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A rare combination of pheochromocytoma and gastrointestinal stromal tumour in a patient with neurofibromatosis 1 syndrome—a case report

Neurofibromatosis 1 is a rare inherited autosomal dominant syndrome. It comprises 90 % of neurofibromatosis cases. These patients may develop various types of tumours in early age, especially multiple neurofibromas with a high risk of developing malignant peripheral nerve sheath tumours. Other tumou...

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Detalles Bibliográficos
Autores principales: Jayalakshmy, P S, Mohan, A. Anish, Kumar, Rajesk K., Beevi, P. Junaina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605922/
https://www.ncbi.nlm.nih.gov/pubmed/26943426
http://dx.doi.org/10.1186/s40792-015-0107-4