LymphedemaV1, Main, Exploration, bibRecord, 001922

Rare Case of Spindle Cell Haemangioma

Identifieur interne : 001922 ( Main/Exploration ); précédent : 001921; suivant : 001923

Rare Case of Spindle Cell Haemangioma

Auteurs : Sunanda Chavva ; M. Hima Priya ; Komali Garlapati ; G. Siva Prasad Reddy ; Ashalata Gannepalli

Source :

Journal of Clinical and Diagnostic Research : JCDR [ 2249-782X ] ; 2015.

RBID : PMC:4525619

Abstract

Spindle cell haemangioma (SCH) is a benign vascular lesion which usually occurs on distal extremities. It was previously regarded as haemangioendothelioma and was initially perceived to be low grade angiosarcoma.They are characterized by cavernous blood vessels and spindle cell proliferation. It is now considered as a reactive lesion and conservative surgical excision is preferred treatment. Intraoral occurrence is rare; hence we present a case of SCH in a 33-year-old male that presented as a swelling below the tongue. Histopathology showed well circumscribed proliferating spindle cells attached to vessel walls, dilated vascular spaces. The lesion was positive for CD31 and CD34 markers suggesting it to be of endothelial cell origin.

Url:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525619

DOI: 10.7860/JCDR/2015/11998.6080
PubMed: 26266229
PubMed Central: 4525619

Affiliations:

Le document en format XML

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<author><name sortKey="Gannepalli, Ashalata" sort="Gannepalli, Ashalata" uniqKey="Gannepalli A" first="Ashalata" last="Gannepalli">Ashalata Gannepalli</name>
<affiliation><nlm:aff id="aff5"> Professor, Department of Oral & Maxillofacial Pathology,<institution>Panineeya Institute of Dental Sciences</institution>
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<front><div type="abstract" xml:lang="en"><p>Spindle cell haemangioma (SCH) is a benign vascular lesion which usually occurs on distal extremities. It was previously regarded as haemangioendothelioma and was initially perceived to be low grade angiosarcoma.They are characterized by cavernous blood vessels and spindle cell proliferation. It is now considered as a reactive lesion and conservative surgical excision is preferred treatment. Intraoral occurrence is rare; hence we present a case of SCH in a 33-year-old male that presented as a swelling below the tongue. Histopathology showed well circumscribed proliferating spindle cells attached to vessel walls, dilated vascular spaces. The lesion was positive for CD31 and CD34 markers suggesting it to be of endothelial cell origin.</p>
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Rare Case of Spindle Cell Haemangioma

Rare Case of Spindle Cell Haemangioma

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