Still's disease and myocarditis associated with recent mumps infection.

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Still's disease and myocarditis associated with recent mumps infection.

We describe a 16 year old patient who developed Still's disease with evidence of myocarditis. A rise in the mumps 'V' antigen indicated that the disease was associated with recent mumps infection.

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Fatal mumps myocarditis.

The case of a 9 year old boy with acute renal failure and myocarditis as complications of mumps is reported. The cardiac rhythm and conduction disorders which appeared after admission were refractory to treatment and the outcome was fatal. On necropsy, minimal interstitial nephritis and myocarditis were seen, confirming the clinical diagnosis.

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Acute pancreatitis and haemolytic anaemia associated with mumps-virus infection.

Because of its various manifestations mumps is now considered to be a generalized infection characterized principally by involvement of the parotid and submaxillary glands. Among the complications of mumps-virus infection are meningoencephalitis, gastro-enteritis, orchitis, mastitis, pancreatitis, and subacute thyroiditis. Sometimes one of these disorders constitutes the only manifestation of i...

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Celiac disease associated with autoimmune myocarditis.

BACKGROUND Both celiac disease (CD) and myocarditis can be associated with systemic autoimmune disorders; however, the coexistence of the 2 entities has never been investigated, although its identification may have a clinical impact. METHODS AND RESULTS We screened the serum of 187 consecutive patients with myocarditis (118 males and 69 females, mean age 41.7+/-14.3 years) for the presence of...

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Opsoclonus-Myoclonus Syndrome Associated with Mumps Virus Infection

BACKGROUND Opsoclonus-myoclonus syndrome (OMS) is a rare neurological disorder that is characterized by involuntary eye movements and myoclonus. OMS exhibits various etiologies, including paraneoplastic, parainfectious, toxic-metabolic, and idiopathic causes. The exact immunopathogenesis and pathophysiology of OMS are uncertain. CASE REPORT We report the case of a 19-year-old male who develop...

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ژورنال

عنوان ژورنال: Postgraduate Medical Journal

سال: 1988

ISSN: 0032-5473

DOI: 10.1136/pgmj.64.755.693