Zobrazeno 1 - 10
of 1 013
pro vyhledávání: '"Rare tumors"'
Publikováno v:
Клинический разбор в общей медицине, Vol 4, Iss 12, Pp 25-28 (2024)
Rare breast neoplasms are found by physicians in clinical practice. Phyllodes tumor of the breast accounting for 0.3–1% of all breast neoplasms is one of these neoplasms. Today, the phyllodes tumor etiology is unclear, the same as its pathogenesis.
Externí odkaz:
https://doaj.org/article/9a80b5bbf0054d1daba647259f1e013b
Publikováno v:
Case Reports in Women's Health, Vol 43, Iss , Pp e00640- (2024)
A case is described of Ewing sarcoma of the uterus, an atypical presentation of an already rare cancer.A 55-year-old woman presented with abdominal pain, abnormal uterine bleeding and a uterine mass that measured 11 × 10 × 14.5 cm and demonstrated
Externí odkaz:
https://doaj.org/article/83a27f34aa9d4c98b2ae89d45c27f42c
Publikováno v:
Amrita Journal of Medicine, Vol 20, Iss 2, Pp 78-82 (2024)
Peripheral nerve sheath tumors are very rare to arise from the obturator nerve. As such, they are usually not considered one of the imaging diagnostic possibilities for a cystic-solid pelvic mass. The present case involves a 32-year-old man with a kn
Externí odkaz:
https://doaj.org/article/567fe50b88f04d7fb2f6d500518a14f0
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Nephroblastoma or Wilms’ tumor (WT) is the most common pediatric renal malignancy but rare in adults. Treatment protocols for adults are typically extrapolated from pediatric guidelines, but there are no standard guidelines for adults due to the ra
Externí odkaz:
https://doaj.org/article/d7bb86c57ad14ceabe590aecd7e303b4
Autor:
Malgorzata A. Krawczyk, Malgorzata Styczewska, Carla Fernandez, Rita Alaggio, Jaroslaw Szydlowski, Ines B. Brecht, Daniel Orbach, Dominik T. Schneider, Jelena Roganovic, Gianni Bisogno, Calogero Virgone, Jan Godzinski, Andrea Ferrari, Nuno Jorge Farinha, Tal Ben Ami, Luca Bergamaschi, Yves Réguerre, Ewa Bien
Publikováno v:
EJC Paediatric Oncology, Vol 3, Iss , Pp 100141- (2024)
Melanotic neuroectodermal tumor of infancy (MNTI) is a very rare benign neoplasm of probable neurocristic origin. It primarily affects children in the first year of life, with the median age at diagnosis of 4.5 months (range 0–804 months). It usual
Externí odkaz:
https://doaj.org/article/8f796361f1dc4e45bfa1999b29c96f1d
Publikováno v:
EJC Paediatric Oncology, Vol 3, Iss , Pp 100144- (2024)
Externí odkaz:
https://doaj.org/article/1141daafdeff46c8b51b2b661fdd417f
Autor:
Dominik T. Schneider, Andrea Ferrari, Daniel Orbach, Calogero Virgone, Yves Reguerre, Jan Godzinski, Ewa Bien, Jelena Roganovic, Nuno Reis Farinha, Tal Ben-Ami, Teresa Stachowicz-Stencel, Tabea Blessing, Antje Redlich, Apostolos Pourtsidis, Kris Ann P. Schultz, Ines B. Brecht, Gianni Bisogno
Publikováno v:
EJC Paediatric Oncology, Vol 3, Iss , Pp 100137- (2024)
Background: Very rare tumors (VRTs) in children and adolescents are orphan diseases defined by an annual incidence of
Externí odkaz:
https://doaj.org/article/f8238ed80f0344d38345f67c73645da6
Autor:
Giselle L. Saulnier Sholler, Genevieve Bergendahl, Elizabeth C. Lewis, Jacqueline Kraveka, William Ferguson, Abhinav B. Nagulapally, Karl Dykema, Valerie I. Brown, Michael S. Isakoff, Joseph Junewick, Deanna Mitchell, Jawhar Rawwas, William Roberts, Don Eslin, Javier Oesterheld, Randal K. Wada, Devang Pastakia, Virginia Harrod, Kevin Ginn, Raya Saab, Kevin Bielamowicz, Jason Glover, Eugenia Chang, Gina K. Hanna, Daniel Enriquez, Tyler Izatt, Rebecca F. Halperin, Abigail Moore, Sara A. Byron, William P. D. Hendricks, Jeffrey M. Trent
Publikováno v:
Genome Medicine, Vol 16, Iss 1, Pp 1-18 (2024)
Abstract Background Children with relapsed central nervous system (CNS tumors), neuroblastoma, sarcomas, and other rare solid tumors face poor outcomes. This prospective clinical trial examined the feasibility of combining genomic and transcriptomic
Externí odkaz:
https://doaj.org/article/aabaaa1d731d43219ab2b7d7fb61c753
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Due to their unique location, airway tumors have a significant impact on patient quality of life and survival. Current research has focused extensively on malignant airway tumors; however, benign airway tumors, especially rare ones, are less understo
Externí odkaz:
https://doaj.org/article/312093c4ff324b2e90fb98e76624ed47
Autor:
Da Fonseca LG, Yamamoto VJ, Trinconi Cunha M, Torre GS, Araujo RL, Fonseca GM, Chen ATC, Chagas AL, Herman P, Alves VAF, Carrilho FJ
Publikováno v:
Journal of Hepatocellular Carcinoma, Vol Volume 10, Pp 1923-1933 (2023)
Leonardo G Da Fonseca,1,* Victor Junji Yamamoto,1,* Mateus Trinconi Cunha,1 Giovanna Sawaya Torre,2 Raphael LC Araujo,3 Gilton Marques Fonseca,4 Andre Tsin Chih Chen,5 Aline Lopes Chagas,6 Paulo Herman,4 Venancio Avancini Ferreira Alves,7 Fla
Externí odkaz:
https://doaj.org/article/d6909c10dc294a02aac07cb4ecc06eff