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Angiomatoid fibrosis histiocytoma in the pulmonary artery: A case report

Angiomatoid fibrosis histiocytoma in the pulmonary artery: A case report

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3f3db651a369422d9805cb933b078cb9

Angiomatoid fibrosis histiocytoma in the pulmonary artery: A case report

About this item

Full title

Angiomatoid fibrosis histiocytoma in the pulmonary artery: A case report

Publisher

Melbourne: Wiley

Journal title

Thoracic Cancer, 2021-05, Vol.12 (9), p.1453-1456

Language

English

Formats

Publication information

Publisher

Melbourne: Wiley

More information

Scope and Contents

Contents

Angiomatoid fibrosis histiocytoma (AFH) is a rare neoplastic disease. Only one report has demonstrated an intraluminal tumor of the pulmonary artery (PA) corresponding to AFH to date. We describe the case of AFH with EWSR1‐CREB1 fusion occurring in the ascending artery. A 42‐year‐old man exhibited an abnormal nodule on chest computed tomography (CT...

Alternative Titles

Full title

Angiomatoid fibrosis histiocytoma in the pulmonary artery: A case report

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_3f3db651a369422d9805cb933b078cb9

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3f3db651a369422d9805cb933b078cb9

Other Identifiers

ISSN

1759-7706,1759-7714

E-ISSN

1759-7714

DOI

10.1111/1759-7714.13929

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