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假性血管瘤样间质增生。一名12岁女孩双侧乳房切除术病例。

Pseudoangiomatous stromal hyperplasia. A case for bilateral mastectomy in a 12-year-old girl.

作者信息

Singh Kimberly A, Lewis Melinda M, Runge Robyn L, Carlson Grant W

机构信息

Department of Surgery, Emory University School of Medicine, Atlanta, Georgia, USA.

出版信息

Breast J. 2007 Nov-Dec;13(6):603-6. doi: 10.1111/j.1524-4741.2007.00499.x.

Abstract

Pseudoangiomatous stromal hyperplasia (PASH) is a benign proliferation of breast stromal cells with a complex pattern of interanastomosing spaces lined by myofibroblasts and is most commonly seen in women of child-bearing age. PASH is a frequent incidental microscopic finding in breast biopsies. Nodular PASH, however, resulting in a clinically appreciable mass and rapid growth is a rare entity, with only four such patients cited in the literature. Surgical excision results in a cure in the majority of cases, with a recurrence rate of approximately 7-22%. We report a case of a 12-year-old girl with nodular PASH who presented with bilateral breast enlargement refractory to surgical excisions, eventually requiring bilateral mastectomies. To our knowledge, our patient is the youngest patient to have nodular PASH and to undergo bilateral mastectomies.

摘要

假血管瘤样间质增生(PASH)是一种乳腺间质细胞的良性增生,具有由肌成纤维细胞衬里的相互吻合的复杂间隙模式,最常见于育龄妇女。PASH是乳腺活检中常见的偶然微观发现。然而,导致临床上可察觉的肿块和快速生长的结节性PASH是一种罕见的情况,文献中仅引用了4例此类患者。手术切除在大多数病例中可治愈,复发率约为7%-22%。我们报告一例12岁患有结节性PASH的女孩,她出现双侧乳腺肿大,手术切除无效,最终需要双侧乳房切除术。据我们所知,我们的患者是患有结节性PASH并接受双侧乳房切除术的最年轻患者。

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