Superficial malignant peripheral nerve sheath tumor from recurrent neurofibroma in the abdominal wall of a patient without neurofibromatosis type 1

Malignant peripheral nerve sheath tumor (MPNST) is rare, accounting for 5–10% of all soft tissue sarcomas. MPNST is characteristically aggressive and has a poor prognosis. Fifty percent of patients with MPNST have neurofibromatosis type 1 (NF1). NF-associated MPNST occurs more often at younger ages...

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Detalles Bibliográficos
Autores principales: Jung, Chang Yeon, Bae, Jung Min, Choi, Joon Hyuk, Jung, Ki Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yeungnam University College of Medicine 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784618/
https://www.ncbi.nlm.nih.gov/pubmed/31620615
http://dx.doi.org/10.12701/yujm.2019.00031

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