Severe combined immunodeficiency
7,128views
Flashcards
Severe combined immunodeficiency
of complete
Questions
USMLE® Step 1 style questions USMLE
of complete
Complete blood count | |
Leukocyte count | 8,100 /mm3 |
Platelet count | 300,000/mm3 |
Lymphocytes | 5% |
CD 19+ | low |
CD 3+ | absent |
Immunoglobulins | |
IgG | 220mg/dL |
IgA | 40 mg/dL |
IgM | 15 mg/dL |
Chest X-ray demonstrates bilateral diffuse interstitial infiltrates. Which of the following is the most likely diagnosis?
Memory Anchors and Partner Content
External References
First Aid
2024
2023
2022
2021
Autosomal recessive disorders
severe combined immunodeficiency p. 115
Bone marrow transplant
severe combined immunodeficiency p. 115
SCID (severe combined immunodeficiency disease) p. 96, 115
adenosine deaminase deficiency as cause p. 35
lymphopenia caused by p. 429
Summary
Severe combined immunodeficiency (SCID) is a severe form of primary immunodeficiency, caused by a genetic mutation that affects the development and function of white blood cells, which are responsible for fighting off infections. It may result from an X-linked recessive defect in IL-2R (interleukin-2 receptor) gamma chain or an autosomal recessive defect in adenosine deaminase deficiency. As a result, individuals with SCID are highly susceptible to infections, particularly bacterial and viral infections, and often present with failure to thrive, chronic diarrhea, thrush, and recurrent infections. Treatment involves HSCT (hematopoietic stem cell transplantation, avoiding live vaccines, antimicrobial prophylaxis, and isolation to prevent catching an infection.