Pulmonary Epithelioid Hemangioendothelioma Mimicking Hamartoma: A case report / 대한흉부외과학회지
The Korean Journal of Thoracic and Cardiovascular Surgery
; : 937-941, 2004.
Article
in Ko
| WPRIM
| ID: wpr-13268
Responsible library:
WPRO
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.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Biopsy
/
Chest Pain
/
Endothelium, Vascular
/
Adenocarcinoma
/
Follow-Up Studies
/
Hemangioendothelioma, Epithelioid
/
Diagnosis
/
Hamartoma
/
Hemangioendothelioma
/
Lung
Type of study:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
Limits:
Adult
/
Female
/
Humans
/
Male
Language:
Ko
Journal:
The Korean Journal of Thoracic and Cardiovascular Surgery
Year:
2004
Type:
Article