Year: 2015
Type: article
Study design: Case Report
Abstract: Cutaneous leiomyomas, which originate in the arrector pili muscles of the skin are rarely seen benign cutaneous tumors. Sometimes familial cutaneous and uterine leiomyomatosis can occur together, an autosomal dominant genetic condition called Reed syndrome or familial leiomyomatosis cutis et uteri. This disorder can be accompanied by malignancies, particularly by renal carcinoma. In this paper, two sisters with Reed syndrome are presented in view of the rarity of the disorder and good response to pregabalin therapy.
Source: Dermatology Online Journal
DOI: 10.5070/d3219028697
Authors: Mahizer Yaldiz, Murcan Metin, Mustafa Teoman Erdem, Bahar Sevimli Dikicier, Zeynep Kahyaoglu
Institution: Sakarya Eğitim ve Araştırma Hastanesi
Language: English
Subfield: Pathology and Forensic Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $300
OpenAlex ID: W1642482425
