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Adrenal cortical carcinoma with extension into the inferior vena cava – case report and literature review

Adrenocortical carcinoma (ACC) is a rare endocrine malignancy with an incidence rate of 1 to 2 per million person-years. ACC most commonly arises sporadically, but may be associated with familial tumour syndromes. Clinical symptoms are mainly related to an excess of steroid hormones. We present an u...

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Main Authors: Fulawka, Lukasz, Patrzalek, Dariusz, Halon, Agnieszka
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2014
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3973845/
https://ncbi.nlm.nih.gov/pubmed/24602387
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1746-1596-9-51
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