2022
DOI: 10.1016/j.ajoc.2022.101645
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Alveolar soft part sarcoma of the superior rectus muscle: Case report and review of literature

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Cited by 2 publications
(4 citation statements)
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“…Less than 1% of all STSs are ASPSs, which is a rare and distinctive STS subtype [ 5 ]. Only 267 patients with this diagnosis were found in a surveillance, epidemiology, and results database search in the United States population between 1973 and 2014 [ 6 ]. Before the age of 30, there is a female predominance with a reverse ratio for older ages [ 7 ].…”
Section: Discussionmentioning
confidence: 99%
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“…Less than 1% of all STSs are ASPSs, which is a rare and distinctive STS subtype [ 5 ]. Only 267 patients with this diagnosis were found in a surveillance, epidemiology, and results database search in the United States population between 1973 and 2014 [ 6 ]. Before the age of 30, there is a female predominance with a reverse ratio for older ages [ 7 ].…”
Section: Discussionmentioning
confidence: 99%
“…Before the age of 30, there is a female predominance with a reverse ratio for older ages [ 7 ]. In young female patients, ASPS most commonly manifests as a painless mass [ 5 , 6 ]. Christopherson et al first described ASPS in 1952 as an entity with distinct clinical and pathologic features [ 7 ].…”
Section: Discussionmentioning
confidence: 99%
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“…When PEComa immunohistochemistry reveals the presence of TFE3, it is easy to confuse it with ASPS, a frequent orbital tumor. 6,10 ASPS histology is characterized by alveolar-like nests of cells with rich pink cytoplasm. 2 ASPS always tests negative for melanotic markers such as HMB-45.…”
Section: Ocular Transcription Factor E3-associated Perivascular Epith...mentioning
confidence: 99%