Radiology Department, Clínica Alemana de Santiago, Vitacura 5951, 7630000, Santiago, RM, Chile.
Eur Radiol. 2023 Dec;33(12):8399-8406. doi: 10.1007/s00330-023-09877-6. Epub 2023 Jun 29.
To determine the upgrade rate of radial scar (RS) and complex sclerosing lesions (CSL) diagnosed with percutaneous biopsy. The secondary objectives were to determine the new atypia rate after surgery and to assess the diagnosis of subsequent malignancy on follow-up.
This single-institution retrospective study had IRB approval. All image-targeted RS and CSL diagnosed with percutaneous biopsy between 2007 and 2020 were reviewed. Patient demographics, imaging presentation, biopsy characteristics, histological report, and follow-up data were collected.
During the study period, 120 RS/CSL were diagnosed in 106 women (median age, 43.5 years; range, 23-74), and 101 lesions were analyzed. At biopsy, 91 (90.1%) lesions were not associated with another atypia or malignancy and 10 (9.9%) were associated with another atypia. Out of the 91 lesions that were not associated with malignancy or atypia, 75 (82.4%) underwent surgical excision, and one upgrade to low-grade CDIS was detected (1.3%). Among the 10 lesions initially associated with another atypia, 9 were surgically excised and no malignancy was detected. After a median follow-up of 47 months (range: 12-143 months), two (1.98%) developed malignancy in a different quadrant; in both cases, another atypia was present at biopsy.
We found a low upgrade rate on image-detected RS/CSL, with or without another atypia associated. Associated atypia was underdiagnosed at biopsy in almost one-third of cases. Subsequent cancer risk could not be established because the only two cases were associated with another high-risk lesion (HRL), which might have increased the patient's risk of developing malignancy.
Our upgrade rates of RS/CSL with or without atypia diagnosed with core needle biopsy are almost as low as the ones reported with larger sampling methods. This result has particular importance in places with limited accessibility to US-guided vacuum-assisted biopsy.
•New evidence is showing lower upgrade rates of RS and CSL after surgery, leading to a more conservative management with extensive sampling using VAB or VAE. •Our study showed only one upgrade to a low-grade DCIS after surgery, yielding an upgrade rate of 1.33%. •During follow-up, no new malignancy was detected in the same quadrant where RS/CSL was diagnosed, including patients without surgery.
确定经皮活检诊断的放射状瘢痕(RS)和复杂硬化性病变(CSL)的升级率。次要目标是确定手术后新的非典型率,并评估随访中后续恶性肿瘤的诊断。
这项单机构回顾性研究获得了 IRB 的批准。回顾了 2007 年至 2020 年间经皮活检诊断的所有图像靶向 RS 和 CSL。收集了患者人口统计学、影像学表现、活检特征、组织学报告和随访数据。
在研究期间,106 名女性中诊断出 120 例 RS/CSL(中位年龄 43.5 岁;范围 23-74 岁),其中 101 例病变进行了分析。在活检时,91 例(90.1%)病变与另一种非典型或恶性肿瘤无关,10 例(9.9%)与另一种非典型有关。在与恶性肿瘤或非典型性无关的 91 例病变中,75 例(82.4%)接受了手术切除,1 例(1.3%)升级为低级别 CDIS。在最初与另一种非典型性相关的 10 例病变中,9 例接受了手术切除,未发现恶性肿瘤。中位随访 47 个月(范围 12-143 个月)后,有 2 例(1.98%)在不同象限发生恶性肿瘤;在这两种情况下,活检时均存在另一种非典型性。
我们发现,经影像学检测的 RS/CSL 无论是否伴有另一种非典型性,其升级率均较低。在近三分之一的病例中,活检时对相关非典型性的诊断不足。由于仅有的两例病例均与另一种高危病变(HRL)相关,这可能增加了患者发生恶性肿瘤的风险,因此无法确定后续癌症的风险。
我们使用核心针活检诊断的伴有或不伴有非典型性的 RS/CSL 的升级率几乎与使用更大取样方法报告的升级率一样低。这一结果在 US 引导下真空辅助活检可及性有限的地方尤为重要。
•新证据显示,RS 和 CSL 手术后的升级率较低,这导致采用 VAB 或 VAE 进行广泛取样的更保守治疗。•我们的研究显示,手术后仅有一例升级为低级别 DCIS,升级率为 1.33%。•在随访期间,在诊断出 RS/CSL 的同一象限未发现新的恶性肿瘤,包括未接受手术的患者。