P3.04-040 A Rare Case of Intrathoracic Mass: Intrathoracic Desmoid Tumor
نویسندگان
چکیده
منابع مشابه
A Rare Intrathoracic Desmoid Type Fibromatosis Tumor: A Case Report
In August, 2013, a 76 year old African American female presented to her family physician with chest pain. A computed tomography (CT) scan identified a 4 cm, well-circumscribed mass of the left lung. Subsequently, on August 23, 2013, the patient underwent a left lung CT-directed fine needle aspiration (FNA) and core biopsy of the mass. An immediate adequacy check of the FNA revealed scant cellul...
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Assistant Professor of Surgery, Department of Surgery, King Edward Medical University/Mayo Hospital, Lahore, Pakistan Professor and Chairman, Department of Surgery, King Edward Medical University/Mayo Hospital, Lahore, Pakistan Department of Internal Medicine, University of Tennessee College of Medicine, Tennessee, USA Department of Surgery, King Edward Medical University/Mayo Hospital, Lahore,...
متن کاملIntrathoracic desmoid tumor with invasion of the great vessels.
A desmoid tumor of the mediastinum was diagnosed and treated in a 35-year-old white male who presented with a right supraclavicular mass. He was treated with resection, which involved several vascular structures, requiring multiple vascular reconstructions followed by post-operative radiotherapy. The authors concluded that, when located in the mediastinum, the invasive character of such tumors ...
متن کاملChest wall desmoid tumor with life-threatening intrathoracic extension.
Fig. 1. The tumor, originating from the right posterior chest wall and involving the 8th, 9th and 10th ribs, had invaded the right thoracic cavity and was causing compression of the right lung and leftward displacement of the mediastinum. The patient had no history of pregnancy or surgical trauma in her chest wall. Preoperatively, the patient’s vital capacity was 940 ml (34% of normal) and echo...
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Abstracts: Dural ectasia is circumferential expansion or dilatation of the dural sac, and has been frequently reported in association with type 1 neurofibromatosis (NF1). It should be differentiated from posterior mediastinal tumors such as neurofibroma, neuroblastoma, and ganglioneuroma because NF-1 has a high risk of tumor formation. In the spinal deformities of NF-1 patients, despite the sco...
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ژورنال
عنوان ژورنال: Journal of Thoracic Oncology
سال: 2017
ISSN: 1556-0864
DOI: 10.1016/j.jtho.2016.11.2155