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Multiple primary dermatofibrosarcoma protuberans tumors in a single patient with chromosomal microarray analysis: A case report and review.
Durgin, Joseph S; Whittington, Carli P; Joseph, Mallory; Harms, Paul W; Andea, Aleodor A; Pedersen, Elisabeth A; Smith, Emily H; Harms, Kelly L.
Affiliation
  • Durgin JS; Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Whittington CP; Department of Pathology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Joseph M; Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Harms PW; Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Andea AA; Department of Pathology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Pedersen EA; Department of Pathology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Smith EH; Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Harms KL; Department of Dermatology, Michigan Medicine, University of Michigan, Ann Arbor, Michigan, USA.
J Cutan Pathol ; 51(7): 490-495, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38548658
ABSTRACT
Dermatofibrosarcoma protuberans (DFSP) is a cutaneous sarcoma with a high propensity for local invasion and recurrence. Although it is a rare event, the occurrence of multiple tumors in a single patient raises a diagnostic dilemma, as metastatic disease should be differentiated from multiple primary malignant events. In more than 90% of DFSP, a pathogenic t(17;22) translocation leads to the expression of COL1A1PDGFB fusion transcripts. Karyotype analysis, fluorescence in situ hybridization, and RT-PCR can be useful ancillary studies in detecting this characteristic rearrangement, and sequencing of the fusion transcript can be used to support a clonal origin in metastatic and multifocal disease. However, previous reports have demonstrated variable sensitivity of these assays, in part due to the high sequence variability of the COL1A1PDGFB fusion. Here, we report a patient who developed two distinct DFSP tumors over the course of 7 years. Chromosomal microarray analysis identified distinctive genomic alterations in the two tumors, supporting the occurrence of multiple primary malignant events.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / Oncogene Proteins, Fusion / Dermatofibrosarcoma Limits: Humans / Male / Middle aged Language: En Journal: J Cutan Pathol Year: 2024 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / Oncogene Proteins, Fusion / Dermatofibrosarcoma Limits: Humans / Male / Middle aged Language: En Journal: J Cutan Pathol Year: 2024 Document type: Article Affiliation country: Estados Unidos