Article Text

Download PDFPDF
Intestinal lymphangiectasia associated with angiofollicular lymph node hyperplasia (Castleman's disease).
  1. S F Moss,
  2. D M Thomas,
  3. C Mulnier,
  4. I G McGill,
  5. H J Hodgson
  1. Department of Medicine, Royal Postgraduate Medical School, Hammersmith Hospital, London.


    A patient presenting with predominantly gastrointestinal symptoms and a history of myocardial infarction was found to have ascites, hepatosplenomegaly, para-aortic lymphadenopathy, thrombocytosis, and a paraproteinaemia. A jejunal biopsy specimen showed lymphangiectasia and histology of the spleen and lymph nodes showed angiofollicular hyperplasia or Castleman's disease of the hyaline vascular type. This association has not previously been described and, moreover, systemic symptoms are unusual in this variant of Castleman's disease.

    Statistics from

    Request Permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.