Primary Solitary Intra-thyroid Myofibroma in a Pediatric Patient

Myofibromas are benign soft tissue tumors, mostly seen in young children, and characterized histologically by fibroblasts/myofibroblasts arranged in fascicles. Clinical presentation of this tumor is highly variable, based on the location and extent of organ involvement. Myofibromas most commonly involve skin and subcutaneous tissue, though they may appear in any location and may be multiple. Nearly all thyroid lesions in children are derived from thyroid follicular cells or C-cells. Solitary myofibroma occurring in the thyroid is exceptionally rare. This case report describes a three-year-old male presenting with a right neck mass. Fine needle aspiration (FNA) revealed spindle cells without evidence of malignancy. Resection of the right thyroid lobe and isthmus revealed a myofibroma, which was completely excised. The patient remained healthy without recurrence two years after the surgery. This case highlights that a solitary myofibroma can present as an intra-thyroid lesion in a pediatric patient. Histological evaluation is critical to establish the diagnosis of myofibroma, and ancillary studies may be necessary to differentiate it from other potential differential diagnoses of spindle cell morphology.

Authors

Institutions

Publication Details

Journal
Cureus
Published
2025-12-22
DOI
https://doi.org/10.7759/cureus.99847
Primary Topic
Soft tissue tumor case studies
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Primary Solitary Intra-thyroid Myofibroma in a Pediatric Patient

Tamarah J. Westmoreland, Lili Miles, Lillie Jensen, Gleidson Silva
Cureus
Soft tissue tumor case studies
article

Primary Solitary Intra-thyroid Myofibroma in a Pediatric Patient

Tamarah J. Westmoreland, Lili Miles, Lillie Jensen, Gleidson Silva
article en

Abstract

Myofibromas are benign soft tissue tumors, mostly seen in young children, and characterized histologically by fibroblasts/myofibroblasts arranged in fascicles. Clinical presentation of this tumor is highly variable, based on the location and extent of organ involvement. Myofibromas most commonly involve skin and subcutaneous tissue, though they may appear in any location and may be multiple. Nearly all thyroid lesions in children are derived from thyroid follicular cells or C-cells. Solitary myofibroma occurring in the thyroid is exceptionally rare. This case report describes a three-year-old male presenting with a right neck mass. Fine needle aspiration (FNA) revealed spindle cells without evidence of malignancy. Resection of the right thyroid lobe and isthmus revealed a myofibroma, which was completely excised. The patient remained healthy without recurrence two years after the surgery. This case highlights that a solitary myofibroma can present as an intra-thyroid lesion in a pediatric patient. Histological evaluation is critical to establish the diagnosis of myofibroma, and ancillary studies may be necessary to differentiate it from other potential differential diagnoses of spindle cell morphology.

CureusVol. 17(12)
University of Central Florida (US), Nemours Children's Clinic (US)
Good health and well-being
Openalex Percentile: Top 29%
Soft tissue tumor case studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Primary Solitary Intra-thyroid Myofibroma in a Pediatric Patient — Tamarah J. Westmoreland, Lili Miles, et al. · Cureus (2025) | TGRS Research Map | TGRS