Publication:
Rare histological subtype of pulmonary artery intimal sarcoma diagnosed by multidisciplinary approach

dc.contributor.authorStojšić, Jelena (23006624300)
dc.contributor.authorPopović, Marko (57191370403)
dc.contributor.authorAdžić-Vukicevic, Tatjana (56888756300)
dc.contributor.authorKovač, Jelena (52563972900)
dc.contributor.authorMarković, Jelena (54793088700)
dc.contributor.authorBlanka-Protic, Ana (57201503514)
dc.contributor.authorRadovanović, Dragan (36087908200)
dc.date.accessioned2025-06-12T16:48:01Z
dc.date.available2025-06-12T16:48:01Z
dc.date.issued2018
dc.description.abstractPulmonary artery intimal sarcoma (PAS) is a rare mesenchymal tumor mostly diagnosed in middle-aged women. In a 63-year-old female, the radiological findings showed cavitation in the left upper lobe of the lung and infiltrative tumor mass around the left pulmonary artery. PAS consisted of small, round tumor cells with about 80% of mitotic activity and with myxoid background and specific immunoprofile and diagnosed as undifferentiated sarcoma with round cell features type. The final diagnosis of PAS was established according to the pathohistological, chest computed tomography scan, and surgery finding. © 2018 Journal of Research in Medical Sciences | Published by Wolters Kluwer - Medknow.
dc.identifier.urihttps://doi.org/10.4103/jrms.jrms_102_18
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85060612941&doi=10.4103%2fjrms.jrms_102_18&partnerID=40&md5=c42b1f5d4329fc5e885b30fc658795d2
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/6630
dc.subjectArtery thrombosis
dc.subjectpulmonary artery intimal sarcoma
dc.subjectpulmonary infarction
dc.subjectthromboembolism
dc.titleRare histological subtype of pulmonary artery intimal sarcoma diagnosed by multidisciplinary approach
dspace.entity.typePublication

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