Solitary Fibrous Tumor: A Giant Pleural Mass

Loading...
Thumbnail Image

Date

2016-10-10

Journal Title

Journal ISSN

Volume Title

Repository Usage Stats

4
views
1
downloads

Citation Stats

Abstract

INTRODUCTION: Solitary fibrous tumor of pleura (SFTP) is a rare tumor, which represents less than 5% of all pleural tumors. We present a case of SFTP presented to with progressive dyspnea and subsequently work up found out to have SFTP. CASE PRESENTATION: 55- year-old man presented to our institution with slowly progressive exertional dyspnea over the preceding five weeks in conjunction with loss of appetite and 10 kilograms weight loss. Chest CT(computed tomography ) demonstrated a large mass in the right hemithorax (Fig.1A), Characterization by MRI (magnetic resonance imaging) revealed massive 19.0 x 13.8 x 19.3cm heterogeneously enhancing mass with slightly lobulated margins (Fig. 1B) and 18FDG PET (Fluorodeoxyglucose positron emission tomography) scan showed heterogeneously FDG avid mass fills the lower one half of the right thoracic cavity(Fig. 1C). Ultrasound-guided biopsies of the mass were taken and subsequently transsternal resection of huge tumor of the pleura was performed. Gross examination (Fig. 2A) and microscopic histopathology (Fig. 2B) demonstrated malignant solitary fibrous tumor. Currently, the patient remains well without clinical or radiographic evidence of disease recurrent. DISCUSSION: SFTP is mostly isolated, well-defined masses while multifocal ones are rare.[1] The most common symptoms are cough, chest pain, or dyspnea.[2] Sometimes, large tumors can produce symptomatic atelectasis or in rare cases hemoptysis by compression of a bronchus.[2] After an initial approach with chest x-rays, CT scan and MRI of the chest are the best procedure in order to study more clearly the size and location of the tumor and to plan surgery. SFTP cannot be diagnosed only by radiological tools[2] and transthoracic tissue biopsy is essential to reach a diagnosis.[2] The only effective treatment of SFTP is surgical resection removing pulmonary parenchyma compression and allowing the reexpansion of the lung.[1,2] CONCLUSIONS: In conclusion, SFTP is rare benigh tumor. Our patient illustrates the importance of careful clinical evaluation, interpretion of imaging and role of early biopsy to get accurate diagnosis and prompt surgical treatment.

Department

Description

Provenance

Subjects

Citation

Published Version (Please cite this version)

10.1016/j.chest.2016.08.769

Scholars@Duke

Srivali

Narat Srivali

Assistant Professor of Medicine

Material is made available in this collection at the direction of authors according to their understanding of their rights in that material. You may download and use these materials in any manner not prohibited by copyright or other applicable law.