CT abdominal imaging findings in patients with sickle cell disease: acute vaso-occlusive crisis, complications, and chronic sequelae.

Published

Journal Article (Review)

Sickle cell disease (SCD) is the most prevalent hemoglobinopathy. Survival in patients with SCD has improved over the past few decades. These patients experience a lifetime of repeated acute pain crises, which are thought to result from sickling and microvascular occlusions; acute abdominal pain is common. Moreover, repeated crises often lead to organ dysfunction, such as asplenia, hepatic failure, and renal failure. The spleen, liver, biliary system, kidneys, and gastrointestinal tract can all be affected. Patients may undergo CT to further direct clinical management. We review the spectrum of CT imaging findings of abdominal manifestations in patients with SCD, from the acute microvascular occlusive pain crisis to the potential complications and chronic sequelae.

Full Text

Duke Authors

Cited Authors

  • Gardner, CS; Boll, DT; Bhosale, P; Jaffe, TA

Published Date

  • December 2016

Published In

Volume / Issue

  • 41 / 12

Start / End Page

  • 2524 - 2532

PubMed ID

  • 27600384

Pubmed Central ID

  • 27600384

Electronic International Standard Serial Number (EISSN)

  • 2366-0058

Digital Object Identifier (DOI)

  • 10.1007/s00261-016-0890-9

Language

  • eng

Conference Location

  • United States