ArticlePDF Available

Extra-skeletal osteochondroma adjacent to the medial malleolus A case report

Authors:

Abstract and Figures

The extra-skeletal osteochondroma is a rare clinical entity, only described as sporadic reports in the medical literature. The usual clinical feature is a painless mass adjacent to a bone but not having any connection with it. The osteochondroma is a closely resembling differential that has the characteristic connection to the underlying bone appreciated in radiological assessment. We report our experience with a case of a 19-year-old male patient with a painless lump over medial ankle causing difficulty in wearing shoes. No functional impairment or distal neuromuscular deficit was noted. The imaging revealed a well-defined, discrete ossified mass distal to the medial malleolus and adjacent to the talus, having no connection with the underlying bones. Excision of the mass led to the histopathological confirmation of the mass as an extra-skeletal osteochondroma. Despite being uncommon, extra-skeletal osteochondroma should be in the differential diagnosis of a well-defined solid lump with varying amount of calcification on the imaging. Excision biopsy, however, has diagnostic and therapeutic value and usually is curative. Keywords: Benign lesion, extra-skeletal osteochondroma, foot, lump, osteochondroma
Content may be subject to copyright.
64 © 2023 Journal of the Uttaranchal Orthopaedic Association | Published by Wolters Kluwer - Medknow
Case Report
Access this article online
Website:
https://journals.lww.com/JUOA/
DOI: 10.4103/juoa.juoa_3_23
Quick Response Code:
Abstract
The extra-skeletal osteochondroma is a rare clinical entity, only described as sporadic reports
in the medical literature. The usual clinical feature is a painless mass adjacent to a bone but not
having any connection with it. The osteochondroma is a closely resembling differential that has the
characteristic connection to the underlying bone appreciated in radiological assessment. We report
our experience with a case of a 19-year-old male patient with a painless lump over medial ankle
causing difculty in wearing shoes. No functional impairment or distal neuromuscular decit was
noted. The imaging revealed a well-dened, discrete ossied mass distal to the medial malleolus
and adjacent to the talus, having no connection with the underlying bones. Excision of the mass
led to the histopathological conrmation of the mass as an extra-skeletal osteochondroma. Despite
being uncommon, extra-skeletal osteochondroma should be in the differential diagnosis of a well-
dened solid lump with varying amount of calcication on the imaging. Excision biopsy, however,
has diagnostic and therapeutic value and usually is curative.
Keywords: Benign lesion, extra-skeletal osteochondroma, foot, lump, osteochondroma
Introduction
The extra-skeletal osteochondroma is
an unusual clinical entity presenting as a
benign mass lesion at various locations
including hand and feet region.[1] These
are extra-osseous or extra-synovial lesions
consisting of predominant mature hyaline
cartilage with an extensive enchondral
ossification.[2] These are discrete lesions
having no connection to the adjacent bone
unlike the osteochondroma or exostosis,
which are one of the commonest resembling
bone lesions. There are many hypotheses
regarding their formation but the exact
etiology is still unclear. Metaplasia of
mesenchymal fibroblast of the loose
connective tissues is one theory, whereas
other relates to their origin from pluripotent
cell lines from tenosynovium, synovium,
or other adjacent tissues.[3] Apart from it,
theories such as adipose tissue metaplasia
or association of repeated trauma as an
inciting event are also suggested. The usual
presentation is of a painless mass with or
without pressure effects on the adjacent
structures. These may be confused with
solitary osteochondroma, which chiefly
presents with painless growing mass with
location-specic symptoms and their painful
presentation is rarely encountered with
associated bursitis, fracture, or malignant
transformation.[4] The extra-skeletal lesions
are still not fully understood and limited to
sporadic care reports or small series in the
literature. Their presence as a mass at ankle
region is a rare occurrence.
CaseReport
A 19-year-old male presented to us with
an atraumatic swelling, noted over the
medial aspect of his right ankle for the
last 4 years. Initially, there was a history
of swelling being smaller in size before
it started growing slowly, but for the last
2years, the size has been relatively static.
There was a hard, nontender mass located
just below and anterior to the medial
malleolus with well-defined border and
irregular surface [Figure 1A and B]. There
was neither overlying skin problems nor any
raised temperature or overlying vascular
engorgement. The mass was not mobile
in any direction and underlying aspect of
the mass could not be palpated. There was,
Address for correspondence:
Dr. Ganesh Singh Dharmshaktu,
Department of orthopaedics,
Government Medical College,
Haldwani, Uttarakhand 263139,
India.
E-mail: drganeshortho@gmail.
com
Extra-Skeletal Osteochondroma Adjacent to the Medial Malleolus:
ACaseReport
How to cite this article: Dharmshaktu GS,
Agarwal N, Dharmshaktu IS, Pangtey T.Extra-
skeletal osteochondroma adjacent to the medial
malleolus: Acase report. J Uttaranchal Ortho Assoc
2022;1:64-7.
