Pathology, Kasturba Medical College Manipal, Manipal, India.
Pathology, Manipal Academy of Higher Education, Manipal, India.
Fetal Pediatr Pathol. 2022 Feb;41(1):134-140. doi: 10.1080/15513815.2020.1745972. Epub 2020 Apr 10.
Epithelioid sarcoma is a malignant mesenchymal neoplasm with evidence of epithelial differentiation. All the cases reported in the solid organs are of "proximal type" occurring in adults. We report a primary epithelioid sarcoma arising in the adrenal gland of a young male. An 11-year-old male patient presented with right loin pain. Imaging revealed a 10.8 × 10.8 × 13.5 cm complex cystic mass with obscured right adrenal gland. Clinical and radiological studies did not reveal metastases. Histologic features were those of proximal type epithelioid sarcoma with extensive central necrosis. Immunohistochemistry showed strong positivity for pancytokeratin, vimentin, and CD34. Nuclear expression of SMARCB1 (INI-1) protein was lost. Proximal type of epithelioid sarcoma can arise from solid organs such as the adrenal.
上皮样肉瘤是一种具有上皮分化证据的恶性间叶性肿瘤。所有在实体器官中报道的病例均为“近端型”,发生于成年人。我们报告了一例发生在年轻男性肾上腺的原发性上皮样肉瘤。
一名 11 岁男性患者因右侧腰痛就诊。影像学检查显示一个 10.8×10.8×13.5cm 的复杂囊性肿块,右侧肾上腺模糊不清。临床和影像学研究未发现转移。组织学特征为具有广泛中央坏死的近端型上皮样肉瘤。免疫组织化学显示广谱细胞角蛋白、波形蛋白和 CD34 强阳性。SMARCB1(INI-1)蛋白核表达缺失。
上皮样肉瘤的近端型可发生于肾上腺等实体器官。