Pleuropulmonary Solitary Fibrous Tumour with Paraneoplastic Syndrome
نویسندگان
چکیده
منابع مشابه
Solitary fibrous tumour of lung.
Fibrous tumours arising entirely within the substance of the lung are rare. We report one such rare case in whom the diagnosis was established after surgical removal.
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Most pleural neoplasms are metastatic in origin. Primary tumours of the pleura are rare and categorized as diffuse or localized. Diffuse or malignant mesothelioma is more common, related to asbestos exposure, and associated with a poor prognosis. Localized or solitary fibrous tumour (SFT), of the pleura is a less common neoplasm of controversial histogenesis and is unrelated to asbestos exposur...
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Solitary fibrous tumours are rare mesenchymal neoplasms usually arising in the pleura. Extra-pleural locations are uncommon although some cases of head and neck involvement have been reported in the recent literature. In such cases, nose, paranasal cavities and parapharyngeal spaces are the most frequently affected sites. The Authors present a case of a solitary fibrous tumour involving the lat...
متن کاملSolitary fibrous tumour of the pleura.
Solitary fibrous tumour (SFT) of the pleura is a rare, usually benign primary tumour of the pleura. Spectrum of presentation can vary from an incidental finding on chest radiograph done for some other purpose, features of compression of surrounding structures to symptoms resulting from the tumour per se. We report a case of a female who presented with complaints of cough and chest pain in whom ...
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BACKGROUND Solitary fibrous tumour (SFT) is an uncommon mesenchymal neoplasm that most frequently affects the pleura, although it has been reported with increasing frequency in various other sites such as in the peritoneum, pericardium and in non-serosal sites such as lung parenchyma, upper respiratory tract, orbit, thyroid, parotid gland, or thymus. Liver parenchyma is rarely affected. Clinica...
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ژورنال
عنوان ژورنال: International Journal of Human and Health Sciences (IJHHS)
سال: 2020
ISSN: 2523-692X
DOI: 10.31344/ijhhs.v5i2.269