Anaplasia in Wilms tumor: A critical review.

Autor: Vujanić GM; Department of Pathology, Sidra Medicine, Doha, Qatar.; Weill Cornell Medicine - Qatar, Doha, Qatar., Mifsud W; Department of Pathology, Sidra Medicine, Doha, Qatar.; Weill Cornell Medicine - Qatar, Doha, Qatar.

Publikováno v: Pediatric blood & cancer [Pediatr Blood Cancer] 2024 Jul; Vol. 71 (7), pp. e31000. Date of Electronic Publication: 2024 Apr 11.

Bilateral Wilms tumor with anaplasia: A report from the Children's Oncology Group Study AREN0534.

Autor: Romao RLP; Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada., Aldrink JH; Nationwide Children's Hospital, The Ohio State University, Columbus, Ohio, USA., Renfro LA; Division of Biostatistics, University of Southern California and Children's Oncology Group, Los Angeles, California, USA., Mullen EA; Boston Children's Hospital and Dana Farber Cancer Institute, Boston, Massachusetts, USA., Murphy AJ; St Jude's Children's Research Hospital, Memphis, Tennessee, USA., Brzezinski J; Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada., Malek MM; Children's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, Pennsylvania, USA., Benedetti DJ; Monroe Carell Jr Children's Hospital at Vanderbilt, Vanderbilt University Medical Center, Nashville, Tennessee, USA., Cost NG; The Surgical Oncology Program at the Children's Hospital of Colorado, University of Colorado, Denver, Colorado, USA., Smith E; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Dome JS; Children National Hospital, George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, USA., Davidoff AM; St Jude's Children's Research Hospital, Memphis, Tennessee, USA., Treece A; Children's Hospital of Alabama, Birmingham, Alabama, USA., Parsons LN; Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA., Fernandez CV; IWK Health, Dalhousie University, Halifax, Nova Scotia, Canada., Tornwall B; Department of Biostatistics, University of Florida, Gainesville, Florida, USA., Shamberger RC; Boston Children's Hospital and Dana Farber Cancer Institute, Boston, Massachusetts, USA., Paulino A; MD Anderson Cancer Center Houston, Houston, Texas, USA., Kalapurakal JA; Ann & Robert H. Lurie Children's Hospital, Chicago, Illinois, USA., Geller JI; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA., Ehrlich PF; Section of Pediatric Surgery, C.S. Mott Children's Hospital University of Michigan, Ann Arbor, Michigan, USA.

Publikováno v: Pediatric blood & cancer [Pediatr Blood Cancer] 2024 Jul; Vol. 71 (7), pp. e30981. Date of Electronic Publication: 2024 Apr 18.

A case of a pilocytic astrocytoma with histological features of anaplasia and unprecedent genetic alterations.

Autor: Moritsubo M; Department of Pathology, Kurume University School of Medicine, Kurume, Japan., Furuta T; Department of Pathology, Kurume University School of Medicine, Kurume, Japan., Negoto T; Department of Neurosurgery, Kurume University School of Medicine, Kurume, Japan., Nakamura H; Department of Neurosurgery, Kurume University School of Medicine, Kurume, Japan., Uchiyama Y; Department of Radiology, Kurume University School of Medicine, Kurume, Japan., Morioka M; Department of Neurosurgery, Kurume University School of Medicine, Kurume, Japan., Oshima K; Department of Pathology, Kurume University School of Medicine, Kurume, Japan., Sugita Y; Department of Pathology, Kurume University School of Medicine, Kurume, Japan.; Department of Neuropathology, St. Mary's Hospital, Kurume, Japan.

Publikováno v: Neuropathology : official journal of the Japanese Society of Neuropathology [Neuropathology] 2024 Apr; Vol. 44 (2), pp. 161-166. Date of Electronic Publication: 2023 Oct 01.

Anaplasia in childhood rhabdomyosarcoma: An under reported entity

Autor: Manisha Ahuja, Reena Tomar, Shruti Thakur, Varuna Mallya, Shramana Mandal, Nita Khurana, Y K Sarin

Publikováno v: Indian Journal of Pathology and Microbiology, Vol 65, Iss 4, Pp 864-868 (2022)

Background: Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children. Anaplasia is a rare phenomenon seen in childhood RMS. The most common histologic subtype was Embryonal followed by Alveolar and spindle subtype. Design: A total of

Externí odkaz: https://doaj.org/article/81558c97469f4195a95fefd996b022bd

Anaplasia in childhood rhabdomyosarcoma: An under reported entity.

Autor: Ahuja, Manisha¹ (AUTHOR), Tomar, Reena¹ (AUTHOR), Thakur, Shruti¹ (AUTHOR), Mallya, Varuna¹ (AUTHOR), Mandal, Shramana¹ (AUTHOR), Khurana, Nita¹ (AUTHOR), Sarin, Y² (AUTHOR), Sarin, Y K³ (AUTHOR)

Publikováno v: Indian Journal of Pathology & Microbiology. Oct-Dec2022, Vol. 65 Issue 4, p864-868. 5p.