Literature DB >> 16971354

Ultrastructure of low-grade intraosseous osteosarcoma of bone: a comparative study with fibrous dysplasia and parosteal osteosarcoma.

German C Steiner1, Michael Forest, Marie C Vacher-Lavenu.   

Abstract

The ultrastructure of low-grade intraosseous osteosarcoma (LGOS) is not well documented in the literature. Four cases of LGOS are described with an emphasis on its distinguishing characteristics as well those it shares with other lesions. The predominant cells of LGOS are fibroblasts with well-developed rough endoplasmic reticulum and mild focal immunoreactivity to SMA and MSA. Few osteoblasts and myofibroblasts are present. Transition cells between fibroblasts and osteoblasts are also noted. The fibroblasts are closely related to osteoblasts from a histological and functional point of view, and phenotypically are probably modified osteoblasts. Comparative ultrastructural studies between LGOS and fibrous dysplasia (FD) reveal basic similarities, although the cells in LGOS are larger with more of an abundance of organelles. Therefore, accurate differentiation between these two lesions rests at the histological and radiological levels. LGOS and parosteal osteosarcomas (PO) also share similar ultrastructural features. In the case samples in this study, an unusual type of multilayered amorphous material was found in the osteoid matrix of a case of LGOS and one of PO. This probably emphasizes the morphologic similarities between these 2 tumors.

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Year:  2006        PMID: 16971354     DOI: 10.1080/019131290969479

Source DB:  PubMed          Journal:  Ultrastruct Pathol        ISSN: 0191-3123            Impact factor:   1.094


  6 in total

1.  Fibrous dysplasia: an unusual case of a very aggressive form with costo-vertebral joint destruction and invasion of the contralateral D7 vertebral body.

Authors:  Carmine Zoccali; Dario Attala; Barbara Rossi; Giovanni Zoccali; Virginia Ferraresi
Journal:  Skeletal Radiol       Date:  2018-05-23       Impact factor: 2.199

2.  Multifocal low-grade central osteosarcoma: a rare case.

Authors:  Richard Boyle; Bruno Giuffre; S Fiona Bonar
Journal:  Skeletal Radiol       Date:  2016-04-05       Impact factor: 2.199

3.  Smooth muscle actin expression in primary bone tumours.

Authors:  F Hemingway; T G Kashima; G Mahendra; A Dhongre; P C W Hogendoorn; F Mertens; N A Athanasou
Journal:  Virchows Arch       Date:  2012-04-28       Impact factor: 4.064

Review 4.  Utility of transmission electron microscopy in small round cell tumors.

Authors:  Na Rae Kim; Seung Yeon Ha; Hyun Yee Cho
Journal:  J Pathol Transl Med       Date:  2015-03-12

5.  Spontaneous extraskeletal osteosarcoma with various histological growth patterns in the abdominal wall of an ICR mouse.

Authors:  Tsuyoshi Ito; Yoshitaka Katoh; Yuko Shimada; Aya Ohnuma-Koyama; Naofumi Takahashi; Maki Kuwahara; Takanori Harada
Journal:  J Toxicol Pathol       Date:  2015-10-05       Impact factor: 1.628

6.  Secretory defects in pediatric osteosarcoma result from downregulation of selective COPII coatomer proteins.

Authors:  Rachael K Wood; Ashley R Flory; Melissa J Mann; Lindsay J Talbot; Linda M Hendershot
Journal:  iScience       Date:  2022-03-17
  6 in total

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