Chhabra Raja, Vidushi Aditya, Rajpurohit Sajjan, Singh Jasbir, Osama Md Ali
Department of Medical Oncology, BLK-MAX Super Speciality Hospital, Pusa Road, New Delhi, India.
Department of Pathology, BLK-MAX Super Speciality Hospital, Pusa Road, New Delhi, India.
Indian J Surg Oncol. 2024 Jun;15(2):370-374. doi: 10.1007/s13193-024-01895-0. Epub 2024 Feb 13.
Sarcomatoid hepatocellular carcinoma is a rare histologic variant of primary liver cancer comprising of malignant spindle cells and typical hepatocellular carcinoma (HCC). In terms of clinical presentation, they usually exhibit extensive tumor burden due to their larger size and a metastatic disease at the time of diagnosis as compared to conventional HCC. Tumor lysis syndrome is an oncological emergency, usually seen after cytotoxic chemotherapy in haematological malignancies. Here, we highlight a case of 76-year old male with no comorbidities, presenting with an excruciating backache and a paravertebral soft tissue mass and multiple osteolytic lesions, was clinically suspected to be a plasma cell neoplasm. On further evaluation, the patient was diagnosed of a sarcomatoid variant of hepatocellular carcinoma. This report showcases multiple rare findings by the presence of non-specific symptoms, non-cirrhotic liver, normal serum alpha protein levels and the occurrence of a spontaneous tumor lysis syndrome in a solid malignancy.
肉瘤样肝细胞癌是原发性肝癌一种罕见的组织学变体,由恶性梭形细胞和典型的肝细胞癌(HCC)组成。在临床表现方面,与传统肝细胞癌相比,它们通常因体积较大且在诊断时已发生转移而表现出广泛的肿瘤负荷。肿瘤溶解综合征是一种肿瘤急症,通常见于血液系统恶性肿瘤的细胞毒性化疗后。在此,我们重点介绍一例76岁男性患者,无合并症,因剧烈背痛、椎旁软组织肿块和多处溶骨性病变就诊,临床怀疑为浆细胞肿瘤。进一步评估后,该患者被诊断为肝细胞癌的肉瘤样变体。本报告展示了多个罕见发现,包括出现非特异性症状、非肝硬化肝脏、血清甲胎蛋白水平正常以及在实体恶性肿瘤中发生自发性肿瘤溶解综合征。