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Primary Alveolar Soft Part Sarcoma of Uterine Corpus: a Case Report with Immunohistochemical, Ultrastructural Study and Review of Literature

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Publisher Biomed Central
Date 2016 Feb 4
PMID 26837430
Citations 3
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Abstract

Background: Alveolar soft part sarcoma (ASPS) is a rare mesenchymal malignancy. ASPS usually occurs most commonly in the deep soft tissues of the thigh and buttock or the head and neck regions. ASPS that originate from the uterine corpus are even more rare, with only 10 previous cases reported in the English literature.

Case Presentation: In our case, the alveolar features were completely lost and the tumour shows a solid, non-alveolar pattern and the nuclei have marked variation in nuclear size, and multinucleation. The correct pathological diagnosis has been made by immuno- histochemical and ultrastructural features, which rvealed overexpression of TFE3 and peculiar cytoplasmic crystalline inclusions. In this paper, an additional case of primary ASPS of uterine corpus is reported with immunohistochemical, ultrastructural study and review of literature in the effort to delineate its clinical and pathological features. In this unusual site, the diagnosis can be problematic because ASPS can mimic other primary or metastatic uterine neoplasms.

Conclusions: Thus, in this unusual presentation an essential diagnostic marker is the nuclear over-expression of TFE3 as well as ultrastructural study, which reveals the presence of peculiar cytoplasmic crystalline inclusions.

Citing Articles

Alveolar Soft Part Sarcoma in the Female Genital Tract: Case Series with Literature Review and SEER Database Analysis.

Long X, Jiang Q, Li R, Wang D, Zou D Int J Womens Health. 2024; 16:17-30.

PMID: 38204972 PMC: 10778149. DOI: 10.2147/IJWH.S435135.


Lingual Alveolar Soft Part Sarcoma in a 78-Year-Old Woman: A Case Report and Comprehensive Review of the Literature from 1952 to 2022.

Aksionau A, Dela Cruz N, Meram A, Cuellar-Saenz H, Aveni J, Takei H Head Neck Pathol. 2022; 17(1):265-274.

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Alveolar soft part sarcoma occurring in the penis of a 3-year-old boy: A rare case report.

Qiu L, Li Y, Ali S, Xie M Medicine (Baltimore). 2017; 96(45):e8383.

PMID: 29137020 PMC: 5690713. DOI: 10.1097/MD.0000000000008383.

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