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Updated: Jan 16, 2026

Endoscopic Approach for Colloid Cyst Resection
Published on: May 23, 2025
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.
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.
Abstract:
A previously healthy male infant presented with a painless skin-coloured subcutaneous upper midline back mass overlying the spine. Initial differential diagnosis included dermoid cyst and pilomatrixoma. He underwent wide excision, with histopathology confirming a plexiform fibrohistiocytic tumour with positive margins. Re-excision achieved clear margins. This case highlights a rare presentation and emphasises the importance of including this tumour in the differential diagnosis of paediatric cystic masses.
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