Cheryl M. Coffin
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Cheryl M. Coffin has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
- David M. Parham
Department of Pathology and Laboratory Medicine, Children's Hospital of Los Angeles and University of Southern California, Keck School of Medicine, Los Angeles, CA
2 shared publications - Mary Beth McCarville
Department of Radiology, St Jude Children's Research Hospital, Memphis, TN
2 shared publications - Sheri L. Spunt
Department of Pediatrics Stanford University School of Medicine Stanford California USA
2 shared publications - Simon Ching-Shun Kao
University of Iowa Carver College of Medicine, Iowa City, IA
2 shared publications Aurore Coulomb-L’hErmine
Chief, Department of Pathology and Cytology, Hôpital Armand-Trousseau, Paris, France
1 shared publication- Douglas S. Hawkins
Seattle Children's Hospital Seattle Washington USA
1 shared publication
Latest Publications
- 29 January 2018
- Published by SAGE Publications in Pediatric and Developmental Pathology
- Vol. 21 (1) , 3-5
In Memoriam: Liliane Boccon-Gibod, M.D., 1941–2017
- 29 January 2018
- Published by SAGE Publications in Pediatric and Developmental Pathology
- Vol. 21 (1) , 3-5
In Memoriam: Liliane Boccon-Gibod, M.D., 1941–2017
- 1 November 2015
- Published by SAGE Publications in Pediatric and Developmental Pathology
- Vol. 18 (6) , 481-494
The Evolution of Pediatric Soft Tissue Sarcoma Classification in the Last 50 Years
This review discusses the history of the classification of soft tissue sarcomas in children and adolescents, the current transition toward integration of morphology and molecular genetics as new entities emerge, and future perspectives.
- 1 November 2015
- Published by SAGE Publications in Pediatric and Developmental Pathology
- Vol. 18 (6) , 481-494
The Evolution of Pediatric Soft Tissue Sarcoma Classification in the Last 50 Years
This review discusses the history of the classification of soft tissue sarcomas in children and adolescents, the current transition toward integration of morphology and molecular genetics as new entities emerge, and future perspectives.
- 1 August 2015
- Published by American Roentgen Ray Society in American Journal of Roentgenology
- Vol. 205 (2) , 414-420
MRI and CT of Low-Grade Fibromyxoid Sarcoma in Children: A Report From Children's Oncology Group Study ARST0332
OBJECTIVE. The purpose of this article is to determine the MRI and CT features of low-grade fibromyxoid sarcoma in children. MATERIALS AND METHODS. We retrospectively analyzed images of 11 pediatri...
- 1 August 2015
- Published by American Roentgen Ray Society in American Journal of Roentgenology
- Vol. 205 (2) , 414-420
MRI and CT of Low-Grade Fibromyxoid Sarcoma in Children: A Report From Children's Oncology Group Study ARST0332
OBJECTIVE. The purpose of this article is to determine the MRI and CT features of low-grade fibromyxoid sarcoma in children. MATERIALS AND METHODS. We retrospectively analyzed images of 11 pediatri...
- 1 December 2014
- Published by American Roentgen Ray Society in American Journal of Roentgenology
- Vol. 203 (6) , 1345-1352
Imaging Features of Alveolar Soft-Part Sarcoma: A Report From Children's Oncology Group Study ARST0332
OBJECTIVE. There are few studies in the literature regarding the imaging features of alveolar soft-part sarcoma (ASPS). We performed a comprehensive assessment of the imaging characteristics of this rare tumor to determine whether there are features that suggest the diagnosis. MATERIALS AND METHODS. Twenty-two subjects with ASPS underwent pretherapy imaging as part of enrollment in Children's Oncology Group protocol ARST0332 for the treatment of nonrhabdomyosarcoma soft-tissue sarcomas: 16 patients underwent MRI; three, CT; and three, both MRI and CT. Two radiologists retrospectively reviewed the imaging studies by consensus and recorded tumor location, size, contour, internal architecture, signal characteristics, presence of flow voids, and enhancement patterns. RESULTS. The 12 females and 10 males in the study group ranged in age from 8 to 23 years 7 months (mean, 15 years 8 months). The most common anatomic site was the lower extremity (12/22, 55%) followed by the upper extremity (4/22, 18%). The maxim...
- 1 December 2014
- Published by American Roentgen Ray Society in American Journal of Roentgenology
- Vol. 203 (6) , 1345-1352
Imaging Features of Alveolar Soft-Part Sarcoma: A Report From Children's Oncology Group Study ARST0332
OBJECTIVE. There are few studies in the literature regarding the imaging features of alveolar soft-part sarcoma (ASPS). We performed a comprehensive assessment of the imaging characteristics of this rare tumor to determine whether there are features that suggest the diagnosis. MATERIALS AND METHODS. Twenty-two subjects with ASPS underwent pretherapy imaging as part of enrollment in Children's Oncology Group protocol ARST0332 for the treatment of nonrhabdomyosarcoma soft-tissue sarcomas: 16 patients underwent MRI; three, CT; and three, both MRI and CT. Two radiologists retrospectively reviewed the imaging studies by consensus and recorded tumor location, size, contour, internal architecture, signal characteristics, presence of flow voids, and enhancement patterns. RESULTS. The 12 females and 10 males in the study group ranged in age from 8 to 23 years 7 months (mean, 15 years 8 months). The most common anatomic site was the lower extremity (12/22, 55%) followed by the upper extremity (4/22, 18%). The maxim...