1: Department of pediatric orthopedics
Kassab Institute, Tunis, Tunisia
2: College of Medicine, Tunis, Tunisia
* Corresponding author
** Academic Editor
Correspondence to:
arfa.wajdi@gmail.com
Publication Data:
Submitted: May 27,2023
Accepted: June 28,2023
Online: November 30,2023
This article was subject to full peer-
review.
This is an open access article distributed
under the terms of the Creative Commons
Attribution Non-Commercial License 4.0
(CCBY-NC) allowing sharing and adapting.
Share: copy and redistribute the material in
any medium or format.
Adapt: remix, transform, and build upon the
licensed material.
The work provided must be properly cited and
cannot be used for commercial purpose.
Tenosynovial Giant Cell Tumor (TGCT) is a rare benign soft tissue tumor arising
from the synovium and peri-articular structures. This tumor is usually diagnosed
in adult age, the hands are the most frequent location. The gold standard for
TCGT treatment is the adequate surgical excision. We herein report a case of a
TGCT of the hallux in a 5-year-old patient.
Keywords
Giant cell tumors ; Child; foot; soft tissue neoplasms.
Introduction
Tenosynovial Giant-cell tumor (TGCT) is a benign solitary tumor arising in the
extremities, more commonly in the flexor tendons of the hands [1]. It usually
affects individuals between the third and fifth decade and is reported incidentally
in children [2]. We present a rare case of a TGCT affecting the hallux extensor
tendon in a 5-year-old patient.
Observation
A 5-year-old girl, with no previous medical history presented to the outpatient
clinic for swelling on the dorsal aspect of her right hallux evolving for two years.
The mass was firm, painless, mobile and the skin was normal (Figure 1).
The mobility of interphalangeal articulation wasn’t affected. No bone lesions were
seen in the standard X-rays.
The MRI revealed well circumscribed mass measuring 16*16*6 mm, encountering
the hallux extensor tendons, with hemosiderin deposit, suggesting a giant cell
tumor (Figure 2). Patient underwent complete surgical resection. Intraoperatively,
the mass was encapsulated and had macroscopic encephaloid aspect. It had an
intimate contact with the tendon sheath and the articulation capsule which were
excised (Figure 3). Histopathological examination revealed giant cell tumor of the
tendon sheath without malignant cells and clear resection margins. Postoperative
course was uneventful, and no recurrence were noted during the follow up.
Comments
TGCT are benign soft tissue lesions of the extremities arising from the synovium,
tendon sheath, bursae and small joint periarticular structures [2,3]. These tumors
are very rare in children. Reported pediatric incidence is up to 4% for both upper
and lower extremities.
Painless slow-growing soft tissue mass is the most frequent clinical presentation
[4,5]. MRI is a gold standard examination for the preoperative diagnosis. Specific
findings of hemosiderin deposit are evocative of TGCT [6]. Complete surgical
excision with sufficient safe margins is the best management option. tyrosine-
kinase inhibitors are indicated for some diffuse or recurrent forms [7].
Significant risk factors for recurrence include radiographic presence of osseous
pressure erosion, incomplete excision, increased cellularity or mitosis, cytogenetic
abnormalities such as trisomy 7 and inhibited expression of nm23 gene [8].