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血小板增多症作为肝细胞癌中一种罕见的副肿瘤综合征:一例报告

Thrombocytosis as a Rare Paraneoplastic Syndrome Occurring in Hepatocellular Carcinoma: A Case Report.

作者信息

Abbas Hafsa, Hanif Sana, Tariq Hassan, Chilimuri Sridhar

机构信息

Division of Gastroenterology, Department of Medicine, Bronxcare Hospital Center, Bronx, NY 10457, USA.

Department of Medicine, Bronxcare Hospital Center, Bronx, NY 10457, USA.

出版信息

Gastroenterology Res. 2019 Apr;12(2):96-99. doi: 10.14740/gr1137. Epub 2019 Apr 7.

Abstract

Hepatocellular carcinoma (HCC) affects more than half a million people worldwide each year. Paraneoplastic syndromes associated with HCC include erythrocytosis, hypercalcemia, hypercholesterolemia, hypoglycemia and thrombocytosis. Thrombocytosis is a rare paraneoplastic syndrome in HCC mediated by thrombopoietin (TPO) production. We report a case of thrombocytosis as a paraneoplastic syndrome in a patient with HCC and hepatitis C cirrhosis. A 56-year-old patient was evaluated with abdominal distension and pain of 1-month duration. He had a history of hepatitis C infection with liver cirrhosis, CTP (Child-Turcotte-Pugh) class C, MELD (model for end-stage liver disease) score 22, methadone dependence, alcohol abuse and depression. His physical examination was remarkable for distended abdomen with shifting dullness, palpable hepatomegaly and scleral icterus. Routine laboratory tests showed a platelet count of 754 k/µL, white blood cell count 12.4 k/µL, serum sodium level 128 mEq/L, alanine aminotransferase 93 U/L, aspartate aminotransferase 871 U/L, total serum bilirubin 4.3 mg/dL, direct serum bilirubin 2.8mg/dL and albumin 2.6 g/dL. Computed tomography of the abdomen and pelvis revealed hepatomegaly with numerous hypodensities suspicious for HCC. Abdominal paracentesis was done, serum ascites albumin gradient (SAAG) was 2.4 g/dL consistent with portal hypertension, and spontaneous bacterial peritonitis was ruled out. Magnetic resonance imaging of the liver was consistent with infiltrating HCC, portal vein thrombosis and retroperitoneal lymphadenopathy. His alpha fetoprotein (AFP) level was 79,102 ng/mL and TPO level was 126 pg/mL. mutation was negative and no other cause of reactive thrombocytosis could be identified. One year prior to this admission, the patient was noted to have a normal platelet count and AFP level. He was not considered a candidate for liver transplantation due to ongoing substance abuse, and expired 1 month later. Thrombocytosis is a rare paraneoplastic condition seen in HCC. It is presumed to be secondary to increased production of TPO by the tumor. We observed an elevated level of TPO in our patient. Thrombocytosis in HCC is associated with a high tumor burden, portal vein thrombosis (PVT), serum AFP levels and a poor prognosis. Thrombocytosis in a cirrhotic patient should alert the presence of HCC and is associated with poor outcomes.

摘要

肝细胞癌(HCC)每年在全球影响着超过50万人。与HCC相关的副肿瘤综合征包括红细胞增多症、高钙血症、高胆固醇血症、低血糖症和血小板增多症。血小板增多症是HCC中一种由血小板生成素(TPO)产生介导的罕见副肿瘤综合征。我们报告一例HCC合并丙型肝炎肝硬化患者出现血小板增多症作为副肿瘤综合征的病例。一名56岁患者因腹胀和腹痛1个月前来就诊。他有丙型肝炎感染合并肝硬化病史,Child-Turcotte-Pugh(CTP)分级为C级,终末期肝病模型(MELD)评分22分,美沙酮依赖,酗酒和抑郁症。体格检查发现腹部膨隆,有移动性浊音,可触及肝脏肿大和巩膜黄染。常规实验室检查显示血小板计数为754 k/µL,白细胞计数12.4 k/µL,血清钠水平128 mEq/L,丙氨酸转氨酶93 U/L,天冬氨酸转氨酶871 U/L,总血清胆红素4.3 mg/dL,直接血清胆红素2.8mg/dL,白蛋白2.6 g/dL。腹部和盆腔计算机断层扫描显示肝脏肿大,有许多低密度区,怀疑为HCC。进行了腹腔穿刺,血清腹水白蛋白梯度(SAAG)为2.4 g/dL,符合门静脉高压,排除了自发性细菌性腹膜炎。肝脏磁共振成像与浸润性HCC、门静脉血栓形成和腹膜后淋巴结病相符。他的甲胎蛋白(AFP)水平为79,102 ng/mL,TPO水平为126 pg/mL。 突变呈阴性,未发现其他反应性血小板增多症的原因。此次入院前一年,该患者的血小板计数和AFP水平正常。由于持续存在药物滥用,他未被视为肝移植候选者,1个月后死亡。血小板增多症是HCC中一种罕见的副肿瘤情况。推测它继发于肿瘤产生的TPO增加。我们观察到我们的患者TPO水平升高。HCC中的血小板增多症与高肿瘤负荷、门静脉血栓形成(PVT)、血清AFP水平及不良预后相关。肝硬化患者出现血小板增多症应警惕HCC的存在,且与不良结局相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5bd/6469898/50e8d1f85038/gr-12-096-g001.jpg

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