Received: 15-Feb-2023, Accepted: 02-Aug-2023,
Published: 09-Nov-2023
This is an open access journal, and arcles are distributed under
the terms of the Creave Commons Aribuon-NonCommercial-
ShareAlike 4.0 License, which allows others to remix, tweak, and
build upon the work non-commercially, as long as appropriate
credit is given and the new creaons are licensed under the
idencal terms.
For reprints contact: WKHLRPMedknow_reprints@wolterskluwer.com
GaneshSingh
Dharmshaktu,
Naveen Agarwal,
IshwarSingh
Dharmshaktu,
Tanuja Pangtey1
Departments of Orthopaedics
and 1Pathology and Blood Bank,
Government Medical College,
Haldwani, Uttarakhand, India
Downloaded from http://journals.lww.com/juoa by BhDMf5ePHKav1zEoum1tQfN4a+kJLhEZgbsIHo4XMi0hCywCX1AW
nYQp/IlQrHD3i3D0OdRyi7TvSFl4Cf3VC1y0abggQZXdgGj2MwlZLeI= on 11/15/2023
Dharmshaktu, etal.: Extra-skeletal osteochondroma
65Journal of the Uttaranchal Orthopaedic Association | Volume 1 | Issue 2 | July-December 2022
Figure 1: The clinical image showing a lump over medial aspect of the
ankle adjacent to the medial malleolus (A and B) and the ankle radiographs
showing the presence of a well-defined mass below the medial malleolus
with calcification (C)
however, no interference with daily activities and the ankle
and toe movements were normal along with intact distal
neuromuscular status. The problem in wearing shoes was
the main concern of the patient because of the bumpy mass.
The ankle radiograph of the patient showed no signicant
bony abnormality except a heterogeneously calcied mass
present adjacent to the medial malleolus [Figure 1C]. The
lesion appeared well-dened and without any connection
to adjacent bones. The computerized tomography (CT)
scan of the ankle region better delineated the lesion [Figure
2A] as a discreet extra-skeletal mass adjacent to the medial
malleolus distally and medial to the talus bone. There was,
however, no bony connection noted with the underlying
bones [Figure 2B]. The excision biopsy of the lesion was
planned through an incision centered over the mass and
dissection of the skin and subcutaneous tissues revealed a
whitish capsule covering the mass lesion [Figure 2C and D].
The lesion was excised to reveal a solid, white mass with
irregular border measuring about 3 × 3× 2 cm [Figure 2E].
The mass was carefully dissected en bloc as it was loosely
adherent to the adjacent soft tissues. The wound was
closed in layers following a thorough lavage. No immediate
or remote postoperative complication or wound-related
problems were noted in the follow-up [Figure 3A]. The
biopsy results were suggestive of the presence of a lesion
composed of mature cartilage tissues with osteochondroma
as the histological diagnosis [Figure 3B]. On the basis of
clinicoradiological ndings, the nal diagnosis of an extra-
skeletal osteochondroma was made. No recurrence of the
lesion was noted in a follow-up of about 8months.
Discussion
The extra-skeletal osteochondroma presents as a
discrete, ossied mass within the soft tissues and may
need CT or magnetic resonance imaging (MRI) scans
for the diagnosis.[5] We also performed CT scan as the
patient could not afford MRI, and it delineated the
mass as separate entity from underlying bone and
exclude osteochondroma as differential. This is also
referred to as a variant of extra-skeletal chondroma, a
benign cartilaginous tumor with extensive enchondral
ossication.[2] Afew differential diagnoses need exclusion
like an acquired osteochondroma or Turret exostosis
that also presents like a mass besides the bone.[6] Usually,
these exostoses have posttraumatic history, which was
absent in our case. Benign parosteal osteochondromatous
proliferation or Nora’s lesion is a similar lesion along with
other mimics that resemble a mass similar to our case.[7]
Nora’s lesion presents with localized pain and swelling
with a cluster of variably calcied lesion. These also
do not have any connection with underlying bone, thus
providing a diagnostic dilemma only to be resolved by
histopathological conrmation. Histopathology in our
case was in favor of an osteochondroma.
Little is understood regarding etiopathogenesis of these
lesions. Afew articles, however, describe genetic involvement
or chromosomal rearrangements noted in association with
these lesions.[8] Usually, these lesions present as small
lumps but giant lesions are also reported. Occasionally,
the lesion may adapt to the shape of the underlying bone
and cover it like a hard shell without any clinical problem
other than apparent mass.[9] The diagnosis of extra-skeletal
osteochondroma requires clinical suspicion, knowledge
of the condition, judicious use of imaging modalities, and
histopathological correlation, like any other mass lesion.
