771233008: Inflammatory myofibroblastic tumor (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Neoplastic disease of uncertain behaviour\Inflammatory myofibroblastic tumour

Status: current, Defined. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3705179017	Inflammatory myofibroblastic tumour	en	Synonym	Active	Case insensitive	SNOMED CT core
3705180019	Inflammatory myofibroblastic tumor	en	Synonym	Active	Case insensitive	SNOMED CT core
3705181015	Inflammatory myofibroblastic tumor (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3705182010	A rare neoplastic lesion of the submucosal stroma, which can develop in any organ, often occurring in the lung, mesentery, omentum and the retroperitoneal region. It is histologically heterogenous, composed of spindle-shaped cells, myofibroblasts and inflammatory cells. It is usually benign, however local invasion, recurrence, malignant transformation with vascular invasion and metastases may occur. The presentation is nonspecific and depends on the organ involved. Some patients may present with paraneoplastic syndrome (fever, malaise, weight loss, thrombocytosis) or symptoms related to compression of adjacent organs, such as bowel obstruction.	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

Back to Start