侵袭性血管粘液瘤经术前激素治疗完全切除并保留器官1例。

Q4 Medicine
Masato Kambe, Sumito Sato, Makoto Tatsumi, Tatsuya Kinjo, Takashi Hamano, Yasuyuki Kobayashi
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引用次数: 0

摘要

34岁女性首次怀孕时出现盆腔肿瘤,最初怀疑为硬纤维瘤,随后进行了治疗。第二胎剖宫产活检证实为侵袭性血管粘液瘤(AAM)。产后肿瘤生长促使患者接受为期16个月的促性腺激素释放激素激动剂治疗(醋酸leuprorelin,每4周1.88 mg), 12次剂量后肿瘤大小从20×13 cm缩小到10×7.5 cm。然而,出现了疲劳和恶心等不良反应,肿瘤进一步缩小很小,需要手术干预。左侧骶骨后入路可以完全切除肿瘤,同时保留直肠、生殖器官和自主神经。AAM是一种发生在年轻女性骨盆或外生殖器的罕见肿瘤。虽然手术切除仍然是主要的治疗方法,但没有标准化的方法。该病例证明了术前激素治疗在显著缩小肿瘤大小,从而促进器官保存的完全切除方面的作用,并强调了其在AAM治疗中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A Case of Aggressive Angiomyxoma Completely Resected with Organ Preservation by Preoperative Hormone Therapy].

A 34‒year‒old woman presented with a pelvic tumor in the Douglas pouch during her first pregnancy, initially suspected to be a desmoid tumor and managed subsequently. Biopsy during cesarean section in her second pregnancy confirmed aggressive angiomyxoma (AAM). Postpartum tumor growth prompted a 16‒month course of gonadotropin‒releasing hormone agonist therapy (leuprorelin acetate, 1.88 mg every 4 weeks), which reduced tumor size from 20×13 cm to 10×7.5 cm after 12 doses. However, adverse effects, such as fatigue and nausea occurred, and further tumor shrinkage was minimal, necessitating surgical intervention. A left posterior sacral approach allowed complete tumor resection while preserving the rectum, reproductive organs, and autonomic nerves. AAM is a rare tumor of the pelvis or external genitalia in young women. Although surgical excision remains the primary treatment, no standardized approach exists. This case demonstrates the role of preoperative hormone therapy in significantly reducing tumor size, thereby facilitating complete excision with organ preservation, and underscore its potential role in AAM management.

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