joven , Esteatocistoma Múltiple/patología , Glándulas Sebáceas/patología , Supuración , Biopsia , Hidradenitis Supurativa/patología , Enfermedades Raras/patología , Diagnóstico Diferencial , Quiste Epidérmico/patologíaRESUMEN
Abstract: Blue nevi are benign melanocytic lesions located in the deeper reticular dermis, consequence of failure of melanocytic migration into the dermal-epidermal junction from the neural crest. Lesions are usually asymptomatic and solitary, but may present in a multiple or agminated (grouped) pattern. The agminated subtype is formed when bluish-pigmented lesions cluster together in a well-defined area. Lesions can be flat or raised. We report the case of a patient who presented multiple bluish macules (1-3 mm in diameter) grouped on the left upper back. Dermoscopy and anatomic pathological examination were consistent with blue nevus.