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Zorluk: OrtaInterpreting Laboratory Results

A 42-year-old woman is evaluated in the intensive care unit for new-onset oozing of blood from her intravenous catheter sites and a widespread petechial rash. She was admitted two days ago for severe sepsis secondary to acute pyelonephritis. Her temperature is 38.8°C (101.8°F), blood pressure is 90/55 mmHg, and pulse is 118/min.

Laboratory studies show:

TestResultReference Range
Hemoglobin8.4 g/dL12.0-15.5 g/dL
Platelet count35,000/mm³150,000-400,000/mm³
Leukocyte count18,500/mm³4,500-11,000/mm³
Prothrombin time (PT)24 seconds11-15 seconds
Partial thromboplastin time (PTT)58 seconds25-40 seconds
Fibrinogen85 mg/dL200-400 mg/dL
D-dimer8,400 ng/mL< 500 ng/mL

Peripheral blood smear reveals numerous schistocytes.

Based on the laboratory findings, which of the following is the most likely diagnosis?

  1. Disseminated intravascular coagulationCevap
  2. B
    Thrombotic thrombocytopenic purpura
  3. C
    Immune thrombocytopenia
  4. D
    Vitamin K deficiency
  5. E
    Heparin-induced thrombocytopenia

Cevap

Disseminated intravascular coagulation
The correct diagnosis is disseminated intravascular coagulation (DIC). DIC is characterized by widespread, systemic activation of the coagulation cascade, leading to the formation of microthrombi throughout the microvasculature. This massive coagulation effort consumes platelets and clotting factors, resulting in thrombocytopenia, prolonged prothrombin time (PT), prolonged partial thromboplastin time (PTT), and low fibrinogen. Simultaneously, the fibrinolytic system is activated to break down these clots, leading to highly elevated levels of fibrin degradation products, such as D-dimer. As red blood cells are forced through small vessels partially occluded by fibrin strands, they are sheared, producing schistocytes (fragmented red blood cells) on the peripheral smear. Severe sepsis is one of the most common triggers for DIC.

Adım Adım Çözüm

1
Analyze the hematologic profile and peripheral smear.
The patient has severe thrombocytopenia and schistocytes.
This combination indicates a microangiopathic hemolytic anemia (MAHA), where red blood cells are sheared by microthrombi in small vessels.
2
Evaluate the coagulation panel (PT, PTT, fibrinogen, D-dimer).
The PT and PTT are markedly prolonged, fibrinogen is critically low, and D-dimer is significantly elevated.
These findings point to systemic activation of the coagulation cascade with subsequent consumption of coagulation factors and active fibrinolysis.
3
Synthesize the laboratory data with the clinical presentation.
A consumptive coagulopathy alongside MAHA in a patient with a known trigger (severe sepsis) confirms the diagnosis.
Only disseminated intravascular coagulation perfectly explains the simultaneous consumption of platelets and clotting factors leading to both bleeding (oozing) and thrombosis.

Anahtar Kavram

The diagnosis of disseminated intravascular coagulation requires identifying both a consumptive coagulopathy (prolonged PT/PTT, low fibrinogen, elevated D-dimer) and a microangiopathic hemolytic anemia (thrombocytopenia, schistocytes).
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