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Pulmonary Epithelioid Hemangioendothelioma Mimicking Hamartoma: A case report / 대한흉부외과학회지
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 937-941, 2004.
Article in Korean | WPRIM | ID: wpr-13268
ABSTRACT
Epithelioid hemangioendothelioma, originating from the vascular endothelium, is a very rare and low-grade malignancy. World-wide, about 50 cases of pulmonary epithelioid hemangioendothelioma have been reported. This is more common in female and is usually shown as multiple nodules in both lung fields. A 41-year-old male, who had suffered from right pleuritic chest pain for 3 months, was initially diagnosed as adenocarcinoma under bronchofiberscopic biopsy. At that time, the stage of tumor according to the TNM staging was IIIa. He received bronchoscopic biopsy again during follow-up period and it was diagnosed as hamartoma. After surgery, the final diagnosis was pulmonary epithelioid hemangioendothelioma.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Biopsy / Chest Pain / Endothelium, Vascular / Adenocarcinoma / Follow-Up Studies / Hemangioendothelioma, Epithelioid / Diagnosis / Hamartoma / Hemangioendothelioma / Lung Type of study: Diagnostic study / Observational study / Prognostic study Limits: Adult / Female / Humans / Male Language: Korean Journal: The Korean Journal of Thoracic and Cardiovascular Surgery Year: 2004 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Biopsy / Chest Pain / Endothelium, Vascular / Adenocarcinoma / Follow-Up Studies / Hemangioendothelioma, Epithelioid / Diagnosis / Hamartoma / Hemangioendothelioma / Lung Type of study: Diagnostic study / Observational study / Prognostic study Limits: Adult / Female / Humans / Male Language: Korean Journal: The Korean Journal of Thoracic and Cardiovascular Surgery Year: 2004 Type: Article