Routine histologic features in complex atypical hyperplasia can predict the presence of endometrial carcinoma: a clinicopathological study of 222 cases

• Published in: Human pathology Vol. 80; pp. 40 - 46
• Main Authors: Zhang, Cunxian, Wang, Edmond Y., Liu, Fang, Sung, C. James, Quddus, M. Ruhul, Ou, Joyce, Lomme, Michele, Lawrence, W. Dwayne
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.10.2018; Elsevier Limited
• Subjects: Adenocarcinoma - pathology; Adult; Age; Aged; Clinicopathologic study; Complex atypical hyperplasia; Endometrial cancer; Endometrial carcinoma; Endometrial Hyperplasia - pathology; Endometrial Neoplasms - pathology; Endometrium - pathology; Female; Human subjects; Humans; Hyperplasia; Hyperplasia - pathology; Hysterectomy; Middle Aged; Patients; Precancerous Conditions - pathology; Predict; Routine histologic features; Uterine Neoplasms - pathology; Predict; Clinicopathologic study; Endometrial carcinoma; Routine histologic features; Complex atypical hyperplasia
• ISSN: 0046-8177; 1532-8392; 1532-8392
• DOI: 10.1016/j.humpath.2018.03.009

There is a wide range of finding endometrial adenocarcinoma (ADCA) in the uterus after a diagnosis of complex atypical hyperplasia (CAH), likely due to a poor diagnostic reproducibility and an inherent heterogeneity in CAH. We evaluated whether histologic subtyping of CAH would help predict ADCA. Our study consisted of 222 cases of CAH diagnosed by endometrial biopsy or curettage. ADCA was seen in 38.3% of these cases at hysterectomy. We divided CAH into 2 subtypes: type A was defined as back-to-back glands in a focus smaller than 2.1 mm, and type B as crowded glands with cytologic atypia but with still-intervening stroma regardless of lesional size. Type A was associated with a significantly higher frequency of ADCA (75.9%) compared with type B (26.2%). Lesions containing neutrophilic/cellular debris showed a higher association of ADCA (60.0%) compared with those without neutrophilic/cellular debris (35.5%). CAH present outside endometrial polyp was associated with a higher frequency of ADCA (42.5%) than that confined to endometrial polyp (19.5%). Within type B cases, lesions greater than 3 mm had a higher association of ADCA (34.3%) than did smaller ones (13.6%). Patients older than 50 years were more likely to have ADCA in the uterus compared with younger women with a preoperative diagnosis of CAH (43.2% versus 28.3%). CAH made on office biopsy showed a higher association of ADCA (46.6%) compared with a diagnosis made on curettage (31.1%). Recognition of these clinicopathological features in CAH may prove useful in predicting the likelihood of ADCA in the uterus. •Histologic features in complex atypical hyperplasia can predict the risk of endometrial cancer.