A Case of Desmoid-Type Fibromatosis Arising after Thoracotomy for Lung Cancer with a Review of the English and Japanese Literature

Chest wall desmoid-type fibromatoses are rare, locally aggressive tumors that occasionally arise from previous thoracotomy sites. Tumors arising from previous sites of thoracotomy to treat malignant disease should be discriminated from the pleural dissemination of the previous malignancy. In this st...

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Veröffentlicht in:Annals of Thoracic and Cardiovascular Surgery 2014, Vol.20(Supplement), pp.465-469
Hauptverfasser: Mori, Takeshi, Yamada, Tatsuya, Ohba, Yasuomi, Yoshimoto, Kentaro, Ikeda, Koei, Shiraishi, Kenji, Suzuki, Makoto
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container_end_page 469
container_issue Supplement
container_start_page 465
container_title Annals of Thoracic and Cardiovascular Surgery
container_volume 20
creator Mori, Takeshi
Yamada, Tatsuya
Ohba, Yasuomi
Yoshimoto, Kentaro
Ikeda, Koei
Shiraishi, Kenji
Suzuki, Makoto
description Chest wall desmoid-type fibromatoses are rare, locally aggressive tumors that occasionally arise from previous thoracotomy sites. Tumors arising from previous sites of thoracotomy to treat malignant disease should be discriminated from the pleural dissemination of the previous malignancy. In this study, we report a case of desmoid-type fibromatosis arising from a site for thoracotomy to treat lung cancer. Additionally we reviewed 15 reported cases of desmoid-type fibromatosis following thoracotomy and summarized their features. A 62-year-old woman was found to have a tumor on computed tomography (CT) at a 1-year routine checkup for lung cancer. The tumor (diameter, 3.4 cm) was located at the previous thoracotomy site. Positron emission tomography (PET) revealed mild 18F-fluorodeoxyglucose (FDG) accumulation in the tumor, with a maximal standardized uptake value (SUVmax) of 1.9. CT-guided biopsy revealed only fibrous tissue. Eighteen months after the biopsy, CT revealed apparent tumor growth, and a biopsy revealed the same histology observed previously. The tumor was removed and diagnosed as desmoid-type fibromatosis. Currently, the patient is alive without recurrence 4 years after desmoid surgery.
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subjects desmoid-type fibromatosis
FDG-PET
Female
Fibroma - etiology
Fibromatosis, Aggressive
Fluorodeoxyglucose F18
Humans
Lung Neoplasms - diagnostic imaging
Lung Neoplasms - surgery
Middle Aged
Positron-Emission Tomography
Postoperative Complications
previous thoracotomy site
Thoracic Neoplasms - etiology
Thoracic Wall
Thoracotomy
Tomography, X-Ray Computed
title A Case of Desmoid-Type Fibromatosis Arising after Thoracotomy for Lung Cancer with a Review of the English and Japanese Literature
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