Repository logo
 
Loading...
Thumbnail Image
Publication

Cutaneous Leiomyomatosis in a Mother and Daughter

Use this identifier to reference this record.
Name:Description:Size:Format: 
An Bras Dermat 2013 s124.pdf272.88 KBAdobe PDF Download

Advisor(s)

Abstract(s)

A 34-year-old woman with no known medical history was evaluated for multiple painful brown nodules and papules on the anterior aspect of the trunk. She mentioned a history of similar cutaneous findings on her mother. Biopsies of three lesions revealed piloleiomyomata. Renal and adrenal ultrasound revealed an isolated simple cortical cyst, and pelvic and endovaginal ultrasound revealed two uterine myomata. The clinical diagnosis of hereditary leiomyomatosis and renal cell cancer was corroborated by the identification of a heterozygous variant on exon 5 of the fumarate hydratase gene (c.578C>T p.T193I). Identification of the tumor piloleiomyoma should alert the dermatologist to this rare genodermatosis, which is associated with an increased risk of renal cell tumors, demanding multidisciplinary follow-up, and personal and family counseling.

Description

Keywords

HSAC DER Biópsia Carcinoma de Células Renais Neoplasias do Útero Fumarato Hidratase Predisposição Genética para a Doença Neoplasias Renais Leiomiomatose Pele Neoplasias da Pele HDE GEN

Citation

An Bras Dermatol. 2013 Nov-Dec;88(6 Suppl 1):124-7

Research Projects

Organizational Units

Journal Issue

Publisher

Scielo

Collections

CC License