13-year-old tuberous sclerosis patient with renal cell carcinoma associated with multiple renal angiomyolipomas developing multifocal micronodular pneumocyte hyperplasia

BACKGROUND: The autosomal dominant tumor syndrome tuberous sclerosis complex is caused by the mutated TSC1 gene, hamartin, and the TSC2 gene, tuberin. Patients with this complex develop typical cutaneus symptoms such as peau chagrin or angiofibromas of the skin as well as other lesions such as astro...

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Detalles Bibliográficos
Autores principales: Behnes, Carl Ludwig, Schütze, Gunther, Engelke, Christoph, Bremmer, Felix, Gunawan, Bastian, Radzun, Heinz-Joachim, Schweyer, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568416/
https://www.ncbi.nlm.nih.gov/pubmed/23379654
http://dx.doi.org/10.1186/1472-6890-13-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568416/
https://www.ncbi.nlm.nih.gov/pubmed/23379654
http://dx.doi.org/10.1186/1472-6890-13-4

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