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Solitary fibrous tumor of the lung: a case report

Solitary fibrous tumors (SFTs) are relatively rare neoplasms that commonly occur in the pleura. The pathological feature of SFTs is a proliferation of spindle-shaped cells in interlacing or storiform fascicles. SFTs appear to derived from pluripotential submesothelial cells, but not the covering mes...

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Autores principales: Ichiki, Yoshinobu, Kakizoe, Keisei, Hamatsu, Takayuki, Matsuyama, Atsuji, Suehiro, Taketoshi, Tanaka, Fumihiro, Hisaoka, Masanori, Sugimachi, Keizo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5218951/
https://www.ncbi.nlm.nih.gov/pubmed/28063145
http://dx.doi.org/10.1186/s40792-016-0286-7
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author Ichiki, Yoshinobu
Kakizoe, Keisei
Hamatsu, Takayuki
Matsuyama, Atsuji
Suehiro, Taketoshi
Tanaka, Fumihiro
Hisaoka, Masanori
Sugimachi, Keizo
author_facet Ichiki, Yoshinobu
Kakizoe, Keisei
Hamatsu, Takayuki
Matsuyama, Atsuji
Suehiro, Taketoshi
Tanaka, Fumihiro
Hisaoka, Masanori
Sugimachi, Keizo
author_sort Ichiki, Yoshinobu
collection PubMed
description Solitary fibrous tumors (SFTs) are relatively rare neoplasms that commonly occur in the pleura. The pathological feature of SFTs is a proliferation of spindle-shaped cells in interlacing or storiform fascicles. SFTs appear to derived from pluripotential submesothelial cells, but not the covering mesothelium. SFTs distinctively show diffuse staining for CD34 but lack staining for smooth muscle markers. We herein report a relatively rare case of a 68-year-old male patient without symptoms, who underwent resection for what was considered to be SFT.
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spelling pubmed-52189512017-01-18 Solitary fibrous tumor of the lung: a case report Ichiki, Yoshinobu Kakizoe, Keisei Hamatsu, Takayuki Matsuyama, Atsuji Suehiro, Taketoshi Tanaka, Fumihiro Hisaoka, Masanori Sugimachi, Keizo Surg Case Rep Case Report Solitary fibrous tumors (SFTs) are relatively rare neoplasms that commonly occur in the pleura. The pathological feature of SFTs is a proliferation of spindle-shaped cells in interlacing or storiform fascicles. SFTs appear to derived from pluripotential submesothelial cells, but not the covering mesothelium. SFTs distinctively show diffuse staining for CD34 but lack staining for smooth muscle markers. We herein report a relatively rare case of a 68-year-old male patient without symptoms, who underwent resection for what was considered to be SFT. Springer Berlin Heidelberg 2017-01-07 /pmc/articles/PMC5218951/ /pubmed/28063145 http://dx.doi.org/10.1186/s40792-016-0286-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Report
Ichiki, Yoshinobu
Kakizoe, Keisei
Hamatsu, Takayuki
Matsuyama, Atsuji
Suehiro, Taketoshi
Tanaka, Fumihiro
Hisaoka, Masanori
Sugimachi, Keizo
Solitary fibrous tumor of the lung: a case report
title Solitary fibrous tumor of the lung: a case report
title_full Solitary fibrous tumor of the lung: a case report
title_fullStr Solitary fibrous tumor of the lung: a case report
title_full_unstemmed Solitary fibrous tumor of the lung: a case report
title_short Solitary fibrous tumor of the lung: a case report
title_sort solitary fibrous tumor of the lung: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5218951/
https://www.ncbi.nlm.nih.gov/pubmed/28063145
http://dx.doi.org/10.1186/s40792-016-0286-7
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