Allergy Immunology Flashcards

(35 cards)

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
Severe progressive infectious mononucleosis and Epstein–Barr virus (EBV) fulminant hepatitis
X-linked lymphoproliferative | syndrome (Duncan syndrome)
26
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
X-linked agammaglobulinemia (Usually starts after first 6 months of life)
27
Persistent thrush, nail dystrophy, endocrinopathies
Chronic mucocutaneous | candidiasis
28
Short stature, fine hair, severe Varicella infection
Cartilage hair hypoplasia with | short limbed dwarfism
29
Oculocutaneous albinism, recurrent infection
Chédiak–Higashi syndrome
30
Adolescent presents with recurrent sinus and pulmonary infections due to encapsulated bacteria, malabsorption, hepatosplenomegaly, and low level of immunoglobulins (IgG, IgM, and IgA)
Common variable | immunodeficiency
31
Candidiasis with raw egg ingestion
Biotin-dependent carboxylases | deficiency
32
The best treatment for a child with asymptomatic transient hypogammaglobulinemia of infancy
Observation (no treatment is | necessary)
33
Induration reaction to TB testing after 72 h is an example of
Type IV: cell-mediated | hypersensitivity
34
A 4-year-old with short stature, micrognathia, telangiectasia, immunodeficiency, learning disability, deficiency of DNA ligase I
Bloom syndrome
35
An 8-year-old boy presents with recurrent ear and sinus infections, ataxia, oculocutaneous telangiectasia, elevated α1-fetoprotein
Ataxia-telangiectasia | autosomal recessive