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Books on the topic 'Rhabdomyosarcoma'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Parker, James N., and Philip M. Parker. The official parent's sourcebook on childhood rhabdomyosarcoma. Icon Health Publications, 2002.

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2

M, Maurer Harold, Ruymann Frederick B, and Pochedly Carl, eds. Rhabdomyosarcoma and related tumors in children and adolescents. CRC Press, 1991.

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3

Agnes, Chan Sze Wah. Identification of differentially expressed genes in rhabdomyosarcoma. 2002.

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4

Gee, Matthew Frederick William. Studies of autocrine VEGF signalling in rhabdomyosarcoma. 2004.

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5

Semel, Robert L. The Third Strike: A Father's Story of His Son's Struggle With Cancer. Booklocker.com, 2003.

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6

Pandita, Ajay. Molecular cytogenetic analysis and gene amplification in rhabdomyosarcoma and neuroblastoma. 2000.

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7

Bhumbra, Rej S., Panagiotis D. Gikas, Sammy Hanna, Jakub Jagiello, and Stephen R. Cannon. Malignant tumours of soft tissues. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199550647.003.002004.

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♦ Malignant vascular tumours of soft tissue♦ Synovial sarcoma♦ Malignant peripheral nerve sheath tumours♦ Rhabdomyosarcoma♦ Leiomyosarcoma♦ Epithelioid sarcoma♦ Clear cell sarcoma♦ Malignant fibrous histiocytoma♦ Chordoma.

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8

Taylor, Roger E. Principles of paediatric radiation oncology. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199696567.003.0020.

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Chapter 15 discusses the principles of paediatric radiation oncology, and addresses quality assurance, chemotherapy/radiotherapy interactions, Leukaemia, Hodgkin lymphoma, Non-Hodgkin lymphoma, Neuroblastoma, Rhabdomyosarcoma, Ewing’s sarcoma/peripheral primitive neuroectodermal tumour, Osteosarcoma, central nervous system tumours, Intensity-modulated radiotherapy, and proton therapy for paediatric tumours.

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9

Publications, ICON Health. The Official Parent's Sourcebook on Childhood Rhabdomyosarcoma: A Revised and Updated Directory for the Internet Age. ICON Health Publications, 2002.

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10

Wang, Weiguang. The study of the oncogenic of PAX3, PAX3-FKHR and IGF-11 genes in rhabdomyosarcoma and medulloblastoma. 1998.

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11

Robertson-Höhne, Joan. The role of residual structure in imaging at the end of therapy for the outcome in parameningeal rhabdomyosarcoma. 2008.

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12

Cassidy, Jim, Donald Bissett, Roy A. J. Spence OBE, Miranda Payne, and Gareth Morris-Stiff. Spinal cord compression and bone marrow suppression. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199689842.003.0030.

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Childhood cancer in adults outlines the uncommon challenge presented by the occurrence of these pathologies in young adults, and the need for shared expertise in their successful management. The embryonal tumours, medulloblastoma, retinoblastoma, neuroblastoma, and Wilms’ tumour are considered first, emphasising similarities and differences in the pathology and management of each when adults are compared with children. The soft tissue sarcoma, rhabdomyosarcoma, is frequently best managed with chemotherapy and surgery. The important role of specialist cytogenetics in all these tumours is emphas

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13

Genini, Michele. Isolation and characterization of candidate tumor suppressor genes: Cloning of DRAL, a novel LIM domain protein down-regulated in embryonal rhabdomyosarcoma cells. 1995.

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14

Barlow, Jason William. Studies of p53 regulated genes in Li-Fraumeni syndrome and analysis of the effects of retinoic acid on pediatric rhabdomyosarcoma cell lines. 2003.

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15

Cassidy, Jim, Donald Bissett, Roy A. J. Spence OBE, Miranda Payne, and Gareth Morris-Stiff. Malignancy of unknown primary. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199689842.003.0026.

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Bone and soft tissue malignancies describes a large group of sarcomas, some of which require highly specialist management, including osteosarcoma, Ewing’s sarcoma, and rhabdomyosarcoma, so that referral to an appropriate multidisciplinary team (MDT) is mandatory. Limb conserving surgery combined with pre- and postoperative chemotherapy is curative in the majority of osteosarcomas, and similar approach which may include local radiotherapy also holds for Ewing’s. Other primary bone tumours are reviewed including malignant fibrous histiocytoma, chondrosarcoma, chordoma, solitary plasmacytoma, and

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16

Cassoni, Anna. Sarcomas of soft tissue and bone. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199696567.003.0019.

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