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1362026000: Nodal T-follicular helper cell lymphoma follicular type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5443908015 Follicular helper T-cell lymphoma, follicular type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5443909011 Nodal T-follicular helper cell lymphoma follicular type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5443910018 nTFHL-F - nodal T-follicular helper cell lymphoma follicular type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5443911019 Nodal T-cell lymphoma with TFH phenotype en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5443912014 Nodal T-follicular helper cell lymphoma follicular type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5443915011 A rare T-cell non-Hodgkin lymphoma characterized by generalized lymphadenopathy and predominantly follicular or perifollicular growth pattern, consistent with the expression of T-follicular helper markers. Affected individuals distinctly lack histologic features (such as proliferation of high endothelial venules and expanded follicular dendritic meshworks) typically associated to angioimmunoblastic T-cell lymphoma. It affects elderly individuals (mostly at the sixth decade of life) that present with advanced-stage disease. Majority of the cases have disseminated nodal involvement, whereas involvement of extranodal sites including skin, liver, spleen and bone marrow are also reported. Patients may therefore develop skin rash and immune manifestations. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5443916012 A rare T-cell non-Hodgkin lymphoma characterised by generalised lymphadenopathy and predominantly follicular or perifollicular growth pattern, consistent with the expression of T-follicular helper markers. Affected individuals distinctly lack histologic features (such as proliferation of high endothelial venules and expanded follicular dendritic meshworks) typically associated to angioimmunoblastic T-cell lymphoma. It affects elderly individuals (mostly at the sixth decade of life) that present with advanced-stage disease. Majority of the cases have disseminated nodal involvement, whereas involvement of extranodal sites including skin, liver, spleen and bone marrow are also reported. Patients may therefore develop skin rash and immune manifestations. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nodal T-follicular helper cell lymphoma follicular type (disorder) Is a T-cell lymphoma (clinical) true Inferred relationship Some
Nodal T-follicular helper cell lymphoma follicular type (disorder) Associated morphology Follicular T-cell lymphoma (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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