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Case report: Pulmonary sarcomatoid carcinoma demonstrating rapid growth on follow-up CT.
Tu, Li; Xie, Hong; Zhan, Lianshan; Yang, Yushi; Chen, Tingting; Hu, Na; Du, Xiaojun; Zhou, Shi.
Afiliação
  • Tu L; General Practice Department, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
  • Xie H; Radiology Department, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
  • Zhan L; Nuclear Medicine Department, Guiqian International General Hospital, Guiyang, Guizhou, China.
  • Yang Y; Pathology Department, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
  • Chen T; Radiology Department, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
  • Hu N; Radiology Department, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
  • Du X; Thoracic Surgery Department, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
  • Zhou S; Interventional Radiology Department, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Front Oncol ; 14: 1393203, 2024.
Article em En | MEDLINE | ID: mdl-39040455
ABSTRACT

Background:

The tumor growth rate and tumor volume doubling time are crucial parameters in diagnosing and managing lung lesions. Pulmonary sarcomatoid carcinoma (PSC) is a unique and highly malignant subtype of lung cancer, with limited documentation on its growth feature. This article aims to address the gap in knowledge regarding a PSC's growth patterns by describing the characteristics of a confirmed case using computed tomography, thereby enhancing the understanding of this rare disease. Case presentation A 79-year-old man was transferred to our center presenting with a mild cough, blood-tinged sputum, and a malignant nodule in the left upper lobe. Chest CT revealed a solid nodule in the left upper lobe. A follow-up CT ten days later showed a significant increase in the size of the nodule, accompanied by ground-glass opacity in the surrounding lung. The rapid preoperative growth of the nodule suggested a non-neoplastic lesion, and intraoperative frozen pathology also considered the possibility of tuberculosis. Subsequently, a left upper apical-posterior segment (S1 + 2) resection was performed. Postoperative tumor pathology confirmed the diagnosis of pulmonary sarcomatoid carcinoma with extensive giant cell carcinoma and necrosis. Immunohistochemistry indicated approximately 60% PD-L1 positive and genetic testing revealed a MET mutation. The patient was discharged with oral crizotinib targeted therapy, and his condition remained stable postoperatively. The patient is currently undergoing regular follow-up at our hospital, with no evidence of distant metastasis or recurrence.

Conclusion:

Pulmonary sarcomatoid carcinoma can exhibit rapid tumor growth on imaging, and PSC should be considered in the differential diagnosis for lesions that present with a fast growth rate. Timely and appropriate treatment for PSC may lead to a good prognosis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Suíça