Contributed by Randall G. Lee, M.D.
PATIENT HISTORY: Per referral letter, the patient is a 48-year-old white female with an increased serum bilirubin of 3.12 with indirect bilirubin of 2.29. The patient also has a normal haptoglobin level. R/O Gilbert's disease. Special stains were negative for acid-fast bacilli and fungal organisms. Review of outside material.

Final Diagnosis (Case 5)

LIVER, NEEDLE BIOPSY -
  1. SCATTERED EPITHELIOID GRANULOMAS WITH PERIPHERAL FIBROSIS AND MILD INFLAMMATORY ACTIVITY.
  2. FOCAL SINUSOIDAL DILATATION.

COMMENT:

The size, associated fibrosis, and multinodularity of the granulomas suggest the possibility of sarcoidosis. This possibility needs to be correlated with clinical and radiographic studies. Other differential considerations include infectious and drug-induced causes of granulomas. In a large minority of cases, however, no specific cause can be identified.

Previous Biopsies on this Patient:
NONE

TPIS Related Resources:
Knodell Scoring
Liver Transplant Topics


Gross Description - Case 5

The specimen consists of one (1) consult slide and one (1) paraffin block . No surgical pathology report was received with the specimen.


Microscopic Description - Case 5

The liver biopsy shows intact hepatic architecture. There are several irregular foci of sinusoidal dilatation. The most striking finding is the presence of scattered well-formed epithelioid granulomas. These granulomas are present both within the lobules and within portal tracts, and they are associated with peripheral and segmentalizing fibrosis as well as, in some instances, a peripheral cuff of mononuclear cells. No bile duct loss or other features of primary biliary cirrhosis is seen. Otherwise, mild nuclear glycogenation of liver cell nuclei is identified. There is no significant hepatitis or other abnormality. The sinusoidal dilatation is presumably of local effect, resulting from the presence of granulomas.

The causes of hepatic granulomas are legion. Nonetheless, several features of this case suggest the possibility of sarcoidosis, and this should be further investigated. Features of primary biliary cirrhosis are not seen, but other differential considerations would include infectious and drug-induced granulomatous reactions. I understand that microbial stains are negative in this case. The extent to which this granuloma should be worked further will depend largely on the clinical findings.


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