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Updated: Jul 10, 2026

Bone Marrow Transplantation Platform to Investigate the Role of Dendritic Cells in Graft-versus-Host Disease
Published on: March 17, 2020
Vulvovaginal chronic graft-versus-host disease with allogeneic hematopoietic stem cell transplantation
Pamela Stratton1, Maria L Turner, Richard Childs
1Reproductive Biology and Medicine Branch, National Institute of Child Health and Human Development, NIH, Bethesda, Maryland 20892-1109, USA. ps79c@nih.gov
Insights
Female genital chronic graft-versus-host (GVH) disease, a complication of stem cell transplants, causes pain and scarring. Topical glucocorticoids and estrogen effectively treat vulvovaginal GVH disease, improving symptoms and preventing surgery.
Area of Science:
- Gynecologic Oncology
- Hematology
- Transplantation Immunology
Background:
- Female genital chronic graft-versus-host (GVH) disease is a significant complication following hematopoietic stem cell transplantation (HSCT).
- This condition can lead to debilitating vulvar and vaginal symptoms, impacting quality of life.
Purpose of the Study:
- To delineate the diagnostic criteria and management strategies for female genital chronic GVH disease.
- To evaluate the efficacy of various therapeutic interventions for vulvovaginal manifestations of chronic GVH disease.
Main Methods:
- A cohort of 33 women with vulvar symptoms or undergoing evaluation for chronic GVH disease post-HSCT were assessed.
- Gynecologic evaluations included history, laboratory tests, and physical examinations.
- Treatment involved superpotent topical glucocorticoids, topical estrogen, vaginal dilators, and estrogen vaginal rings.
Main Results:
- Most patients presented with vulvar pain and dyspareunia.
- Common findings included vulvar erythema, erosions, and scarring; vaginal scarring also developed in several patients.
- Topical glucocorticoids and estrogen improved symptoms, reduced friability, and nonsurgical treatments were effective for vaginal synechiae.
Conclusions:
- Combination therapy with topical superpotent glucocorticoids and estrogen is effective for vulvovaginal chronic GVH disease.
- Vaginal dilators and estrogen rings aid in managing vaginal scarring.
- Early diagnosis and treatment can alleviate pain, heal mucosal erosions, and potentially prevent surgical intervention.
Objective:
To describe the diagnosis and management of female genital chronic graft-versus-host (GVH) disease, a complication of hematopoietic stem cell transplantation.
Methods:
From 1999 to 2006, 33 women with vulvar symptoms or undergoing systematic evaluation for chronic GVH disease were referred 267 (median, range 29-6,117) days after transplantation for gynecologic evaluation. Pertinent histories, laboratory tests, and skin and genital area-directed examinations were performed. Vulvar disease was treated with superpotent topical glucocorticoids and topical estrogen. Sexually active, menopausal women used vaginal dilators, topical glucocorticoids and estrogen, and estrogen vaginal rings for vaginal synechiae.
Results:
At presentation, most patients complained of vulvar pain during urination and pain that prevented sexual intercourse. Twenty-nine of 33 presenting with vulvovaginal chronic GVH disease had vulvar erythema, with additional signs including vulvar vestibulitis syndrome (n=9), vulvar erosions (n=12), vulvar scarring (n=2), and vaginal scarring (n=6); over time, eight additional patients developed vaginal scarring. Topical glucocorticoids improved vulvar symptoms, and estrogen decreased vulvar mucosal friability. Eleven of 12 patients, who wanted to resume having intercourse, responded to nonsurgical treatment for vaginal synechiae.
Conclusion:
A combination of topical superpotent glucocorticoids and estrogen was effective in the treatment of vulvovaginal chronic GVH disease. In those with vaginal scarring, use of a vaginal dilator and estrogen ring was helpful. Early identification and treatment of vulvovaginal chronic GVH disease ameliorates vulvar pain by healing eroded vulvar mucosa and may prevent the need for surgery for hematocolpos.
Level Of Evidence:
III.
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