雄激素不敏感综合征的双侧乳腺叶状瘤。

IF 0.8 Q4 SURGERY
Aishwarya Sunil Dutt, Girish Bakhshi, Chandrakant Sabale, Ravi Landge, Sushrut Baligar, Rajalakshmi V, Madhu Jha, Sampada Joshi, Chettubattina Ravi Teja
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引用次数: 0

摘要

叶状瘤是一种罕见的肿瘤,只在女性中发现。它可以根据疾病的侵袭性分为良性、中度或恶性。术前充分的临床评估,结合组织病理学和影像学检查,可以制定适当的治疗策略,以避免未来复发。完全雄激素不敏感综合征(CAIS)与基因型男性相关,可通过核型分析证实,具有表型女性特征。本病例是CAIS患者中第一例双侧乳腺叶状瘤。术前评估提示双侧叶状肿瘤伴双侧性腺位于腹股沟区,术后病理分析证实为睾丸。一个简短的病例报告,回顾文献提出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bilateral Breast Phyllodes Tumor in Androgen Insensitivity Syndrome.

Bilateral Breast Phyllodes Tumor in Androgen Insensitivity Syndrome.

Bilateral Breast Phyllodes Tumor in Androgen Insensitivity Syndrome.

Bilateral Breast Phyllodes Tumor in Androgen Insensitivity Syndrome.

Phyllodes is a rare tumor found exclusively in females. It can be classified into benign, intermediate, or malignant variety based on the aggressive nature of the disease. With adequate preoperative clinical assessment combined with histopathology and radiological investigations the adequate treatment strategy can be formulated to avoid future recurrences. Complete androgen insensitivity syndrome (CAIS) is associated with a genotypic male, which can be confirmed by karyotyping, with phenotypic female characteristics. The present case is the first case of bilateral breast phyllodes tumor in a patient with CAIS. Preoperative assessment was suggestive of bilateral phyllodes tumor with bilateral gonads in the inguinal region which was confirmed to be testis postoperatively on histopathological analysis. A brief case report with review of literature is presented.

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来源期刊
Surgery Journal
Surgery Journal SURGERY-
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