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desmoïd-type fibromatose (aandoening)
desmoïd-type fibromatose
agressieve fibromatose
desmoïd
Dit is een goedaardig, regelmatig terugkerend bindweefselgezwel.
Aggressive fibromatosis
Desmoid tumor
Desmoid fibromatosis
Deep fibromatosis
Desmoid type fibromatosis
Desmoid tumor can occur in any part of the body: extra-abdominally (neck, shoulders, upper limbs, gluteal region), abdominally (originating from muscle fascia or the abdominal/chest wall), and more rarely intra-abdominally in the mesentery or retroperitoneum. Depending on the location of the tumor, symptoms may include pain, fever and functional impairment or loss of function of the organ involved. Desmoid tumor results from the proliferation of well-differentiated myofibroblasts. The exact etiopathogenetic mechanism is still unknown, but they seem to have a multi-factorial origin with hormonal and genetic factors being involved. Somatic mutations in the CTNNB1 gene (3q21) encoding beta-catenin have been found in about 85 % of sporadic cases.
Id725049005
StatusDefined
Associated morphologydesmoïd-type fibromatose
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetD48.1
TermNeoplasma met onzeker of onbekend gedrag van bindweefsel en overige weke delen
SNOMED CT to Orphanet simple map873
SNOMED CT to ICD-10 extended map
TargetD48.1
RuleTRUE
AdviceALWAYS D48.1 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE
CorrelationSNOMED CT source code to target map code correlation not specified
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