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罕见的外阴血管肌纤维母细胞瘤:病例系列和文献回顾
Authors Chen L, Sun Q, Zhang J, Xu X, Fan X
Received 13 January 2023
Accepted for publication 13 March 2023
Published 22 March 2023 Volume 2023:15 Pages 427—431
DOI https://doi.org/10.2147/IJWH.S403121
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Professor Elie Al-Chaer
Background: Angiomyofibroblastoma (AMFB) is an uncommon disease with few literature reports, leading to the poor understanding of its diagnosis, treatment, and postoperative follow-up plans among gynecologists.
Objective: To study the clinical and pathological features of vulvar AMFB and discuss its treatment and prognosis.
Case Summary: The 3 cases were characterized by a gradually increasing painless mass in the vulva. Preoperative diagnosis was difficult and mainly depended on ultrasonic examination. Immunohistochemistry confirmed clear boundaries of AMFB. This condition could be completely cured by surgery, and the prognosis was good.
Conclusion: The vulvar AMFB is a rare tumor that is frequently misdiagnosed before surgery. Ultrasound is preferred in auxiliary diagnosis, and surgery remains the best treatment, and long-term follow-up is necessary to avoid recurrence or other complications.
Keywords: angiomyofibroblastoma, diagnosis, surgery, follow-up