These uncommon lesions require an acknowledgement for
early identication of the cases and robust studies to better
comprehend them for the optimal management.
Declaration of patient consent
The authors certify that they have obtained all appropriate
patient consent forms. In the form the patient(s) has/have
given his/her/their consent for his/her/their images and
other clinical information to be reported in the journal. The
patients understand that their names and initials will not
be published and due efforts will be made to conceal their
identity, but anonymity cannot be guaranteed.
Downloaded from http://journals.lww.com/juoa by BhDMf5ePHKav1zEoum1tQfN4a+kJLhEZgbsIHo4XMi0hCywCX1AW
nYQp/IlQrHD3i3D0OdRyi7TvSFl4Cf3VC1y0abggQZXdgGj2MwlZLeI= on 11/15/2023
Dharmshaktu, etal.: Extra-skeletal osteochondroma
66 Journal of the Uttaranchal Orthopaedic Association | Volume 1 | Issue 2 | July-December 2022
Figure2: The CT images showing the lesion in details as a calcified mass medial to the talus and below the medial malleolus (A). The axial images showing
no connection of the lesion with the underlying bone (B). The intraoperative images showing the lesion covered with a thin capsule (C) overlying a solid,
white mass (D) that was excised en masse measuring about 3 × 3× 2 cm (E)
Figure3: The postoperative clinical image following the removal of the mass (A) and the histopathology image (B) showing the presence of a lesion laden
with mature cartilage tissue in the stroma (×40, hematoxylin and eosin)
Downloaded from http://journals.lww.com/juoa by BhDMf5ePHKav1zEoum1tQfN4a+kJLhEZgbsIHo4XMi0hCywCX1AW
nYQp/IlQrHD3i3D0OdRyi7TvSFl4Cf3VC1y0abggQZXdgGj2MwlZLeI= on 11/15/2023
Dharmshaktu, etal.: Extra-skeletal osteochondroma
67Journal of the Uttaranchal Orthopaedic Association | Volume 1 | Issue 2 | July-December 2022
Financial support and sponsorship
Nil.
Conicts of interest
There are no conicts of interest.
References
1. SheffJS, WangS. Extra skeletal osteochondroma of the foot. J
Foot Ankle Surg 2005;44:57-9.
2. UenoT, AnsaiS, OmiT, KawanaS. Extraskeletal osteochondroma
arising on the plantar region. Case Rep Dermatol 2011;3:147-50.
3. Kransdorf MJ, MeisJM. From the archives of the AFIP:
Extraskeletal osseous and cartilaginous tumors of the extremities.
Radiographics 1993;13:853-84.
4. BhardwajA, RaichandaniK, Jain H, Surana R, Bishnoi H,
RaichandaniS, etal. Giant extra skeletal osteochondroma of
foot. Acase report with review of literature. J Clin Orthop
Trauma 2017;8:S78-81.
5. GayleEL, MorrisonWB, CarrinoJA, ParsonsTW, LiangCY,
StevensonA. Extraskeletal osteochondroma of the foot. Skelet
Radiol 1999;28:594-8.
6. Dharmshaktu GS, Pangtey T. Turret exostosis of proximal
phalanx of thumb. N Niger J Chin Res 2016;5:64-5.
7. Dharmshaktu GS, Dharmshaktu IS, Agarwal N, PangteyT.
Bizarre parosteal osteochondromatous proliferation or Nora’s
lesion affecting the extremities: Aconcise update. J Musculoskelet
Surg Res 2022;6:200-6.
8. PanagopoulosI, BjerkehagenB, GorunovaL, TaksdalI, HeimS.
Rearrangements of chromosome bands 12q14-15 causing
HMGA2-SOX5 fusion and HMGA2 expression in extraskeletal
osteochondroma. Oncol Rep 2015;34:577-84.
9. DharmshaktuGS, PangteyT. A cap over the kneecap. Indian J
Med Res 2020;152:S80-1.
Downloaded from http://journals.lww.com/juoa by BhDMf5ePHKav1zEoum1tQfN4a+kJLhEZgbsIHo4XMi0hCywCX1AW
nYQp/IlQrHD3i3D0OdRyi7TvSFl4Cf3VC1y0abggQZXdgGj2MwlZLeI= on 11/15/2023
ResearchGate has not been able to resolve any citations for this publication.
