Cargando…
Rare triad of periampullary carcinoid, duodenal gastrointestinal stromal tumor and plexiform neurofibroma at hepatic hilum in neurofibromatosis type 1: a case report
BACKGROUND: Neurofibromatosis type 1 is a relatively common inherited disorder. Patients with neurofibromatosis type 1 are at high risk of developing neurogenic, neuroendocrine and mesenchymal intra-abdominal tumors. Although coexistence of multiple tumors of different types is frequent in neurofibr...
Autores principales: | Abdessayed, Nihed, Gupta, Rahul, Mestiri, Sarra, Bdioui, Ahlem, Trimech, Mounir, Mokni, Moncef |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575842/ https://www.ncbi.nlm.nih.gov/pubmed/28851321 http://dx.doi.org/10.1186/s12885-017-3567-z |
Ejemplares similares
-
Immunohistochemical Characterization Improves the Reproducibility of the Histological Diagnosis of Ovarian Carcinoma
por: Missaoui, Nabiha, et al.
Publicado: (2018) -
Ossifying fibromyxoid tumor of the trunk mimicking hydatid cyst: A case report
por: Abdessayed, Nihed, et al.
Publicado: (2017) -
Plexiform neurofibroma in the hepatic hilum associated with neurofibromatosis type 1: a case report
por: Hoshimoto, Sojun, et al.
Publicado: (2009) -
Retroperitoneal unicentric Castleman’s disease: A case report
por: Abdessayed, Nihed, et al.
Publicado: (2017) -
A case of portal hypertension by presumed as plexiform neurofibroma at the hepatic hilum
por: Lee, Kyung Han, et al.
Publicado: (2016)