Immunosuppressive therapy in transplanted recipients increases the incidence of tuberculosis, because of suppressive effects against the cell mediated immunity (
9). Most cases of post-transplant tuberculosis in the literature have been among the renal transplant patients and reports of post liver transplant tuberculosis are not common (
10). Isolated TB in the allograft liver is extremely rare and until now only three cases have been reported (
6-
8).
Table 2 shows clinical characteristics of previous and current cases of isolated TB in the transplanted liver in detail.
Two of the previous cases as well as our case have been in the patients above 40 years of age who have been transplanted by a cadaveric liver (
6,
8). However, the patient reported by Kiuchit et al. From Japan has received the liver from her mother (who finally turned out to be PPD positive). In the adult cases of allograft TB, the diagnosis has been made in 8 to 18 months, but in the pediatric cases, this duration was much shorter i.e. 3 months post transplantation (
6-
8). All of the previous cases were PPD negative before transplantation, so it seems that they have got the infection from the graft (
6-
8). However, pre-transplant PPD test may underestimate the infection, because cirrhosis as chronic disease may result in cutaneous anergy which declines the sensitivity of the test, especially in our case with a history of diabetes mellitus (
3). Addition of pre-transplantion chest imaging would be helpful (
1). It is also important to perform PPD test and chest X-ray in the donor if it’s feasible (living related transplant) (
3). Most common presenting symptoms have been fever and night sweat which in combination with abnormal LFT has led to perform a liver biopsy (
7,
8). The intensity of immunosuppression is a possible risk factor for the development of post-transplant TB i.e. OKT3 or anti-T lymphocyte antibodies (
4). However none of the previous post-liver transplant tuberculosis cases has been receiving these types of medication. Presence of other accompanying diseases such as diabetes (as in our case) is also another predisposing factor (
4). Tissue biopsy is critical for the establishment of the diagnosis (
1). All the previous cases have been diagnosed by liver biopsy or fine needle aspiration and the presence of acid fast bacilli and caseating granuloma (
6-
8). Treatment of the hepatic TB in the allografts of previous cases has been successful by anti TB regimens composed of INH, refampin, and ethambutol. In none of them INH hepatotoxicity has been reported despite of at least 6 months of therapy (
6-
8). It is very important to monitor the patients with liver transplant on both anti TB and immunosuppressive drugs, in order to prevent graft rejection and maintain an effective anti TB therapy, because of high mortality of untreated TB in a transplant recipient (
11). As a conclusion high degree of suspicion is necessary for diagnosis of post-liver hepatic transplant TB and should be considered in the patients with fever and night sweat as well as abnormal LFT.