Collapsing glomerulopathy in sickle cell disease: a case report
2011

Collapsing Glomerulopathy in Sickle Cell Disease: A Case Report

Sample size: 1 publication Evidence: low

Author Information

Author(s): Ramidi Ganga B, Kurukumbi Mohan K, Sealy Peter L

Primary Institution: Howard University Hospital

Conclusion

This case highlights a rare instance of collapsing glomerulopathy in a patient with sickle cell disease, which has a very poor prognosis.

Supporting Evidence

  • Collapsing glomerulopathy is a rare condition in patients with sickle cell disease.
  • The patient experienced acute renal failure requiring dialysis.
  • Collapsing glomerulopathy has a very poor prognosis and often leads to end-stage renal disease.

Takeaway

A 21-year-old woman with sickle cell disease developed a serious kidney problem called collapsing glomerulopathy, which made her kidneys stop working well and required dialysis.

Methodology

Case report detailing the clinical presentation, diagnosis, and treatment of a patient with collapsing glomerulopathy.

Limitations

The study is based on a single case report, limiting generalizability.

Participant Demographics

21-year-old African-American woman with a history of sickle cell disease and asthma.

Digital Object Identifier (DOI)

10.1186/1752-1947-5-71

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication