Spontaneous splenic rupture: A rare complication of acute myeloid leukemia. Report of a case

Amal Hajri1,2, Karim Yaqine1,2, Salaheddine El Massi1,2

  • 1Departement of General Surgery, University Hospital Centre Ibn Rochd, Casablanca, Morocco.

Abstract

Insights

Spontaneous splenic rupture is a rare but serious condition, often linked to hematologic malignancies like acute myeloid leukemia. Early diagnosis and splenectomy are crucial for improving patient outcomes.

Area of Science:

  • Hematology
  • Gastroenterology
  • Emergency Medicine

Background:

  • Spontaneous splenic rupture (SPR) is a rare, severe condition with diverse causes, frequently associated with infectious and hematologic disorders.
  • Acute myeloid leukemia (AML) is identified as a significant underlying cause of SPR in patients with hematologic malignancies.

Observation:

  • A 48-year-old male undergoing chemotherapy for AML presented with acute abdominal pain, hemodynamic instability, and signs of splenic rupture on CT scan.
  • CT imaging revealed splenic rupture with hemoperitoneum and bilateral pleural effusion, necessitating immediate surgical intervention.

Findings:

  • Splenic rupture, particularly in the context of hematologic malignancy, can manifest with severe abdominal symptoms.
  • Diagnostic tools such as CT and ultrasound are essential for identifying splenic rupture, while Kehr's and Balance's signs may be suggestive.
  • Splenectomy is the primary treatment for splenic rupture, with prognosis dependent on care quality and etiology.

Implications:

  • Clinicians must consider spontaneous splenic rupture in the differential diagnosis of acute abdominal pain, especially in patients with hematologic malignancies.
  • Prompt recognition and management of splenic rupture significantly enhance patient survival rates and improve overall prognosis.