Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Department of Anatomic Pathology, University of California, San Francisco, CA, USA.
Histopathology. 2019 Dec;75(6):833-842. doi: 10.1111/his.13957. Epub 2019 Oct 13.
Limited data exist on atypical lipomatous tumour (ALT)/well-differentiated liposarcoma (WDL) and de-differentiated liposarcoma (DDLPS) in children and young adults.
Cases of ALT/WDL/DDLPS arising in patients aged ≤ 40 years were collected from multiple institutional and consultation archives. A total of 116 cases of ALT/WDL (75) and DDLPS (41) were identified, representing fewer than 5% of these tumours seen at our institutions during this time-period. The patients (59 male/57 female) ranged in age from 8 to 40 years. Sites included deep central (abdomen/retroperitoneum/pelvis/groin) (n = 60), extremity (n = 42), trunk (n = 5), head/neck (n = 8) and mediastinum (n = 1). De-differentiated patterns included: high-grade pleomorphic sarcoma, myxofibrosarcoma-like, heterologous rhabdomyoblastic differentiation, low-grade spindle cell sarcoma and homologous lipoblastic differentiation. Forty-one patients experienced a local recurrence and 11 patients with DDLPS developed metastasis. ALT arising in the extremities had lower recurrence rates than deep central WDL (5-year recurrence-free survival 88.9% versus 59.0%; P = 0.002), while patients with deep central DDLPS experienced significantly more adverse events compared to WDL at this site (5-year event-free survival 11.9% versus 59.0%) (P < 0.0001). Seven (of eight) head/neck tumours had follow-up available; five recurred, and one patient (DDLPS) with recurrence also experienced a metastasis. The single mediastinal tumour (DDLPS) recurred and metastasised.
ALT/WDL and DDLPS occurring in patients aged ≤ 40 years is rare, but exhibits similar morphological features to its counterparts in older adults, including potential for heterologous and homologous de-differentiation in the latter. Although case numbers are limited, tumours arising in the head and neck exhibit high rates of adverse events, suggesting that classification as WDL rather than ALT is more appropriate.
关于儿童和青年的非典型性脂肪肿瘤(ALT)/高分化脂肪肉瘤(WDL)和去分化脂肪肉瘤(DDLPS),目前仅有有限的数据。
从多个机构和咨询档案中收集了年龄≤40 岁的患者中发生的 ALT/WDL/DDLPS 病例。共鉴定出 116 例 ALT/WDL(75 例)和 DDLPS(41 例),这不到我们机构在此期间所见这些肿瘤的 5%。患者(59 名男性/57 名女性)年龄 8 至 40 岁。部位包括深部中央(腹部/腹膜后/骨盆/腹股沟)(n=60)、四肢(n=42)、躯干(n=5)、头颈部(n=8)和纵隔(n=1)。去分化模式包括:高级多形性肉瘤、黏液纤维肉瘤样、异源性横纹肌样分化、低度梭形细胞肉瘤和同源性脂肪样分化。41 例患者发生局部复发,11 例 DDLPS 患者发生转移。四肢发生的 ALT 复发率低于深部中央 WDL(5 年无复发生存率 88.9%对 59.0%;P=0.002),而深部中央 DDLPS 患者的不良事件发生率明显高于该部位的 WDL(5 年无事件生存率 11.9%对 59.0%)(P<0.0001)。8 例头颈部肿瘤中有 7 例(7 例)有随访结果;5 例复发,1 例(DDLPS)复发患者也发生转移。唯一的纵隔肿瘤(DDLPS)复发并转移。
年龄≤40 岁的患者中发生的 ALT/WDL 和 DDLPS 很少见,但表现出与老年患者相似的形态学特征,包括后者潜在的异源性和同源性去分化。尽管病例数有限,但发生在头颈部的肿瘤不良事件发生率较高,这表明分类为 WDL 而不是 ALT 更为合适。