Literature DB >> 11676337

Portal hypertension secondary to Langerhans cell histiocytosis.

D Bansal1, R K Marwaha, A Trehan, U Poddar, B D Radotra.   

Abstract

We report two children, aged 2 and 2 1/2 years, with multisystem Langerhans cell histiocytosis (LCH). Both were administered chemotherapy, with apparently good response. However, hepatic fibrosis and portal hypertension were detected 5 and 1 1/2 years after therapy, respectively. The first child died after a bout of hematemesis. Hepatic fibrosis can proceed despite apparently successful chemotherapy in LCH.

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Mesh:

Year:  2001        PMID: 11676337

Source DB:  PubMed          Journal:  Indian J Gastroenterol        ISSN: 0254-8860


  2 in total

1.  Imaging findings in hepatic Langerhans' cell histiocytosis.

Authors:  Alka Chaudhary; Jyotindu Debnath; Sanjay Thulkar; Tulika Seth; Anindita Sinha
Journal:  Indian J Pediatr       Date:  2006-11       Impact factor: 1.967

Review 2.  Current perspectives on the role of liver transplantation for Langerhans cell histiocytosis: A narrative review.

Authors:  Jagadeesh Menon; Ashwin Rammohan; Mukul Vij; Naresh Shanmugam; Mohamed Rela
Journal:  World J Gastroenterol       Date:  2022-08-14       Impact factor: 5.374

  2 in total

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