Literature DB >> 16260572

Hematometra in a patient with Cornelia De Lange syndrome.

Joseph O Doyle1, Christopher D Williams, Colleen A Raymond.   

Abstract

BACKGROUND: Hematometra is usually the result of developmental anomalies or may be secondary to cervical obstruction. Abnormal uterine contractile function (atony) would be an uncommon cause of hematometra. CASE: An 18-year-old female with Cornelia De Lange syndrome and abdominal pain was found to have a hematometra on ultrasound examination. On pelvic examination, her cervical canal was patent and was easily dilated, but the hematometra did not drain until suprapubic pressure was applied. Two weeks postoperatively, pelvic magnetic resonance imaging showed a markedly thinned uterine myometrium and a recurrent hematometra, prompting the decision to perform a hysterectomy.
CONCLUSION: Hematometra in a patient with Cornelia De Lange syndrome may be the result of abnormal uterine contractile function.

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Year:  2005        PMID: 16260572     DOI: 10.1097/01.AOG.0000160512.24767.08

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  2 in total

Review 1.  Natural history of aging in Cornelia de Lange syndrome.

Authors:  Antonie D Kline; Marco Grados; Paul Sponseller; Howard P Levy; Natalie Blagowidow; Christianne Schoedel; Joni Rampolla; Douglas K Clemens; Ian Krantz; Amy Kimball; Carmen Pichard; David Tuchman
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-08-15       Impact factor: 3.908

2.  Congenital vaginal obstruction in a female with Cornelia de Lange syndrome: A case report.

Authors:  Yiding Shen; Dongyan Zhao; Long Sun; Xiuzhen Yang; Xiang Yan
Journal:  Front Endocrinol (Lausanne)       Date:  2022-08-25       Impact factor: 6.055

  2 in total

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