Gastric Plexiform Fibromyxoma

Preferred Label : Gastric Plexiform Fibromyxoma;

NCIt synonyms : Plexiform Fibromyxoma;

NCIt definition : A rare soft tissue neoplasm arising from the stomach. It occurs in the antrum and pyloric region and it may extend into the duodenum. It occurs in all ages and affects men and women equally. Morphologically it is characterized by a multinodular plexiform mass that involves the muscular layer. The neoplastic cells are spindle-shaped and the mitotic activity is low. It follows a benign clinical course.;

Neoplastic status : Benign;

NCI Metathesaurus CUI : CL497919;

ICD-O code : 8811/0;

Details

Origin ID

C95902;

UMLS CUI

C3272426;

Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
Excludes anatomical site(s)
- Bone [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
- Digestive System [NCIt concept]
- Stomach [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
Validated automatic mappings to NTBT
- Plexiform fibromyxoma [ICD-11 Extension code]
disease_excludes_finding
- Malignant Cellular Infiltrate [NCIt concept]
disease_excludes_normal_tissue_origin
- Lymphoid Tissue [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Spindle Cell [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Indolent Clinical Course [NCIt concept]
- Multinodular Pattern [NCIt concept]
- Plexiform Growth Pattern [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Digestive System [NCIt concept]
- Stomach [NCIt concept]
disease_mapped_to_gene
- MALAT1/GLI1 Fusion Gene [NCIt concept]
pathogenesis_of_disease_involves_gene
- MALAT1/GLI1 Fusion Gene [NCIt concept]

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