Zobrazeno 1 - 10
of 1 296
pro vyhledávání: '"Rare cancer"'
Autor:
Tamsin Farrugia, Saskia F. A. Duijts, Carlene Wilson, Laura Hemming, Christine Cockburn, Evelien Spelten
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-16 (2024)
Abstract Objective Providing current, evidence-based information to cancer survivors is critical for informed decision making. People diagnosed with a rare cancer report higher unmet information needs compared to common cancer survivors. However, int
Externí odkaz:
https://doaj.org/article/0b1ed23e655c4e138d2a192293dccab2
Autor:
Jetty A. M. Weijers, Gerald W. Verhaegh, G. Lassche, Adriana C. H. van Engen-van Grunsven, Chantal M. L. Driessen, Nielka P. van Erp, Marianne A. Jonker, Jack A. Schalken, Carla M. L. van Herpen
Publikováno v:
BMC Cancer, Vol 24, Iss 1, Pp 1-10 (2024)
Abstract Background Salivary duct carcinoma (SDC) is a rare and aggressive subtype of salivary gland cancer, frequently associated with incurable recurrences and distant metastases (R/M). Proliferation of SDC relies on androgen receptor (AR) signalli
Externí odkaz:
https://doaj.org/article/a5bc0409b05e44f287a00260be8d6cfe
Autor:
Shoichi Inokuchi, Kohjiro Shirabe, Satoshi Tsutsumi, Hiroomi Takayama, Takahiro Terashi, Kazuhiro Yasuda, Masahiko Ikebe, Toshio Bandoh, Junpei Wada, Shogo Urabe, Tohru Utsunomiya
Publikováno v:
Surgical Case Reports, Vol 10, Iss 1, Pp 1-5 (2024)
Abstract Background Malignant neoplasms arising from Meckel’s diverticulum are rare and an adenocarcinoma in Meckel’s diverticulum originating from ectopic pancreatic tissue is even rarer. Herein, we report a patient with an ectopic pancreatic ad
Externí odkaz:
https://doaj.org/article/57cbd095aeaa418ca8043d0a822afaae
Incidence of hematologic cancer types in Japan by ICD-O-3 code: analysis of National Cancer Registry
Autor:
Ayako Muramatsu, Tetsuji Kawakami
Publikováno v:
Future Science OA, Vol 10, Iss 1 (2024)
Aim: We classified subtypes of hematologic cancer in Japan’s National Cancer Registry (NCR) in 2016 by ICD-O-3 code and compared numbers with the Japanese Society of Hematology’s Blood Diseases Registry (BDR).Materials & methods: We reviewed data
Externí odkaz:
https://doaj.org/article/6351eaf2d6394b918ee5988022562969
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Sarcomas comprise between 10–15% of all pediatric malignancies. Osteosarcoma and Ewing sarcoma are the two most common pediatric bone tumors diagnosed in children and young adults. These tumors are commonly treated with surgery and/or radiation the
Externí odkaz:
https://doaj.org/article/6a5ae4eae1054e239f87be40f11f3d15
Publikováno v:
European Journal of Case Reports in Internal Medicine (2024)
Positron emission tomography (PET) has gained widespread acceptance as a valuable diagnostic tool for cancer. It is rare for a PET/CT scan to overlook the presence of metastatic disease. Sebaceous carcinoma is an uncommon malignant tumour that typica
Externí odkaz:
https://doaj.org/article/37353abe34cc4da2ad049b2ba600f0db
Autor:
Emily A. Hatanaka, Joshua J. Breunig
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Ependymomas are rare brain tumors that can occur in both children and adults. Subdivided by the tumors’ initial location, ependymomas develop in the central nervous system in the supratentorial or infratentorial/posterior fossa region, or the spina
Externí odkaz:
https://doaj.org/article/b7c836d1f04649dea07e86982669f055
Autor:
Kelly G. Paulson, Vinod Ravi, Brian P. Rubin, Min Park, Elizabeth T. Loggers, Lee D. Cranmer, Michael J. Wagner
Publikováno v:
Cancer Medicine, Vol 12, Iss 14, Pp 15101-15106 (2023)
Abstract Background Malignant hemangioendothelioma is an endothelial cancer with heterogeneous clinical behavior that can range from indolent to aggressive, of which the majority are epithelioid (EHE). Its incidence and demographics have not been pre
Externí odkaz:
https://doaj.org/article/b3ec2e3c2c0f43889a2818e3d3728470
Autor:
Kris Ann P. Schultz, Murali Chintagumpala, Jin Piao, Kenneth S. Chen, Rachana Shah, Robyn D. Gartrell, Emily Christison-Lagay, Farzana Pashnakar, Jesse L. Berry, Allison F. O’Neill, Lauren M. Vasta, Ashley Flynn, Sarah G. Mitchell, Brittani KN. Seynnaeve, Jeremy Rosenblum, Samara L. Potter, Junne Kamihara, Carlos Rodriguez-Galindo, Douglas S. Hawkins, Theodore W. Laetsch
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100024- (2023)
While all childhood cancers are rare, tumors that are particularly infrequent or underrepresented within pediatrics are studied under the umbrella of the Children’s Oncology Group Rare Tumor committee, divided into the Retinoblastoma and Infrequent
Externí odkaz:
https://doaj.org/article/1d78ae7efc7f48d693fb7d9771fddd5b
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Rare cancers represent only 5% of newly diagnosed malignancies. However, in some cases, they account for up to 50% of the deaths attributed to cancer in their corresponding organ. Part of the reason is that treatment options are generally quite limit
Externí odkaz:
https://doaj.org/article/9c95bff8c09741c793f5d4d10bf412ef