| Literature DB >> 31662549 |
Christos F Kampolis1, Christos Damaskos2, Angeliki A Loukeri3, Nikolaos Garmpis4, Anna Garmpi5, Ioannis Tomos6, Eleftherios Spartalis7, Dimitrios Dimitroulis4, Alexandros Patsouras8, Marousa Douskou9, Spyros A Papiris6, Periklis Tomos10.
Abstract
BACKGROUND/AIM: Extralobar pulmonary sequestration (EPS) is an unusual congenital defect characterized by the presence of non-functioning lung tissue receiving arterial supply from the systemic arteries. Primary hemangiopericytoma (HPC) is an uncommon potentially malignant tumor of vascular origin that usually involves the soft tissue of the extremities or retroperitoneum, but extremely rarely affects the lung. We present the rare case of a primary pulmonary HPC arising in an EPS. CASE REPORT: A 65-year-old woman, with dyspnea and pleuritic chest pain, was referred for further investigation. Radiological evaluation demonstrated a well-circumscribed mass above the right hemidiaphragm, receiving its arterial supply from the descending thoracic aorta. The patient underwent a right posterolateral thoracotomy and a middle lobectomy. The intraoperative finding was a well-encapsulated solid mass. The histological evaluation described HPC.Entities:
Keywords: Hemangiopericytoma; extralobar; pulmonary; sequestration
Mesh:
Substances:
Year: 2019 PMID: 31662549 PMCID: PMC6899116 DOI: 10.21873/invivo.11715
Source DB: PubMed Journal: In Vivo ISSN: 0258-851X Impact factor: 2.155