[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.205.0.26. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Contempo Updates
Clinician's Corner
November 19, 2003

Chronic Graft-vs-Host Disease

Author Affiliations

Author Affiliation: Hematopoietic Cell Transplantation Program, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas.

 

Contempo Updates Section Editor: Catherine Meyer, MD, Fishbein Fellow.

JAMA. 2003;290(19):2599-2603. doi:10.1001/jama.290.19.2599

Allogeneic hematopoietic cell transplantation (HCT) is a treatment used increasingly for a variety of malignant and nonmalignant diseases of the bone marrow and immune system.1 Although the procedure cures many patients with otherwise incurable diseases, it is often associated with serious immunological complications, particularly graft-vs-host disease (GVHD).2 A chronic form of GVHD afflicts many allogeneic HCT recipients, resulting in dysfunction of numerous organ systems and an oftentimes profound state of immunodeficiency.35 Chronic GVHD is the most frequent cause of poor long-term outcome and quality of life after allogeneic HCT. The syndrome typically develops several months after transplantation, when the patient may no longer be under the direct care of the transplant team. The patient's primary physician plays an important role in diagnosis and treatment of the patient with chronic GVHD.

First Page Preview View Large
First page PDF preview
First page PDF preview
×