الاثنين، 11 فبراير 2013

MCQs In Pediatric Infections -Part II

Q 1:

A 15-year-old boy from Missouri develops prolonged low-grade fever, cough, chest pain, and fatigue. Chest radiography reveals hilar adenopathy and scattered pulmonary infiltrates. Results of a skin test with purified protein derivative are negative.
Of the following, the MOST likely diagnosis is:

A. allergic bronchopulmonary aspergillosis
B. atypical mycobacterial infection
C. histoplasmosis
D. sporotrichosis
E.  tuberculosis

Answer

C

Histoplasmosis 

 Clinical manifestations may be classified according to site (pulmonary, extrapulmonary, or disseminated), duration of infection (acute, chronic), and pattern of infection (primary versus reactivation). Acute pulmonary histoplasmosis is an influenza-like illness that is characterized by nonpleuritic chest pain, pulmonary infiltrates, and hilar adenopathy, as described for the boy in the vignette. Symptoms persist for 2 or 3 days to 2 weeks. Erythema nodosum (Figure 189A) can occur in adolescents, but erythema nodosum and chronic pulmonary histoplasmosis are uncommon in children. Primary cutaneous infections can occur after trauma.

            Acute disseminated histoplasmosis is most common in children whose cell-mediated immunity is impaired, including patients who have human immunodeficiency virus (HIV) infection, solid-organ transplant recipients, and infants younger than 1 year of age. Features include prolonged fever, failure to thrive, cough, hepatosplenomegaly, adenopathy, pneumonia, skin lesions, and pancytopenia. Central nervous system involvement is common. Chronic disseminated infection is rare. Histoplasmosis may reactivate years after primary infection in isolated tissues, particularly in the central nervous system, adrenal glands, and mucocutaneous surfaces, as well as in other sites. Disseminated or extrapulmonary histoplasmosis is an acquired immunodeficiency syndrome–defining condition in an HIV-infected person. Histoplasmosis may be diagnosed by culture, antigen detection in body fluids, or serology. T

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Q 2:


A 12-year-old girl complains of pain in a 3 cm linear distribution along the course of a vein in the dorsum of her right forearm. She was recently hospitalized because of cellulitis of her left hand, which was treated with intravenous nafcillin.

Of the following, the MOST likely cause for her symptom is:



A.  an allergic reaction

B.  ascending lymphangitis

C.  carpal tunnel syndrome
D.  deep vein thrombosis
E.   thrombophlebitis

Answer

E


Penicillinase-resistant penicillins can cause thrombophlebitis and an acute interstitial nephritis. Intravenous infusion, particularly of nafcillin, has been associated with thrombophlebitis of the infused vein, which is the most likely diagnosis for the girl described in the vignette.

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Q 3:


A child is being treated with intravenous antibiotics for culture-proven Staphylococcus aureus osteomyelitis.

Of the following, the MOST important factor in determining the likelihood of success of oral antibiotic therapy in the management of this child is:



A. absence of bacteremia at diagnosis
B. age of the child
C. location of osteomyelitis
D. need for surgical drainage
E. patient compliance

Answer

E



The steps in managing patients who have osteomyelitis are to: 1) identify the location, 2) isolate the organism, 3) select the appropriate antibiotic, 4) deliver the antibiotic to the bacterial organisms, and 5) prevent further tissue destruction.

            The route of antibiotic administration is not critical as long as appropriate serum concentrations are attained. The advantages of oral administration, such as ease of administration and relatively low cost, must be balanced by adequacy of absorption from the gut and parental-patient compliance.

 Absence of bacteremia at diagnosis, the age of the child, the location of the osteomyelitis, and the need for surgical drainage are not important factors in determining the likelihood of success of oral antibiotic therapy in culture-proven osteomyelitis.

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Q 4:


A 5-year-old boy has been ill for 2 days with fever, decreased appetite, and a rash. On physical
examination, you note ulcers on the tongue  and soft palate, but the gingivae are
spared. You also see oval vesicles with surrounding erythema on the hands

Of the following, the MOST likely diagnosis is

A. aphthae
B. hand-foot-and-mouth disease
C. herpangina
D. herpetic gingivostomatitis
E. thrush

Answer

B



Hand-foot-and-mouth disease is a distinctive syndrome usually caused by infection with Coxsackievirus A16 or enterovirus 71, although other Coxsackievirus types and echoviruses have been implicated. Hand-foot-and-mouth disease typically occurs during the summer and fall and is characterized by fever, sore throat, and rash. Oral involvement precedes the appearance of skin lesions. Shallow ulcers, measuring 1 to 5 mm, surrounded by a red border, are observed on the soft palate, uvula, tonsillar pillars, and tongue, as described for the boy in the vignette.

Cutaneous lesions are erythematous papules or vesicles that typically are oval and surrounded by a rim of erythema. They are located acrally, involving the palms  soles, and digits, particularly the lateral aspects. The thighs and buttocks also may be affected, but the trunk and face generally are spared. Approximately two thirds of patients exhibit this typical presentation, 20% have only oral lesions, and 11% have acral lesions without mucosal involvement. Hand-foot-and-mouth disease generally is a mild illness and is self-limited, resolving in about 1 week.

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Q 5


A mother brings in her child because she found a tick on the girl’s shoulder yesterday and is
worried about Lyme disease. The mother found a site on the Internet that suggests her daughter
needs an antibiotic called ceftriaxone. You assure the mother that only very few children who
suffer tick bites actually develop a tick-associated disease.
Of the following, the manifestation of Lyme disease for which ceftriaxone administration is MOST
appropriate is

A. acute arthritis
B. carditis
C. disseminated erythema migrans
D. isolated facial palsy
E. peripheral neuropathy

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