2010Experimental PathologyRequires access

Extrapleual solitary fibrous tumors:a clinicopathologic study of 39 cases

Na Jiang

Open publisher page 1 citations

Abstract

Purpose To investigate the clinicopathologic and immunohistochemical features of extrapleural solitary fibrous tumors (E-SFT) and their biologic behaviors. Methods The clinical pathologic data were reviewed retrospectively and immunohistochmical stains were performed in 39 case of E-SFT. Results 25 cases were females and 14 cases were males,affected age ranged from 15 to 81 years (mean,41.2 years). The sites of E-SFT involvement were soft tissue (15 cases),orbit (8 cases),retroperitoneum (4 cases),pelvis (3 cases),cranial cavity (4 cases),kidney (2 cases),urinary bladder (1 case),lung (1 case),and nasal cavity (1 case). Histologically,the tumors showed a wide range of growth patterns,varied form predominantly fibrous lesions containing large collagenized areas to more cellular and less fibrous areas,with thick-walled branching vessels showing HPC-like growth pattern. Myxoid degeneration and fat-forming areas were noted. There were four categories,including fibrous SFT,cellular SFT,giant-cell-rich SFT and fat-forming SFT. Immunohistochemically,all cases of the tumor cells showed diffusely and strongly positive for both vimentin and CD34,less frequently positive for CD99 (20/24),bcl-2 (18/24). Conclusion SFTs are rare mesenchymal spindle cell tumors,which could be found in various sites of human body and need to be distinguished from other spindle cell tumors.

About this research paper

What this paper is about

Purpose To investigate the clinicopathologic and immunohistochemical features of extrapleural solitary fibrous tumors (E-SFT) and their biologic behaviors. Methods The clinical pathologic data were reviewed retrospectively and immunohistochmical stains were performed in 39 case of E-SFT. Results 25 cases were females and 14 cases were males,affected age ranged from 15 to 81 years (mean,41.2 years). The sites of E-SFT involvement were soft tissue (15 cases),orbit (8 cases),retroperitoneum (4 cases),pelvis (3 cases),cranial cavity (4 cases),kidney (2 cases),urinary bladder (1 case),lung (1 case),and nasal cavity (1 case). Histologically,the tumors showed a wide range of growth patterns,varied form predominantly fibrous lesions containing large collagenized areas to more cellular and less fibrous areas,with thick-walled branching vessels showing HPC-like growth pattern. Myxoid degeneration and fat-forming areas were noted. There were four categories,including fibrous SFT,cellular SFT,giant-cell-rich SFT and fat-forming SFT. Immunohistochemically,all cases of the tumor cells showed diffusely and strongly positive for both vimentin and CD34,less frequently positive for CD99 (20/24),bcl-2 (18/24). Conclusion SFTs are rare mesenchymal spindle cell tumors,which could be found in various sites of human body and need to be distinguished from other spindle cell tumors.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Purpose To investigate the clinicopathologic and immunohistochemical features of extrapleural solitary fibrous tumors (E-SFT) and their biologic behaviors. Methods The clinical pathologic data were reviewed retrospectively and immunohistochmical stains were performed in 39 case of E-SFT. Results 25 cases were females and 14 cases were males,affected age ranged from 15 to 81 years (mean,41.2 years). The sites of E-SFT involvement were soft tissue (15 cases),orbit (8 cases),retroperitoneum (4 cases),pelvis (3 cases),cranial cavity (4 cases),kidney (2 cases),urinary bladder (1 case),lung (1 case),and nasal cavity (1 case). Histologically,the tumors showed a wide range of growth patterns,varied form predominantly fibrous lesions containing large collagenized areas to more cellular and less fibrous areas,with thick-walled branching vessels showing HPC-like growth pattern. Myxoid degeneration and fat-forming areas were noted. There were four categories,including fibrous SFT,cellular SFT,giant-cell-rich SFT and fat-forming SFT. Immunohistochemically,all cases of the tumor cells showed diffusely and strongly positive for both vimentin and CD34,less frequently positive for CD99 (20/24),bcl-2 (18/24). Conclusion SFTs are rare mesenchymal spindle cell tumors,which could be found in various sites of human body and need to be distinguished from other spindle cell tumors.

Key concepts: Solitary fibrous tumor, CD34, CD99, Vimentin, Pathology, Nasal cavity, Immunohistochemistry, Mesenchymal stem cell

Related papers

Back to paper searchBrowse research topicsOriginal source
Extrapleual solitary fibrous tumors:a clinicopathologic study of 39 cases — Research Paper | ScholarLens