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Information Journal Paper

Title

EPITHELIOID HEMANGIOENDOTHELIOMA: A CASE WITH LARGE SOLITARY PULMONARY MASS AND HYPERTROPHIC OSTEOARTHROPATHY

Pages

  73-78

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.      

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    APA: Copy

    RAHIMIRAD, M.H., & MILANI, M.. (2005). EPITHELIOID HEMANGIOENDOTHELIOMA: A CASE WITH LARGE SOLITARY PULMONARY MASS AND HYPERTROPHIC OSTEOARTHROPATHY. TANAFFOS, 4(16), 73-78. SID. https://sid.ir/paper/530100/en

    Vancouver: Copy

    RAHIMIRAD M.H., MILANI M.. EPITHELIOID HEMANGIOENDOTHELIOMA: A CASE WITH LARGE SOLITARY PULMONARY MASS AND HYPERTROPHIC OSTEOARTHROPATHY. TANAFFOS[Internet]. 2005;4(16):73-78. Available from: https://sid.ir/paper/530100/en

    IEEE: Copy

    M.H. RAHIMIRAD, and M. MILANI, “EPITHELIOID HEMANGIOENDOTHELIOMA: A CASE WITH LARGE SOLITARY PULMONARY MASS AND HYPERTROPHIC OSTEOARTHROPATHY,” TANAFFOS, vol. 4, no. 16, pp. 73–78, 2005, [Online]. Available: https://sid.ir/paper/530100/en

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