2017JAAD Case ReportsOpen access

Treatment of cutaneous leiomyomas with 5% lidocaine patches in a patient with hereditary leiomyomatosis and renal cell cancer (Reed syndrome)

Tina Hsu, Lynn A. Cornelius, Ilana S. Rosman, Kathleen M. Nemer

Open full text 5 citations

Abstract

Hereditary leiomyomatosis and renal cell cancer (HLRCC) (formerly known as Reed syndrome, multiple cutaneous and uterine leiomyomatosis, leiomyomatosis cutis et uteri, and multiple leiomyomatosis) is an autosomal dominant syndrome comprising cutaneous leiomyomas, uterine leiomyomas, or renal tumors. The cutaneous leiomyomas of HLRCC are classically painful and difficult to treat. We report the first case, to our knowledge, of cutaneous leiomyomas symptomatically treated with 5% lidocaine patches.

Open-access reader

About this research paper

What this paper is about

Hereditary leiomyomatosis and renal cell cancer (HLRCC) (formerly known as Reed syndrome, multiple cutaneous and uterine leiomyomatosis, leiomyomatosis cutis et uteri, and multiple leiomyomatosis) is an autosomal dominant syndrome comprising cutaneous leiomyomas, uterine leiomyomas, or renal tumors. The cutaneous leiomyomas of HLRCC are classically painful and difficult to treat. We report the first case, to our knowledge, of cutaneous leiomyomas symptomatically treated with 5% lidocaine patches.

Why it matters

OpenAlex reports 5 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Hereditary leiomyomatosis and renal cell cancer (HLRCC) (formerly known as Reed syndrome, multiple cutaneous and uterine leiomyomatosis, leiomyomatosis cutis et uteri, and multiple leiomyomatosis) is an autosomal dominant syndrome comprising cutaneous leiomyomas, uterine leiomyomas, or renal tumors. The cutaneous leiomyomas of HLRCC are classically painful and difficult to treat. We report the first case, to our knowledge, of cutaneous leiomyomas symptomatically treated with 5% lidocaine patches.

Key concepts: Leiomyomatosis, Medicine, Leiomyoma, Uterine leiomyoma, Pathology

Related papers

Back to paper searchBrowse research topicsOriginal source
Treatment of cutaneous leiomyomas with 5% lidocaine patches in a patient with hereditary leiomyomatosis and renal cell cancer (Reed syndrome) — Research Paper | ScholarLens