What laboratory profile is expected in a 2-year-old boy with sickle cell anemia (SCA) presenting with pallor, decreased responsiveness, marked splenomegaly, and signs of shock, including hypotension, tachycardia, and impaired peripheral circulation?

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Differential Diagnosis for a 2-year-old boy with Sickle Cell Anemia

The patient's presentation with pallor, decreased responsiveness, abdominal pain, and marked splenomegaly suggests a severe complication of sickle cell anemia. The following differential diagnoses are considered:

  • Single most likely diagnosis
    • Sickle Cell Sequestration Crisis: This condition is characterized by the sudden enlargement of the spleen due to trapping of red blood cells, leading to a significant drop in hemoglobin level and potentially life-threatening anemia. The patient's marked splenomegaly, pallor, and decreased responsiveness support this diagnosis.
  • Other Likely diagnoses
    • Sickle Cell Pain Crisis with Sepsis: Although the patient does not have a fever, the abdominal pain and decreased energy could be indicative of a pain crisis, and the presence of prophylactic penicillin suggests a concern for infection.
    • Acute Splenic Sequestration Crisis with Hypovolemic Shock: The patient's low blood pressure, tachycardia, and delayed capillary refill suggest hypovolemic shock, which could be caused by acute splenic sequestration.
  • Do Not Miss (ddxs that may not be likely, but would be deadly if missed.)
    • Sepsis: Despite the lack of fever, sepsis is a significant concern in patients with sickle cell anemia, particularly those taking prophylactic antibiotics. Sepsis can present with non-specific symptoms, such as abdominal pain and decreased energy.
    • Acute Chest Syndrome: Although the patient has clear breath sounds, acute chest syndrome is a life-threatening complication of sickle cell anemia that can present with non-specific symptoms, such as abdominal pain and decreased energy.
  • Rare diagnoses
    • Hepatic Sequestration Crisis: This is a rare complication of sickle cell anemia, characterized by the trapping of red blood cells in the liver, leading to liver enlargement and potentially life-threatening anemia.
    • Acute Multi-Organ Failure: This is a rare but potentially life-threatening complication of sickle cell anemia, characterized by the failure of multiple organs, such as the liver, kidneys, and lungs.

The laboratory profile that would most likely be seen in this patient is D. Increased Reticulocytes, Decreased Platelets, indicating a response to anemia (increased reticulocytes) and possible splenic sequestration (decreased platelets).

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This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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