Intrathoracic Desmoid Tumor

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Intrathoracic 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 ...

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Chest 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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Intrathoracic Desmoid Tumor Presenting as Multiple Lung Nodules 13 Years after Previous Resection of Abdominal Wall Desmoid Tumor

Desmoid tumors are rare soft tissue tumors considered to have locally infiltrative features without distant metastasis until now. Although they are most commonly intraabdominal, very few cases have extra-abdominal locations. The origin of intrathoracic desmoid tumors is predominantly the chest wall with occasional involvement of pleura. True intrathoracic primary desmoid tumors with no involvem...

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Largest recorded non-invasive true intrathoracic desmoid tumour.

Intrathoracic desmoid tumours are rare soft-tissue neoplasms arising from fascial or musculo-aponeurotic structures, accounting for less than 0.03% of all neoplasms. Most cases in fact represent intrathoracic extension of chest wall tumours. This case report describes the largest recorded true intrathoracic desmoid tumour without mediastinal or chest wall invasion. The tumour was completely exc...

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ژورنال

عنوان ژورنال: Journal of the Belgian Society of Radiology

سال: 2015

ISSN: 1780-2393

DOI: 10.5334/jbr-btr.834