Gestational gigantomastia with pseudoangiomatous stromal hyperplasia - a case report of rare entities.

IF 0.4 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI:10.1093/jscr/rjae835
Sophia Moore, Carlos Neblett, Kenneth Appiah, Rory Thompson
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引用次数: 0

Abstract

Gestational gigantomastia (GG) is a rare and severe clinical complication of pregnancy. It is characterized by dramatic and uncontrolled growth of the breasts, often leading to physical discomfort, psychological distress and significant surgical complications. Its pathophysiology is poorly understood; management options include conservative pharmacological and surgical interventions. Pseudoangiomatous stromal hyperplasia of the breast is a very rare, incidental, and histological diagnosis seen predominantly in women aged 30-40 years old, with the management generally involving surgical excision. The authors herein discuss an unusual case of bilateral GG complicated by pseudoangiomatous stromal hyperplasia in a premenopausal Caribbean woman, which is the second reported case in this population, with the first reported by one of our authors.

妊娠期巨乳瘤合并假性血管瘤间质增生1例。
妊娠期巨乳症(GG)是一种罕见而严重的妊娠并发症。它的特点是乳房急剧和不受控制的生长,经常导致身体不适,心理困扰和严重的手术并发症。其病理生理机制尚不清楚;治疗方案包括保守的药物和手术干预。乳腺假性血管瘤间质增生是一种非常罕见的、偶发的组织学诊断,主要见于30-40岁的女性,治疗通常涉及手术切除。作者在此讨论一个不寻常的病例双侧GG合并假性血管瘤间质增生在绝经前加勒比妇女,这是第二例报告的情况下,与第一个报告的作者之一。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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