妊娠期假性血管瘤间质增生表现为巨乳症:一罕见乳腺实体病例报告及多学科团队的临床推荐。

IF 0.6 Q4 SURGERY Case Reports in Surgery Pub Date : 2023-01-01 DOI:10.1155/2023/9279934
S Jennifer Wang, Shivi Maheswaran, Rosemary Reiss, Leah H Portnow, Jane Brock, Lara Novak, Jessica Erdmann-Sager, Thanh U Barbie
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引用次数: 0

摘要

假性血管瘤间质增生(PASH)在妊娠期表现为巨乳症是罕见的,但可对母亲和胎儿造成严重的临床后果。案例演示。43岁女性,活检证实有双侧PASH病史,于妊娠22 3/7周出现双侧乳房肿大,有症状。经过多学科的治疗,她接受了双侧乳房切除术,足月分娩,没有其他并发症。结论:妊娠中期因pash诱发的巨乳症而行乳房切除术的孕妇恢复较快,胎儿风险低。鉴于这种乳腺实体的罕见性,管理指南很少。我们的病例报告是全面审查这种情况的努力,并分享由我们机构的多学科团队提出的临床建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Gestational Pseudoangiomatous Stromal Hyperplasia Presenting as Gigantomastia: A Case Report of a Rare Breast Entity with Clinical Recommendations by a Multidisciplinary Team.

Introduction: Pseudoangiomatous stromal hyperplasia (PASH) presenting as gigantomastia is rare in pregnancy but can result in severe clinical consequences for both mother and fetus. Case Presentation. A 43-year-old female with a history of biopsy-proven bilateral PASH presented at 22 3/7 weeks gestation with massive bilateral breast enlargement that was symptomatic. After multidisciplinary care, she underwent bilateral mastectomies and delivered at term with no additional complications.

Conclusion: Pregnant women who undergo mastectomies for PASH-induced gigantomastia during their second trimesters will likely recover quickly, and fetal risks are low. Given the rarity of this breast entity, management guidelines are sparse. Our case report is an effort to comprehensively review this condition and share the clinical recommendations made by our institution's multidisciplinary team.

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