725049005: Aggressive fibromatosis (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Fibromatosis\Aggressive fibromatosis
• \Neoplasm and/or hamartoma\Neoplastic disease\Neoplastic disease of uncertain behaviour\Aggressive fibromatosis

Status: current, Defined. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3437473018	Aggressive fibromatosis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3437474012	Aggressive fibromatosis	en	Synonym	Active	Case insensitive	SNOMED CT core
3437475013	Desmoid type fibromatosis	en	Synonym	Active	Case insensitive	SNOMED CT core
3437476014	Desmoid tumor	en	Synonym	Active	Case insensitive	SNOMED CT core
3437477017	Desmoid tumour	en	Synonym	Active	Case insensitive	SNOMED CT core
3773008016	Desmoid fibromatosis	en	Synonym	Active	Case insensitive	SNOMED CT core
3773009012	Deep fibromatosis	en	Synonym	Active	Case insensitive	SNOMED CT core
3437478010	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.	en	Definition	Active	Case sensitive	SNOMED CT core
3437479019	Desmoid tumour 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 tumour, symptoms may include pain, fever and functional impairment or loss of function of the organ involved. Desmoid tumour results from the proliferation of well-differentiated myofibroblasts. The exact aetiopathogenetic 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.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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