Literature DB >> 26171068

Radiological and clinical findings of osseous peripheral primitive neuroectodermal tumors.

Chao Wang1, Bin Li1, Xin-Feng Yu1, Min Xuan1, Quan-Quan Gu1, Wei Qian1, Tian-Tian Qiu1, Zhu-Jing Shen1, Min-Ming Zhang1.   

Abstract

Peripheral primitive neuroectodermal tumor (pPNET) is a rare and highly malignant undifferentiated type of tumor. The aim of the present study was to analyze the computed tomography (CT), magnetic resonance imaging (MRI) and clinical findings of osseous pPNET. The present study retrospectively analyzed the clinical data and CT findings from 15 patients with osseous pPNET; the MRI findings from 11 of these 15 patients were confirmed by histopathological examination. The 15 patients included 9 men and 6 women. The mean patient age was 29 years (range, 16-64 years) and 11 cases were aged <30 years. A CT scan was performed in 15 cases and the findings included a lytic lesion (13 cases), a lytic lesion with irregular sclerosis and dilation (2 cases), a soft tissue mass (15 cases), calcification (2 cases) and periosteal reaction (5 cases). A total of 9 cases of soft tissue mass were heterogeneous, with different sizes of lower-density necrotic areas. An enhanced MRI scan was performed in 11 cases. On T1-weighted images (WI), the soft tissue mass was isointense (8 cases) and marginally hyperintense (3 cases). On T2WI, aggressive soft tissue masses were heterogeneous iso- or hyperintense (11 cases). On contrast-enhanced T1WI, marked heterogeneous enhancement was present in 10 cases and intermediate heterogeneous enhancement in 1 case. The results indicated that osseous pPNET mainly affects male adolescents and young adults. The CT findings of osseous pPNET were destructive lesions with a soft tissue mass and, occasionally, with periosteal reaction. The tumor was often isodense, with patchy hypodense areas. Tumor calcification was uncommon. The MRI findings were those of an aggressive soft tissue mass exhibiting isointensity on T1WI and iso- or hyperintensity on T2WI, with marked heterogeneous enhancement. Although the imaging characteristics of pPNETs may be non-specific, CT and MRI may be useful in delineating the extent of the tumor, identifying distant metastases, predicting resectability and monitoring treatment.

Entities:  

Keywords:  bone neoplasm; computed tomography; magnetic resonance imaging; primitive neuroectodermal neoplasm

Year:  2015        PMID: 26171068      PMCID: PMC4487181          DOI: 10.3892/ol.2015.3233

Source DB:  PubMed          Journal:  Oncol Lett        ISSN: 1792-1074            Impact factor:   2.967


  14 in total

Review 1.  Molecular biology of the Ewing's sarcoma/primitive neuroectodermal tumor family.

Authors:  E de Alava; W L Gerald
Journal:  J Clin Oncol       Date:  2000-01       Impact factor: 44.544

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Journal:  Eur J Radiol       Date:  1996-02       Impact factor: 3.528

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4.  Computed tomography and magnetic resonance imaging findings of peripheral primitive neuroectodermal tumors of the head and neck.

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Journal:  Eur J Radiol       Date:  2011-02-26       Impact factor: 3.528

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Journal:  Eur Radiol       Date:  2000       Impact factor: 5.315

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Authors:  P L Khong; G C F Chan; T W H Shek; P K H Tam; F L Chan
Journal:  Clin Radiol       Date:  2002-04       Impact factor: 2.350

8.  Sequestra in primary lymphoma of bone: prevalence and radiologic features.

Authors:  M E Mulligan; M J Kransdorf
Journal:  AJR Am J Roentgenol       Date:  1993-06       Impact factor: 3.959

9.  Imaging findings of abdominal peripheral primitive neuroectodermal tumor: report of four cases with pathological correlation.

Authors:  Jingshan Gong; Yue Zhang; Min Zuo; Zhong Yang; Da Zang; Shiyun Bao; Jianmin Xu; Xiaofang Yu; Xiaomei Wang
Journal:  Clin Imaging       Date:  2009 May-Jun       Impact factor: 1.605

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Authors:  J E Jones; T McGill
Journal:  Arch Otolaryngol Head Neck Surg       Date:  1995-12
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  1 in total

1.  Huge peripheral primitive neuroectodermal tumor of the small bowel mesentery at nonage: A case report and review of the literature.

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Journal:  World J Clin Cases       Date:  2016-09-16       Impact factor: 1.337

  1 in total

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