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Descriptor English: Steatocystoma Multiplex
Descriptor Spanish: Esteatocistoma Múltiple
Descriptor esteatocistoma múltiple
Scope note: Trastorno caracterizado por múltiples quistes cutáneos, de distribución amplia, que a menudo se inflaman y se rompen. Este cuadro está provocado por determinadas mutaciones genéticas en la codificación de KRT-17, causantes de las mutaciones de la Paquioniquia congénita tipo 2. La existencia de dientes natales suele estar asociada con el esteatocistoma múltiple.
Descriptor Portuguese: Esteatocistoma Múltiplo
Descriptor French: Sébocystomatose
Entry term(s): Cyst, Multiple Sebaceous
Cysts, Multiple Sebaceous
Multiple Sebaceous Cyst
Multiple Sebaceous Cysts
Multiplex Steatocystoma
Multiplex Steatocystomas
Sebaceous Cyst, Multiple
Sebaceous Cysts, Multiple
Steatocystoma Multiplices
Steatocystoma, Multiplex
Steatocystomas, Multiplex
Tree number(s): C16.131.831.350.856.500
C16.320.850.250.856.500
C17.800.529.594.500
C17.800.804.350.856.500
C17.800.827.250.856.500
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D062685
Scope note: A disorder characterized by multiple, wide spread cutaneous cysts that often become inflamed and rupture. It is caused by the same mutations in the gene coding for KRT-17 that are causative mutations for Pachyonychia congenita, Type 2. Natal teeth involvement is sometimes associated with steatocystoma multiplex.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
TM transmission
UR urine
VE veterinary
VI virology
Public MeSH Note: 2013
History Note: 2013
Related: Keratin-17 MeSH
DeCS ID: 54893
Unique ID: D062685
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2013/01/01
Date of Entry: 2012/07/03
Revision Date: 2015/06/18
Steatocystoma Multiplex - Preferred
Concept UI M0528908
Scope note A disorder characterized by multiple, wide spread cutaneous cysts that often become inflamed and rupture. It is caused by the same mutations in the gene coding for KRT-17 that are causative mutations for Pachyonychia congenita, Type 2. Natal teeth involvement is sometimes associated with steatocystoma multiplex.
Preferred term Steatocystoma Multiplex
Entry term(s) Cyst, Multiple Sebaceous
Cysts, Multiple Sebaceous
Multiple Sebaceous Cyst
Multiple Sebaceous Cysts
Multiplex Steatocystoma
Multiplex Steatocystomas
Sebaceous Cyst, Multiple
Sebaceous Cysts, Multiple
Steatocystoma Multiplices
Steatocystoma, Multiplex
Steatocystomas, Multiplex



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