Pediatric Neurotrophic Tyrosine Receptor Kinase-rearranged Neoplasm Resembling a Vascular Malformation

Author:

Sadic Mohammad1,Vu Alexander Hien1,Bayraktar Erol2,Strubel Naomi3,Sharma Sheel4,Blei Francine5,Jour George2,Tomita Sandra1

Affiliation:

1. Department of General Surgery, NYU Grossman School of Medicine, New York, New York

2. Department of Pathology, NYU Grossman School of Medicine, New York, New York

3. Department of Radiology, NYU Grossman School of Medicine, New York, New York

4. Department of Plastic Surgery, NYU Grossman School of Medicine, New York, New York

5. Department of Pediatrics, Hematology/Oncology, NYU Grossman School of Medicine, New York, New York

Abstract

Pediatric neurotrophic tyrosine receptor kinase-rearranged spindle cell neoplasms are soft tissue neoplasms whose behaviors are not well understood. We provide a case presentation of such a tumor sharing features of a vascular malformation. Our patient is an 11-year-old female referred for a lesion clinically and radiologically concerning for a vascular tumor or malformation. Upon excision, next-generation sequencing revealed a laminA-neurotrophic tyrosine receptor kinase 1 fusion. Neurotrophic tyrosine receptor kinase-rearranged spindle cell neoplasms represent an emerging entity in children now being diagnosed with a variety of techniques including immunohistochemistry, fluorescence in situ hybridization, and next-generation sequencing. Consideration for this tumor should be in the differential diagnosis of vascular skin lesions with unusual features on physical examination.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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