Histological and immunohistochemical evaluation of leiomyoma and endometrial tissue in patients with uterine leiomyoma and endometrial hyperplasia.

Authors

  • V. A. Potapov ДЗ «Дніпропетровська медична академія МОЗ України», Ukraine
  • Yu. V. Donskaya ДЗ «Дніпропетровська медична академія МОЗ України», Ukraine
  • M. V. Medvedev ДЗ «Дніпропетровська медична академія МОЗ України», Ukraine

DOI:

https://doi.org/10.26641/1997-9665.2014.1.80-84

Keywords:

leiomyoma, endometrial hyperplasia, immunohistochemical analysis

Abstract

Background. Uterine leiomyoma and endometrial hyperplasia are commonly found disorders because of quite similar pathogenic pathways associated with action of sex steroids such as estradiol and progesterone. The gold standard of treatment of combination of uterine leiomyoma and endometrial hyperplasia is myomectomy with further prescription of gestagens. Objective. Histological and immunohistochemical evaluation of leiomyoma and endometrial tissue in patients with uterine leiomyoma and endometrial hyperplasia. Methods. In this study histological and immunohistochemical analysis of leiomyoma and endometrium samples were conducted in 30 patients with uterine leiomyoma and endometrial hyperplasia. Further evaluation with transvaginal ultrasound end endometrial biopsy was conducted in 6 and 12 months after surgery. Results. In women with combined endometrial hyperplasia and uterine leiomyoma there is an increased risk of myoma relapse (23.3%) and treatment failure of endometrial hyperplasia (36.7%) after traditional treatment with gestagens. Among 7 patients with leiomyoma recurrence there was persistence of endometrial hyperplasia what was associated with increased proliferation, angiogenesis and decreased apoptosis. Conclusion. During a comprehensive immunohistochemical study of endometrial biopsies and uterine leiomyoma in women with histologically verified uterine leiomyoma and endometrial hyperplasia common immunohistochemical features had been identified such as increased expression of ki-67 and VEGF and bcl-2. It was proposed that traditional scheme using derivatives of progesterone should be avoided in such patients. In order to optimize treatment outcomes in women with such findings proposed treatment of choice should be drugs with severe suppressive action on proliferation, angiogenesis with simultaneous stimulating action on apoptosis. Drug of choice in such case should be GnRH agonist what should be assessed in future research.

References

  1. De Leo V, Morgante G, La Marca A, Musacchio MC, Sorace M, Cavicchioli C, Petraglia F. A benefit-risk assessment of medical treatment for uterine leiomyomas. Drug Saf. 2002;25(11):759-79. Cited in: PubMed; PMID: 12222988.
  2. Lethaby A, Vollenhoven B, Sowter M. Efficacy of pre-operative gonadotrophin hormone releasing analogues for women with uterine fibroids undergoing hysterectomy or myomectomy: a systematic review. BJOG. 2002 Oct;109(10):1097-108. Cited in: PubMed; PMID: 12387461.
  3. Vu K1, Greenspan DL, Wu TC, Zacur HA, Kurman RJ. Cellular proliferation, estrogen receptor, progesterone receptor, and bcl-2 expression in GnRH agonist-treated uterine leiomyomas. Hum Pathol. 1998 Apr;29(4):359-63. Cited in: PubMed; PMID: 9563785.
  4. Bozzini N, Rodrigues CJ, Petti DA, Bevilcqua RG, Gonçalves SP, Pinotti JA. Effects of treatment with gonadotropin releasing hormone agonist on the uterine leiomyomata structure. Acta Obstet Gynecol Scand. 2003 Apr;82(4):330-4. Cited in: PubMed; PMID: 12716317.
  5. Regidor PA, Schmidt M, Callies R, Kato K, Schindler AE. Estrogen and progesterone receptor content of GnRH analogue pretreated and untreated uterine leiomyomata. Eur J Obstet Gynecol Reprod Biol. 1995 Nov;63(1):69-73. PMID: Cited in: PubMed; 8674569.

How to Cite

Potapov, V. A., Donskaya, Y. V., & Medvedev, M. V. (2014). Histological and immunohistochemical evaluation of leiomyoma and endometrial tissue in patients with uterine leiomyoma and endometrial hyperplasia. Морфологія / Morphologia / Morfologìâ, 8(1), 80–84. https://doi.org/10.26641/1997-9665.2014.1.80-84

Issue

Section

Статті