The ability of endometrial biopsies with atypical complex hyperplasia to guide surgical management

Objective This study was undertaken to determine the clinical relevance of “qualifying comments” on pathology reports of complex atypical endometrial hyperplasia. Study Design A retrospective review of endometrial biopsy specimens with atypical hyperplasia at our institutions was performed if subseq...

Full description

Saved in:
Bibliographic Details
Published inAmerican journal of obstetrics and gynecology Vol. 199; no. 1; pp. 69.e1 - 69.e4
Main Authors Miller, Caela, MD, Bidus, Michael A., MD, Pulcini, Joseph P., MD, Maxwell, G. Larry, MD, Cosin, Jonathan A., MD, Rose, G. Scott, MD
Format Journal Article
LanguageEnglish
Published Philadelphia, PA Mosby, Inc 01.07.2008
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Objective This study was undertaken to determine the clinical relevance of “qualifying comments” on pathology reports of complex atypical endometrial hyperplasia. Study Design A retrospective review of endometrial biopsy specimens with atypical hyperplasia at our institutions was performed if subsequent hysterectomy results were available for review. Endometrial biopsy results were graded on an ordinal scale (complex atypical endometrial hyperplasia vs atypical endometrial hyperplasia “cannot rule out a more severe lesion”) and compared with pathology obtained at hysterectomy. Data were analyzed by using Fisher's exact test. Results Endometrial biopsy specimens were associated with carcinoma in 37.5% (18/48) of complex atypical endometrial hyperplasia cases and in 60% (18/30) of atypical endometrial hyperplasia-cancer cases. Atypical endometrial hyperplasia-cancer on biopsy was associated with an increased risk of discovering a malignancy at intermediate/high-risk for lymph node involvement (odds ratio 4.71, P = .0256). Conclusion Biopsy specimens that show atypical endometrial hyperplasia-cancer are associated with an increased risk of finding a cancer at intermediate or high risk for nodal metastasis.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0002-9378
1097-6868
DOI:10.1016/j.ajog.2007.11.070