Results 31 to 40 of about 113,085 (229)

Primary renal carcinoid tumor [PDF]

open access: yes, 2013
Primary renal carcinoid tumor is extremely rare and, therefore, its pathogenesis and prognosis is not well known.
V B Kute   +6 more
core   +1 more source

Rare Case of Neuroendocrine Metastasis to the Left Ventricle

open access: yesJACC: Case Reports
Carcinoid syndrome is a constellation of signs and symptoms caused by different hormones produced by carcinoid tumors. Very rarely, those tumors can metastasize to the heart and cause cardiac involvement of the tumor. This study presents a very rare case
Said Hajouli, MD   +7 more
doaj   +1 more source

Primary Carcinoid Tumor of the Testis: A Case Report and Review of the Literature

open access: yesCase Reports in Urology, 2018
Carcinoid tumors usually arise in the gastrointestinal tract. Immunocytohistochemical and radiologic studies are important in detecting the primary tumor site.
Rawad Abou Zahr   +5 more
doaj   +1 more source

Primary Testicular Carcinoid Tumor presenting as Carcinoid Heart Disease [PDF]

open access: yes, 2015
Primary carcinoid tumors of the testis are very rare, and they seldom present with carcinoid syndrome. We report a hereto unreported instance, where a patient with a long-standing testicular mass presented with carcinoid heart disease, an uncommon form ...
Manjunath Shetty   +2 more
core   +1 more source

Primary ovarian mucinous carcinoid tumor: A case report and review of literature

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2019
Objective: Only a few cases of primary ovarian mucinous carcinoid tumor have been documented in the literature till date. We present a case of primary ovarian mucinous carcinoid tumor, atypical type, and review the reported cases.
Wen-Wei Hsu, Tsui-Lien Mao, Chi-Hau Chen
doaj   +1 more source

European Standard Clinical Practice Guideline and EXPeRT Recommendations for the Diagnosis and Management of Gastroenteropancreatic Neuroendocrine Neoplasms in Children and Adolescents

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Pediatric gastroenteropancreatic neuroendocrine neoplasms (GEP‐NENs) are extremely rare and clinically heterogeneous. Management has largely been extrapolated from adult practice. This European Standard Clinical Practice Guideline (ESCP), developed by the EXPeRT network in collaboration with adult NEN experts, provides (adult) evidence ...
Michaela Kuhlen   +23 more
wiley   +1 more source

Risk Prediction Models for Recurrence After Curative Treatment of Early‐Stage or Locally Advanced Lung Cancer: A Systematic Review

open access: yesAging and Cancer, EarlyView.
This systematic review synthesizes prognostic models for survival and recurrence in resected non‐small cell lung cancer. While many models demonstrate moderate to good discrimination, few are externally validated and reporting quality is variable, limiting clinical applicability and highlighting the need for robust, transparent model development ...
Evangeline Samuel   +4 more
wiley   +1 more source

Primary Renal Carcinoid Tumor Mimicking Non-Clear Cell Renal Cell Carcinoma: A Case Report

open access: yes대한영상의학회지, 2016
Carcinoid tumors are neoplasms with neuroendocrine differentiation, and they are most commonly found in the gastrointestinal and respiratory systems. Primary renal carcinoid tumor has rarely been reported.
Leehi Joo   +3 more
doaj   +1 more source

Paediatric development of radiopharmaceutical imaging agents and radioligand therapeutics

open access: yesBritish Journal of Clinical Pharmacology, EarlyView.
Abstract This review focuses on the development of radiopharmaceutical imaging agents and radioligand therapeutics for paediatric use. Nuclear medicine plays an important role in the diagnosis and treatment of various childhood conditions, including cancers, infections and brain disorders.
Justin L. Hay   +5 more
wiley   +1 more source

Disseminated typical bronchial carcinoid tumor [PDF]

open access: yes, 2013
Introduction. Bronchial carcinoids belong to a rare type of lung tumors. If they do not expose outstanding neuroendocrine activity, they develop without clearly visible symptoms. They are often detected during a routine examination. According to their
Cerović Snežana   +6 more
core   +1 more source

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