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Quoted phrase not found in phrase index: "Multiple intestinal neurofibromatosis"
Page 1
Pancreatic endocrine tumors.
Oberg K. Oberg K. Semin Oncol. 2010 Dec;37(6):594-618. doi: 10.1053/j.seminoncol.2010.10.014. Semin Oncol. 2010. PMID: 21167379 Review.
They represent a heterogeneous group with very varying tumor biology and prognosis. About half of the patients present clinical symptoms and syndromes related to substances released from the tumors (Zollinger-Ellison syndrome, insulinoma, glucagonoma, etc) and the other ha …
They represent a heterogeneous group with very varying tumor biology and prognosis. About half of the patients present clinical sympt …
The genetics of neuroendocrine tumors.
Öberg K. Öberg K. Semin Oncol. 2013 Feb;40(1):37-44. doi: 10.1053/j.seminoncol.2012.11.005. Semin Oncol. 2013. PMID: 23391111
The majority of these tumors are sporadic, but there are several familial (inherited) syndromes to consider, such as multiple endocrine neoplasia type 1 and type 2 (MEN-1 and MEN-2), von Hippel-Lindau syndrome (VHL), tuberosclerosis, and neurofibromatosis syndromes. …
The majority of these tumors are sporadic, but there are several familial (inherited) syndromes to consider, such as multiple endocri …
Rectal carcinoma and multiple gastrointestinal stromal tumors (GIST) of the small intestine in a patient with neurofibromatosis type 1: a case report.
Hakozaki Y, Sameshima S, Tatsuoka T, Okuyama T, Yamagata Y, Noie T, Oya M, Fujii A, Ueda Y, Shimura C, Katagiri K. Hakozaki Y, et al. World J Surg Oncol. 2017 Aug 23;15(1):160. doi: 10.1186/s12957-017-1231-3. World J Surg Oncol. 2017. PMID: 28835241 Free PMC article.
BACKGROUND: Neurofibromatosis type 1 (NF1) is an autosomally dominant inherited disorder characterized by multiple pigmented skin spots (cafe-au-lait spots) and neurofibroma. ...The resected rectal tumor was a well-differentiated adenocarcinoma with multiple …
BACKGROUND: Neurofibromatosis type 1 (NF1) is an autosomally dominant inherited disorder characterized by multiple pigmented s …
Volar melanotic macules in a gardener: a case report and review of the literature.
Blossom J, Altmayer S, Jones DM, Slominski A, Carlson JA. Blossom J, et al. Am J Dermatopathol. 2008 Dec;30(6):612-9. doi: 10.1097/DAD.0b013e318184bc57. Am J Dermatopathol. 2008. PMID: 19033941 Review.
She was healthy without any medical conditions or medications. No family history of intestinal polyposis or mucosal melanosis existed. At presentation, she had less than 20 brownish-black, 2- to 10-mm irregular macules over the volar aspect of the thumbs and index fingers, …
She was healthy without any medical conditions or medications. No family history of intestinal polyposis or mucosal melanosis existed …
Primary Effusion Lymphoma-like Lymphoma in a Patient with Neurofibromatosis Type 1.
Oki M, Nanao T, Shinoda T, Tsuda A, Yasuda A, Seki T, Ozawa H, Nakamura N, Takagi A. Oki M, et al. Tokai J Exp Clin Med. 2016 Sep 20;41(3):123-9. Tokai J Exp Clin Med. 2016. PMID: 27628603 Free article.
To date, there are only 15 case reports of lymphoma in patients with neurofibromatosis type 1 (NF1), a common autosomal dominant tumor predisposition syndrome. ...The woman presented with pleural effusion following surgery for a small intestinal gastrointestinal str …
To date, there are only 15 case reports of lymphoma in patients with neurofibromatosis type 1 (NF1), a common autosomal dominant tumo …