Plaque-like myofibroblastic tumor: report of three cases

Ann L Marqueling1, David Dasher, Sheila F Friedlander

  • 1Department of Dermatology, University of California at San Francisco, San Francisco, California.

Pediatric Dermatology
|July 16, 2013
PubMed

Insights

Plaque-like myofibroblastic tumor of infancy (PMTI) can also present in early childhood, not just infancy. This rare tumor may exhibit ulceration and aggressive growth, warranting a name change to plaque-like myofibroblastic tumor.

Area of Science:

  • Oncology
  • Dermatopathology

Background:

  • Plaque-like myofibroblastic tumor of infancy (PMTI) is a rare condition first described in 2007.
  • Initial reports detailed infantile cases with features of dermatofibroma and myofibroblastic lineage.

Observation:

  • Three new cases of PMTI are presented, expanding the known clinical spectrum.
  • These cases demonstrate presentation in early childhood, a feature not noted in initial descriptions.
  • Additional clinical observations include tumor ulceration and aggressive growth patterns.

Findings:

  • PMTI exhibits variable clinical presentation, extending beyond infancy into early childhood.
  • Microscopic and immunohistochemical features remain consistent with myofibroblastic differentiation.
  • The observed aggressive features necessitate careful monitoring and management.

Implications:

  • The findings suggest renaming the condition to "plaque-like myofibroblastic tumor" to encompass its broader age range of presentation.
  • Further research is needed to understand the biological behavior and optimal treatment strategies for PMTI.
  • Increased awareness among clinicians may improve early diagnosis and patient outcomes.

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