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01-09-2020 | Hypoxemia | Case Report

Intravascular Papillary Endothelial Hyperplasia of the Maxillary Sinus in Patient with Tricuspid Atresia

Authors: Peter Cooke, David Goldrich, Alfred Marc Iloreta, Abeer Salama, Raj Shrivastava

Published in: Head and Neck Pathology | Issue 3/2020

Abstract

Intravascular papillary endothelial hyperplasia (IPEH) is a benign, highly vascularized, endothelial growth that can be mischaracterized as a malignancy. While hundreds of IPEH cases are reported, only four occurred in the maxillary sinus. We present the case of a 28-year-old male who underwent surgical resection of IPEH of the right maxillary sinus. An additional consideration was the patient’s condition of univentricular tricuspid atresia which contributed to chronic hypoxemia and polycythemia. After complete resection from the maxillary sinus, post-operational workup determined the lesion to be IPEH. Given the potential for misdiagnosis of IPEH, careful histopathologic evaluation is required in order to avoid improper treatment.

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Title: Intravascular Papillary Endothelial Hyperplasia of the Maxillary Sinus in Patient with Tricuspid Atresia
Authors: Peter Cooke
David Goldrich
Alfred Marc Iloreta
Abeer Salama
Raj Shrivastava
Publication date: 01-09-2020
Publisher: Springer US
Keyword: Hypoxemia
Published in: Head and Neck Pathology / Issue 3/2020
Electronic ISSN: 1936-0568
DOI: https://doi.org/10.1007/s12105-019-01070-w

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Intravascular Papillary Endothelial Hyperplasia of the Maxillary Sinus in Patient with Tricuspid Atresia

Abstract

Keynote webinar | Spotlight on sleep in brain health

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Abstract

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