19岁女孩子宫内膜缪勒氏腺肉瘤一例报告及文献复习

A. Miyoshi, Y. Ueda, K. Sato, T. Kimura
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引用次数: 0

摘要

青春期女孩发生子宫内膜缪勒氏腺肉瘤极为罕见,迄今为止仅报道了15例20岁以下的病例。我们在此报告一例青少年缪勒氏腺肉瘤,并对以往有关此类罕见肿瘤的文献作一最新回顾。我们的19岁的病例提出了六个月的月经延长的历史。她还没有任何性关系。经肉眼检查,发现阴道内有易碎的肿块,易出血。磁共振成像(MRI)显示4.0×2.0 cm肿块。肿瘤似乎轻微侵犯子宫体肌层。经阴道超声检查证实在子宫颈和阴道有一个4.0厘米的肿块。肿瘤活检诊断为子宫内膜缪勒氏腺肉瘤。我们进行了全腹子宫切除术(TAH)和双侧输卵管切除术(BS)。术后标本被诊断为pT1aNXM0子宫内膜苗勒氏腺肉瘤。患者不需要辅助化疗。每3个月监测一次,28个月无复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mullerian Adenosarcoma of the Endometrium in a 19-Year-Old Girl: Case Report and a Literature Review
Mullerian adenosarcoma of the endometrium in adolescent girls is extremely rare, with only fifteen cases under 20 years old having been reported to date. We describe here a new case of adolescent Mullerian adenosarcoma and provide an updated review of the previous literature on such rare tumors. Our 19-year-old case presented with a six-month history of prolonged menstruation. She had not yet had any sexual relationship. On gross examination, a fragile mass was seen in her vagina that bled easily. A 4.0×2.0 cm mass was visualized with Magnetic Resonance Imaging (MRI). The tumor seemed to slightly invade the myometrium of the uterine corpus. Transvaginal ultrasound sonography confirmed the presence of a 4.0 cm mass located in the cervix and vagina. The tumor biopsy was diagnosed as a Mullerian adenosarcoma of the endometrium. We performed a Total Abdominal Hysterectomy (TAH) and Bilateral Salpingectomy (BS). The post-surgical specimen was diagnosed as a pT1aNXM0 Mullerian adenosarcoma of the endometrium. The patient did not require adjuvant chemotherapy. She has been monitored every 3 months and has been without recurrence now for 28 months.
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