RESUMO
Malignant atrophic papulosisis is a rare, multisystem obliterative vasculopathy of unknown etiology, occasionally involving the cranial nerve. We describe the first case of malignant atrophic papulosisis with cranial nerve and peripheral nerve involvement in China. A 47-year-old woman presented to our hospital with atrophic porcelain white papules over the trunk and extremities, numbness in the right calf, vision decrease and impaired movement of the right eye. She was diagnosed with malignant atrophic papulosisis, based on characteristic symptoms and histopathologic examination. The patient was treated with dipyridamole and aspirin for 9 months, but later died of gastrointestinal hemorrhage. We reviewed currently available case reports on cranial nerve involvement in malignant atrophic papulosisis and emphasized the importance of skin biopsy in diagnosing this disease.
.Assuntos
Feminino , Humanos , Pessoa de Meia-Idade , Doenças dos Nervos Cranianos/patologia , Papulose Atrófica Maligna/patologia , Doenças do Sistema Nervoso Periférico/patologia , Biópsia , Doenças dos Nervos Cranianos/tratamento farmacológico , Evolução Fatal , Papulose Atrófica Maligna/tratamento farmacológico , Doenças do Sistema Nervoso Periférico/tratamento farmacológico , Pele/patologiaRESUMO
Degos disease, also known as malignant atrophic papulosis, is a rare occlusive vasculopathy of unknown etiology characterized by infarcts in the dermis, gastrointestinal tract, central nervous system, and other organs. It is characterized by papules, which become umbilicated and evolve with a depressed porcelain-white central area, with an erythematous halo with telangiectasias. Histological findings include wedge-shaped dermoepidermal necrosis and blood vessel thrombosis. Approximately 50-60% of patients with systemic symptoms die within 2-3 years, most due to gastrointestinal perforation. We report a typical case, with lethal outcome, in a 45-year-old woman.
Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Pele/patologia , Papulose Atrófica Maligna/patologia , Biópsia , Evolução Fatal , Trombose Venosa/patologia , Papulose Atrófica Maligna/complicações , Perfuração Intestinal/complicaçõesRESUMO
Presentamos una paciente de sexo femenino, de 53 años de edad, con manifestaciones cutáneas de enfermedad de Degos, sin compromiso sistémico asociado. Se realiza una revisión actualizada de la bibliografía médica mundial, con una descripción clínica, histopatológica, diagnóstica y terapéutica de la enfermedad.
