Acalculous Cholecystitis Associated withPlasmodium falciparumInfection
نویسندگان
چکیده
منابع مشابه
Brucellosis Associated with Acute Acalculous Cholecystitis
Brucellosis is a rare cause of acute acalculous cholecystitis. We report a 45-year-old, previously healthy, man with brucellosis who presented with abdominal pain due to cholecystitis.
متن کاملAcute acalculous perforated cholecystitis.
A case of acute acalculous perforated cholecystitis with acute generalized peritonitis in a middle aged cachectic man, presenting late in a moribund condition, is reported. He underwent emergency laparotomy (subtotal cholecystectomy), went into multi-organ failure and was managed accordingly. The patient recovered in about 2 weeks and was followed-up regularly.
متن کاملbrucellosis associated with acute acalculous cholecystitis
brucellosis is a rare cause of acute acalculous cholecystitis. we report a 45-year-old, previously healthy, man with brucellosis who presented with abdominal pain due to cholecystitis.
متن کاملEpstein-Barr virus – associated acute acalculous cholecystitis in an adult
BACKGROUND Gallbladder involvement during primary Epstein-Barr virus (EBV) infection in adults is rare. CASE REPORT We report the case of a 29-year-old female with acute acalculous cholecystitis associated with EBV infection. The patient was successfully treated with conservative therapy. CONCLUSIONS Clinicians should be aware that acute acalculous cholecystitis may be present during viral ...
متن کاملAcute and chronic acalculous cholecystitis associated with aortic dissection
Acalculous cholecystitis is a rare but life-threatening disease, but its pathogenesis is not fully revealed yet. We experienced two acalculous cholecystitis cases associated with aortic dissection. In Case 1, acalculous cholecystitis occurred just after the exacerbation of the aortic dissection. Laparotomy showed necrotized cholecystitis with fresh thrombi formation. Case 2 developed acalculous...
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ژورنال
عنوان ژورنال: Clinical Infectious Diseases
سال: 1999
ISSN: 1058-4838,1537-6591
DOI: 10.1086/520474