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hooggradig B-cellymfoom met herschikking van MYC, BCL2 en/of BCL6 (aandoening)
hooggradig B-cellymfoom met herschikking van MYC, BCL2 en/of BCL6
hooggradig B-cellymfoom met herschikking van MYC-, BCL2- en/of BCL6-gen
High grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements
A rare aggressive B-cell non-Hodgkin lymphoma with characteristics of rearrangement in MYC and BCL2 and/or BCL6 (so-called double-hit or triple-hit lymphoma). The category includes double-hit cases with features intermediate between diffuse large B-cell lymphoma (DLBCL) and Burkitt lymphoma, blastoid cases with a double-hit, and cases with a DLBCL not otherwise specified morphology with a double-hit. It refers only to de novo cases, not to lymphomas with a history of pre-existing or coexistent indolent lymphoma. Patients typically present with widespread disease, including involvement of lymph nodes, bone marrow and central nervous system.
Id1172704005
StatusDefined
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetC85.1
TermB-cel-lymfoom, niet gespecificeerd
SNOMED CT to Orphanet simple map480541
SNOMED CT to ICD-10 extended map
TargetC85.7
RuleTRUE
AdviceALWAYS C85.7 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE
CorrelationSNOMED CT source code to target map code correlation not specified