| Literature DB >> 29299105 |
Fadi Nemeh1, Anderson H Kuo1, Jenny Ross2, Carlos S Restrepo1.
Abstract
Pulmonary blastomas are rare malignancies, representing 0.25% to 0.5% of all primary lung neoplasms with often aggressive progression and poor prognosis. Clinical management of pulmonary blastomas depends on histologic subtype, staging, and presentation, and may consist of surgery, chemotherapy, and radiation. Biphasic pulmonary blastoma is a subtype of pulmonary blastoma that exhibits biphasic histology, with both epithelial and mesenchymal malignant elements. We report a case of biphasic pulmonary blastoma in a 33-year-old female with 1 pack per day history of smoking for approximately 16 years, who presented with left-sided pleuritic chest pain on deep inspiration without otherwise significant pat medical history. Imaging evaluation using chest radiography, computed tomography, and magnetic resonance imaging identified a heterogenous, well-circumscribed, left lower lobe mass with extensive necrosis and hemorrhage. No lymphadenopathy or distant metastasis was detected through imaging evaluation. Surgical resection of the tumor followed by histopathological analysis confirmed a biphasic pulmonary blastoma.Entities:
Keywords: Biphasic Pulmonary Blastoma; Computed Tomography; Magnetic Resonance Imaging; Pulmonary Blastoma; Pulmonary Neoplasm
Mesh:
Year: 2017 PMID: 29299105 PMCID: PMC5743140 DOI: 10.3941/jrcr.v11i9.3153
Source DB: PubMed Journal: J Radiol Case Rep ISSN: 1943-0922