# Simultaneous Onset of Acute Myeloid Leukemia and Decompensated Cirrhosis: A Rare Case

**Authors:** Wilfredo J Javier-Rojas, Alvin B Newman-Caro, Yizhi Lin, Carlos Montero

PMC · DOI: 10.7759/cureus.86990 · 2025-06-29

## TL;DR

A rare case of a patient with both acute myeloid leukemia and decompensated cirrhosis is presented, highlighting the difficulty in diagnosing overlapping symptoms.

## Contribution

This paper reports a rare concurrent case of newly diagnosed AML and cirrhosis, emphasizing diagnostic challenges and the need for multidisciplinary care.

## Key findings

- A 78-year-old female presented with symptoms of both AML and decompensated cirrhosis.
- AML was confirmed via peripheral blood flow cytometry showing blasts with specific markers.
- The case underscores the importance of a multidisciplinary approach for accurate diagnosis and management.

## Abstract

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.

## Linked entities

- **Proteins:** CD34 (CD34 molecule), KIT (KIT proto-oncogene, receptor tyrosine kinase), CD33 (CD33 molecule), ANPEP (alanyl aminopeptidase, membrane)
- **Diseases:** acute myeloid leukemia (MONDO:0015667), hereditary hemochromatosis (MONDO:0006507)

## Full-text entities

- **Genes:** CD33 (CD33 molecule) [NCBI Gene 945] {aka CD33rSiglec, SIGLEC-3, SIGLEC3, p67}, CD34 (CD34 molecule) [NCBI Gene 947], KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815] {aka C-Kit, CD117, MASTC, PBT, SCFR}, ANPEP (alanyl aminopeptidase, membrane) [NCBI Gene 290] {aka AP-M, AP-N, APN, CD13, GP150, LAP1}
- **Diseases:** esophageal varices (MESH:D004932), cirrhosis (MESH:D005355), abdominal distension (MESH:D000007), thrombocytopenia (MESH:D013921), extremity edema (MESH:D004487), hematologic malignancy (MESH:D019337), anorexia (MESH:D000855), ascites (MESH:D001201), Decompensated Cirrhosis (MESH:D006333), cirrhotic liver (MESH:D008103), leukocytosis (MESH:D007964), dyspnea (MESH:D004417), hyperbilirubinemia (MESH:D006932), fatigue (MESH:D005221), infarct (MESH:D007238), splenomegaly (MESH:D013163), hypoalbuminemia (MESH:D034141), AML (MESH:D015470), portal hypertension (MESH:D006975), hereditary hemochromatosis (MESH:D006432), Chronic liver disease (MESH:D008107), macrocytic anemia (MESH:D000748), fever (MESH:D005334)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12206544/full.md

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Source: https://tomesphere.com/paper/PMC12206544