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Response of pulmonary artery intimal sarcoma to surgery, radiotherapy and chemotherapy: a case report

INTRODUCTION: Pulmonary artery intimal sarcoma is a rare disease with no characteristic symptoms. It is difficult to diagnose early and is frequently misdiagnosed as a pulmonary embolism. CASE PRESENTATION: Here we report a case of pulmonary artery intimal sarcoma in a 54-year-old woman presenting w...

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Detalles Bibliográficos
Autores principales: Long, Hong-qing, Qin, Qin, Xie, Cong-hua
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443155/
https://www.ncbi.nlm.nih.gov/pubmed/18577236
http://dx.doi.org/10.1186/1752-1947-2-217
Descripción
Sumario:INTRODUCTION: Pulmonary artery intimal sarcoma is a rare disease with no characteristic symptoms. It is difficult to diagnose early and is frequently misdiagnosed as a pulmonary embolism. CASE PRESENTATION: Here we report a case of pulmonary artery intimal sarcoma in a 54-year-old woman presenting with complaints of shortness of breath on exertion. Echocardiography and a computed tomography scan showed that the right pulmonary artery trunk was blocked by a low-density mass. The patient was diagnosed with pulmonary artery intimal sarcoma by pathology and a complete mass resection was performed. After experiencing 10 months of disease-free survival, she was re-admitted because of the recurrence and metastasis of the tumor. Radiotherapy and chemotherapy were performed; however, only limited success was achieved. The patient died 15 months after the initial onset of symptoms. CONCLUSION: Some patients with intimal sarcoma of the pulmonary artery can benefit from radiotherapy and chemotherapy as well as surgery.