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787036009: Monomorphic epitheliotropic intestinal T-cell lymphoma (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3773563016 Monomorphic epitheliotropic intestinal T-cell lymphoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3773564010 Monomorphic epitheliotropic intestinal T-cell lymphoma (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Monomorphic epitheliotropic intestinal T-cell lymphoma Is a T-cell lymphoma morphology false Inferred relationship Some
Monomorphic epitheliotropic intestinal T-cell lymphoma Is a Mature (peripheral) T-cell neoplasm (morphologic abnormality) false Inferred relationship Some
Monomorphic epitheliotropic intestinal T-cell lymphoma Is a Intestinal T-cell lymphoma true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
A rare T-cell non-Hodgkin lymphoma characterized by monomorphic cytomorphology and epitheliotropism. It is mostly detected in the small intestine but can also be present in the colon, duodenum or stomach. It is an aggressive tumor that can disseminate to mesenteric lymph nodes, lung, liver, brain and skin. Major clinical features include abdominal pain, gastrointestinal bleeding, obstruction or perforation, diarrhea, and weight loss. It is not associated to celiac disease. Associated morphology True Monomorphic epitheliotropic intestinal T-cell lymphoma Inferred relationship Some 1

This concept is not in any reference sets

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