Uterine Adenosarcoma: a Review

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This review covers uterine adenosarcomas, rare tumors with benign epithelium and malignant mesenchyme, detailing their diagnosis, prognosis, and standard treatment of hysterectomy with bilateral salpingo-oophorectomy.

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This review describes uterine adenosarcoma, a rare female genital tract malignancy, summarizing epidemiology, clinicopathologic features, diagnostic criteria, immunohistochemical markers (notably CD10 and WT1), and prognostic factors. It reports that most patients present with stage I disease and cites overall survival around 60–80%, with survival and recurrence strongly influenced by myometrial invasion, sarcomatous overgrowth, lymphovascular invasion, necrosis, and heterologous elements; it also notes that sarcomatous overgrowth is associated with higher recurrence and lower 5-year overall survival. The review explicitly cautions that standard prognostic and treatment evidence is limited, including insufficient data to routinely recommend neoadjuvant or adjuvant chemotherapy and retrospective data not showing a survival benefit from adjuvant pelvic radiotherapy. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index, though it briefly notes that extra-uterine adenosarcoma may be related to endometriosis.

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Abstract

Adenosarcomas are rare malignancies of the female genital tract, accounting for approximately 5 % of uterine sarcomas. Occasionally, adenosarcoma occurs in the ovaries or in extra-uterine tissue, which may be related to endometriosis. These tumors are characterized by benign epithelial elements and a malignant mesenchymal component. Pathologic diagnosis is dependent on the identification of the characteristic morphologic features. The most common immunohistochemical markers for adenosarcoma are CD10 and WT1, but these are not specific. The most frequent presenting symptom is abnormal uterine bleeding. The majority of patients present with stage I disease, with a 5-year overall survival of 60 to 80 %. Survival is influenced by the presence of myometrial invasion, sarcomatous overgrowth, lymphovascular invasion, necrosis, and the presence of heterologous elements including rhabdomyoblastic differentiation. Patients with sarcomatous overgrowth have significantly increased risk of recurrence 23 versus 77 % and decreased 5-year overall survival 50 to 60 %. Standard of care treatment is total hysterectomy with bilateral salpingo-oophorectomy without lymphadenectomy, as the incidence of lymph node metastasis is rare. Retrospective data does not support the use of adjuvant pelvic radiotherapy in uterine adenosarcomas as no survival benefit is seen. Insufficient data exists to recommend routinely neoadjuvant or adjuvant chemotherapy for uterine adenosarcomas. Limited evidence exists for the role of hormonal therapy in uterine adenosarcomas. The PIK3/AKT/PTEN pathway is mutated in ∼70 % of adenosarcomas, and this may represent a possible therapeutic target. This article reviews the current state of knowledge concerning uterine adenosarcoma and discusses the management of this rare tumor.
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Abstract

Adenosarcomas are rare malignancies of the female genital tract, accounting for approximately 5 % of uterine sarcomas. Occasionally, adenosarcoma occurs in the ovaries or in extra-uterine tissue, which may be related to endometriosis. These tumors are characterized by benign epithelial elements and a malignant mesenchymal component. Pathologic diagnosis is dependent on the identification of the characteristic morphologic features. The most common immunohistochemical markers for adenosarcoma are CD10 and WT1, but these are not specific. The most frequent presenting symptom is abnormal uterine bleeding. The majority of patients present with stage I disease, with a 5-year overall survival of 60 to 80 %. Survival is influenced by the presence of myometrial invasion, sarcomatous overgrowth, lymphovascular invasion, necrosis, and the presence of heterologous elements including rhabdomyoblastic differentiation. Patients with sarcomatous overgrowth have significantly increased risk of recurrence 23 versus 77 % and decreased 5-year overall survival 50 to 60 %. Standard of care treatment is total hysterectomy with bilateral salpingo-oophorectomy without lymphadenectomy, as the incidence of lymph node metastasis is rare. Retrospective data does not support the use of adjuvant pelvic radiotherapy in uterine adenosarcomas as no survival benefit is seen. Insufficient data exists to recommend routinely neoadjuvant or adjuvant chemotherapy for uterine adenosarcomas. Limited evidence exists for the role of hormonal therapy in uterine adenosarcomas. The PIK3/AKT/PTEN pathway is mutated in ∼70 % of adenosarcomas, and this may represent a possible therapeutic target. This article reviews the current state of knowledge concerning uterine adenosarcoma and discusses the management of this rare tumor. Similar content being viewed by others

References

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Nathenson, Vinod Ravi, Nicole Fleming, Wei-Lien Wang, and Anthony Conley declare that they have no conflict of interest. Human and Animal Rights and Informed Consent This article does not contain any studies with human or animal subjects performed by any of the authors. Additional information This article is part of the Topical Collection on Sarcomas Rights and permissions About this article Cite this article Nathenson, M.J., Ravi, V., Fleming, N. et al. Uterine Adenosarcoma: a Review. Curr Oncol Rep 18, 68 (2016). https://doi.org/10.1007/s11912-016-0552-7 Published: DOI: https://doi.org/10.1007/s11912-016-0552-7

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endometriosis

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Adenosarcoma Uterine Neoplasms Adenosarcoma Adenosarcoma Female Humans Prognosis Uterine Neoplasms Uterine Neoplasms

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