Case Description: A 28-year old woman receiving thiopurine treatment for Crohn’s disease presented with a systemic primo cytomegalovirus (CMV) infection affecting the gut (colitis), liver (hepatitis), lungs (pneumonitis) and eyes (retinitis). Secondary to this systemic infection, she developed splenomegaly, pancytopenia and lymphadenopathy. Anti-viral treatment resulted in complete resolution of clinical, biochemical and radiological abnormalities within 6 weeks.
Conclusion: Early recognition is crucial since CMV infection in a patient receiving thiopurine treatment may result in serious complications.
Cytomegalovirus, thiopurine, pneumonitis, colitis, hepatitis
A 28-year-old Caucasian woman was referred to our emergency department with fever, diarrhoea, cough and visual disturbances. Her medical history reported Crohn’s disease, which had been remission with 6-mercaptopurine (Puri-nethol, Aspen, KwaZulu-Natal, South Africa) for the previous 4 years.
Physical examination revealed no abnormalities. Laboratory assessment showed pancytopenia and elevated liver enzymes, but was otherwise unremarkable. The initial chest x-ray showed an infiltrate in the right middle lobe (Fig. 1a). Abdominal ultrasound showed splenomegaly, enlarged para-aortal lymph nodes and a thickened wall of the ascending colon.
During admission, the patient’s condition deteriorated and she developed high fever (>40°C) and progressive shortness of breath. She also still had diarrhoea. Blood cultures remained negative. Faeces PCR testing was negative for viruses, bacteria and parasites. A follow-up chest x-ray showed an interstitial pattern suggestive for lymphangitis and, retrospectively, pneumonitis (Fig. 1b). A chest CT scan confirmed lymphangitis with a suspicion of lymphoma (Fig. 1c,d).
Bone marrow biopsy showed no evidence of a haemophagocytic syndrome or haematological malignancy. The tuberculin skin test was negative. Serological testing revealed a primo cytomegalovirus (CMV) infection (IgM-positive, IgG-positive) with a viral load of 870,000 IU/ml. The consulted ophthalmologist noticed a cotton wool spot on the retina of the right eye.
Figure 1. (a) Chest x-ray showing right middle lobe pneumonia. (b) Chest x-ray taken 3 days later showing pleural fluid on the right side with bilateral interlobular septal thickening. (c,d) A high resolution CT scan of the lungs confirming diffuse interlobular thickening fitting lymphangitis with a suspicion of lymphoma. The interstitial pattern turned out to be CMV pneumonitis.
Systemic CMV infection affecting the gut (colitis), liver (hepatitis), eyes (retinitis) and lungs (pneumonitis) was diagnosed. The patient had also developed splenomegaly, pancytopenia and lymphadenopathy secondary to this infection.
The patient was treated with intra-venous ganciclovir for 14 days followed by oral valganciclovir for 4 weeks, resulting in complete resolution of her clinical, biochemical, radiographic and ophthalmological abnormalities.
Seropositivity for CMV in the adult population can vary between 45% and 100% [1]. The rate of positivity is higher in non-Caucasian populations and in older adults [1]. In Western Europe, the majority of young adults are seronegative for CMV. In immunocompetent individuals, CMV infection is usually asymptomatic or causes non-specific viral symptoms.
The risk of a severe systemic CMV infection is increased among individuals on immunosuppressive medication, like thiopurines [2, 3]. In case of systemic disease, there can be involvement of the gastrointestinal tract and central nervous system, and haematological disorders [4–6]. Less frequently, retinitis, pneumonitis and vascular thrombosis can occur [6, 7].
A review by Cascio et al. found 13 cases of CMV pneumonitis in subjects receiving thiopurines for inflammatory bowel disease, of whom eight were transferred to intensive care and four (30%) died [8]. In previously published cases, pneumonitis was seen as infiltrates or an interstitial pattern on chest radiography [8]. In our case, the second x-ray and following CT scan of the lungs showed diffuse interlobular septal thickening with a pattern fitting lymphangitis suggestive for lymphoma. As thiopurines have been associated with an increased risk of lymphoma, haematological malignancies should be considered in patients on immunosuppressive medication with enlarged lymph nodes [9]. However, benign diffuse lymph node enlargement can be seen as well in CMV infection [10]. In our patient, these anomalies resolved after she completed anti-viral treatment.
Primary or reactivated CMV infection is preferably diagnosed using a PCR test with CMV DNA [11]. Histological evaluation of biopsy specimens from involved organs also has high sensitivity [11]. IgM and IgG serology is not recommended [11]. Viral cultures are not advised due to their time-consuming nature [11]. The possibility of monitoring viral load is an additional benefit of PCR testing. Treatment should be continued until an undetectable viral load is achieved [8].
The European Crohn’s and Colitis Organization recommends treating CMV infection with ganciclovir [11]. Primary treatment should be initiated intravenously with a switch to oral valganciclovir whenever possible [11]. In severe cases, early treatment is recommended to improve outcomes [8, 11]. Haemophagocytic lymphohistiocytosis is the most severe complication associated with thiopurine treatment for Crohn’s disease. It is mostly observed in cases of primo Epstein–Barr virus (EBV) infection, but may occur in primo CMV infection as well[12,13]. Therefore, a bone marrow biopsy should be performed in individuals receiving thiopurines who present with pancytopenia, elevated ferritin levels and unexplained fever. In our case, bone marrow evaluation excluded haemophagocytic lymphohistiocytosis.
Screening for previous EBV and CMV infection before initiation of thiopurine treatment is not routinely recommended in the Dutch guideline for Crohn’s disease [3]. Therefore, a primo infection might occur during treatment with possibly severe complications[14]. As the occurrence of a severe primo infection seems to be rare, in our opinion there is no reason for withholding thiopurine treatment if screening is negative for previous infection. However, a patient on thiopurine treatment presenting with symptoms that might fit EBV or CMV infection should be tested early as long as there is no other proven cause of the symptoms.
We present a case of severe generalized primo CMV infection in an immunocompromised patient receiving thiopurines for Crohn’s disease. This case illustrates the risks related to thiopurine treatment, and so early recognition of possible complications is crucial.