Woolner Kathryn, O'Toole Ashley, LaBerge Lauren
University of Ottawa, Ontario, Canada
The Ottawa Hospital Civic Campus, Parkdale Clinic, Ottawa, Ontario, Canada.
J Cutan Med Surg. 2016 Jul;20(4):334-6. doi: 10.1177/1203475416634091. Epub 2016 Feb 22.
Reed's syndrome, also known as hereditary leiomyomatosis and renal cell cancer (HLRCC) syndrome, is an autosomal dominant condition in which affected individuals may develop cutaneous leiomyomas, uterine fibroids, and renal cell carcinoma.
This report describes a unique case of HLRCC because it presented in pregnancy with development of cutaneous pilar leiomyomas.
Review of the literature for previous cases of Reed's syndrome during pregnancy including PubMed and Medline search.
Genetic testing of this patient demonstrated a mutation in the fumarate hydratase (FH) gene. Review of the literature showed only 1 previous case series that described the onset of cutaneous lesions during pregnancy.
This case serves as a reminder that there may exist a correlation between pregnancy and the first manifestation of cutaneous lesions in patients with HLRCC, and thus an increased clinical suspicion is warranted during this period.
里德综合征,也称为遗传性平滑肌瘤病和肾细胞癌(HLRCC)综合征,是一种常染色体显性疾病,患病个体可能会出现皮肤平滑肌瘤、子宫肌瘤和肾细胞癌。
本报告描述了一例独特的HLRCC病例,因为它在孕期出现了皮肤毛发平滑肌瘤。
回顾包括PubMed和Medline检索在内的既往孕期里德综合征病例的文献。
该患者的基因检测显示延胡索酸水合酶(FH)基因突变。文献回顾显示,之前仅有1个病例系列描述了孕期皮肤病变的发作。
该病例提醒我们,孕期与HLRCC患者皮肤病变的首次表现之间可能存在关联,因此在此期间应提高临床怀疑度。