Epithelioid haemangioendothelioma arising in the nasal cavity

We report here the case of an epithelioid haemangioendothelioma (EHE) arising in the nasal cavity which is, to the best of our knowledge, the first ever described example in the world literature in that particular site. The patient is a 23-year-old male who presented with repeated episodes of epista...

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Veröffentlicht in:Journal of laryngology and otology 2003-01, Vol.117 (1), p.75-77
Hauptverfasser: Girolamo, Alberto Di, Giacomini, Pier Giorgio, Coli, Antonella, Castri, Federica, de Padova, Alessandro, Bigotti, Giulio
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container_issue 1
container_start_page 75
container_title Journal of laryngology and otology
container_volume 117
creator Girolamo, Alberto Di
Giacomini, Pier Giorgio
Coli, Antonella
Castri, Federica
de Padova, Alessandro
Bigotti, Giulio
description We report here the case of an epithelioid haemangioendothelioma (EHE) arising in the nasal cavity which is, to the best of our knowledge, the first ever described example in the world literature in that particular site. The patient is a 23-year-old male who presented with repeated episodes of epistaxis from the nasal cavity and with a 1.5 cm reddish, polypoid, smooth, spontaneously bleeding nodule in the rightmiddle meatus. This lesion was histologically diagnosed as epithelioid haemangioendothelioma. Immunohistochemically the neoplasm displayed striking positivity for CD31, CD34 and vimentin. A surgical approach was performed by ’facial degloving’, removing the right inferior turbinate, the anterior two-thirds of the middle turbinate and the medial wall of the ethmoid bone. After 12 months follow-up the patient is disease-free, without any local or distant recurrence.
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The patient is a 23-year-old male who presented with repeated episodes of epistaxis from the nasal cavity and with a 1.5 cm reddish, polypoid, smooth, spontaneously bleeding nodule in the rightmiddle meatus. This lesion was histologically diagnosed as epithelioid haemangioendothelioma. Immunohistochemically the neoplasm displayed striking positivity for CD31, CD34 and vimentin. A surgical approach was performed by ’facial degloving’, removing the right inferior turbinate, the anterior two-thirds of the middle turbinate and the medial wall of the ethmoid bone. 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Laryngol. Otol</addtitle><description>We report here the case of an epithelioid haemangioendothelioma (EHE) arising in the nasal cavity which is, to the best of our knowledge, the first ever described example in the world literature in that particular site. The patient is a 23-year-old male who presented with repeated episodes of epistaxis from the nasal cavity and with a 1.5 cm reddish, polypoid, smooth, spontaneously bleeding nodule in the rightmiddle meatus. This lesion was histologically diagnosed as epithelioid haemangioendothelioma. Immunohistochemically the neoplasm displayed striking positivity for CD31, CD34 and vimentin. A surgical approach was performed by ’facial degloving’, removing the right inferior turbinate, the anterior two-thirds of the middle turbinate and the medial wall of the ethmoid bone. 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Laryngol. Otol</addtitle><date>2003-01</date><risdate>2003</risdate><volume>117</volume><issue>1</issue><spage>75</spage><epage>77</epage><pages>75-77</pages><issn>0022-2151</issn><eissn>1748-5460</eissn><coden>JLOTAX</coden><abstract>We report here the case of an epithelioid haemangioendothelioma (EHE) arising in the nasal cavity which is, to the best of our knowledge, the first ever described example in the world literature in that particular site. The patient is a 23-year-old male who presented with repeated episodes of epistaxis from the nasal cavity and with a 1.5 cm reddish, polypoid, smooth, spontaneously bleeding nodule in the rightmiddle meatus. This lesion was histologically diagnosed as epithelioid haemangioendothelioma. Immunohistochemically the neoplasm displayed striking positivity for CD31, CD34 and vimentin. A surgical approach was performed by ’facial degloving’, removing the right inferior turbinate, the anterior two-thirds of the middle turbinate and the medial wall of the ethmoid bone. After 12 months follow-up the patient is disease-free, without any local or distant recurrence.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>12590863</pmid><doi>10.1258/002221503321046711</doi><tpages>3</tpages></addata></record>
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subjects (RF) Otorhinolaryngology
Adult
Biological and medical sciences
Epitheloid
Haemangioendothelioma
Hemangiosarcoma - pathology
Hemangiosarcoma - surgery
Humans
Male
Medical sciences
Nasal Cavity
Nasal Cavity - pathology
Nasal Cavity - surgery
Nose Neoplasms - pathology
Nose Neoplasms - surgery
Otorhinolaryngology. Stomatology
Tomography, X-Ray Computed
Tumors
Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology
title Epithelioid haemangioendothelioma arising in the nasal cavity
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