Fertility and Sterility
Volume 94, Issue 3 , Pages 862-868, August 2010

Diagnosis, laparoscopic management, and histopathologic findings of juvenile cystic adenomyoma: a review of nine cases

Department of Obstetrics and Gynecology, Juntendo University School of Medicine, Tokyo, Japan

Received 1 May 2008; received in revised form 27 April 2009; accepted 7 May 2009. published online 19 June 2009.

Objective

To define diagnostic criteria for juvenile cystic adenomyoma (JCA), describe the histologic features of the condition and evaluate laparoscopic excision for treating associated dysmenorrhea and pelvic pain.

Design

Prospective long-term follow-up study.

Setting

University-affiliated hospital.

Patient(s)

Nine consecutive patients with JCA.

Intervention(s)

Patients meeting the diagnostic criteria for JCA underwent laparoscopic enucleation of the lesion. The severity of dysmenorrhea was evaluated before surgery and every 6 months after surgery. Five patients underwent second-look laparoscopy (SLL) 6 months after surgery.

Main Outcome Measure(s)

Relief of dysmenorrhea as measured by a visual analog scale, postoperative healing at SLL, and subsequent pregnancy when desired by the patient.

Result(s)

Laparoscopic enucleation of the cystic adenomyoma resulted in a statistically and clinically significant reduction in dysmenorrhea and improved chronic pelvic pain. Neither cystic adenomyoma nor severe dysmenorrhea recurred during the follow-up period. Adhesions were minimal at SLL. Two of the three patients who desired pregnancy conceived after surgery. The histologic findings of the JCA lesion and adenomyosis were similar, and the endometrial glands and stroma infiltrating the surrounding myometrium in all patients were consistent with the appearance of adenomyosis.

Conclusion(s)

We defined the diagnostic criteria for JCA, and demonstrated significant improvement of dysmenorrhea after laparoscopic excision of the lesion.

Key Words: Cystic adenomyoma, laparoscopy, cystic lesion, uterus, cystic adenomyosis, Medline search, adolescent, congenital

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 H.T. has nothing to disclose. M.K. has nothing to disclose. I.K. has nothing to disclose. J.K. has nothing to disclose. K.K. has nothing to disclose. M.J. has nothing to disclose.

PII: S0015-0282(09)01086-3

doi:10.1016/j.fertnstert.2009.05.010

Fertility and Sterility
Volume 94, Issue 3 , Pages 862-868, August 2010