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Folio edition · Set in Instrument Serif & Archivo

Paeds SAQsallergy-and-immunology

Paeds SAQs · allergy-and-immunology

Secondary immunodeficiency — formative SAQs

Formative SAQs on recognising secondary immunodeficiency, sorting the cause into the six mechanism-based categories, linking cause to immune arm to organism to prophylaxis, applying the five-step management ladder, and deciding who needs immunoglobulin replacement.

20 marks30 min
On this page & tools

Target exams

RACP General PaediatricsMRCPCH ClinicalRACP DWE

Target exams

RACP General PaediatricsMRCPCH ClinicalRACP DWE
Prompt
Secondary immunodeficiency in children

SAQ 1 (10)

A seven-year-old boy with acute lymphoblastic leukaemia, day twelve of induction chemotherapy, presents with fever of 39 °C. His absolute neutrophil count is 0.2 × 10⁹ per litre. He looks flushed and tachycardic but is normotensive. [1] [4]

a) Define secondary immunodeficiency and state why this child is immunodeficient. (2 marks) [1]

b) Outline your immediate management, including the timing of key interventions. (3 marks) [1] [4]

c) Explain how the cause predicts the infecting organism, giving the predicted organism class for chemotherapy-induced neutropenia. (2 marks) [1]

d) Describe the prophylaxis and vaccination principles that belong in his long-term plan as he proceeds through treatment. (3 marks) [4] [1]

SAQ 2 (10)

A four-year-old girl who underwent splenectomy for hereditary spherocytosis is brought in with a six-hour history of high fever and rigors. She is fully vaccinated for her age but has been inconsistent with prophylaxis. [5] [1]

a) What is the immediate threat, and what emergency management is required? (3 marks) [5] [1]

b) Explain the mechanism by which asplenia disables immunity and the organisms it predicts. (2 marks) [5]

c) Outline the long-term prevention plan: prophylaxis, vaccination, and the family's sick-day action plan. (3 marks) [5] [1]

d) State two other secondary causes of immunodeficiency that, unlike asplenia, may be reversible when the cause is treated, and name the mechanism in each. (2 marks) [1] [3]

References

  1. [1]Chinen J, Shearer WT. Secondary immunodeficiencies, including HIV infection. J Allergy Clin Immunol, 2010.PMID 20042227
  2. [2]Tuano KS, Seth N, Chinen J. Secondary immunodeficiencies: An overview. Ann Allergy Asthma Immunol, 2021.PMID 34481993
  3. [3]Otani IM, Lehman HK, Jongco AM, et al. Practical guidance for the diagnosis and management of secondary hypogammaglobulinemia: A Work Group Report. J Allergy Clin Immunol, 2022.PMID 35176351
  4. [4]Maertens J, Cesaro S, Maschmeyer G, et al. ECIL guidelines for preventing Pneumocystis jirovecii pneumonia in haematological malignancies and stem cell transplant recipients. J Antimicrob Chemother, 2016.PMID 27550992
  5. [5]Lee GM. Preventing infections in children and adults with asplenia. Hematology Am Soc Hematol Educ Program, 2020.PMID 33275684