Fumarate Hydratase Mutation in a Young Woman With Uterine Leiomyomas and a Family History of Renal Cell Cancer

Merry Lynn Mann, Mohammad Ezzati, Edward D. Tarnawa, Bruce R. Carr

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Background: Heterozygous gene mutations in fumarate hydratase can result in a syndrome characterized by hereditary (cutaneous and uterine) leiomyomatosis and renal cell cancer. This disorder has been described in more than 200 families, but the prevalence of the disease is unknown. Case: A 22 year-old woman of Bangladeshi lineage presented with menorrhagia and pelvic pain secondary to uterine leiomyomas and underwent an abdominal myomectomy. Because of a family history of renal cell cancer, she was tested for fumarate hydratase mutations and found to be a carrier. As a result of the risk of renal cell cancer associated with this mutation, an annual surveillance plan was initiated. Conclusion: Fumarate hydratase gene mutations should be considered in women presenting with leiomyomas and a family history of renal cancer.

Original languageEnglish (US)
Pages (from-to)90-92
Number of pages3
JournalObstetrics and Gynecology
Volume126
Issue number1
DOIs
StatePublished - Jul 23 2015

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Fumarate Hydratase
Leiomyoma
Renal Cell Carcinoma
Mutation
Uterine Myomectomy
Leiomyomatosis
Menorrhagia
Pelvic Pain
Kidney Neoplasms
Genes
Skin

ASJC Scopus subject areas

  • Obstetrics and Gynecology

Cite this

Fumarate Hydratase Mutation in a Young Woman With Uterine Leiomyomas and a Family History of Renal Cell Cancer. / Mann, Merry Lynn; Ezzati, Mohammad; Tarnawa, Edward D.; Carr, Bruce R.

In: Obstetrics and Gynecology, Vol. 126, No. 1, 23.07.2015, p. 90-92.

Research output: Contribution to journalArticle

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