An intrathoracic giant tumour and vanishing lung cyst after tumour resection

Abstract A 65‐year‐old woman was brought to the emergency unit with an approximately 6‐month history of persistent fever and cough. Chest computed tomography (CT) demonstrated a 16‐cm heterogeneous mass with adjacent large cyst (approximately 4.0 cm). The patient underwent CT‐guided biopsy, and beni...

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Main Authors: Masashi Nishimura, Shinichiro Ota, Sumitaka Yamanaka, Kanako Shinada, Masaharu Shinkai
Format: Article
Language:English
Published: Wiley 2021-10-01
Series:Respirology Case Reports
Subjects:
Online Access:https://doi.org/10.1002/rcr2.848
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spelling doaj-3237d6a8071a44589ded9adada4f14622021-09-27T08:52:29ZengWileyRespirology Case Reports2051-33802021-10-01910n/an/a10.1002/rcr2.848An intrathoracic giant tumour and vanishing lung cyst after tumour resectionMasashi Nishimura0Shinichiro Ota1Sumitaka Yamanaka2Kanako Shinada3Masaharu Shinkai4Department of Respiratory Medicine Tokyo Shinagawa Hospital Tokyo JapanDepartment of Respiratory Medicine Tokyo Shinagawa Hospital Tokyo JapanDepartment of Thoracic Surgery Tokyo Shinagawa Hospital Tokyo JapanDepartment of Respiratory Medicine Tokyo Shinagawa Hospital Tokyo JapanDepartment of Respiratory Medicine Tokyo Shinagawa Hospital Tokyo JapanAbstract A 65‐year‐old woman was brought to the emergency unit with an approximately 6‐month history of persistent fever and cough. Chest computed tomography (CT) demonstrated a 16‐cm heterogeneous mass with adjacent large cyst (approximately 4.0 cm). The patient underwent CT‐guided biopsy, and benign solitary fibrous tumour (SFT) was immunohistochemically diagnosed. As the symptoms were thought to be due to enlargement of the tumour, surgery was deemed necessary, and the tumour was successfully resected. Based on morphological and immunohistochemical examination of the resected specimen, the final diagnosis was dedifferentiated SFT (DSFT). Follow‐up CT verified disappearance of the pulmonary cyst. The cyst was speculated to be caused by a check valve mechanism, which may also suggest a rapid growth of the tumour. At the time of writing, 2 years post‐operatively, no tumour recurrence has been identified. This represents the first report of intrathoracic giant DSFT with a cystic lesion returning to normal lung parenchyma.https://doi.org/10.1002/rcr2.848cystdedifferentiated solitary fibrous tumour (DSFT)giant tumourthree‐dimensional computed tomography (3D‐CT)
collection DOAJ
language English
format Article
sources DOAJ
author Masashi Nishimura
Shinichiro Ota
Sumitaka Yamanaka
Kanako Shinada
Masaharu Shinkai
spellingShingle Masashi Nishimura
Shinichiro Ota
Sumitaka Yamanaka
Kanako Shinada
Masaharu Shinkai
An intrathoracic giant tumour and vanishing lung cyst after tumour resection
Respirology Case Reports
cyst
dedifferentiated solitary fibrous tumour (DSFT)
giant tumour
three‐dimensional computed tomography (3D‐CT)
author_facet Masashi Nishimura
Shinichiro Ota
Sumitaka Yamanaka
Kanako Shinada
Masaharu Shinkai
author_sort Masashi Nishimura
title An intrathoracic giant tumour and vanishing lung cyst after tumour resection
title_short An intrathoracic giant tumour and vanishing lung cyst after tumour resection
title_full An intrathoracic giant tumour and vanishing lung cyst after tumour resection
title_fullStr An intrathoracic giant tumour and vanishing lung cyst after tumour resection
title_full_unstemmed An intrathoracic giant tumour and vanishing lung cyst after tumour resection
title_sort intrathoracic giant tumour and vanishing lung cyst after tumour resection
publisher Wiley
series Respirology Case Reports
issn 2051-3380
publishDate 2021-10-01
description Abstract A 65‐year‐old woman was brought to the emergency unit with an approximately 6‐month history of persistent fever and cough. Chest computed tomography (CT) demonstrated a 16‐cm heterogeneous mass with adjacent large cyst (approximately 4.0 cm). The patient underwent CT‐guided biopsy, and benign solitary fibrous tumour (SFT) was immunohistochemically diagnosed. As the symptoms were thought to be due to enlargement of the tumour, surgery was deemed necessary, and the tumour was successfully resected. Based on morphological and immunohistochemical examination of the resected specimen, the final diagnosis was dedifferentiated SFT (DSFT). Follow‐up CT verified disappearance of the pulmonary cyst. The cyst was speculated to be caused by a check valve mechanism, which may also suggest a rapid growth of the tumour. At the time of writing, 2 years post‐operatively, no tumour recurrence has been identified. This represents the first report of intrathoracic giant DSFT with a cystic lesion returning to normal lung parenchyma.
topic cyst
dedifferentiated solitary fibrous tumour (DSFT)
giant tumour
three‐dimensional computed tomography (3D‐CT)
url https://doi.org/10.1002/rcr2.848
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