Korean Journal of Radiology

  • 제16권4호
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  • Pages.783-790
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  • 2015
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  • 1229-6929(pISSN)
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  • 2005-8330(eISSN)
대한영상의학회 (The Korean Society of Radiology)
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Imaging Features of Primary Tumors and Metastatic Patterns of the Extraskeletal Ewing Sarcoma Family of Tumors in Adults: A 17-Year Experience at a Single Institution

  • Huh, Jimi (Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine) ;
  • Kim, Kyung Won (Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine) ;
  • Park, Seong Joon (Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine) ;
  • Kim, Hyoung Jung (Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine) ;
  • Lee, Jong Seok (Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine) ;
  • Ha, Hyun Kwon (Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine) ;
  • Tirumani, Sree Harsha (Department of Imaging, Dana-Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School) ;
  • Ramaiya, Nikhil H. (Department of Imaging, Dana-Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School)
  • 투고 : 2015.01.03
  • 심사 : 2015.03.28
  • 발행 : 2015.08.01
⟨ 이전 논문 다음 논문 ⟩

초록

Objective: To comprehensively analyze the spectrum of imaging features of the primary tumors and metastatic patterns of the Extraskeletal Ewing sarcoma family of tumors (EES) in adults. Materials and Methods: We performed a computerized search of our hospital's data-warehouse from 1996 to 2013 using codes for Ewing sarcoma and primitive neuroectodermal tumors as well as the demographic code for ${\geq}18$ years of age. We selected subjects who were histologically confirmed to have Ewing sarcoma of extraskeletal origin. Imaging features of the primary tumor and metastatic disease were evaluated for lesion location, size, enhancement pattern, necrosis, margin, and invasion of adjacent organs. Results: Among the 70 patients (mean age, $35.8{\pm}15.6$ years; range, 18-67 years) included in our study, primary tumors of EES occurred in the soft tissue and extremities (n = 20), abdomen and pelvis (n = 18), thorax (n = 14), paravertebral space (n = 8), head and neck (n = 6), and an unknown primary site (n = 4). Most primary tumors manifested as large and bulky soft-tissue masses (mean size, 9.0 cm; range, 1.3-23.0 cm), frequently invading adjacent organs (45.6%) and showed heterogeneous enhancement (73.7%), a well-defined (66.7%) margin, and partial necrosis/cystic degeneration (81.9%). Notably, 29 patients had metastatic disease detected at their initial diagnosis. The most frequent site of metastasis was lymph nodes (75.9%), followed by bone (31.0%), lung (20.7%), abdominal solid organs (13.8%), peritoneum (13.8%), pleura (6.9%), and brain (3.4%). Conclusion: Primary tumors of EES can occur anywhere and mostly manifest as large and bulky, soft-tissue masses. Lymph nodes are the most frequent metastasis sites.

키워드

과제정보

연구 과제 주관 기관 : National Research Foundation of Korea (NRF)

참고문헌

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피인용 문헌

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  2. Imaging in Soft Tissue Sarcomas vol.25, pp.4, 2016, https://doi.org/10.1016/j.soc.2016.05.002
  3. Rhabdomyosarcoma in Children and Adolescents: Patterns and Risk Factors of Distant Metastasis vol.209, pp.2, 2015, https://doi.org/10.2214/ajr.16.17466
  4. Primitive Neuroectodermal Tumor of Lung in Adult with Hemorrhagic Brain Metastasis: An Extremely Rare Case Scenario vol.38, pp.1, 2015, https://doi.org/10.4103/0971-5851.203491
  5. Extraosseous Ewing’s sarcoma, a case report on a rare diagnosis in an 80-year-old woman with a large abdominal mass vol.21, pp.1, 2015, https://doi.org/10.4102/sajr.v21i1.1183
  6. Extraosseous Ewing's Sarcoma Presented as a Rectal Subepithelial Tumor: Radiological and Pathological Features vol.21, pp.1, 2015, https://doi.org/10.13104/imri.2017.21.1.51
  7. Sarcoma de Ewing extraóseo en cabeza y cuello: revisión de la literatura a propósito de un caso vol.39, pp.2, 2015, https://doi.org/10.1016/j.maxilo.2016.03.003
  8. Rare extraskeletal Ewing’s sarcoma mimicking as adenocarcinoma of the sigmoid vol.117, pp.3, 2015, https://doi.org/10.1080/00015458.2016.1239799
  9. Comparison of clinical features and outcomes in patients with extraskeletal vs skeletal Ewing sarcoma: an SEER database analysis of 3,178 cases vol.10, pp.None, 2018, https://doi.org/10.2147/cmar.s178979
  10. EWING SARCOMA: FEATURES OF LYMPHOGENOUS METASTASIS AND PROGNOSTIC FACTORS vol.18, pp.5, 2015, https://doi.org/10.21294/1814-4861-2019-18-5-29-37
  11. Mediastinal lymph node metastasis as a single expression of disease relapse in Ewing's sarcoma: multidisciplinary approach of two consecutive cases vol.10, pp.3, 2015, https://doi.org/10.5582/irdr.2021.01063
  12. EWSR1(22q12) Translocation Positive Pediatric Adrenal Tumor with Loss of 1p, 11q, and Unbalanced Gain of 17q: Neuroblastoma or Ewing Sarcoma? vol.40, pp.6, 2015, https://doi.org/10.1080/15513815.2020.1745971