Bendimerad Mehdi Aymen, Meilhac-Fournier Catherine, Nika Eleni, Piolat Christian, Giovannini Diane, Valmary-Degano Séverine
Service d'anatomie pathologique, CHU de Grenoble-Alpes, 38000 Grenoble, France.
Service de chirurgie pédiatrique, CHU de Grenoble-Alpes, 38000 Grenoble, France.
Ann Pathol. 2024 Sep;44(5):372-377. doi: 10.1016/j.annpat.2024.05.001. Epub 2024 May 29.
We report the case of a 14 year-old teenager who has SC hemoglobinosis and presented with a tumor syndrome with a retro-peritoneal mass, a supraclavicular lymph node and a mid-renal lesion. The microscopic examination revealed an undifferentiated tumor proliferation infiltrating the lymph node parenchyma. This tumor proliferation was INI1/SMARCB1-deficient, and expressed cytokeratins. Given the fact that the histopathological data showed an undifferentiated INI1-deficient carcinoma and that the patient has a kidney lesion and a sickle cell trait, the final diagnosis was lymph node metastasis of SMARCB1-deficient renal medullary carcinoma (OMS 2022).
我们报告了一例14岁青少年,患有SC血红蛋白病,表现为肿瘤综合征,伴有腹膜后肿块、锁骨上淋巴结和肾中部病变。显微镜检查显示未分化肿瘤增殖浸润淋巴结实质。这种肿瘤增殖缺乏INI1/SMARCB1,并表达细胞角蛋白。鉴于组织病理学数据显示为未分化的INI1缺乏型癌,且患者有肾脏病变和镰状细胞性状,最终诊断为SMARCB1缺乏型肾髓质癌的淋巴结转移(2022年版《肿瘤学》)。