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Asymptomatic fibrous dysplasia of the temporal bone

Published online by Cambridge University Press:  23 February 2015

T Kimitsuki*
Affiliation:
Department of Otorhinolaryngology, Kyushu Central Hospital, Fukuoka, Japan
S Komune
Affiliation:
Department of Otorhinolaryngology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan
*
Address for correspondence: T Kimitsuki, Department of Otorhinolaryngology, Kyushu Central Hospital, 3-23-1 Shiobaru, Minami-ku, Fukuoka 815-8588, Japan Fax: +81 92 541 4540 E-mail: [email protected]

Abstract

Introduction:

Fibrous dysplasia is a bone disorder of unknown origin in which normal bone is replaced with fibrotic tissue and disorganised bone trabeculae. The temporal bone is rarely affected. Because of the slowly progressive course of the disease, many mild cases may never be recognised and are found incidentally. We present a patient with fibrous dysplasia of the right temporal bone, who had few complaints.

Objective:

A 62-year-old man was incidentally found to have fibrous dysplasia of the temporal bone on routine computed tomography scan.

Method:

One case report.

Results:

Computed tomography showed a thickening of the right temporal bone with a ground-glass appearance. The 62-year-old man opted for watchful waiting.

Conclusion:

We have presented an asymptomatic fibrous dysplasia of the temporal bone. Mild cases may never be recognised and are found incidentally because of their slow progression.

Type
Main Articles
Copyright
Copyright © JLO (1984) Limited 2015 

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References

1McCune, DJ, Bruch, H. Osteodystrophia fibrosa: report of a case in which the condition was combined with precocious puberty, pathologic pigmentation of the skin and hyperthyroidism, with a review of the literature. Am J Dis Child 1937;54:806–48CrossRefGoogle Scholar
2Nager, GT, Kennedy, DW. Kopstein, E. Fibrous dysplasia: a review of the disease and its manifestations in the temporal bone. Ann Otol Rhinol Laryngol 1982;91(suppl 92):152Google Scholar
3Windolz, F. Cranial manifestation of fibrous dysplasia of bone. Am J Roentgenol 1947;58:5163Google Scholar
4Magerian, CA, Sofferman, RA, McKenna, MJ, Eavey, RD, Nadol, JB Jr. Fibrous dysplasia of the temporal bone: ten new cases demonstrating the spectrum of otologic sequelae. Am J Otol 1995;16:408–19Google Scholar
5Morrissey, DD, Talbot, JM, Schleuning, AJ. Fibrous dysplasia of the temporal bone: reversal of sensorineural hearing loss after decompression of the internal auditory canal. Laryngoscope 1997;107:1336–40CrossRefGoogle ScholarPubMed
6Van Horn, PE, Dahlin, DC, Bickel, WH. Fibrous dysplasia: a clinical pathologic study of orthopaedic surgical cases. Mayo Clin Proc 1963;38:175–89Google Scholar
7Yaunus, M, Haleem, A. Monostotic fibrous dysplasia of the temporal bone. J Laryngol Otol 1987;101:1070–4Google Scholar
8Barrionuevo, CE, Marcallo, FA, Coelho, A, Cruz, GA, Mocellin, M, Patrocinio, JA. Fibrous dysplasia and the temporal bone. Arch Otolaryngol 1980;106:298301CrossRefGoogle ScholarPubMed
9Abe, T, Suzuki, M, Ueyama, T, Ina, K, Mogi, G. A case of monostotic fibrous dysplasia of the temporal bone [in Japanese]. Practica Oto-Rhino-Laryngologica 1999;92:713–19CrossRefGoogle Scholar
10Wang, YC, Chen, YA. Fibrous dysplasia of the temporal bone presenting as an external auditory canal mass. Otolaryngol Head Neck Surg 2009;141:655–6CrossRefGoogle ScholarPubMed
11Tochino, R, Sunami, K, Yamane, H. Fibrous dysplasia of the temporal bone with cholesteatoma. Acta Otolaryngol Suppl 2004;554:47–9Google Scholar
12McCall, AA, Curtin, HD, McKenna, MJ. Posterior semicircular canal dehiscence arising from temporal bone fibrous dysplasia. Otol Neurotol 2010;31:1516–17Google Scholar
13Sakamoto, M, Hayashida, T, Sugasawa, M. A case of fibrous dysplasia of the temporal bone: evaluation of treatment performed 23 years ago. Otolaryngol Head Neck Surg 2001;125:563–4Google Scholar
14Reddy, KTV, Vinayak, BC, Jefferis, AF, Grieve, DV. Fibrous dysplasia of the temporal bone. Ann Otol Rhinol Laryngol 1994;103:74–6Google Scholar
15Pouwels, ABPM, Cremers, CWRJ. Fibrous dysplasia of the temporal bone. J Laryngol Otol 1988;102:171–2CrossRefGoogle ScholarPubMed
16Lambert, PR, Brackmann, DE. Fibrous dysplasia of the temporal bone: the use of computed tomography. Otolaryngol Head Neck Surg 1984;92:461–7Google Scholar
17Chee, GH, Chen, JM. Fibrous dysplasia of the temporal bone. Otol Neurotol 2002;23:405–6Google Scholar
18Casselman, JW, De Jonge, I, Neyt, I, De Clercq, C, D'Hont, G. MRI in craniofacial fibrous dysplasia. Neuroradiol 1993;35:234–7CrossRefGoogle ScholarPubMed
19Kim, YH, Song, JJ, Choi, HG, Lee, JH, Oh, SH, Chang, SO et al. Role of surgical management in temporal bone fibrous dysplasia. Acta Otolaryngol 2009;129:1374–9Google Scholar
20Yang, H, Chen, S, Zheng, Y, Xu, Y, Zhang, X, Xiong, H et al. Surgical treatment of monostotic fibrous dysplasia of the temporal bone: a retrospective analysis. Am J Otolaryngol 2012;33:697701Google Scholar
21Yagoda, MR, Selesnick, SH. Temporal bone fibrous dysplasia and cholesteatoma leading to the development of a parapharyngeal abscess. J Laryngol Otol 1994;108:51–3Google Scholar
22Slow, IN, Stern, D, Friedman, EW. Osteogenic sarcoma arising in preexisting fibrous dysplasia: report of a case. J Oral Surg 1971;29:126–9Google Scholar
23Kaushik, S, Smoker, WR, Frable, WJ. Malignant transformation of fibrous dysplasia into chondroblastic osteosarcoma. Skeletal Radiol 2002;31:103–6CrossRefGoogle ScholarPubMed
24Schwartz, DT, Alpert, M. The malignant transformation of fibrous dysplasia. Am J Med Sci 1964;247:120Google Scholar