There was no enanthema.

The patient reported slight eye pain, myalgia, and loose stools, but no headache or fever. The temperature was 36.5°C axillary. What is the diagnosis? Solution: Acute probable Coxsackie virus infection. In the patient presented rubella infection was initially assumed, as there was no documented vaccination and no history of rubella infection during childhood either. Rubella serology was negative for IgM and IgG, although IgM may not be detectable during the early stages of illness. Measles serology showed a high IgG titer but a negative IgM titer, and there was one documented measles vaccination 30 years ago. In contrast, Coxsackie virus serology was positive with an IgM titer of 130 U/mL (normal check details value <30 U/mL) and an IgG titer of 56 U/mL (normal value <80 U/mL). Routine blood tests showed normal C-reactive protein and lactate dehydrogenese levels. Erythrocyte sedimentation rate was not accelerated. White blood count showed leukocytopenia Selleck PARP inhibitor (3,200 cells/µL) with a relative monocytosis

of 10%, and thrombocytopenia (116,000 cells/µL). Creatinine kinase was elevated (247 U/L; normal value <171 U/L), troponin and myoglobin levels were within normal range. Liver and kidney function tests were unremarkable, ECG showed no abnormalities. The patient was treated symptomatically and the rash faded within 4 days. Coxsackie viruses are RNA viruses of the Picornaviridae family, genus enterovirus.

The incubation period of Coxsackie virus infection is usually 2 to 6 days, rarely up to 35 days. Transmission occurs by droplets and feco-orally. Like the closely related ECHO viruses and other enteroviruses, Coxsackie viruses can cause a variety of different clinical presentations.1 Coxsackie A viruses have been associated with rash, herpangina, and hand-foot-mouth disease. Coxsackie B viruses have been linked to pleurodynia, diabetes, and other diseases. However, large overlapping clinical pictures can be caused by both Coxsackie virus groups, such as influenza-like illness, meningoencephalitis and myocarditis.1 Coxsackie virus infections occur Nintedanib (BIBF 1120) worldwide, and in the case presented the locale of infection was Hong Kong. Diagnosis is usually accomplished by serology. In this case, the Coxsackie virus infection was only probable (positive serology) and not definitely proven, because it was not confirmed by polymerase chain reaction (PCR). Viruses can be isolated or detected by reverse transcriptase (RT)-PCR from feces and pharyngeal secretions.1 Because of the exanthema, Coxsackie A virus was more likely the aetiological agent than Coxsackie B virus in this case.2 There is no specific treatment for Coxsackie virus infections. The differential diagnoses of the exanthematous illness shown in this patient encompass dengue fever and chikungunya virus infection because of the recent travel history.