Allergy Immunology Flashcards

1
Q

Primary defense against exogenous antigens

A

CD4+ T cells

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2
Q

Cytotoxic cells against viruses and neoplastic cells

A

CD8+ T cells

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3
Q

A child received penicillin 10 days ago for the first time, presents with fever, nausea, vomiting, pruritic skin rash, urticaria, angioedema, joint pain, lymphadenopathy, myalgia, and proteinuria

A

Serum sickness

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4
Q

A common trigger of allergic reactions in a patient with spina bifida or congenital urogenital problems

A

Latex

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5
Q

Antibody that has a major role in allergic conditions, e.g., anaphylaxis, atopy, asthma, allergic rhinitis, food allergies

A

IgE

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6
Q

Antibody that mediates Type I hypersensitivity reaction

A

IgE

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7
Q

First antibody produced in an infection

A

IgM

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8
Q

Antibody found in body mucosal secretions

A

IgA

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9
Q

Sudden onset of lip swelling, abdominal pain, swelling of both feet, non pruritic erythematous skin rash, one family member have the same condition

A

Hereditary angioedema

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10
Q

What is the cause of hereditary angioedema?

A

Low levels of plasma protein C1 inhibitor (C1-INH). (Autosomal dominant)

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11
Q

Initial screening test for patient with suspected hereditary angioedema

A

C4 levels

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12
Q

The test that can differentiate between various types of hereditary angioedema

A

C1-INH functional assay

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13
Q

Patient with recurrent meningococcal meningitis

A

Terminal complement C5-C9 deficiency

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14
Q

Initial screening test for a patient with suspected complement deficiency, e.g., recur- rent ( Neisseria meningitidis) meningitis

A

(CH50) test

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15
Q

Complement deficiency that increases the risk of SLE

A

C2 deficiency

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16
Q

A 4-year-old boy with recurrent skin abscesses, spleen and liver abscesses, and
osteomyelitis

A

Chronic granulomatous disease

X-linked

17
Q

Test of choice in a patient with suspected chronic granulomatous disease?

A

DHR oxidation is preferred, NBT

reduction can be used

18
Q

An 8-year old boy presents with eczema, recurrent Staphylococcus aureus skin infections
without inflammatory response “cold abscess,” pneumatoceles, coarse facial
feature, eosinophilia, IgE level is 80,000 IU

A
Job syndrome (hyper-IgE
syndrome)
19
Q

Highly elevated white blood count in a 10-weeks-old infant who still has an umbilical
cord

A

Leukocyte adhesion defect type I

20
Q

Test of choice in a patient with suspected leukocyte adhesion defect

A

Flow cytometry beta 2 integrin

CD11b/CD18 on leukocytes

21
Q

Newborn with hypocalcemia, tetralogy of Fallot, interrupted aortic arch, and abnormal
facial features

A

DiGeorge anomaly
(Deletion of chromosome
22q11.2)

22
Q

An 8-week-old boy presents with diarrhea, pneumonia, persistent oral thrush,
eczematous-like skin lesions, sepsis, lymphopenia, and failure to thrive

A

Severe combined

immunodeficiency

23
Q

Recurrent ear infections, eczema, profuse bleeding during circumcision procedure,
thrombocytopenia, and small platelets

A

Wiskott–Aldrich syndrome

24
Q

A 5-month-old presents with Pneumocystis jiroveci pneumonia, mouth ulcers, severe
neutropenia, recurrent sinusitis, and otitis media, chronic diarrhea, failure to thrive,
negative HIV

A

X-linked hyper IgM syndrome

25
Q

Severe progressive infectious mononucleosis and Epstein–Barr virus (EBV) fulminant
hepatitis

A

X-linked lymphoproliferative

syndrome (Duncan syndrome)

26
Q

A 9-month-old boy, previously healthy, presents with recurrent otitis media, two
episodes of pneumonia in the last 2 months, persistent giardiasis. On examination,
the lymph nodes, the tonsils are absent

A

X-linked agammaglobulinemia
(Usually starts after first 6 months
of life)

27
Q

Persistent thrush, nail dystrophy, endocrinopathies

A

Chronic mucocutaneous

candidiasis

28
Q

Short stature, fine hair, severe Varicella infection

A

Cartilage hair hypoplasia with

short limbed dwarfism

29
Q

Oculocutaneous albinism, recurrent infection

A

Chédiak–Higashi syndrome

30
Q

Adolescent presents with recurrent sinus and pulmonary infections due to encapsulated
bacteria, malabsorption, hepatosplenomegaly, and low level of immunoglobulins
(IgG, IgM, and IgA)

A

Common variable

immunodeficiency

31
Q

Candidiasis with raw egg ingestion

A

Biotin-dependent carboxylases

deficiency

32
Q

The best treatment for a child with asymptomatic transient hypogammaglobulinemia
of infancy

A

Observation (no treatment is

necessary)

33
Q

Induration reaction to TB testing after 72 h is an example of

A

Type IV: cell-mediated

hypersensitivity

34
Q

A 4-year-old with short stature, micrognathia, telangiectasia, immunodeficiency,
learning disability, deficiency of DNA ligase I

A

Bloom syndrome

35
Q

An 8-year-old boy presents with recurrent ear and sinus infections, ataxia, oculocutaneous
telangiectasia, elevated α1-fetoprotein

A

Ataxia-telangiectasia

autosomal recessive