martes, 31 de agosto de 2010

Austrian Syndrome Associated with Pandemic (H1N1) 2009 in Child | CDC EID



EID Journal Home > Volume 16, Number 9–September 2010

Volume 16, Number 9–September 2010
Letter
Austrian Syndrome Associated with Pandemic (H1N1) 2009 in Child
Waseem Alhushki and Chokechai Rongkavilit
Author affiliation: Wayne State University, Detroit, Michigan, USA


To the Editor: In 1957, an American internist reported the preference of Streptococcus pneumoniae for the aortic valve and its frequent association with meningitis and pneumonia (1), an association now known as Austrian syndrome. This syndrome mainly occurs in middle-age men who have predisposing factors, such as chronic alcoholism, altered immune state, dural fistula, and ear or sinus infections.

One case of Austrian syndrome has been reported in the pediatric age group, in a 7-year-old girl in whom aortic valve endocarditis developed after pneumococcal meningitis infection (2). In pneumococcal endocarditis, the native aortic valve is the most frequent location of vegetation. Valve replacement must be considered to avoid development of cardiogenic shock, whereas medical treatment alone may be adequate in some cases of mitral endocarditis (3,4).

We report a previously healthy adolescent with Austrian syndrome associated with pandemic (H1N1) 2009 infection. Cardiac involvement resulted in extensive mitral valve destruction requiring surgical valve replacement.

A 13-year-old boy had cough, nasal congestion, and a fever ≥103°F for 2 weeks before being seen at a hospital. On the day he was admitted to hospital, he became unarousable, and weakness was noted on his left side. His medical history included mild asthma requiring no therapy over the past 3 years. His immunizations were up to date except for seasonal influenza and pandemic (H1N1) 2009 vaccination.

When admitted to hospital, his temperature was 38.7°C, blood pressure 97/47 mm Hg, respiratory rate 77 breaths/min, and heart rate 150 beats/min. Pupils were 3 mm in diameter and reactive to light and accommodation. Weakness and hypertonia of the left upper and lower extremities were noted. He had neck stiffness without Kernig sign or Brudzinski sign. Complete blood count showed a leukocyte count of 26,400 cells/mm3 and differential of 92.1% neutrophils, 5.3% lymphocytes, 2.6% monocytes, and 0.1% eosinophils; hemoglobin level of 12.9 g/dL; hematocrit 38.6%; and a thrombocyte count of 102,000 cells/mm3. A plain chest radiograph showed a left lower lobe infiltrate. Computed tomography of the head showed a large infarction involving the right frontal lobe at the distribution of the right middle cerebral artery; small infarcts involved the left frontal lobe and the right parietal lobe.

Lumbar puncture showed a leukocyte count of 100 cells/mm3, 71% neutrophils, 8% bands, 15% lymphocytes, 5% monocytes, and 1% eosinophils; protein 195 mg/dL, and glucose 6 mg/dL, with a blood glucose level of 140 mg/dL. Gram stain of the cerebrospinal fluid showed gram-positive cocci in pairs. The patient was treated with intravenous ceftriaxone, vancomycin, and dexamethasone. He subsequently became unconscious and hypotensive and required intubation with mechanical ventilation and intravenous dopamine. His nasal wash sample was positive for pandemic (H1N1) 2009 RNA by real-time reverse transcription–PCR; oseltamivir (75 mg) through a nasogastric tube every 12 h for 5 days was administered. Because of heart murmur, a 2-dimensional echocardiography was conducted; it showed a large mitral valve vegetation 1.6 cm ´ 2.1 cm attached to the posterior mitral leaflet and mild to moderate mitral insufficiency. Because of this finding, he was transferred to Children’s Hospital of Michigan for surgical intervention.


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Austrian Syndrome Associated with Pandemic (H1N1) 2009 in Child | CDC EID

Suggested Citation for this Article
Alhushki W, Rongkavilit C. Austrian syndrome associated with pandemic (H1N1) 2009 in child [letter]. Emerg Infect Dis [serial on the Internet]. 2010 Sep [date cited].
http://www.cdc.gov/EID/content/16/9/1493.htm


DOI: 10.3201/eid1609.091779

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