2019, Number 3
<< Back Next >>
Rev Cent Dermatol Pascua 2019; 28 (3)
Reed syndrome
Trejo-Acuña JR, Ramos-Garibay JA, Ríos-Garza Z, Valdés-Morales KL
Language: Spanish
References: 16
Page: 127-131
PDF size: 4976.47 Kb.
ABSTRACT
Cutaneous leiomyomas are benign neoplasms arising from smooth muscle. Piloleiomyomas are a subtype of leiomyomas arising from the piloerector muscle, which can be solitary or multiple. Reed’s syndrome consists of the association of multiple familial piloleiomyomas and uterine fibroids. In this article, we present the case of a 75 year old woman with the diagnosis of Reed’s syndrome, and we made a brief review of the literature.
REFERENCES
Çaliskan E, Bodur S, Ulubay M, Özmen I, Çiçek AF, Deveci G et al. Hereditary leiomyomatosis and renal cell carcinoma syndrome: a case report and implications of early onset. An Bras Dermatol. 2017; 92: 88-91. doi:10.1590/abd1806-4841.20175380
Pastor MA, Carrasco L, Izquierdo MJ, Fariña MC, Martín L, Requena L. Piloleiomiomas faciales múltiples no familiares. Actas Dermosifiliogr. 2001; 92: 510-514.
Emer JJ, Solomon S, Mercer SE. Reed’s syndrome: a case of multiple cutaneous and uterine leiomyomas. J Clin Aesthet Dermatol. 2011; 4: 37-42.
Morales-Barrera ME, Galván-Soria LA, Novales-Santa Coloma J, Ramos-Garibay A. Piloleiomiomas múltiples. Presentación de un caso. Rev Cent Dermatol Pascua. 2001; 10: 138-140.
Diluvio L, Torti C, Terrinoni A, Candi E, Piancatelli R, Piccione E et al. Dermoscopy as an adjuvant tool for detecting skin leiomyomas in patient with uterine fibroids and cerebral cavernomas. BMC Dermatol. 2014; 14: 7. doi:10.1186/1471-5945-14-7.
Hinostroza DD, Rodríguez AM, Ramos-Garibay A. Piloleiomiomas cutáneos múltiples. Comunicación de un caso. Rev Cent Dermatol Pascua. 2002; 11: 91-93.
Basendwh MA, Fatani M, Baltow B. Reed’s syndrome: a case of multiple cutaneous leiomyomas treated with liquid nitrogen cryotherapy. Case Rep Dermatol. 2016; 8: 65-70. doi:10.1159/000445042
Collgros H, Iglesias-Sancho M, Tribó-Boixareu MJ, Creus-Vila L, Umbert-Millet P, Salleras-Redonnet M. Multiple cutaneous and uterine leiomyomatosis or reed syndrome: a retrospective study of 13 cases. Actas Dermosifiliogr. 2015; 106: 117-125. doi:10.1016/j.adengl.2014.12.013
Patel VM, Handler MZ, Schwartz RA, Lambert WC. Hereditary leiomyomatosis and renal cell cancer syndrome: An update and review. J Am Acad Dermatol. 2017; 77: 149-158. doi:10.1016/j.jaad.2017.01.023
Nagarajan P, Kenney B, Drost P, Galan A. An unusual case of sporadic hereditary leiomyomatosis and renal cell carcinoma syndrome. Cutis. 2015; 95: E7-E9.
Lehtonen HJ. Hereditary leiomyomatosis and renal cell cancer: update on clinical and molecular characteristics. Fam Cancer. 2011; 10: 397-411. doi:10.1007/s10689-011-9428-z
Rongioletti F, Fausti V, Ferrando B, Parodi A, Mandich P, Pasini B. A novel missense mutation in fumarate hydratase in an Italian patient with a diffuse variant of cutaneous leiomyomatosis (Reed’s syndrome). Dermatology. 2010; 221: 378-380. doi:10.1159/000321336
Schmidt LS, Linehan WM. Hereditary leiomyomatosis and renal cell carcinoma. Int J Nephrol Renovasc Dis. 2014; 7: 253-260. doi:10.2147/ijnrd.s42097
van Spaendonck-Zwarts KY, Badeloe S, Oosting SF, Hovenga S, Semmelink HJ, van Moorselaar RJ et al. Hereditary leiomyomatosis and renal cell cancer presenting as metastatic kidney cancer at 18 years of age: implications for surveillance. Fam Cancer. 2012; 11: 123-129. doi:10.1007/s10689-011-9491-9495
Laufer CB, Green LB, Whittemore DE. A case of reed syndrome with a novel mutation in the fumarate hydratase gene. Case Rep Med. 2013; 2013: 926896. doi.org/10.1155/2013/926896
Valdivia Z, Tolentino J, Galarza V, Vela C, Delgado V. Leiomiomatosis cutánea y uterina: síndrome de Reed. Folia Dermatol. 2009; 20: 32-34.