RESUMO
Lipofibromatosis is a slow-growing, childhood soft-tissue neoplasm that is often confused with other conditions. We report a patient with lipofibromatosis causing extremity enlargement at birth. The lesion initially was thought to be a vascular anomaly or lipedema on clinical and MRI examination. When involving the lower extremity, diffuse lipofibromatosis must be differentiated from more common causes of lower limb enlargement in children: lymphatic malformation, lymphedema, or lipedema. Compared with these more frequent conditions, lipofibromatosis usually causes less morbidity. Management of the tumor includes observation or excision. Because complete extirpation of the lesion is difficult, the recurrence rate is high.
Assuntos
Fibroma/diagnóstico , Lipomatose/diagnóstico , Neoplasias de Tecidos Moles/diagnóstico , Malformações Vasculares/diagnóstico , Diagnóstico Diferencial , Humanos , Lactente , Extremidade Inferior , Imageamento por Ressonância Magnética , MasculinoRESUMO
While abdominoplasty has a long history of development, we have recently had several cases where a lateral hip lift was requested. The goal is to raise and tighten the skin and subcutaneous tissue of the lateral thigh after weight loss or to improve cellulite. We have modified the excellent technique of Ted Lockwood by eliminating undermining and suturing the resulting flaps only to the deep dermal layers. The complications have been limited to the spreading of scars as a result of so much tension, and the occasional delayed healing of those tense wounds.
