ArticleJournal of clinical and diagnostic research : JCDR2015
Rare Case of Spindle Cell Haemangioma.
Article in Journal of clinical and diagnostic research : JCDR, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 13 citations in OpenAlex.
- Immunohistochemical Analysis of Oral Spindle Cell Hemangioma.Journal of dentistry (Shiraz, Iran) · 2025Article
- Spindle Cell Hemangioma of Lower Lip: The Fourth Case Report with Review of Literature.Journal of maxillofacial and oral surgery · 2023Article
- A Rare Case of a Primary Leiomyoma of the Clivus in an Immunocompetent Patient and a Review of the Literature Regarding Clival Lesions.Diagnostics (Basel, Switzerland) · 2022Review
- Rare case of spindle cell haemangioma of oral cavity.BMJ case reports · 2022Article
- Successful Outcome After Intralesional Curettage for Spindle Cell Hemangioma of Fibula in an Infant: A Case Report.Frontiers in pediatrics · 2021Article
- Spindle Cell Hemangioma in the Mucosa of the Upper Lip: A Case Report and Review of the Literature.Case reports in dentistry · 2018Article
- [Spindle-shaped hemangioma: an unusual location].The Pan African medical journal · 2016Article
- Spindle cell haemangioma - Report of a rare entity.Journal of oral and maxillofacial pathology : JOMFPArticle
Corrections and comments
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
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.
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