Primary pleural epithelioid haemangioendothelioma with metastases to the skin. A case report and literature review. Issue 1 (27th December 2004)

• Record Type: Journal Article
• Authors: Al-Shraim, M; Mahboub, B; Neligan, P C; Chamberlain, D; Ghazarian, D
• Is Part Of: Journal of clinical pathology. Volume 58:Issue 1(2005)
• Page Start: 107
• Page End: 109
• Publication Date: 2004-12-27
• Subjects: CEA, carcinoembryonic antigen -- CT, computed tomography -- EHE, epithelioid haemangioendothelioma; epithelioid haemangioendothelioma -- skin -- pleura -- asbestos; Pathology -- Periodicals; Pathology, Molecular -- Periodicals; 616.0705
• DOI: 10.1136/jcp.2004.018937
• Languages: English
• ISSNs: 0021-9746

Abstract

Abstract : Epithelioid haemangioendothelioma (EHE) is a rare vascular tumour of intermediate behaviour. It can arise from various sites including the liver, spleen, pleura, or lung. Cutaneous EHE can be primary or secondary. This report describes the case of a 51 year old man who presented with a history of dry cough, shortness of breath, and pleural effusion, and who developed two cutaneous nodules in the anterior abdominal wall a few weeks later. He had a previous history of asbestos exposure. Computed tomography scan showed a left sided pleural effusion and nodular pleural mass. Histology of both the pleural and cutaneous lesions was compatible with EHE. Electron microscopic examination demonstrated the presence of Weibel-Palade bodies. The patient underwent elliptical excision of the metastatic cutaneous nodules after decortication of the primary pleural tumour and adjuvant treatment. A few reports have described metastasis of intrathoracic EHE to the skin. Despite treatment with interferon, the patient developed more cutaneous lesions two years after the initial diagnosis. Even though the tumour has the classic light histological and ultrastructural features of EHE, it behaved in an aggressive manner.