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年轻女性巨大外阴血管肌纤维母细胞瘤罕见病例。

Rare case of huge vulvar angiomyofibroblastoma in a young female.

作者信息

Anggraeni Tricia Dewi, Nuranna Laila, Luthfiyanto Muhammad, Siregar Nuryati Chairani, Hellyanti Tantri, Siregar Trifonia Pingkan, Alexandra Leonardo

机构信息

Department of Obstetrics and Gynecology, Dr. Cipto Mangunkusumo National General Hospital, Jakarta, Indonesia.

Department of Pathological Anatomy, Dr. Cipto Mangunkusumo National General Hospital, Jakarta, Indonesia.

出版信息

Gynecol Oncol Rep. 2021 Mar 22;36:100751. doi: 10.1016/j.gore.2021.100751. eCollection 2021 May.

DOI:10.1016/j.gore.2021.100751
PMID:33869711
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8040263/
Abstract

Mesenchymal tumours of the vulva are rare and consist of two types, difficult to distinguish but with different prognoses. Angiomyofibroblastoma (AMFB) is a benign tumour, whereas Aggressive Angiomyxoma (AA) is an infiltrating tumour. We describe a 22-year-old nulliparous patient with a vulvar mass sized 19 cm in diameter. After preoperative assessment by ultrasound, chest X-ray, and MRI, wide excision on the tumour was done and diagnosed as AMFB. Differentiation from AA is being discussed.

摘要

外阴间叶性肿瘤较为罕见,由两种类型组成,难以区分但预后不同。血管肌纤维母细胞瘤(AMFB)是一种良性肿瘤,而侵袭性血管黏液瘤(AA)是一种浸润性肿瘤。我们描述了一名22岁未生育的患者,其外阴有一个直径为19厘米的肿块。在通过超声、胸部X线和MRI进行术前评估后,对肿瘤进行了广泛切除,并诊断为AMFB。目前正在讨论与AA的鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b76e/8040263/429545103fda/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b76e/8040263/a631c7aeb4d7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b76e/8040263/1d4622d9d495/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b76e/8040263/429545103fda/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b76e/8040263/a631c7aeb4d7/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b76e/8040263/1d4622d9d495/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b76e/8040263/429545103fda/gr3.jpg

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