急性髓性白血病和失代偿性肝硬化同时发病:一例罕见病例。

IF 1.3 Q3 MEDICINE, GENERAL & INTERNAL
Cureus Pub Date : 2025-06-29 eCollection Date: 2025-06-01 DOI:10.7759/cureus.86990
Wilfredo J Javier-Rojas, Alvin B Newman-Caro, Yizhi Lin, Carlos Montero
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摘要

急性髓性白血病(AML)是一种血液系统恶性肿瘤,其特征是异常髓性前体细胞不受控制的增殖,而肝硬化则涉及进行性肝纤维化和结构扭曲。尽管不同的病理生理,两者都可以呈现重叠的临床特征,使诊断过程复杂化。我们报告一位78岁的女性,有一个月的双侧下肢水肿、呼吸困难、疲劳、厌食、低烧和进行性腹胀的病史。入院时,综合代谢检查显示轻度转氨炎、高胆红素血症和低白蛋白血症。全血细胞计数与差异显示中度白细胞增多,大细胞性贫血低于输血阈值,严重血小板减少,10%循环母细胞。腹部和骨盆的增强计算机断层扫描显示肝硬化、门脉高压、食管静脉曲张、脾肿大伴梗死和少量腹水。慢性肝病检查也显示可能有遗传性血色素沉着症。包括外周血流式细胞术在内的血液学评估证实,11.4%的细胞表达CD34、CD117、HLA-DR、CD33和CD13。该病例突出了新诊断的急性髓性白血病和肝硬化同时出现的罕见情况,强调了重叠症状带来的诊断挑战以及及时识别和管理多学科方法的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Simultaneous Onset of Acute Myeloid Leukemia and Decompensated Cirrhosis: A Rare Case.

Acute myeloid leukemia (AML) is a hematologic malignancy marked by uncontrolled proliferation of abnormal myeloid precursor cells, while cirrhosis involves progressive hepatic fibrosis and architectural distortion. Despite differing pathophysiologies, both can present with overlapping clinical features, complicating the diagnostic process. We present the case of a 78-year-old female with a one-month history of bilateral lower extremity edema, dyspnea, fatigue, anorexia, low-grade fever, and progressive abdominal distension. Upon admission, a comprehensive metabolic panel revealed mild transaminitis, hyperbilirubinemia, and hypoalbuminemia. Complete blood count with differential revealed moderate leukocytosis, macrocytic anemia below the transfusion threshold, severe thrombocytopenia, and 10% circulating blasts. A contrast-enhanced computed tomography scan of the abdomen and pelvis showed cirrhotic liver morphology, portal hypertension, esophageal varices, splenomegaly with infarct, and minimal ascites. Chronic liver disease workup also indicated possible hereditary hemochromatosis. Hematologic evaluation, including peripheral blood flow cytometry, confirmed AML with 11.4% blasts expressing CD34, CD117, HLA-DR, CD33, and CD13. This case highlights the rare concurrent presentation of newly diagnosed AML and cirrhosis, emphasizing the diagnostic challenges posed by overlapping symptoms and the necessity of a multidisciplinary approach for timely identification and management.

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