2
Department of Pathology, Imam-Khomeini Hospital, Urmia University of Medical Sciences and Health Services, URMIA- IRAN
Abstract
We describe a case of pulmonary epithelioid hemangioendothelioma (PEH), previously known as intravascular bronchoalveolar tumor, in a 48- year-old woman with an initial diagnosis made by CT-guided transthoracic needle biopsy. This is a rare disease, with approximately 50 cases described in the literature. To our knowledge, this has not been previously described in the English-language literature. This tumor can affect multiple organs. PEH is usually multifocal or small sized; hypertrophic osteoarthropathy is uncommon. This patient presented with hypertrophic osteoarthropathy and large solitary pulmonary mass, rare presentations of this uncommon tumor.(Tanaffos 2005; 4(16): 73-78)
Rahimi Rad, M. H., & Milani, M. (2005). Epithelioid Hemangioendothelioma: A Case with Large Solitary Pulmonary Mass and Hypertrophic Osteoarthropathy. TANAFFOS (Respiration), 4(4(autumn)), 73-78.
MLA
Mohammad Hossein Rahimi Rad; Majid Milani. "Epithelioid Hemangioendothelioma: A Case with Large Solitary Pulmonary Mass and Hypertrophic Osteoarthropathy". TANAFFOS (Respiration), 4, 4(autumn), 2005, 73-78.
HARVARD
Rahimi Rad, M. H., Milani, M. (2005). 'Epithelioid Hemangioendothelioma: A Case with Large Solitary Pulmonary Mass and Hypertrophic Osteoarthropathy', TANAFFOS (Respiration), 4(4(autumn)), pp. 73-78.
VANCOUVER
Rahimi Rad, M. H., Milani, M. Epithelioid Hemangioendothelioma: A Case with Large Solitary Pulmonary Mass and Hypertrophic Osteoarthropathy. TANAFFOS (Respiration), 2005; 4(4(autumn)): 73-78.
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