Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-28T02:28:44.829Z Has data issue: false hasContentIssue false
  • English
  • Français

A rare angiosarcoma: retiform haemangioendothelioma

Published online by Cambridge University Press:  05 September 2011

F O'Duffy ,
C Timon  and
M Toner
F O'Duffy*
Affiliation:
Department of Otorhinolaryngology, Royal Victoria Eye and Ear Hospital, Dublin, Ireland
C Timon
Affiliation:
Department of Otorhinolaryngology, Royal Victoria Eye and Ear Hospital, Dublin, Ireland
M Toner
Affiliation:
Department of Pathology, St James's Hospital, Dublin, Ireland
*
Address for correspondence: Mr Fergal O'Duffy, Royal Victoria Hospital, Adelaide Rd, Dublin 2, Ireland Fax: +353 14900643 E-mail: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

Objective:

We report the case of a rare angiosarcoma, retiform haemangioendothelioma, in an 18-year-old young man, which presented as a recurrent ulcerating lesion of the left pinna.

Method:

Case report and literature review of retiform haemangioendothelioma. This is a low grade angiosarcoma with a high local recurrence rate and low metastasis rate, and was first described in 1994 by Calonje et al.

Results:

This patient represents only the third report of lymph node metastasis in a case of retiform haemangioendothelioma. To date, 31 cases of the tumour have been reported. Histological diagnosis of this group of vascular neoplasms can be challenging, as their histopathological appearance is intermediate between haemangioma and angiosarcoma.

Conclusion:

Surgical excision remains the primary treatment modality, with adjuvant radiotherapy recommended in patients with large tumour size, local recurrence and lymph node metastasis, as seen in this case.

Keywords

EarPinnaRetiform HemangioendotheliomaHemangiosarcomaHemangiomaNeoplasm Metastasis
Type
Clinical Records
Information
The Journal of Laryngology & Otology , Volume 126 , Issue 2 , February 2012 , pp. 200 - 202
Copyright
Copyright © JLO (1984) Limited 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1Calonje, E, Fletcher, CD, Wilson-Jones, E, Rosai, J. Retiform haemangioendothelioma. A distinctive form of low-grade angiosarcoma delineated in a series of 15 cases. Am J Surg Pathol 1994;18:115–25CrossRefGoogle Scholar
2Tan, D, Kraybill, W, Cheney, RT, Khoury, T. Retiform haemangioendothelioma: a case report and review of literature. J Cutan Pathol 2005;32:634–7CrossRefGoogle Scholar
3Bhutoria, B, Konar, A, Chakrabarti, S, Das, S. Retiform hemangioendothelioma with lymph node metastasis: a rare entity. Indian J Dermatol Venereol Leprol 2009;75:60–2CrossRefGoogle ScholarPubMed
4Duke, D, Dvorak, AM, Harris, T, Cohen, LM. Multiple retiform haemangioendotheliomias. A low-grade angiosarcoma. Am J Dermatopathol 1996;18:606–10CrossRefGoogle ScholarPubMed
5Darouti, ME, Marzouk, SA, Sobhi, RM et al. Retiform haemangioendothelioma. Int J Dermatol 2000;42:290–2Google Scholar
6Schommer, M, Herbst, RA, Brodersen, JP, Kiehl, P, Katenkamp, D, Kapp, A et al. Retiform haemangioendothelioma: another tumour associated with human herpes virus type 8? J Am Acad Dermatol 2000;39:365–8Google Scholar
7Caljonje, E, Fletcher, CDM. Tumours of blood vessels and lymphatics. In: Fletcher, CDM, ed. Diagnostic Histopathology of Tumours, 2nd edn.London: Churchill Livingstone, 2000;1:45–86Google Scholar
8Zhang, G, Lu, Q, Yin, H, Wen, H, Su, Y, Li, D et al. A case of retiform-hemangioendothelioma with unusual presentation and aggressive clinical features. Int J Clin Exp Pathol 2010;3:528–33Google ScholarPubMed