Rare thoracic mass lesion--myofibrobastoma.

dc.contributor.authorSahni, Vaibhaven_US
dc.contributor.authorSunandan, Sikdaren_US
dc.contributor.authorAgarwal, Satish Ken_US
dc.contributor.authorSingh, Narinder Pen_US
dc.contributor.authorGanguli, Anirbanen_US
dc.date.accessioned2009-05-28T06:20:37Z
dc.date.available2009-05-28T06:20:37Z
dc.date.issued2005-07-09en_US
dc.description.abstractMesenchymal soft tissue masses are uncommon tumours of the chest. Myofibroblastoma is a recently described entity consisting of cells with origin from the myoepethelial cell, mostly seen as benign well-circumscribed neoplasms of the breast tissue. Though usually classified as a benign lesion, rarely it can be multifocal and prone to recurrence. We describe below the case of a 26-year-old female who presented with exertional dyspnoea and evidence of a massive mass lesion in the left hemithorax causing mediastinal displacement to the opposite side. On histological and immunophenotypic analysis, a diagnosis of the very rare thoracic myofibroblastoma was made. The incidence, salient features, pathological differential diagnoses and treatment are reviewed.en_US
dc.description.affiliationDepartment of Medicine, Maulana Azad Medical College and Associated Lok Nayak Hospital, G. B. Pant Hospital and Guru Nanak Eye Hospital, New Delhi-110 002, India. vaibhavsahni@hotmail.comen_US
dc.identifier.citationSahni V, Sunandan S, Agarwal SK, Singh NP, Ganguli A. Rare thoracic mass lesion--myofibrobastoma. Indian Journal of Cancer. 2005 Jul-Sep; 42(3): 161-4en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/49690
dc.language.isoengen_US
dc.source.urihttps://www.indianjcancer.comen_US
dc.subject.meshAdulten_US
dc.subject.meshDiagnosis, Differentialen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshImmunohistochemistryen_US
dc.subject.meshNeoplasms, Muscle Tissue --diagnosisen_US
dc.subject.meshSoft Tissue Neoplasms --diagnosisen_US
dc.titleRare thoracic mass lesion--myofibrobastoma.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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