11: 4-year-old male with fever and adenopathy Flashcards
normal heart rate for a 4-year-old
65 to 135 beats per minute
Causes of Unilateral Cervical Lymphadenopathy: Reactive cervical adenitis (1/5)
Occurs in response to an oral infectious or inflammatory process
Causes of Unilateral Cervical Lymphadenopathy: Kawasaki disease (2/5)
- LAD with Kawasaki disease is most often unilateral, w/ LN >1.5 cm in diameter; less commonly diffuse LAD can occur.
- Enlarged LN are nonfluctuant.
Causes of Unilateral Cervical Lymphadenopathy: Bacterial cervical adenitis (3/5)
- Typically seen in children ages 1-5yo w/ a h/o a recent upper respiratory tract infection.
- S. aureus and S. pyogenes are the organisms most commonly identified.
- Patients may have high fevers and a toxic appearance.
- Overlying cellulitis and development of fluctuance are common.
Causes of Unilateral Cervical Lymphadenopathy: Cat scratch disease (4/5)
- Infections caused by the bacterium Bartonella henselae can be asymptomatic or symptomatic.
- The infection usually is introduced by a scratch from a cat or kitten, with subsequent infection of the node or nodes draining that site.
- The site most commonly involved is the axilla, followed by cervical, submandibular, and inguinal areas.
- Usually a self-limited disease, with regression of the lymph node in four to six weeks.
Causes of Unilateral Cervical Lymphadenopathy: Mycobacterial infection (5/5)
- Mycobacterial infections can cause diffuse lymphadenopathy or isolated lymphadenitis.
- Lymphadenitis is the most common manifestation of nontuberculous mycobacteria in children, with a peak age of presentation of 2 to 4 years.
- TB is the m/c c/o mycobacterial lymphadenitis in children >12y.
- Children with these infections usually appear well with minimal if any constitutional s/s.
- The overlying skin may be erythematous initially, but left untreated often becomes violaceous as the nodes enlarge.
- Nodes may rupture through the skin, resulting in a draining sinus tract.
- Tx is surgical excision, as incision and drainage can also result in a sinus tract.
Strawberry Tongue
erythematous tongue with prominent papillae, is a characteristic finding of:
- -Streptococcal pharyngitis
- -Kawasaki disease
- -Toxic shock syndrome
In addition to high fever for at least five days, four of the following five criteria are needed for a diagnosis of Kawasaki disease:
- Changes in oral mucosa (i.e.: “strawberry tongue”)
- Extremity changes (redness/swelling)
- Unilateral cervical LAD (least likely)
- Rash
- Conjunctivitis (bilateral, nonpurulent)
Kawasaki Disease: General
- acute inflammatory panvasculitis of unknown etiology.
- It is thought that the disease results from an ai response to a not yet identified infectious trigger.
- KD is a dz of childhood, with the typical age of patients 15-18 mo; 80% of KD patients are <5y.
- KD “outbreaks” follow seasonal patterns, and children of Asian descent have a higher incidence of KD (suggesting both infectious and genetic influences).
Kawasaki Disease: three distinct phases of illness
- Acute phase: onset through ~10 days. Fever and clinical findings are present, with serologic evidence of systemic inflammation (elevated acute phase reactants).
- Subacute phase: 10 days through ~3 weeks. Fever resolves and clinical findings largely subside (often with peeling of hands and feet). Serologic evidence of inflammation continues.
- Convalescent phase: 3 weeks through 6-8 weeks. All clinical findings have resolved. Continued serologic evidence of inflammation.
Kawasaki Disease: Late
- Beyond 6-8 wks, serologic evidence for inflammation has resolved.
- KD causes a panvasculitis, impacting any blood vessels, although there is a predilection for small and medium-sized vessels (especially the coronary arteries for unclear reasons).
- This vasculitis can lead to aneurysmal dilation, particularly during the subacute phase of illness.
Complications of Kawasaki Disease
- Aseptic meningitis or other central nervous system manifestations (90% of pts develop neuro manifestations)
- coronary artery aneurysm (20-25% of untreated pts)
- Liver dysfunction (as evidenced by elevated transaminases and a decreased albumin) (40%)
- Arthritis (30%)
- Hydrops of the gallbladder (10%)
Derm Nomenclature
- Macule=Flat, discolored spot
- Papule=Small, well-defined solid palpable bump
- Vesicle=Small, well-defined, fluid-containing bump
- Pustule=Small, well-defined bump containing purulent material
- Plaque=Small, raised, differentiated patch or area on a body surface
- Desquamation=Shedding of the outer layer of skin surface
Treatment of Kawasaki Disease: ASA (1/2)
- High-dose aspirin (80-100 mg/kg/day, divided into four doses) is administered for its anti-inflammatory properties.
- ASA shortens the febrile course of the illness but has no effect on the development of aneurysms.
- Following defervescence, low-dose aspirin (3-5 mg/kg/day given in a single dose) is administered for its anti-platelet effects.
- ASA is discontinued altogether after a total of 6-8wks if no coronary artery changes are seen in f/u echo. If there are coronary artery abnormalities, low dose aspirin is continued indefinitely as an anti-platelet agent.
Treatment of Kawasaki Disease: IVIG (2/2)
- has dec the incidence of coronary artery aneurysms from 20- 25% to 2-4%.
- A single dose of IVIG at a dose of 2 g/kg administered over 10-12h has been shown to be more effective in reducing the risk of coronary artery aneurysms than multiple lower doses.