POSTGRADUATE
ORTHOPEDIC INSTRUCTION - IMAGING
Case Resolution
Juan Manuel Romero Ante,*
Carlos A. Polo Marulanda, ** Cristian Valderrama,#
Cynthia Delgado Soto*
*Orthopedics
and Traumatology Service, Hospital
Alma Máter, Medellín, Colombia
**Foot and Ankle Department, Orthopedics and Traumatology Service,
Neuromédica,
Medellín, Colombia
#Universidad de Antioquia, Medellín, Colombia
##Laboratorio de Patología y Citología (LAPACI),
Clínica Medellín de Occidente, Medellín, Colombia
Case
Presentation
on page 189.
RESUMEN
Las lesiones óseas ocupantes de espacio de localización endomedular y excéntricas en huesos cortos del pie son infrecuentes, hay escasos reportes de caso
y, hasta hoy, no se han descrito en la falange distal del hallux. Presentamos uno de estos casos, las
evaluaciones clínica y radiológica, y el abordaje terapéutico.
Palabras clave: Neoplasia; localización excéntrica; atípica; endomedular; hallux.
Nivel de Evidencia:
IV
Unusual Intramedullary Lesion in the Distal Phalanx of the Hallux
ABSTRACT
Intramedullary, eccentrically located space-occupying bone lesions in the short
bones of the foot are uncommon. Few cases have been reported in the
literature, and to date, such lesions have
not been described in the distal phalanx of the hallux. We present one such case, including its clinical and radiological evaluation and therapeutic management.
Keywords: Neoplasm; eccentric location; atypical; intramedullary; hallux.
Level of Evidence: IV
Enchondroma
of the distal phalanx of the hallux.
The patient
provided informed consent for surgery.
In the operating room, prophylactic intravenous antibiotics were administered, and a toe tourniquet was applied for 45 minutes. Through an oblique
incision in the lateral eponychium over the distal phalanx of the right hallux,
the nail plate and nail bed were elevated,
the lesion was identified in the central proximal
metaphyseal-diaphyseal region of the phalanx, and curettage was performed with an osteotome, allowing removal of the lesion, which had a gritty, whitish, opaque appearance, with intramedullary involvement and lateral cortical destruction. The lesion was completely excised and submitted for histopathological examination. A
residual bone defect involving less than 30% of the diameter of the distal phalanx remained. The bone cavity was irrigated with a 5% dextrose solution. A second incision was made over the lateral aspect of the ipsilateral heel
to harvest a corticocancellous calcaneal bone graft, which was placed
into the residual cavitary defect of the distal phalanx of the hallux. The wounds were closed in layers, and the limb was immobilized with a below-knee plaster splint.
The patient
was discharged with analgesics and instructed to bear
weight on the heel only. An outpatient follow-up visit was scheduled
once the biopsy results became available.
Histopathological
examination revealed a lesion composed of hyaline cartilage, with no areas of necrosis, no chondrocyte atypia, and no myxoid change, forming well-defined cartilaginous nodules. Most importantly, no permeative growth pattern was identified (Figure 3).
After 4 months of clinical follow-up, the patient reported no pain or mechanical discomfort while wearing shoes, with only residual
nail discoloration. Radiographically, advanced bone healing was observed, with no evidence of recurrence (Figures 4 and 5).
Bone tumors
of the foot and ankle are rare entities, accounting for only 5-10% of all musculoskeletal tumors.1
Enchondroma is a benign neoplasm located within the medullary cavity
that, when occurring in the foot, most commonly
involves the metatarsals and phalanges; in 80%
of cases, the proximal phalanx
is the most
frequent location. It is generally asymptomatic but may cause pain and swelling secondary to pressure from its intracavitary expansion or to a pathological fracture.
Lesions range from 5 mm to 18.7 mm in size and are usually solitary; when multiple lesions are present, the condition is termed enchondromatosis or Ollier disease. When enchondromatosis is associated with soft-tissue hemangiomas, it is known as Maffucci syndrome.2
Histologically,
enchondromas are composed
of nodules of hyaline cartilage within the medullary cavity,
often with peripheral endochondral ossification. The nuclei are round and hyperchromatic, and mitotic activity is absent. Enchondromas of the small bones of the hands and feet
may exhibit increased cellularity and mild cytological atypia. Furthermore, when these cartilaginous nodules are eccentrically located, they may thin the cortex and even breach it,
producing periosteal bulging. Although such findings
may raise suspicion of malignancy, they are still considered features of benign lesions. Therefore, correlation of the clinical presentation,
duration of symptoms, imaging findings, and histological features is essential, making
the diagnosis frequently
challenging.3,4
On
radiographs, enchondroma appears as a well-defined, expansile, lytic lesion located centrally in the diaphysis or metaphyseal-diaphyseal
region. Computed tomography may demonstrate characteristic intralesional calcification patterns and allows assessment of cortical integrity.
