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14岁女孩乳腺假血管瘤样间质增生(PASH)的诊断与治疗挑战:基于病例的综述

Diagnostic and Therapeutic Challenges in Pseudoangiomatous Stromal Hyperplasia (PASH) of the Breast in a 14-Year-Old Girl: A Case-Based Review.

作者信息

Sosnowska-Sienkiewicz Patrycja, Mańkowski Przemysław, Januszkiewicz-Lewandowska Danuta

机构信息

Department of Pediatric Surgery, Medical University of Warsaw, Żwirki i Wigury 63A Street, 02-091 Warsaw, Poland.

Department of Pediatric Surgery, Traumatology and Urology, Poznan University of Medical Sciences, ul. Fredry 10, 61-701 Poznan, Poland.

出版信息

Diagnostics (Basel). 2025 Sep 20;15(18):2395. doi: 10.3390/diagnostics15182395.

Abstract

Pseudoangiomatous stromal hyperplasia (PASH) is a benign breast lesion characterized by stromal myofibroblast proliferation forming slit-like pseudoangiomatous spaces. Although most frequently diagnosed in premenopausal women, it has also been reported in adolescent girls, where it may present as a rapidly enlarging mass that mimics fibroadenoma or phyllodes tumor. The pathogenesis is thought to be hormonally influenced, particularly by progesterone, with a possible role for estrogen. We report the case of a 14-year-old girl who presented with a painless, rapidly growing mass in the left breast, first noticed approximately six months earlier. Clinical examination revealed a mobile lesion about 10 cm in diameter without skin changes, lymphadenopathy, or nipple discharge. Ultrasound and MRI demonstrated a large, well-circumscribed solid tumor (10.4 × 11.2 × 4.2 cm) displacing normal breast tissue but without infiltration; both were classified as BI-RADS 4. Given the tumor size, diagnostic uncertainty, and potential risk of a non-representative core needle biopsy, a decision was made to proceed with primary radical excision. The mass was completely removed with preservation of the glandular tissue. Histopathology confirmed PASH, described macroscopically as a solid, gray-yellow, encapsulated tumor and microscopically as slit-like spaces lined by spindle cells (CD34+, CD31-). Postoperatively, the breast gradually regained symmetry with the contralateral side, and at 14 months of follow-up, no recurrence was observed. PASH, although benign, may present as a large breast tumor in adolescents and clinically mimic both benign and malignant lesions. Histological evaluation based on an adequately performed biopsy is crucial for accurate diagnosis. Complete excision with capsule preservation is recommended to minimize the risk of recurrence. In adolescents, a watchful waiting approach after surgery may be beneficial, as breast tissue often remodels and regains symmetry spontaneously, reducing the need for reconstructive procedures. This case underscores the importance of individualized diagnostic and therapeutic strategies in managing rare benign breast lesions in pediatric patients.

摘要

假血管瘤样间质增生(PASH)是一种良性乳腺病变,其特征为间质肌成纤维细胞增殖,形成裂隙样假血管瘤样腔隙。尽管最常诊断于绝经前女性,但也有在青春期女孩中报道的病例,在青春期女孩中它可能表现为迅速增大的肿块,类似纤维腺瘤或叶状肿瘤。其发病机制被认为受激素影响,尤其是受孕酮影响,雌激素可能也起作用。我们报告一例14岁女孩,她左侧乳房出现一个无痛、迅速生长的肿块,大约6个月前首次被注意到。临床检查发现一个可活动的病变,直径约10厘米,无皮肤改变、淋巴结病或乳头溢液。超声和磁共振成像显示一个大的、边界清楚的实性肿瘤(10.4×11.2×4.2厘米),推移正常乳腺组织但无浸润;两者均分类为BI-RADS 4类。鉴于肿瘤大小、诊断不确定性以及非代表性粗针穿刺活检的潜在风险,决定进行一期根治性切除。肿块被完整切除,同时保留了腺组织。组织病理学证实为PASH,大体上描述为实性、灰黄色、有包膜的肿瘤,显微镜下为梭形细胞(CD34阳性、CD31阴性)衬里的裂隙样腔隙。术后,乳房逐渐与对侧恢复对称,在14个月的随访中,未观察到复发。PASH虽然是良性的,但在青少年中可能表现为大的乳腺肿瘤,在临床上可类似良性和恶性病变。基于充分活检进行的组织学评估对于准确诊断至关重要。建议完整切除并保留包膜以将复发风险降至最低。在青少年中,术后密切观察的方法可能有益,因为乳腺组织常可自发重塑并恢复对称,减少了重建手术的必要性。该病例强调了个体化诊断和治疗策略在处理儿科患者罕见良性乳腺病变中的重要性。

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