Rare tumour presenting as a cystic lesion in an infant

Jonathan M Stern1, Gurinder Kumar2,3, Aparna Roy1

  • 1Paediatrics, Case Western Reserve University Hospital, Cleveland, Ohio, USA.

BMJ Case Reports
|September 29, 2025
PubMed

Insights

A rare plexiform fibrohistiocytic tumour presented as a back mass in an infant. Surgical excision was successful, highlighting the need to consider this in paediatric cystic mass diagnoses.

Area of Science:

  • Paediatric Oncology
  • Dermatopathology
  • Surgical Pathology

Background:

  • Plexiform fibrohistiocytic tumours (PFHT) are rare neoplasms typically affecting the extremities.
  • Presentation in the paediatric population, particularly as a midline back mass, is exceptionally uncommon.

Purpose of the Study:

  • To report a rare case of PFHT in an infant presenting as a subcutaneous back mass.
  • To emphasize the diagnostic considerations for paediatric cystic masses.

Main Methods:

  • Clinical presentation and imaging findings.
  • Surgical wide excision and subsequent re-excision.
  • Histopathological examination for definitive diagnosis.

Main Results:

  • Histopathology confirmed a plexiform fibrohistiocytic tumour with initially positive margins.
  • Re-excision successfully achieved clear margins.
  • The tumour was located subcutaneously in the upper midline back, overlying the spine.

Conclusions:

  • This case underscores the importance of including PFHT in the differential diagnosis of paediatric subcutaneous and cystic masses.
  • Early and accurate diagnosis through histopathology is crucial for appropriate management and complete tumour resection.