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Revista Española de Enfermedades Digestivas
versión impresa ISSN 1130-0108
Rev. esp. enferm. dig. vol.110 no.6 Madrid jun. 2018
https://dx.doi.org/10.17235/reed.2018.5256/2017
LETTERS TO THE EDITOR
Idiopathic portal hypertension with regard to thiopurine treatment
1Servicio de Aparato Digestivo. Corporació Sanitària Parc Taulí. Sabadell, Barcelona
2Universidad Autónoma de Barcelona. Barcelona. Spain
3CIBERhed. Instituto Carlos III. Madrid. Spain
Key words: Portal hypertension; Thiopurine. Azathioprine; Idiopathic portal hypertension; Hepatoportal sclerosis; Inflammatory bowel disease
Dear Editor,
We read with interest the paper "Idiopathic portal hypertension regarding thiopurine treatment in patients with inflammatory bowel disease" 1, which was recently published in this journal. The paper reported four cases of idiopathic portal hypertension (IPH). In this letter, we would like to comment on a recent case treated at our unit.
Case report
We present the case of a 76-year-old male with ileocolic Crohn's disease treated with azathioprine. After ten years of treatment, he presented with a severe outbreak that required a resection of the terminal ileum. During the intervention, non-purulent ascites were observed which were culture negative. One month later, he presented with low-grade fever, abdominal pain and grade 2 ascites. The paracentesis showed a transudate without infection criteria, negative ascites and blood cultures. Empirical treatment with broad-spectrum antibiotics was initiated. The ascitic fluid had a serum ascites albumin gradient of 11 g/l that was compatible with portal hypertension. A computed tomography (CT) scan identified a homogeneous liver of a normal size and appearance, a splenomegaly of 13 cm and ascites. Endoscopy revealed small esophageal varices. The portal hemodynamics had a normal portosystemic gradient of 5 mmHg, compatible with presinusoidal portal hypertension. A liver biopsy identified hepatoportal sclerosis with mild changes due to nodular regenerative hyperplasia (NRH) (Fig. 1).
Discussion
Hepatoportal sclerosis and NRH are part of the spectrum of IPH. The lesion usually occurs insidiously and thrombocytopenia is usually the first manifestation 2. The natural history is not well established. However, cases of histological regression have been described with the withdrawal of the drug 3. However, it is usually diagnosed late due to its asymptomatic nature. Some studies show that lower levels of 6-TGN indicate a lower incidence of IPH and therefore, monitoring is recommended 4. It is important to guide the pathologist in a case of clinical suspicion; one study reported a k = 0.20 for NRH when the clinical information was inadequate 5.
Bibliografía
1. Suárez Ferrer C, Llop Herrera E, Calvo Moya M, et al. Idiopathic portal hypertension regarding thiopurine treatment in patients with inflammatory bowel disease. Rev Esp Enferm Dig 2016;108(2):79-83. [ Links ]
2. Calabrese E, Hanauer SB. Assessment of non-cirrhotic portal hypertension associated with thiopurine therapy in inflammatory bowel disease. J Crohn's Colitis 2011;5:48-53. DOI: 10.1016/j.crohns.2010.08.007 [ Links ]
3. Seiderer J, Zech CJ, Diebold J, et al. Nodular regenerative hyperplasia: a reversible entity associated with azathioprine therapy. Eur J Gastroenterol Hepatol 2006;18:553-5. DOI: 10.1097/00042737-200605000-00018 [ Links ]
4. Gilissen LPL, Derijks LJJ, Driessen A, et al. Toxicity of 6-thioguanine: no hepatotoxicity in a series of IBD patients treated with long-term, low dose 6-thioguanine. Dig Liver Dis 2007;39:156-9. DOI: 10.1016/j.dld.2006.10.007 [ Links ]
5. Jharap B, Van Asseldonk DP, De Boer NKH, et al. Diagnosing nodular regenerative hyperplasia of the liver is thwarted by low interobserver agreement. PLoS One 2015;10:e0120299. DOI: 10.1371/journal.pone.0120299 [ Links ]