Results 91 to 100 of about 1,298,129 (315)

Socio-Demographic Characteristics of Study Subjects by Colorectal Neoplasm Staging. [PDF]

open access: yes, 2013
Note: AJCC = American Joint Committee on Cancer*Significant difference between colorectal neoplasm staging (except unknown stage)by One-Way ANOVA†Significant difference between colorectal neoplasm staging (except unknown stage)by Chi-square Test ...
Dora L. W. Kwong (166235)   +3 more
core   +1 more source

P212 | COMPARATIVE ANALYSIS OF MUTATION LANDSCAPE IN MPN PATIENTS WITH SPLANCHNIC VEIN THROMBOSIS AND OTHER VEIN THROMBOSES

open access: yesHaematologica
Introduction: Myeloproliferative neoplasms (MPNs) are a main cause of splanchnic vein thrombosis (SVT), with JAK2V617F as a known risk factor. The impact of co-occurring mutations on thrombosis risk remains unclear.
L. Fagiolo   +12 more
doaj  

Solid Pseudopapillary Neoplasm of the Pancreas in Children and Adolescents: Expert Recommendations

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Solid pseudopapillary neoplasm of the pancreas (SPN) is a rare low‐grade malignant exocrine pancreatic tumor, mostly discovered during the second decade of life in females, with a very good prognosis, provided microscopically complete surgical excision is achieved.
Sabine Irtan   +18 more
wiley   +1 more source

Poral neoplasm with combined sebaceous and apocrine differentiation [PDF]

open access: yes, 1998
Poromas have been considered the hallmark of benign eccrine neoplasms. The literature describes six cases of poroma differentiating toward apocrine and sebaceous lineage.
A. Coggi, R. Gianotti, E. Alessi
core   +1 more source

Bridging the Gap in Neuroblastoma Care: Consensus‐Based Statements With Recommendations for Improved Patient and Caregiver Experiences

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Neuroblastoma's complex, heterogeneous biology poses significant diagnostic and therapeutic challenges, often requiring caregivers to absorb complex information and participate in time‐sensitive decisions. However, caregivers often feel unprepared to evaluate options.
Vickie Buenger   +8 more
wiley   +1 more source

Unicentric Castleman’s Disease Masquerading Pancreatic Neoplasm [PDF]

open access: yes, 2012
Castleman’s disease is a rare nonclonal proliferative disorder of the lymph nodes with an unknown etiology. Common locations of Castleman’s disease are mediastinum, neck, axilla, and abdomen.
Partha Chakraborty   +5 more
core   +1 more source

Immunophenotypic patterns in precursor T-cell neoplasm [PDF]

open access: yes, 2007
T-cell lymphoproliferative disorders are a heterogeneous group of lymphoid neoplasm that can mimic both benign conditions and non-hematopoietic tumors. In routine clinical practice, morphology and immunophenotyping forms the basis of their diagnosis.
Gupta, R.   +3 more
core   +2 more sources

Imaging Findings of Primary Angiomyolipoma of the Pancreas: A Case Report

open access: yes대한영상의학회지, 2017
Angiomyolipoma (AML), a part of a family of mesenchymal tumors, is a common fat-containing solid neoplasm. Kidney and liver are the main sites of AML; rarely, primary pancreatic AML has also been reported. Here, we present a case of pathologically proven
Hye Hee Kim, Dong Hee Park
doaj   +1 more source

Impact of Metastatic Patterns on Survival and Response to Therapy in Neuroblastoma

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background While the presence of metastases in neuroblastoma (NB) is a well‐established prognostic factor, the clinical significance of dissemination patterns and tumour burden and their impact on response and survival remains poorly understood.
Mariona Morell‐Daniel   +15 more
wiley   +1 more source

Microsatellite instability in ovarian neoplasm. [PDF]

open access: yes, 1997
Microsatellite instability in ovarian ...
Dionigi A   +10 more
core  

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