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http://www.scirp.org/journal/PaperInformation.aspx?PaperID=54058#.VOBXlSzQrzE
ABSTRACT
Following
an elective transphenoidal resection of a pituitary tumor, a
66-year-old Hispanic male acutely developed fulminant hepatic failure
and severe coagulopathy. He received parenteral corticosteroids the day
prior to surgery, and was first noted to have significant coagulopathy
intraoperatively. Despite aggressive workup and treatment for fulminant
hepatic failure, the patient developed multiorgan failure by
post-operative day 2, and expired on post-operative day 3. On
post-mortem examination, hemorrhagic necrosis of the liver was noted and
microscopic examination revealed Cowdry type A inclusions, consistent
with Herpes Simplex Virus (HSV) infection. This diagnosis was
subsequently confirmed by immunehistochemistry. Fulminant hepatic
failure due to HSV is a rare but highly fatal disease if untreated. Most
case reports include only immunocompromised or pregnant patients.
However, the lack of clinical suspicion in this previously healthy
patient may have delayed prompt treatment with antiviral agents. It is
important to raise the awareness of this rare and life-threatening, but
potentially treatable, etiology when clinicians are faced with acute
idiopathic fulminant hepatic failure.
Cite this paper
References
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