Article
Full-text available
The bizarre parosteal osteochondromatous proliferation or Nora’s lesion is an unusual clinical entity that presents with localized swelling and pain. The characteristic radiological appearance includes a cluster of variably calcified lesions adjacent to a particular bone. However, it does not necessarily have direct continuity with its medullary region. The etiopathogenesis of this disorder is not yet fully understood. Various other lesions require careful exclusion and the use of advanced imaging modalities to supplement the diagnosis. The final diagnosis of the lesion, however, is based on the histopathological basis. However, these lesions are reported as sporadic reports or small series in the literature and are also discovered in areas other than the common locations in hands and feet. The recent research aims to throw more advanced knowledge into their causation, including genetic etiology. The symptomatic lesions may require excision for clinical relief, but recurrence is not uncommon. The future research, and preferably multi-center collaboration, is required for more insight into their comprehensive nature and clinical spectrum. A brief and crisp update of the articles published in the past 10 years describing bizarre parosteal oseochondromatous proliferation in the extremities is presented here for educational purposes for orthopedists and generalists alike.
Article
Full-text available
Article
Full-text available
We describe two cases of extraskeletal osteochondroma in which chromosome bands 12q14~15 were visibly rearranged through a pericentric inv(12). Molecular analysis of the first tumor showed that both transcript 1 (NM_003483) and transcript 2 (NM_003484) of HMGA2 were expressed. In the second tumor, the inv(12) detected by karyotyping had resulted in an HMGA2-SOX5 fusion transcript in which exons 1-3 of HMGA2 were fused with a sequence from intron 1 of SOX5. The observed pattern is similar to rearrangements of HMGA2 found in several other benign mesenchymal tumors, i.e., disruption of the HMGA2 locus leaves intact exons 1-3 which encode the AT-hook domains and separates them from the 3'-terminal part of the gene. Our data therefore show that a subset of soft tissue osteochondromas shares pathogenetic involvement of HMGA2 with lipomas, leiomyomas and other benign connective tissue neoplasms.
Article
Full-text available
Extraskeletal osteochondroma is a variant of extraskeletal chondromas that are uncommon soft-tissue cartilaginous tumors. These tumors may undergo extensive enchondral ossification to form an extraskeletal osteochondroma. This report describes the case of a 39-year-old Japanese man with an extraskeletal osteochondroma arising on the plantar aspect of the foot.
Article
The osteochondromatous lesion of the skeleton is common occurrences and may have many variants, the knowledge of which is crucial for identification and treatment. Acquired osteochondroma, also known as Turret exostosis is one such lesion. The clinico-radiological picture often mimics that of a solitary osteocartilagenous exostosis, but the history of minor trauma as triggering event and histopathological correlation concludes the ubiquitous diagnosis. We present a case of Turret exostosis of thumb proximal phalanx on medial aspect with appropriate management. Keywords: Complication, injury, metacarpal, osteochondroma, thumb, treatment, turret exostosis.
Article
Extraskeletal osseous and cartilaginous tumors and tumorlike conditions of the extremities can often be differentiated radiologically; for those that cannot, knowledge of the spectrum of lesions will allow a suitably ordered differential diagnosis. Of the osseous lesions--myositis ossificans, fibro-osseous pseudotumor, fibrodysplasia ossificans progressiva, soft-tissue osteoma, and extraskeletal osteosarcoma--all but myositis ossificans are relatively rare. Myositis ossificans has a distinct mineralization pattern that can be observed radiologically as a peripheral rim of lamellar bone. Fibro-osseous pseudotumor typically occurs in the digits of the hand and lacks the well-defined zoning pattern of myositis ossificans. The cartilaginous entities include the true tumors, soft-tissue chondroma and extraskeletal chondrosarcoma, and the tumorlike process, synovial osteochondromatosis. The tumors are relatively rare; synovial osteochondromatosis commonly affects middle-aged men, especially in the knee, and is associated with osteoarthritis. The differential diagnosis for these extraskeletal osseous and cartilaginous lesions includes soft-tissue sarcoma, benign mesenchymoma, malignant mesenchymoma (rare), calcified tophi in gout, melorheostosis (rare), pilomatricoma (rare), and tumoral calcinosis (rare).
Article
A case of pathologically proven extraskeletal osteochondroma is presented with magnetic resonance imaging (MRI), computed tomography (CT), bone scan and radiographic findings. The diagnosis of extraskeletal osteochondroma should be considered when a discrete, ossified mass is localized in the soft tissues of the distal extremities. Nomenclature surrounding this entity is controversial and is discussed.
Article
An extraskeletal osteochondroma is an infrequently encountered benign cartilaginous tumor with a predilection for the hands and feet that usually does not exceed 3 cm in diameter. This diagnosis can be misleading because it bears the same name as the osseous neoplasm more commonly referred to as an exostosis. The authors present an unusual case of a painful enlarging mass in the foot of a 28-year-old man who was later diagnosed as having an extraskeletal osteochondroma measuring in excess of 4 cm. Clinical, radiographic, and magnetic resonance images are provided along with intraoperative and histopathologic figures. There was no sign of recurrence 1 year after surgical excision. A review of the literature regarding this uncommon lesion is also presented.