Results 31 to 40 of about 991,497 (309)

Prediction of progression-free survival in patients with advanced, well-differentiated, neuroendocrine tumors being treated with a somatostatin analog: the GETNE-TRASGU study [PDF]

open access: yes, 2019
Artículo escrito por un elevado número de autores, sólo se referencian el que aparece en primer lugar, y los autores pertenecientes a la UAMSomatostatin analogs (SSAs) are recommended for the first-line treatment of most patients with well ...
Carmona Bayonas, Alberto   +1 more
core   +1 more source

Patient with recurrent paratesticular malignant mesothelioma and multiple primary neoplasms [PDF]

open access: yesJournal of Men's Health
Paratesticular malignant mesothelioma (MM) is a rare tumor frequently associated with asbestos exposure. Therefore, we present an even rarer case of a 78-year-old male patient diagnosed with multiple primary neoplasms, including prostate cancer, lung ...
Kyung Hwan Kim   +4 more
doaj   +1 more source

Imaging features of rare mesenychmal liver tumours: beyond haemangiomas. [PDF]

open access: yes, 2017
Tumours arising from mesenchymal tissue components such as vascular, fibrous and adipose tissue can manifest in the liver. Although histopathology is often necessary for definitive diagnosis, many of these lesions exhibit characteristic imaging features.
Ahmed, Kareem   +7 more
core   +3 more sources

Synchronous abdominal tumors: is combined laparoscopic surgery in a single approach a safe option?

open access: yesInternational Brazilian Journal of Urology
Background and Purpose: Recent advances in cancer treatment have resulted in bet- ter prognosis with impact on patient's survival, allowing an increase in incidence of a second primary neoplasm.
Marcelo Cartapatti   +9 more
doaj   +1 more source

Multiple Primary Malignant Neoplasms in the Presence of Concomitant Chilaiditi Syndrome

open access: yesTurkish Journal of Colorectal Disease, 2018
Chilaiditi syndrome, jejunal diverticulosis, and multiple primary malignant neoplasms (MPMN) are all relatively rare entities. In this study, clear cell renal cell carcinoma together with adenocarcinoma arising in the rectum were confirmed in an 82-year ...
Ali Ezer, Alper Parlakgümüş
doaj   +1 more source

Evidence-based indications for the planning of PET or PET/CT capacities are needed [PDF]

open access: yes, 2019
Purpose To identify evidence-based indications for PET/PET–CT scans in support of facilities planning and to describe a pilot project in which this information was applied for an investment decision in an Austrian region.
Busse, Reinhard   +4 more
core   +1 more source

Poorly Differentiated Neuroendocrine Carcinoma of Unknown Primary with Metastasis to the Testis: A Case Report

open access: yesCase Reports in Oncology, 2022
Neuroendocrine neoplasms are rare epithelial neoplasms with neuroendocrine differentiation. Few cases of primary testicular poorly differentiated neuroendocrine carcinomas (PD-NECs) have been reported, and secondary testicular neoplasms are rare.
Momoko Sano   +5 more
doaj   +1 more source

Physiopathological Implications of 7TM Receptors [PDF]

open access: yes, 2010
Seven-transmembrane (7TM) receptors are one of the most important proteins involved in perception of extracellular stimuli and regulation of variety of intracellular signaling pathways.
Cygankiewicz, Adam
core   +2 more sources

Clinical Insights Into Hypercalcemia of Malignancy in Childhood

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Hypercalcemia of malignancy (HCM) is a rare but life‐threatening metabolic emergency in children that occurs in less than 1% of pediatric cancer cases, with a reported incidence ranging from 0.4% to 1.0% across different studies. While it is observed in 10%–20% of adult malignancies, pediatric HCM remains relatively uncommon.
Hüseyin Anıl Korkmaz
wiley   +1 more source

Polyneoplasia associated with gastrointestinal stromal tumor: literature review and case report

open access: yesСибирский онкологический журнал, 2020
The purpose of the study was to demonstrate a rare clinical case of polyneoplasia associated with GIST, combining three malignant neoplasms of different nosological affiliation and different tissue origin.
N. V. Vasilyev   +6 more
doaj   +1 more source

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