Monday, April 30, 2012

Acute liver failure in a case of Bancroftian filariasis.



 Acute liver failure in a case of  Bancroftian filariasis.
                                                                                Dr. Dwijesh Kumar Panda, M.D. Ph.D (FILARIA)
Summary:
We report a case of acute liver failure associated with Bancroftian filariasis in a young male. Absence of other etiological factors rule out other causes of liver failure.  Treatment of the filariasis condition improved the liver function.
Introduction:
Bancroftian filarisis is associated with multiple clinical presentations. Peripheral blood eosinophilia is a common association in patients with filariasis. Tropical pulmonary eosinophilia is a common condition in filarial endemic areas wherein peripheral blood eosinophilia is associated with pulmonary symptoms. Acute eosinophilic glomerulonephritis has been described in association with bancroftian filariasis. The presentation of a case of Bancroftian Filarisis with liver failure is described below and an etiological association between the two conditions is discussed.
Case report:
A 10 year old male child presented pain abdomen, fever, loss of appetite, nausea and yellowish discoloration of the skin and eyes for 3 days. Fever was a low grade continuous type.  Pain abdomen was more pronounced in the right upper quadrant. There was no history of trauma  or drug intake of any kind.  There were no complaints pertaining to the respiratory or neurological system.  A provisional diagnosis of acute Viral hepatitis was made and hematological tests including routine hemoglobin count, differential count, leukocyte count, liver function tests, Hbsag , urine for bile salt and pigments and an Ultrasonogram of the abdomen and pelvis was ordered. While the hemoglobin was in normal range, the differential count revealed eosinophilia ( 79%) with a low neutrophil and lymphocyte count( 10% each). Hbsag test was negative. Liver function tests revealed a raised SGOT ( 2039 U/L), SGPT (1670 U/L), Alkaline phosphatase ( 533U/L), LDH ( 495 U/L),  total bilirubin ( 12.24 mg/dl), Bilirubin direct ( 10.27mg/dl), Bilurbin indirect ( 1.97 mg/dl). Serum protein was in normal range and serum globulin was high (4.8g/dl) with a low albumin to globulin ratio (0.7). bile salts and bile pigments were detected in the urine sample. Ultrasonogram of the abdomen revealed a enlarged liver and a distended gall bladder with thickened  walls. Rest of the intraabdominal structures appeared normal. Based on these findings conservative treatment along the line of viral hepatitis was instituted.  At the end of ten days , when the patient did not report any clinical improvement, a repeat of  the liver function tests was carried out.  Repeat tests revealed a mild decrease in liver enzymes with a mild increase in the total and direct bilirubin. The patient was continued under a conservative regimen for 4 weeks and repeat liver function tests performed. At this time the SGOT and SGPT values showed definite improvement, alkaline phosphatase values were normal but total and direct biluribin values were still high.  Differential count repeated at this time showed persistent eosinophilia (75%), elevated total leukocyte count ( 1 lac 12 thousands). No premature cells in peripheral smear or toxic  granules were seen in the neutrophils.  Absolute eosinophil count was 39,640 ( normal  range: 50 – 400/cmm). Since the patient belonged to a filarial endemic zone, a test for filarial antigen  OG4C3 was carried out. The test for filarial antigen was positive ( 512 AU). A diagnosis of  Bancroftian filariasis with acute liver failure was made and patient started on a course of diethylcarbamazine. Over the next three weeks, patient reported rapid clinical improvement with improved appetite, resolution of abdominal pain and fever. At the end of three weeks a repeat of differential and leucocyte count revealed improvement in both the parameters.  A repeat of liver function tests at this time showed normal values of the liver enzymes and bilirubin count.
 

Discussion:
A raise in eosinophil differential count  and absolute eosinophil count in a young male with fever coming from a filarial endemic zone raised the suspicion towards bancroftian filariasis. Persistently high liver enzymes with raised bilirubin values that did not improve with conservative measures prompted us to search for infective causes in absence of othe common etiologic factors for liver failure. Og4c3 antigenic test for filarial has been proven to be of benefit to detect infection with Wuchereria bancrofti  in case of inability to detect microfilaria in peripheral smear. Raised eosinophil values in the absence of any premature cells in peripheral smear ruled out the diagnosis of  eosinophilic leukemia. The improvement of both the clinical and hematological  parameters with a course of diethylcarbamazine clinches the diagnosis of acute liver failure with bancroftian filariasis. The patient was last seen at a six month follow up and a repeat clinical and hematological evaluation showed persistent improvement without any recurrence of symptoms.
Addition-  OG4C3  ELISA Test=  It is a semi-quantitative ELISA test for the detection of adult Filarial antigen on 50 micro-litre of serum. Different titre groups are- 32,000, 8192 , 2048 , 512, 128, 32, <10 Antigen Units. 512 and above antigen Units are considered Positive and less thsn 512  Antigen Units are Negative.