PowerPoint Presentation · Vitamin C Allergies: NKDA. Clinical History November 2016 (OSH) Routine...
Transcript of PowerPoint Presentation · Vitamin C Allergies: NKDA. Clinical History November 2016 (OSH) Routine...
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SH2017-0332
TP53 mutation in a patient with paroxysmal nocturnal hemoglobinuriaLENA STUART, MD
MASSACHUSETTS GENERAL HOSPITAL
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Clinical History74M in overall good health, found to have anemia and thrombocytopeniaPast Medical History◦ Hypertension
Family History◦ CAD (multiple family members)◦ No malignancies or hematologic disorders
Social History◦ Prior smoker (quit 40 years ago)◦ 1x glass red wine per night
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Clinical HistoryMedications◦ Irbesartan (BP)◦ Aspirin◦ Folate◦ Glucosamine◦ Fish oil◦ Vitamin C
Allergies: NKDA
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Clinical HistoryNovember 2016 (OSH)◦ Routine blood work revealed new onset anemia and thrombocytopenia◦ Coombs negative◦ Normal iron, B12, folate◦ No evidence of kidney disease◦ No hypothyroidism◦ Flow cytometry: paroxysmal nocturnal hemoglobinuria (per report)◦ 58% granulocytes (loss of GPI)◦ 52% monocytes (loss of GPI)◦ 0.3% red blood cells (type II)◦ 15% red blood cells (type III)
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Clinical HistoryJanuary 2017◦ Asymptomatic◦ Labs drawn◦ Bone marrow biopsy◦ Molecular studies (NGS)
1/6/17WBC (K/uL) 5.10Hgb (g/dL) 9.6HCT (%) 27.4MCV (fL) 111.4PLT (K/uL) 96Retics (%) 6.2LDH (U/L) 1229T-Bili (mg/dL) 1.1
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Bone Marrow Biopsy, HE
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Bone Marrow Biopsy, HE
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Bone Marrow Biopsy, HE
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Bone Marrow Biopsy, CD61
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Bone Marrow Aspirate, HE
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Bone Marrow BiopsyFINAL DIAGNOSIS:Moderately hypercellular marrow with maturing trilineage hematopoiesis and slight erythroid hyperplasia.
Note: Diagnostic features of MDS are not recognized and there is no evidence of an aplastic process.
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Flow (March 2017)Granulocytes 82.8% Monocytes 79.6% RBC II: 0.6%, III: 16.8%
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Additional TestingCytogenetics:◦ 45,X,-Y[15]/46,XY[5]◦ Loss of the Y chromosome is commonly seen in older men and although it may reflect
a clonal process, and is not considered sufficient to diagnose MDS in a cytopenic patient
SNaPshot @ MGH (1/12/17)◦ TP53 ENSP00000269305.4:p.Tyr163Cys (ENST00000269305.4:c.488A>G)◦ 73% variant allelic frequency◦ Subsequent NGS◦ Rapid Heme Panel @ BWH (6/2/2017) – 51% VAF◦ SNaPshot @ MGH (8/8/2017) – 63% VAF
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Bone Marrow Biopsy, p53
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Patient Follow-UpProgressive anemia resulting in 4U RBC transfusions in 2017
Started on eculizumab in March◦ Marked decrease in LDH, but no response in Hgb/Hct◦ Lab evidence of an autoimmune hemolytic anemia (DAT+)
Started on steroids◦ Side effects not tolerated
Multiple heme-onc consults◦ Increased dose of eculizumab◦ Consider EPO◦ No clear clinical trajectory for controlling hemolysis/symptoms
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DiscussionPNH◦ Non-malignant clonal disease of hematopoietic stem cells associated
with hemolysis, marrow failure and thrombophilia◦ Monogenic disease due to somatic mutation in PIGA (required for
synthesis of GPI-anchored proteins)◦ Confers growth advantage◦ Leaves cells susceptible to complement destruction (loss of CD55 and CD59)◦ Hemolytic anemia
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DiscussionNo PIGA mutation!◦ Whole exome sequencing of PNH identified multiple other genes with mutations
arising as either subclones of PIGA or prior to PIGA (Shen et al, 2014)◦ Similarities to MDS: clonal hematopoiesis, persistent aberrant stem cell clone
Unexpected TP53 mutation◦ Positive strong IHC staining suggestive that mutation is pathogenic◦ Associated with aggressive myeloid neoplasms; concerning for evolution to MDS◦ No prior reports of TP53 mutation in PNH◦ Primarily reported as a somatic mutation (lung, breast, ovary, GI)◦ One report of germline mutation in pediatric patient with osteosarcoma and family
history of malignancies (McIntyre 1994)
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DiscussionFurther workup◦ Given high variant allelic frequency, is the mutation germline?◦ No personal or family history of malignancies
◦ Is the mutation confined to the PNH clone?◦ Attempt at NGS on PNH+ vs. PNH- populations failed (not enough cells sorted)
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Panel Diagnosis
Proposed: Paroxysmal nocturnal hemoglobinuria with a pathogenic TP53 mutation (clonal hematopoiesis of indeterminate potential, CHIP)
?
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AcknowledgementsMGH Flow Cytometry and Center for Integrated Diagnostics
Robert Hasserjian, MD MASSACHUSETTS GENERAL HOSPITAL
Valentina Nardi, MD MASSACHUSETTS GENERAL HOSPITAL
James Weitzman, MD MGH-WEST