| Literature DB >> 28670184 |
Divya Shivdasani1, Natasha Singh1, Melvika Pereira1, Anand Zade2.
Abstract
Sarcomas are a heterogeneous group of rare tumors and arise either from soft tissue or from bone. Soft-tissue sarcomas (STSs) initially metastasize to the lungs. Metastases to extrapulmonary sites such as liver, brain, and soft tissue distant from primary tumor usually develop later. However, cases with isolated adrenal metastasis without disseminated disease have been reported in literature. We present a case of primary myxoid liposarcoma of the lower limb, in which staging 18-F fluorodeoxyglucose positron emission tomography-computed tomography (FDG PET-CT) scan detected a suspicious FDG avid adrenal lesion which eventually on resection was diagnosed as asymptomatic pheochromocytoma. Pheochromocytomas have been reported to demonstrate FDG uptake mimicking metastasis. Hence, while interpreting FDG PET-CT scans in the context of STSs, both the extrapulmonary metastatic potential of aggressive histological subtypes of sarcoma and rare possibility of FDG avid coexistent benign tumor should be taken into consideration.Entities:
Keywords: 18-F fluorodeoxyglucose positron emission tomography-computed tomography; Adrenal lesion; myxoid liposarcoma; pheochromocytoma
Year: 2017 PMID: 28670184 PMCID: PMC5460309 DOI: 10.4103/1450-1147.207275
Source DB: PubMed Journal: World J Nucl Med ISSN: 1450-1147