Pulmonary hemangioendothelioma with osteoclast‑like giant cells: A rare observation.

dc.contributor.authorAdamane, Shraddha A
dc.contributor.authorDeodhar, Kedar K
dc.contributor.authorGupta, Amit M
dc.contributor.authorKarimundackal, George
dc.contributor.authorDesai, Sangeeta B
dc.date.accessioned2016-12-09T05:40:55Z
dc.date.available2016-12-09T05:40:55Z
dc.date.issued2016-07
dc.description.abstractPulmonary epithelioid hemangioendothelioma (PEH) is a rare vascular neoplasm, predominantly encountered in women, more often in the age group of 40 years and below. It is a tumor of borderline malignant potential with a clinical course intermediate between hemangioma and angiosarcoma. The tumor has variable prognosis, and treatment options include surgical excision in operable cases and chemotherapy in disseminated ones. The present report describes complete clinical, radiological, and histopathological features of PEH with osteoclast‑like giant cells and metaplastic ossification in a 20‑year‑old boy who presented with dyspnea and episodes of hemoptysis with review of literature.en_US
dc.identifier.citationAdamane Shraddha A, Deodhar Kedar K, Gupta Amit M, Karimundackal George, Desai Sangeeta B. Pulmonary hemangioendothelioma with osteoclast‑like giant cells: A rare observation. Indian Journal of Pathology & Microbiology. 2016 July-Sept 59(3): 398-400.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/179600
dc.language.isoenen_US
dc.source.urihttps://www.ijpmonline.org/article.asp?issn=0377-4929;year=2016;volume=59;issue=3;spage=398;epage=400;aulast=Adamaneen_US
dc.subjectEpithelioid hemangioendotheliomaen_US
dc.subjectmetaplastic ossificationen_US
dc.subjectosteoclast‑like giant cellen_US
dc.subjectlungen_US
dc.titlePulmonary hemangioendothelioma with osteoclast‑like giant cells: A rare observation.en_US
dc.typeArticleen_US
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