Endometrial Stromal Sarcomas: Case Series of Rare Mesenchymal Uterine Tumour
This paper presents a case series of seven patients with endometrial stromal sarcoma (ESS), describing their clinical presentation and clinical course in a perimenopausal population with symptoms such as abnormal vaginal bleeding, abdominal pain, and rapid abdominal enlargement. The authors report that ESS is often clinically mistaken for conditions including leiomyoma, adenomyosis, or intrauterine polyps and is frequently diagnosed postoperatively based on histopathology, with tumors typically positive for estrogen and progesterone receptors (ER/PR). A key limitation is that the work is a small descriptive case series, without comparative or controlled methodology to establish broader clinical conclusions. The paper mentions adenomyosis as part of the differential diagnosis and diagnostic confusion, making it relevant to adenomyosis research despite its main focus being ESS case descriptions.
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