Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2012 Sep;7(3):211-4.
doi: 10.4103/1817-1745.106483.

Chondromyxoid fibroma of the temporal bone: A rare entity

Affiliations
Case Reports

Chondromyxoid fibroma of the temporal bone: A rare entity

Mayur Sharma et al. J Pediatr Neurosci. 2012 Sep.

Abstract

Chondromyxoid fibroma (CMF) is the least common benign tumor of the cartilaginous origin. It is very unusual to find these tumors in the skull bones. We report one such case involving the temporal bone. Till date, only nine such cases including this patient, involving the temporal bone have been reported to the best of our knowledge. Grant Medical College and Sir J.J Group of Hospitals, Byculla, Mumbai, Maharashtra, India. A 12-year-old female patient presented with a history of headache associated with left earache of 1 month duration. This was followed by swelling over the left preauricular region 15 days later. Imaging was suggestive of an expansile lesion involving the squamous part of the left temporal bone with calcifications suggestive of a benign chondroid lesion. The patient was operated upon with left temporal incision and complete excision of the lesion. The patient had relief from headache, earache and swelling, with no evidence of new neurological deficit in the post-operative period. CMF of the skull bone is an extremely rare tumor. Differential diagnosis should be kept in mind, especially in cases of calcified lesions and includes chordoma, chondroid chondroma, and low-grade myxoid chondrosarcoma. En-bloc complete excision should be the aim to achieve cure.

Keywords: Chondromyxoid; fibroma; temporal.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest: None declared.

Figures

Figure 1
Figure 1
X-ray of the skull was suggestive of a multilobulated radiolucent lesion with well-defined margins in the left temporal region
Figure 2
Figure 2
Computerized tomography scan showing a lesion about 4.1 cm × 3.2 cm arising from the left temporal region. It shows isodense soft tissue within and also shows small, calcific foci
Figure 3
Figure 3
Magnetic resonance imaging scan showing a lobulated mass in the squamous part of the left temporal bone. Cortex is well maintained with no intracranial extension. The lesion shows heterogeneous enhancement on post gadolinium contrast images
Figure 4
Figure 4
On histopathological examination, tumor cells can be seen arranged in a lobular pattern. Individual lobules show central hypocellular and peripheral hypercellular areas comprised of sheets of chondrocytes. Focal areas of dense calcification are also seen, suggestive of chondromyxoid fibroma
Figure 5
Figure 5
Post-operative computerized tomography scan showing complete tumor excision

Similar articles

Cited by

References

    1. Jaffe HL, Lichtenstein L. Chondromyxoid fibroma of bone; a distinctive benign tumor likely to be mistaken especially for chondrosarcoma. Arch Pathol (Chic) 1948;45:541–51. - PubMed
    1. Tarhan NC, Yologlu Z, Tutar NU, Coskun M, Agildere AM, Arikan U. Chondromyxoid fibroma of the temporal bone: CT and MRI findings. Eur Radiol. 2000;10:1678–80. - PubMed
    1. Wu CT, Inwards CY, O’Laughlin S, Rock MG, Beabout JW, Unni KK. Chondromyxoid fibroma of bone: A clinicopathologic review of 278 cases. Hum Pathol. 1998;29:438–46. - PubMed
    1. Haberal AN, Bulezuk B, Coskun M, Altinors N, Demirhan B. Unusual presentation of a chondromyxoid fibroma of the temporal bone. Turk J Med Sci. 2001;31:91–3.
    1. Unni KK. Dahlin's Bone Tumors General Aspects and Data on 11087 Cases. 5th ed. Philadelphia: Lippincott-Raven; 1996. Chondromyxoid fibroma; pp. 59–69.

Publication types