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  1. Leong, Z.P., Watanabe, M., Lim, M.L.
    Jurnal Veterinar Malaysia, 2015;27(1):27-30.
    MyJurnal
    A 4-year-old, male local dog was referred to University Veterinary Hospital-Universiti Putra Malaysia (UVH-UPM) due to
    dyspnoea and ascites. Full diagnostic investigations inclusive of blood haematology, serum biochemistry, blood smear examinations
    for haemopathogens, heartworm antigen test, thoracic and abdominal radiography and echocardiography were conducted. A
    diagnosis of severe heartworm disease was made from the positive heartworm antigen test, the presence of heartworms on
    echocardiography and the accompanying advanced clinical findings. This was the first case of right-sided heart failure due to severe
    heartworm disease with concurrent pulmonary hypertension diagnosed in UVH-UPM from which the moribund dog was
    successfully stabilised during hospitalisation.
  2. Yiew, X.T., Leong, Z.P., Rahman, N., Watanabe, M., Noordin, M.M., Khor, K.H.
    Jurnal Veterinar Malaysia, 2016;28(1):7-11.
    MyJurnal
    A 5-month-old Siamese cross kitten was presented with jaundice and a palpable abdominal mass at the right cranial quadrant. The extra-hepatic biliary system was markedly distended upon abdominal ultrasonography. Complete bile duct obstruction was ruled out due to the presence of urobilinogen, light brown stool, and consistentlynormal alkaline phosphatase (ALP) levels. Head tremors developed on the second day of hospitalization. Tentative diagnoses of congenital biliary anomaly and hepatic encephalopathy werederived and exploratory laparotomy revealed a severely distended and tortuous bile duct indistinguishable from the gallbladder with negative duodenal filling. Modified cholechoduodenostomy was performed however the kitten did not recover from general anaesthesia. Secondary cholangiohepatitis and hepatic encephalopathy were confirmed upon histopathologic examination.Primary congenital biliary atresia or choledochal cyst with secondary cholangiohepatitis was suspected. Biliary anomalies are rare in cats with only two cases reported in the literature. These conditions are often challenging to diagnose and due to the limited treatment options, have a poor prognosis.
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