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伪装成失代偿期肝硬化的急性髓系白血病

Acute Myeloid Leukemia Masquerading as Decompensated Cirrhosis.

作者信息

Ahdi Hardeep S, Mannem Seetharam, Lakha Asif

机构信息

Internal Medicine, Advocate Lutheran General Hospital, Park Ridge, USA.

Gastroenterology, Advocate Lutheran General Hospital, Park Ridge, USA.

出版信息

Cureus. 2022 Jul 31;14(7):e27538. doi: 10.7759/cureus.27538. eCollection 2022 Jul.

Abstract

Patients with known cirrhosis who present with anemia, thrombocytopenia, acute renal failure, and confusion are usually presenting with decompensated cirrhosis. We present a patient with known alcoholic cirrhosis presenting with the above abnormalities, initially thought to be decompensated cirrhosis but found to have acute myeloid leukemia (AML) with acute blast crisis. This case was presented as a poster at the American College of Gastroenterology Annual Scientific Meeting held on October 22-27, 2021. A 59-year-old male with a history of compensated alcoholic cirrhosis presented with unresponsiveness. On physical exam, vitals were normal, he appeared lethargic with generalized pallor, and rectal exam demonstrated an empty rectal vault with no blood or stool noted. Labs were notable for hemoglobin 3.1 g/dL, platelet count 41,000/µL, creatinine 5.2mg/dL, aspartate aminotransferase (AST) 242 U/L, alanine aminotransferase (ALT) 138 U/L, bilirubin 0.8 mg/dL, lactic acid 8.5 mmol/L, international normalized ratio (INR) 1.8, ammonia 51µmol/L. Imaging with CT head was unremarkable and CT abdomen demonstrated cirrhotic morphology of the liver with a small amount of ascites. Upper endoscopy was performed with no evidence of varices. Paracentesis demonstrated a high serum-ascites albumin gradient with low total protein consistent with portal hypertension. He was intubated for airway protection due to worsening encephalopathy. A peripheral smear was performed which showed myeloblasts with no signs of hemolysis. Bone marrow biopsy was subsequently performed which revealed 38% myeloblasts and features of myelodysplastic syndrome suggestive of secondary AML. Chemotherapy was not initiated as he was acutely critically ill and he expired shortly thereafter.  AML can present with symptomatic anemia, bleeding, mental status changes due to central nervous system involvement, organomegaly, and renal insufficiency. Diagnosing AML in the setting of decompensated liver cirrhosis can be difficult as the clinical presentations can be similar at times. Thus, hematological causes should be considered when there is profound anemia with no acute blood loss early in the course.

摘要

已知患有肝硬化且出现贫血、血小板减少、急性肾衰竭和意识障碍的患者通常表现为失代偿期肝硬化。我们报告一例已知酒精性肝硬化患者,出现上述异常情况,最初被认为是失代偿期肝硬化,但后来发现患有急性髓系白血病(AML)伴急性原始细胞危象。该病例于2021年10月22日至27日举行的美国胃肠病学会年度科学会议上以海报形式展示。一名有代偿期酒精性肝硬化病史的59岁男性出现无反应状态。体格检查时,生命体征正常,他看起来嗜睡,全身苍白,直肠指检显示直肠空虚,未发现血液或粪便。实验室检查结果显示血红蛋白3.1g/dL、血小板计数41,000/µL、肌酐5.2mg/dL、天冬氨酸转氨酶(AST)242U/L、丙氨酸转氨酶(ALT)138U/L、胆红素0.8mg/dL、乳酸8.5mmol/L、国际标准化比值(INR)1.8、氨51µmol/L。头颅CT成像未见异常,腹部CT显示肝脏呈肝硬化形态,有少量腹水。进行了上消化道内镜检查,未发现静脉曲张迹象。腹腔穿刺显示血清-腹水白蛋白梯度高,总蛋白低,符合门静脉高压。由于脑病恶化,为保护气道对他进行了插管。进行了外周血涂片检查,显示有原始粒细胞,无溶血迹象。随后进行了骨髓活检,结果显示原始粒细胞占38%,并有骨髓增生异常综合征的特征,提示继发性AML。由于他病情严重危急,未开始化疗,此后不久他就去世了。AML可表现为有症状的贫血、出血、因中枢神经系统受累导致的精神状态改变、器官肿大和肾功能不全。在失代偿期肝硬化的情况下诊断AML可能很困难,因为临床表现有时可能相似。因此,在病程早期出现严重贫血且无急性失血时,应考虑血液学原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef2e/9428419/1385964ea686/cureus-0014-00000027538-i01.jpg

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