نتایج جستجو برای: solid pseudo papillary tumor of the pancreas

تعداد نتایج: 22853501  

2014
Ching hsueh Cheng-Yu Lin Yuan-Chun huang Chi-Kuang Liu

Desmoid tumors, also called deep or aggressive fibromatosis, are uncommon mesenchymal tumors characterized by proliferation of fibroblasts in an abundant collagen extracellular matrix. They rarely involve the pancreas, and the diagnosis is difficult to make if they do. Only eleven cases have previously been reported involving the pancreas in a review of the literature. In these reported cases, ...

Journal: :International Journal of Case Reports and Images 2015

Introduction: Papillary Glioneuronal Tumor (PGNT) is a rare tumor with approximately 70 cases reported in the last decade. This tumor is more common in young adults and is the most common clinical manifestation of headaches and seizures. This tumor has an indolent clinical behavior. Regarding gender prevalence there is no detailed epidemiological information available, because of the rarity and...

Journal: :گوارش 0
homaun vahedi masoud sotoudeh golrokh olfati

endocrine tumors of the pancreas (islet-cell tumors) are rare with neuroendocrine origin. the patient was a 41- year- old man, admitted with chief complains of epigastric mass feeling, dull abdominal pain, lack of appetite and weight loss up to 2-3 kg since 6 months ago. in physical examination, a mass was detected in epigaster and left upper quadrant (luq). in abdominal x-ray, a calcified mass...

Journal: :Revista espanola de medicina nuclear 2007
E Roldán-Valadez A Rumoroso-García I Vega-González G Valdivieso-Cárdenas O Morales-Santillán L Osorio-Cardiel

Solid and papillary epithelial neoplasm of the pancreas (SPEN) is an encapsulated, slowly enlarging abdominal mass that generally shows no evidence of capsular invasion, regional lymph node involvement, or distal metastases. We present a 68 years old Hispanic male diagnosed with SPEN 5 years earlier that refused surgical excision. Presently he underwent a whole-body 18F-FDG PET/CT. Although tum...

Journal: :JOP : Journal of the pancreas 2013
Max V Wohlauer Martine McManus Norio Fukami Csaba Gajdos

CONTEXT Cystic tumors of the pancreas have been diagnosed with increasing frequency. Intraductal oncocytic papillary neoplasm is a rare type of cystic pancreatic tumor. Intraductal oncocytic papillary neoplasm is considered a distinct entity with the potential of developing into invasive carcinoma and it should be differentiated from other cystic tumors of the pancreas, including mucinous cysti...

2014
Ju Hee Lee Jae Ho Byun Jin Hee Kim Seung Soo Lee Hyoung Jung Kim Moon-Gyu Lee

OBJECTIVE To describe the computed tomography (CT) features of neuroendocrine tumors (NETs) and solid pseudopapillary tumors (SPTs) with unilocular cyst-like appearance, and to compare them with those of unilocular cystic tumors of the pancreas. MATERIALS AND METHODS This retrospective study was approved by our Institutional Review Board, and informed consent was waived. We included 112 pancr...

Journal: :JOP : Journal of the pancreas 2013
Hálio Rodrigues-Duarte Helena Torrão Paulo Coelho Maria Noruegas Maria Sanches

CONTEXT Solid pseudopapillary tumor of the pancreas is a rare tumor more common in young girls and rare in males. CASE REPORT We present a case of a solid pseudopapillary tumor of the pancreas in a 13-year-old boy, with typical imaging features. CONCLUSIONS Our case report specifically illustrates the potential of diffusion-weighted imaging findings on solid pseudopapillary tumor in pediatr...

Journal: :The journal of the Japanese Practical Surgeon Society 1988

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