Longitudinal observation of solitary fibrous tumor translation into malignant pulmonary artery intimal sarcoma.
J Cardiothorac Surg
; 15(1): 233, 2020 Sep 01.
Article
em En
| MEDLINE
| ID: mdl-32873341
ABSTRACT
BACKGROUND:
Pulmonary artery intimal sarcoma (PAIS) is a rare malignant tumor that was usually misdiagnosed as chronic pulmonary thromboembolism. CASE PRESENTATION We previously reported a solitary fibrous tumor in the pulmonary artery presented with acute pulmonary embolism, which was identified by 99mTc-Galacto-RGD2 imaging. However, this patient had a recurrence in situ two-year after surgery, post-operative pathology revealed pulmonary artery intimal sarcoma. At one-year post-operation, 18F-FDG PET/CT was performed for exclusion of tumor metastasis, which showed FDG avid lesion in the T5, T10, and L5 vertebral bodies, as well as in bilateral ilium and right ischium.CONCLUSIONS:
This is the first longitudinal observation of a solitary fibrous tumor (SFT) development into a pulmonary artery intimal sarcoma (PAIS) and presented with multiple bone metastases.Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Sarcoma
/
Neoplasias Ósseas
/
Neoplasias Vasculares
/
Tumores Fibrosos Solitários
Tipo de estudo:
Prognostic_studies
Limite:
Aged
/
Female
/
Humans
Idioma:
En
Revista:
J Cardiothorac Surg
Ano de publicação:
2020
Tipo de documento:
Article
País de afiliação:
China