Ren Dong, O'connell Ryan
Departments of Pathology and Laboratory Medicine, University of California Irvine Medical Center, Orange, California, USA.
Case Rep Oncol Med. 2025 Aug 4;2025:5186729. doi: 10.1155/crom/5186729. eCollection 2025.
Small round cell tumors (SRCTs) are characterized by primitive round cells and a broad differential diagnosis due to their undifferentiated nature, making their diagnosis particularly challenging. Molecular testing is often essential for definitive classification; however, subtle histomorphological features can significantly narrow the differential diagnosis. Here, we present the case of a 44-year-old male who presented with a painless mass (up to 15.6 cm) in the left thigh. Histologic examination of the biopsy revealed solid sheets of monotonous small round cells with scant cytoplasm, hyperchromatic nuclei, and conspicuous nucleoli within the edematous to myxoid stroma. Notably, capillary-sized blood vessels were present throughout the tumor, which made BCOR-rearranged sarcomas, myxoid liposarcoma with small cell morphology, and GLI1-altered soft tissue tumors the main differential diagnoses. Classic morphology of myxoid liposarcoma was not present. Immunohistochemical (IHC) staining revealed that the tumor cells were diffusely positive for SOX11 but negative for SATB2, CD56, S100, and TLE1. This immunophenotype, combined with the histological findings, strongly suggested a diagnosis of myxoid liposarcoma with high-grade features. Fluorescence in situ hybridization (FISH) analysis confirmed a DDIT3 rearrangement, supporting this diagnosis. We hope this case will enhance pathologists' understanding and recognition of the importance of utilizing subtle histologic features to establish the differential diagnosis and accurately diagnose SRCTs in biopsy specimens prior to molecular testing.
小圆细胞肿瘤(SRCTs)的特征是原始的圆形细胞,由于其未分化的性质,鉴别诊断范围广泛,这使得其诊断极具挑战性。分子检测对于明确分类通常至关重要;然而,细微的组织形态学特征可显著缩小鉴别诊断范围。在此,我们报告一例44岁男性患者,其左大腿出现无痛性肿块(最大直径达15.6厘米)。活检组织学检查显示,在水肿至黏液样基质内,有实性片状的单调小圆细胞,胞质稀少,核深染,核仁明显。值得注意的是,整个肿瘤内均有毛细血管大小的血管,这使得BCOR重排肉瘤、具有小细胞形态的黏液样脂肪肉瘤以及GLI1改变的软组织肿瘤成为主要的鉴别诊断对象。黏液样脂肪肉瘤的典型形态并不存在。免疫组织化学(IHC)染色显示,肿瘤细胞SOX11弥漫性阳性,但SATB2、CD56、S100和TLE1阴性。这种免疫表型,结合组织学表现,强烈提示诊断为具有高级别特征的黏液样脂肪肉瘤。荧光原位杂交(FISH)分析证实存在DDIT3重排,支持这一诊断。我们希望该病例能增强病理学家对利用细微组织学特征建立鉴别诊断并在分子检测之前准确诊断活检标本中SRCTs重要性的理解和认识。