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BONE MARROW FAILURE! Hemoglobin of 4 gm/dl and Reticulocytes of < 0.5%


High Yield Review - Aplastic Crisis

Case: A 23 y/o African American female with a

medical history of sickle cell anemia, comes to

the emergency department for evaluation of

shortness of breath, fatigue, and

light headedness. She also c/o joint pains in her hands and ankles. All of her symptoms have been worsening over

the past week. She states her baseline hemoglbin is 10 gm/dl.

And she has not had a blood transfusion in many years.

She has pale conjunctiva, and no rash noted, no spleenomegaly noted.

Her Stat Hemogram shows

Hemoglobin of 4 gm/dl ( Her baseline is 10 )

Reticulocytes of 0.5% ( Normal 0.5- 2.5%)

You send for a type and cross, request for packed red blood cells,

and inform the nurse that they patient will need a blood transfusion and supportive care. The patient was also started on IV Fluids, and Oxygen via nasal cannula.

 

Case Clues - Aplastic Crisis in Sickle Cell

- She has a h/o of sickle cell anemia and her symptoms are worsening, implying an acute worsening on chronic anemia

- Very low Hemoglobin of 4 gm/dl from her baseline of 10 gm/dl

- Very low Reticulocytes of < 0.5 %

- Joint Pains

- No Recent Blood Transfusions

Notable Notes - Aplastic Crisis in Sickle Cell

- Hall mark is decrease in bone marrow -->

Decrease in Erythropoiesis --> Low Hemoglobin and Low Reticulocytes

- The culprit is INFECTIONS: ( Parvo B19, EBV, Staph.Pneumonia and Salmonella)

- Parvo B19 Infection is adults mostly p/w joint pains, no rash

- Treatment is supportive ( Blood Transfusions, IV Fluids, Oxygen )

The Differentials ( Why Not? )

Why not Splenic Sequestration Crisis ?

--> Will have Low Hemoglobin

--> Will have Elevated Reticulocytes

--> Spleenomegaly

--> Common in Children ( This patients an adult )

Why not Hemolytic Crisis ?

--> Will have low hemoglobin

--> Will have Elevated Reticulocytes

--> No h/o recent massive blood transfusions

Know it for the Boards- Aplastic Crisis in Sickle Cell!

- Acute worsening of Anemia in a adult with Sickle Cell suspect

Aplastic Crisis

- Clues for Aplastic Crisis is Low Hemoglobin and Low Reticulocytes

-Aplastic Crisis think INFECTION!

 

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