Aggressive Systemic Mastocytosis Related to Germline p.D816V KIT Mutation

Systemic mastocytosis (SM) in adults is, in most cases, caused by a somatic mutation leading to p.D816V in KIT. We report the first proof of this variant as a heterozygous de novo germline mutation in a female infant with severe neonatal SM. The girl presented prenatally with hepatosplenomegaly and postnatally with diffuse cutaneous lesions and organ dysfunction. Histopathologic specimens displayed infiltration with atypical mastocytes. Molecular analyses confirmed the KIT mutation in multiple non-infiltrated tissues, demonstrating the germline nature of the mutation. Despite targeted treatment with pharmacokinetically monitored midostaurin and adjunct therapies, the disease progressed rapidly, resulting in fatal multiorgan failure.

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Publication Details

Journal
Pediatric Blood & Cancer
Published
2025-10-21
DOI
https://doi.org/10.1002/pbc.32129
Primary Topic
Mast cells and histamine
Type
article
Field-Weighted Citation Impact
0.00
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article

Aggressive Systemic Mastocytosis Related to Germline p.D816V KIT Mutation

Martin E. G. Blohm, Ingo Müller, Sofia Apostolidou, Julian Trah et al.
Pediatric Blood & Cancer
Mast cells and histamine
article

Aggressive Systemic Mastocytosis Related to Germline p.D816V KIT Mutation

Martin E. G. Blohm, Ingo Müller, Sofia Apostolidou, Julian Trah, Antonia Kiwit, Ilske Oschlies, Philipp Deindl, Kai Lehmberg, Dominique Singer, Carsten Müller, Nikolas C. C. von Bubnoff, Amelie T. van der Ven
article en

Abstract

Systemic mastocytosis (SM) in adults is, in most cases, caused by a somatic mutation leading to p.D816V in KIT. We report the first proof of this variant as a heterozygous de novo germline mutation in a female infant with severe neonatal SM. The girl presented prenatally with hepatosplenomegaly and postnatally with diffuse cutaneous lesions and organ dysfunction. Histopathologic specimens displayed infiltration with atypical mastocytes. Molecular analyses confirmed the KIT mutation in multiple non-infiltrated tissues, demonstrating the germline nature of the mutation. Despite targeted treatment with pharmacokinetically monitored midostaurin and adjunct therapies, the disease progressed rapidly, resulting in fatal multiorgan failure.

Pediatric Blood & CancerVol. 73(1)
Universität Hamburg (DE), Christian-Albrechts-Universität zu Kiel (DE), University Medical Center Hamburg-Eppendorf (DE), Kinderkrebs-Zentrum Hamburg (DE), University Hospital Schleswig-Holstein (DE), University Hospital Cologne (DE), University of Lübeck (DE)
Openalex Percentile: Top 69%
Mast cells and histamine
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Aggressive Systemic Mastocytosis Related to Germline p.D816V KIT Mutation — Martin E. G. Blohm, Ingo Müller, et al. · Pediatric Blood & Cancer (2025) | TGRS Research Map | TGRS