scholarly journals iCREATE: imaging features of primary and metastatic alveolar soft part sarcoma from the EORTC CREATE study

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Naami Charlotte Mcaddy ◽  
Hind Saffar ◽  
Saskia Litière ◽  
Pieter Jespers ◽  
Patrick Schöffski ◽  
...  

Abstract Background Alveolar Soft Part Sarcoma (ASPS) is a rare, slow-growing, but highly vascular soft tissue sarcoma, characterised by a high rate of metastases at presentation. Although imaging features of the primary are well described, less detail is available on the imaging pattern of metastatic ASPS. The EORTC 90101 (CREATE) study assessed the efficacy of Crizotinib in patients with metastatic ASPS and presents a unique opportunity to describe the imaging phenotype of primary and metastatic ASPS, based on prospectively collected imaging. Methods A retrospective review of the staging CT scans of 32 patients with ASPS from the CREATE study was undertaken and the imaging features of primary and metastatic disease were assessed. Results Imaging of the primary tumour was available in 7/32 cases (28%). All primary tumours demonstrated marked vascularity with prominent feeding vessels (7/7, 100%). The most frequent sites of metastases included lung (30/32, 94%), nodal (7/32, 22%), bone (5/32, 16%) and muscle/subcutaneous (5/32, 16%). Features of hypervascularity were identified at all sites, more appreciable in the lungs, with feeding vessels frequently demonstrated in pulmonary metastases (21/32, 66%). Conclusion Analysis of imaging from the CREATE cohort of patients with metastatic ASPS demonstrates that metastases from ASPS are predominantly hypervascular and demonstrate feeding vessels comparable to primary ASPS, suggesting potential sensitivity of this rare sarcoma for antivascular/antiangiogenic treatment approaches.

2021 ◽  
Vol 15 (10) ◽  
pp. 20-26
Author(s):  
Satyam Satyam ◽  
Alpana Manchanda ◽  
Ramya Kamraj ◽  
Anju Garg ◽  
Kaushik Majumdar

Alveolar soft part sarcoma is a rare soft tissue tumor with uncertain histogenesis. It is a slow growing tumor with a high rate of metastasis. The tumor is not easily identified as clinical symptoms are not pronounced. The retroperitoneum is a rare location of tumor, with a few cases published in literature. Surgical excision is the mainstay of treatment. Here we describe a rare case of a large retroperitoneal Alveolar soft part sarcoma in a young female with radiological and histopathological findings.


2000 ◽  
Vol 1 (1) ◽  
pp. 56 ◽  
Author(s):  
Joon-Il Choi ◽  
Jin Mo Goo ◽  
Joon Beom Seo ◽  
Hyae Young Kim ◽  
Choong Ki Park ◽  
...  

2014 ◽  
Vol 203 (6) ◽  
pp. 1345-1352 ◽  
Author(s):  
M. Beth McCarville ◽  
Sofia Muzzafar ◽  
Simon C. Kao ◽  
Cheryl M. Coffin ◽  
David M. Parham ◽  
...  

Author(s):  
Shilpa Kaushal ◽  
Muninder K. Negi

Alveolar soft-part sarcoma (ASPS) is an extremely rare connective tissue tumor, predominantly seen in adolescents and young adults, with a female preponderance. Alveolar soft-part sarcoma (ASPS) is a slow growing tumor, but with high likelihood of metastasis, leading to high mortality. A classical histopathological feature of an alveolar pattern from the biopsy of the lesion favors the diagnosis. We report a case of 14 years old male patient who presented with a history of single painless swelling over thigh for which surgical excision was done. Histopathology was suggestive of Alveolar soft-part sarcoma (ASPS). There was no evidence of distant metastases. He was treated with external beam radiotherapy in view of vascular invasion.


2011 ◽  
Vol 57 (6) ◽  
pp. 1071-1073 ◽  
Author(s):  
Nuria Conde ◽  
Ofelia Cruz ◽  
Asteria Albert ◽  
Jaume Mora

2014 ◽  
Vol 87 (1036) ◽  
pp. 20130719 ◽  
Author(s):  
S Sood ◽  
A D Baheti ◽  
A B Shinagare ◽  
J P Jagannathan ◽  
J L Hornick ◽  
...  

Author(s):  
Malvika Gulati ◽  
Abhenil Mittal ◽  
Adarsh Barwad ◽  
Rambha Pandey ◽  
Sameer Rastogi ◽  
...  

Abstract Context Alveolar soft part sarcoma (ASPS) is a rare soft tissue tumor most commonly occurring in deep intramuscular plane of lower extremities of adolescents and young adults. It is a highly vascular, slow growing tumor with malignant potential having lung as the most common site of metastases at the time of presentation. Aims The aim is to review the imaging findings of ASPS and determine characteristic imaging features of this rare tumor. Materials and Methods Sixteen patients having histopathological diagnosis and preoperative imaging of ASPS attending the dedicated sarcoma clinic at our institute were included in the study. The demographic, clinical, and imaging data were retrieved from the case records and then evaluated for characteristic imaging features which may raise suspicion of ASPS. Results The patients ranged from 3 to 72 years of age and with a slight male preponderance. Of the eight CECTs evaluated, 62.5% tumors showed well-defined lobulated margins, 87.5% cases showed intense enhancement with presence of feeder vessels. On CEMRI of 10 patients, 70% had well circumscribed lobulated margins with intense enhancement and tortuous flow voids in most of them. All cases showed T2 hyperintense signal. Fourteen of 16 (87.5%) patients had metastatic disease with lung as the most common site (92.8%). Conclusion ASPS is a rare soft tissue sarcoma seen in children and young adults. Imaging may mimic a vascular malformation due to the presence of tortuous feeders. Misdiagnosis at an early stage may lead to later metastatic presentation of the disease, thus emphasizing the need to suspect it on imaging.


1988 ◽  
Vol 27 (6) ◽  
pp. 974-977
Author(s):  
Hideaki MIYAMOTO ◽  
Toshiki HIROSE ◽  
Miharu TSUCHIYA ◽  
Kimiko MAEKAWARA ◽  
Harumi YAMAMURA ◽  
...  

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