Magnetic resonance imaging may reveal
bone and soft-tissue edema,
together with low-to-intermediate signal intensity on T1-weighted images, characteristic of cartilaginous tumors, and high signal intensity on T2-weighted images. Contrast-enhanced MRI readily demonstrates peripheral enhancement and internal
septations.5
Malignant
transformation of a solitary
lesion in the foot and ankle is exceedingly rare. The risk may reach
5% in large lesions of the distal tibia and up to 20% in patients with Ollier disease or Maffucci
syndrome. Conversely, secondary malignant lesions of the foot and ankle are extremely uncommon, accounting for only 1% of cases, and typically occur in advanced lung, breast, or
endometrial cancer.6
Only isolated case
reports have been published. One described a 16-year-old patient with a lesion of the proximal phalanx of the second toe that had been present for 10 years and became symptomatic 3 months before undergoing intralesional resection and bone grafting.7 Similarly, a 27-year-old patient with a 4-month history of pain and a mass involving the proximal
phalanx of the fourth toe underwent local resection, bone grafting, and Kirschner wire stabilization because of the size of the residual defect after resection.8 In both cases, no recurrences were reported, and the patients remained asymptomatic throughout follow-up.
For solitary lesions, intralesional resection, bone grafting, and, in selected cases,
temporary stabilization with a Kirschner wire are established as the most effective treatment for symptomatic lesions that fail conservative management or
are associated with pathological fractures.9
In the
present case, an open resection technique through a direct approach to the
lesion is described. However, minimally invasive and endoscopic
techniques have also been reported
for resection of enchondromatous lesions and placement of a bone graft into the
residual defect.10 To date, no comparative studies have evaluated the outcomes of these techniques; therefore, both remain valid options for the management of these intraosseous lesions.
Solitary
lytic lesions of the toe phalanges are uncommon and generally benign, but they
may cause pain, local deformity, and pathological fracture.
Imaging evaluation is recommended, together with resection, biopsy, and, in selected
cases, stabilization with a
Kirschner wire.
REFERENCES
1.
Toepfer A, Harrasser N, Recker M, Lenze U, Pohlig F, Gerdesmeyer L, et al. Distribution patterns of foot and ankle tumors: a university tumor institute experience. BMC Cancer 2018;18(1):735. https://doi.org/10.1186/s12885-018-4648-3
2.
Chun KA, Stephanie S, Choi JY, Nam JH, Suh JS. Enchondroma of the Foot. J Foot Ankle Surg 2015;54(5):836-9. https://doi.org/10.1053/j.jfas.2015.01.002
3.
Kerr DA, Cipriani
NA. Benign cartilage-forming tumors. Surg Pathol Clin 2021;14(4):585-603.
https://doi.org/10.1016/j.path.2021.06.004
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Afonso PD, Isaac A, Villagrán JM. Chondroid tumors as incidental findings and differential diagnosis between enchondromas and low-grade chondrosarcomas. Sem Musculoskelet Radiol 2019;23(1):3-18. https://doi.org/10.1055/s-0038-1675550
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Cavalcante MM, Silveira
CRS, da Costa CR, Távora
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Teixeira MJD, et al. Tumors and pseudotumors
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2021;49:101845. https://doi.org/10.1016/j.foot.2021.101845
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Scheele C, Toepfer A, Beischl S, Dammerer D, Harrasser N, von
Eisenhart-Rothe R, et al. Insights into the distribution patterns of foot and ankle tumours: Update on the perspective of a University Tumour Institute. J Clin Med 2024;13(2):350. https://doi.org/10.3390/jcm13020350
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Alhosain D, Kouba L, Dandashy A, Jejan W. A painful lump on a teenager’s toe is a benign enchondroma. Lancet 2020;396(10263):1663. https://doi.org/10.1016/S0140-6736(20)32165-6
8.
Edwards SR, Kingsford
AC. Surgical management of an enchondroma of the proximal
phalanx of the foot: An illustrative case report. SAGE Open Med Case Rep
2020;8:2050313X20945894. https://doi.org/10.1177/2050313X20945894
9.
Jasqui Remba S, Álvarez San Martín R, Baley Amiga I, Portman
Santos D. Solitary enchondroma in a metatarsal bone, an incidental discovery. Int J Surg Case Rep 2021;78:254-8. https://doi.org/10.1016/j.ijscr.2020.12.056
10.
Lui TH. (2015).
Endoscopic
curettage and bone grafting of the enchondroma of the proximal
phalanx of the great toe. Foot Ankle Surg 2015;21:137-41. https://doi.org/10.1016/j.fas.2014.06.001
C. A. Polo Marulanda
ORCID ID: https://orcid.org/0000-0002-4736-8393
C. Valderrama ORCID ID: https://orcid.org/0009-0002-3614-6952
C. Delgado
Soto ORCID ID: https://orcid.org/0000-0001-5461-8955
Received on August 22nd, 2025. Accepted after evaluation on December
16th, 2025 • Dr. JUAN MANUEL ROMERO
ANTE • juanmaro04041977@gmail.com • https://orcid.org/0000-0002-9390-9496
How to cite this article: Romero Ante JM, Polo Marulanda CA, Valderrama C, Delgado Soto C. Postgraduate Orthopedic Instruction – Imaging. Case Resolution. Rev Asoc Argent
Ortop Trau-matol 2026;91(3):286-290. https://doi.org/10.15417/issn.1852-7434.2026.91.3.2345
Article
Info
Identification:
https://doi.org/10.15417/issn.1852-7434.2026.91.3.2345
Published: June, 2026
Conflict
of interests: The authors declare no conflicts of interest.
Copyright: © 2026, Revista de la Asociación
Argentina de Ortopedia y Traumatología.
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