Evidence map›Paper›PMID 39517065›Full record

ArticleGeneral thoracic and cardiovascular surgery cases2023

Myxoid solitary fibrous tumor with rapid growth due to increased mucinous components: a case report.

Kaoru Kondo, Toshio Shiotani, Shinichi Furukawa, Mototsugu Watanabe, Kazuhiko Kataoka

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Article in General thoracic and cardiovascular surgery cases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kaoru KondoDepartment of Thoracic Surgery, National Hospital Organization Iwakuni Clinical Center, 1-1-1 Atago-Machi, Iwakuni-City, Yamaguchi, 740-8510, Japan.
Toshio ShiotaniDepartment of Thoracic Surgery, National Hospital Organization Iwakuni Clinical Center, 1-1-1 Atago-Machi, Iwakuni-City, Yamaguchi, 740-8510, Japan. me17036@s.okayama-u.ac.jp.ORCID http://orcid.org/0000-0003-1218-2908
Shinichi FurukawaDepartment of Thoracic Surgery, National Hospital Organization Iwakuni Clinical Center, 1-1-1 Atago-Machi, Iwakuni-City, Yamaguchi, 740-8510, Japan.
Mototsugu WatanabeDepartment of Thoracic Surgery, National Hospital Organization Iwakuni Clinical Center, 1-1-1 Atago-Machi, Iwakuni-City, Yamaguchi, 740-8510, Japan.
Kazuhiko KataokaDepartment of Thoracic Surgery, National Hospital Organization Iwakuni Clinical Center, 1-1-1 Atago-Machi, Iwakuni-City, Yamaguchi, 740-8510, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyxoid solitary fibrous tumors are defined as solitary fibrous tumors with ≥ 50% mucinous components. As they are a rare type of pleural tumor, no reports on their rapid growth before surgery exist. CASE PRESENTATION: Herein, we report the case of a 63-year-old male patient with a myxoid solitary fibrous tumor. The tumor had grown rapidly from 27 to 50 mm over 6 months, and a contrast-enhancing area was observed in approximately one-quarter of the tumor on computed tomography. The tumor was located in the parietal pleura at the ventral part of the left fourth intercostal space without adhesion or invasion into surrounding organs. It was completely resected via video-assisted thoracic surgery. Based on histopathological and immunohistochemical findings, the tumor was identified as a myxoid solitary fibrous tumor. The patient was discharged on postoperative day 2 and has had recurrence-free survival for 6 months postoperatively.

conclusionsTo the best of our knowledge, this is the first case to report the rapid growth of myxoid solitary fibrous tumor despite its predominantly benign nature. Myxoid solitary fibrous tumors should be considered in the differential diagnosis of rapidly growing preoperative tumors.

Indexed as

Myxoid solitary fibrous tumorSolitary fibrous tumorVideo-assisted thoracic surgery

Identifiers

PMID39517065
PMCPMC11533597

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