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Pulmonary blastoma: a comprehensive overview of a rare entity
Ioannis Tsamis1, Stavroula-Porfyria Chachali2, Georgia Gomatou3
1Oncology Unit, Third Department of Medicine, Sotiria General Hospital, National and Kapodistrian University of Athens, Messogion, Athens, Greece.
Pulmonary blastoma, a rare lung cancer with epithelial and mesenchymal parts, is often diagnosed early and treatable with surgery. Further research and collaboration are needed for better management and targeted therapies.
Area of Science:
- Oncology
- Pulmonology
- Pathology
Background:
- Pulmonary blastoma is a rare lung malignancy (<0.5% of primary lung tumors).
- It is characterized by a biphasic pattern of epithelial and mesenchymal components.
- Also known as sarcomatoid carcinoma, only a few hundred cases are reported globally.
Purpose of the Study:
- To conduct a comprehensive literature review and critical assessment of pulmonary blastoma.
- To consolidate current knowledge on this rare lung cancer.
Main Methods:
- A narrative literature review was performed.
- The PubMed database was searched from its inception to January 2021.
- Keywords included "pulmonary blastoma", "biphasic pulmonary blastoma", and "sarcomatoid carcinoma" in English.
Main Results:
- Pulmonary blastoma exhibits both epithelial and mesenchymal malignant components.
- Diagnosis often occurs at a younger age, with many cases non-metastatic at presentation, allowing for surgical intervention.
- Clinical presentation is non-specific, with 40% of patients asymptomatic; immunohistochemistry aids diagnosis.
Conclusions:
- The precise origin of the biphasic cell population in pulmonary blastoma remains unclear.
- Management and survival data are limited, highlighting the need for multicenter collaboration.
- Advances in targeted therapy may offer future treatment avenues for this rare cancer.
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