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Case Studies |
Epithelioid haemangioendotheliomas are rare tumours of endothelial origin. They can develop in any tissue but occur principally in the lung and liver. Their usual course is a slow progression, so that they can be treated by surgery. In aggressive forms, no treatment has proved efficient to date. This study, describes a case of bilateral pleural epithelioid haemangioendothelioma that extended to the peritoneum. The histological diagnosis was confirmed by both conventional examination and immunohistochemistry. After six courses of carboplatine plus etoposide, a complete response was obtained. The complete remission is still lasting at 18 months after the diagnosis and the patient is healthy.
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L. Posligua, F. Anatelli, L. P. Dehner, and J. D. Pfeifer Primary peritoneal epithelioid hemangioendothelioma. International Journal of Surgical Pathology, July 1, 2006; 14(3): 257 - 267. [Abstract] [PDF] |
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P Sanjay, S Raman, J Shannon, G T Williams, and A Woodward Gastric epithelioid haemangioendothelioma: a rare cause of upper gastrointestinal bleeding Postgrad. Med. J., August 1, 2005; 81(958): e7 - e7. [Abstract] [Full Text] [PDF] |
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R. Diaz, A. Segura, V. Calderero, I. Cervera, J. Aparicio, M.V. Jorda, and L. Pellin Central nervous system metastases of a pulmonary epitheloid haemangioendothelioma Eur. Respir. J., March 1, 2004; 23(3): 483 - 486. [Abstract] [Full Text] [PDF] |
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P. Cronin and D. Arenberg Pulmonary Epithelioid Hemangioendothelioma: An Unusual Case and a Review of the Literature Chest, February 1, 2004; 125(2): 789 - 793. [Abstract] [Full Text] [PDF] |
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G.A. Rossi, P. Toma, O. Sacco, B. Fregonese, E. Podesta, P. Dodero, G. Silvestri, and C. Gambini A 14-yr-old male with dyspnoea, productive cough and chest pain Eur. Respir. J., August 1, 2003; 22(2): 387 - 391. [Full Text] [PDF] |
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