Hamartoma mesenquimal rabdomiomatoso

Julio A. Díaz-Pérez; C. A. García-Ramírez; J. A. García-Vera; M. A. Melo-Uribe; C. J. Uribe

doi:10.1016/S1578-2190(08)70292-0

Hamartoma mesenquimal rabdomiomatoso

Translated title of the contribution: Rhabdomyomatous mesenchymal hamartoma

Julio A. Díaz-Pérez, C. A. García-Ramírez, J. A. García-Vera, M. A. Melo-Uribe, C. J. Uribe

Research output: Articles / Notes › Scientific Article › peer-review

13 Scopus citations

Abstract

Rhabdomyomatous mesenchymal hamartoma is an extremely rare congenital lesion, and very few cases have been reported even though its macroscopic and microscopic features make diagnosis easy. An 18-year-old woman consulted with a pedunculated mass in the medial region of her neck. The mass was surgically removed, and rhabdomyomatous mesenchymal hamartoma was diagnosed. The clinical, macroscopic, histologic, and immunochemical characteristics that allow diagnosis of this entity are discussed. Although association with congenital abnormalities is uncommon, this possibility should be assessed by the clinician.

Translated title of the contribution	Rhabdomyomatous mesenchymal hamartoma
Original language	Spanish
Pages (from-to)	474-476
Number of pages	3
Journal	Actas Dermo-Sifiliograficas
Volume	99
Issue number	6
DOIs	https://doi.org/10.1016/S1578-2190(08)70292-0
State	Published - 1 Jul 2008
Externally published	Yes

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10.1016/S1578-2190(08)70292-0

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title = "Hamartoma mesenquimal rabdomiomatoso",

abstract = "Rhabdomyomatous mesenchymal hamartoma is an extremely rare congenital lesion, and very few cases have been reported even though its macroscopic and microscopic features make diagnosis easy. An 18-year-old woman consulted with a pedunculated mass in the medial region of her neck. The mass was surgically removed, and rhabdomyomatous mesenchymal hamartoma was diagnosed. The clinical, macroscopic, histologic, and immunochemical characteristics that allow diagnosis of this entity are discussed. Although association with congenital abnormalities is uncommon, this possibility should be assessed by the clinician.",

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T1 - Hamartoma mesenquimal rabdomiomatoso

AU - Díaz-Pérez, Julio A.

AU - García-Ramírez, C. A.

AU - García-Vera, J. A.

AU - Melo-Uribe, M. A.

AU - Uribe, C. J.

PY - 2008/7/1

Y1 - 2008/7/1

N2 - Rhabdomyomatous mesenchymal hamartoma is an extremely rare congenital lesion, and very few cases have been reported even though its macroscopic and microscopic features make diagnosis easy. An 18-year-old woman consulted with a pedunculated mass in the medial region of her neck. The mass was surgically removed, and rhabdomyomatous mesenchymal hamartoma was diagnosed. The clinical, macroscopic, histologic, and immunochemical characteristics that allow diagnosis of this entity are discussed. Although association with congenital abnormalities is uncommon, this possibility should be assessed by the clinician.

AB - Rhabdomyomatous mesenchymal hamartoma is an extremely rare congenital lesion, and very few cases have been reported even though its macroscopic and microscopic features make diagnosis easy. An 18-year-old woman consulted with a pedunculated mass in the medial region of her neck. The mass was surgically removed, and rhabdomyomatous mesenchymal hamartoma was diagnosed. The clinical, macroscopic, histologic, and immunochemical characteristics that allow diagnosis of this entity are discussed. Although association with congenital abnormalities is uncommon, this possibility should be assessed by the clinician.

KW - Cutaneous tumors

KW - Skeletal muscle

KW - Skin abnormalities

KW - Skin and connective tissue disease

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AN - SCOPUS:47049094814

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EP - 476

JO - Actas Dermo-Sifiliograficas

JF - Actas Dermo-Sifiliograficas

IS - 6

ER -

Hamartoma mesenquimal rabdomiomatoso

Abstract

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