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Br J Dermatol ; 159(2): 473-5, 2008 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-18547304

RESUMEN

Tuberous sclerosis complex (TSC) is an autosomal dominant disorder with an incidence of approximately one in 6000. It arises from a genetic abnormality involving either the TSC1 gene on chromosome 9 or the TSC2 gene on chromosome 16. The protein product of TSC1 is hamartin and that of TSC2 is tuberin. In cells, hamartin and tuberin form a complex which inhibits the mammalian target of rapamycin (mTOR), a central controller of cell growth and proliferation. Angiofibroma affects 70-80% of patients with TSC, typically on the face. We report a patient with TSC with recurrent life-threatening haemorrhage from both kidneys due to extensive angiomyolipoma formation leading to bilateral nephrectomy and renal transplantation. Immunosuppressive treatment with rapamycin, a specific mTOR inhibitor, initiated because of renal transplantation, reduced facial angiofibroma dramatically.


Asunto(s)
Angiofibroma/tratamiento farmacológico , Neoplasias Faciales/tratamiento farmacológico , Sirolimus/uso terapéutico , Neoplasias Cutáneas/tratamiento farmacológico , Esclerosis Tuberosa/complicaciones , Adolescente , Angiofibroma/etiología , Angiofibroma/patología , Antibióticos Antineoplásicos/uso terapéutico , Neoplasias Faciales/etiología , Neoplasias Faciales/patología , Femenino , Humanos , Inhibidores de Proteínas Quinasas/uso terapéutico , Proteínas Quinasas/fisiología , Neoplasias Cutáneas/etiología , Neoplasias Cutáneas/patología , Serina-Treonina Quinasas TOR
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