Graft-versus-host diseaseL99.1/L99.2

Author:Prof. Dr. med. Peter Altmeyer

All authors of this article

Last updated on: 27.04.2022

Dieser Artikel auf Deutsch

Synonym(s)

Cutaneous graft-versus-host disease; Graft-Host-Reaction; graft-versus-host disease; graft-versus-host reaction; GvHD; Transplant recipient response

Requires free registration (medical professionals only)

Please login to access all articles, images, and functions.

Our content is available exclusively to medical professionals. If you have already registered, please login. If you haven't, you can register for free (medical professionals only).


Requires free registration (medical professionals only)

Please complete your registration to access all articles and images.

To gain access, you must complete your registration. You either haven't confirmed your e-mail address or we still need proof that you are a member of the medical profession.

Finish your registration now

DefinitionThis section has been translated automatically.

Complex immunological reaction involving various organs, which may occur mainly as a result of allogeneic hematopoietic stem cell transplantation (HSCT). Rarely, but nevertheless described, is the occurrence of GvHD after transfusions of blood products, organ transplantation (liver, kidney) as well as after autologous HSCT.

In GvHR, it is mainly the donor T lymphocytes contained in the graft that react to the recipient organism. The most common symptoms of GvHR are seen in the skin (epithelial cells), liver, intestine, and eye, with the skin being the most commonly affected organ.

Graft-versus-host (GvH)-like reactions (see pseudoscleroderma below) have also been described (rarely) as adverse reactions to various drugs, including phenobarbital, D-penicillamine, gold preparations, hepatitis B vaccine, captopril, spironolactone, and allopurinol.

ClassificationThis section has been translated automatically.

From a clinical perspective (NIH 2005 consensus conference), GvH reactions, once they occur, are classified as:

  • acute graft-versus-host disease (L99.1-) (onset of disease within first 100 days after transplantation)
    • Persistent acute graft-versus-host disease (disease onset 100 days after transplantation).
    • Recurrent acute graft-versus-host disease (disease onset 100 days after transplantation)
    • Delayed-onset acute graft-versus-host disease
  • chronic graft-versus-host disease (L99.2-) (disease onset >100 days after transplantation)
    • Classic graft versus host disease (>100 days post-transplant)
    • Overlap syndrome (>100 days after transplantation; signs of acute and chronic graft-versus-host disease)

to be subdivided.

Occurrence/EpidemiologyThis section has been translated automatically.

The incidence of unrelated donors is expected to be 4-60%. With HLA incompatibility the risk of GvHD increases to 70-80%.

Clinical featuresThis section has been translated automatically.

In > 90% of allogeneic hematopoietic stem cell transplants, the skin is involved in chronic GVHD.

LiteratureThis section has been translated automatically.

  1. Filipovich AH et al (2005) National Institute of Health consensus development project on criteria for clinical trials in chronic-graft-versus-host-disease. Biol Blood Marrow Transplant 11: 945-956
  2. Travnik R et al (2011) Graft-versus-host-disease (GvHD) - an update. Dermatologist 62: 139-155

Authors

Last updated on: 27.04.2022