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以巨乳症形式表现的妊娠期假性血管瘤样间质增生:一例罕见乳腺病变病例报告及多学科团队的临床建议

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

作者信息

Wang S Jennifer, Maheswaran Shivi, Reiss Rosemary, Portnow Leah H, Brock Jane, Novak Lara, Erdmann-Sager Jessica, Barbie Thanh U

机构信息

Division of Surgical Oncology, Department of Surgery, Brigham and Women's Hospital, Boston, MA, USA.

Division of Breast Surgery, Department of Surgery, Brigham and Women's Hospital, Boston, MA, USA.

出版信息

Case Rep Surg. 2023 Jul 10;2023:9279934. doi: 10.1155/2023/9279934. eCollection 2023.

Abstract

INTRODUCTION

Pseudoangiomatous stromal hyperplasia (PASH) presenting as gigantomastia is rare in pregnancy but can result in severe clinical consequences for both mother and fetus. . 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.

摘要

引言

以巨乳症形式出现的假血管瘤样间质增生(PASH)在孕期罕见,但可对母亲和胎儿造成严重临床后果。一名43岁女性,有活检证实的双侧PASH病史,在妊娠22 3/7周时出现双侧乳房大量增大且有症状。经过多学科治疗,她接受了双侧乳房切除术,并足月分娩,无其他并发症。

结论

在孕中期因PASH引起的巨乳症接受乳房切除术的孕妇可能恢复迅速,且胎儿风险较低。鉴于这种乳腺病变罕见,管理指南稀少。我们的病例报告旨在全面回顾这种情况,并分享我们机构多学科团队提出的临床建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e583/10352531/1d0c101b1d77/CRIS2023-9279934.001.jpg

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