TY - JOUR
T1 - Myometrial Hyperplasia in Pediatric, Adolescent, and Young Adult Uteri
AU - Cramer, Stewart F.
AU - Padela, Aasim I.
AU - Marchetti, Carol E.
AU - Newcomb, Patricia M.
AU - Heller, Debra S.
N1 - Funding Information:
We thank Leon Metlay, M.D., Nicholas Forbes, M.D., and H Ronald Zielke, Ph.D. (Director, Brain and Tissue Bank for Developmental Disorders at the University of Maryland, Contract N01-HD8-3283) for contributing autopsy uteri. This study was supported by the Myoma Project Fund and the Kidd Fund, Rochester General Hospital Foundation.
PY - 2003/10
Y1 - 2003/10
N2 - Objective: To evaluate if myometrial hyperplasia is a congenital variation in myometrial differentiation, or an acquired structural disorder of the myometrium, this study evaluated whether myometrial hyperplasia was present in uteri of children, adolescents, and young adults. Methods: We studied 19 pediatric/young adult uteri in cases with no clinical history of uterine disease. Random photomicrographs at 100x, taken at 1, 5, and 10 mm beneath the endometrium, were assessed for increased cellularity and nucleus/cell ratio, as compared to normal myometrium in the outer third of the same uterus. Results: Myometrial hyperplasia was generally absent in prepubertal uteri, first appeared in adolescent uteri just beneath the endometrium, and was found at 5 mm depth only after age 18. It decreased with depth beneath the endometrium (P < 0.05). Conclusion: Myometrial hyperplasia is not a congenital anatomic variation in myometrial differentiation, but rather an age-related acquired structural variation. Its relationship to common adolescent symptoms of dysmenorrhea and an-ovulatory bleeding remains unknown and unexplored.
AB - Objective: To evaluate if myometrial hyperplasia is a congenital variation in myometrial differentiation, or an acquired structural disorder of the myometrium, this study evaluated whether myometrial hyperplasia was present in uteri of children, adolescents, and young adults. Methods: We studied 19 pediatric/young adult uteri in cases with no clinical history of uterine disease. Random photomicrographs at 100x, taken at 1, 5, and 10 mm beneath the endometrium, were assessed for increased cellularity and nucleus/cell ratio, as compared to normal myometrium in the outer third of the same uterus. Results: Myometrial hyperplasia was generally absent in prepubertal uteri, first appeared in adolescent uteri just beneath the endometrium, and was found at 5 mm depth only after age 18. It decreased with depth beneath the endometrium (P < 0.05). Conclusion: Myometrial hyperplasia is not a congenital anatomic variation in myometrial differentiation, but rather an age-related acquired structural variation. Its relationship to common adolescent symptoms of dysmenorrhea and an-ovulatory bleeding remains unknown and unexplored.
KW - Adolescent
KW - Myometrium Hyperplasia
KW - Uterus
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U2 - 10.1016/S1083-3188(03)00158-X
DO - 10.1016/S1083-3188(03)00158-X
M3 - Article
C2 - 14597019
AN - SCOPUS:0344014298
SN - 1083-3188
VL - 16
SP - 301
EP - 306
JO - Journal of Pediatric and Adolescent Gynecology
JF - Journal of Pediatric and Adolescent Gynecology
IS - 5
ER -