Pathologic features and clinical course of a non-functioning primary pulmonary paraganglioma: A case report

• Published in: Annals of medicine and surgery 2020-07, Vol.55, p.185-189
• Main Authors: Tobón, Angélica, Velásquez, Mauricio, Pérez, Bladimir, Zúñiga, Valeria, Sua, Luz F., Fernández-Trujillo, Liliana
• Format: Article
• Language: English
• Subjects: Case Report; Lung cancer; Neuroendocrine tumor; Paraganglioma; Thoracic surgery video-assisted
• ISSN: 2049-0801; 2049-0801
• DOI: 10.1016/j.amsu.2020.05.027

Paragangliomas (PGGL) are rare neuroendocrine tumors arising from non-epithelial extra-adrenal chromaffin cells. They have been described in different sites: abdomen, pelvis, head, neck and thorax. Incidence is very low, occurring in less than 2–8/million per year. PGGL's of the lung are extremely rare, they have a slow growth and present as painless lesions. Biopsy is the method of choice for diagnosis and prognosis. This is a 70-year-old woman with chronic cough, with a CT-scan showing a 3.3-cm mass in the left lower lobe. After video-assisted thoracic surgery, histologic findings confirmed a non-functioning pulmonary paraganglioma. We present the clinical, radiological, pathological findings and clinical course. Primary pulmonary PGGL's are extremely rare neuroendocrine tumors with low-grade malignancy, difficult to distinguish from other pulmonary tumors relying only on imaging techniques. In this case, PGGL presented as an incidentaloma during the evaluation of chronic cough. After histological diagnosis, genetic testing are ideally performed to identify somatic or germline mutations that may condition a higher risk of malignancy and metastasis. PGGL's must be considered when other diagnoses are unlikely due to immunohistochemistry findings. Larger studies in this field are needed to determine the risk factors for its development and to determine which populations have the greatest potential for malignant transformation •Paragangliomas are rare neuroendocrine tumors derived from non-epithelial extra-adrenal chromaffin cells.•Paragangliomas from the lung are rare, they have a slow growth and present as non-painful lesions.•Complete surgical resection is the diagnostic method of choice for solitary primary pulmonary paragangliomas.•Genetic testing is important to identify somatic or germline mutations.