Elsevier

Auris Nasus Larynx

Volume 28, Issue 1, January 2001, Pages 103-105
Auris Nasus Larynx

Case report
Fibrous dysplasia with cystic appearance in maxillary sinus

https://doi.org/10.1016/S0385-8146(00)00077-8Get rights and content

Abstract

Fibrous dysplasia (FD) in the paranasal sinuses is uncommon, and its management may be difficult. We report the case of a 25-year-old female with FD exhibiting a cystic appearance in the maxillary sinus. The patient had been complaining of facial swelling for few years. Imagery study showed a cystic lesion and dense bone changes in the maxillary bone. Inferior meatal antrostomy with a nasal endoscope failed to confirm a histological diagnosis. After a 3-year follow-up, the degree of facial swelling was unchanged, and the patient underwent middle meatal antrostomy and was diagnosed with FD.

Introduction

Fibrous dysplasia (FD) of the bone is a slowly progressive, benign disease of unknown cause where normal architectures are replaced with fibrous and osteoid tissue. The disease usually develops over several years in the first or second decades of life. Swelling without pain is the most common initial symptom, and malignant changes are rare.

There are three types of FD: monostotic, polyostotic, and McCune–Albright syndrome. Monostotic FD is predominant, and craniofacial involvement occurs in approximately 30% of the cases [1]. FD in the paranasal sinuses is uncommon, and its management may be difficult.

Section snippets

Case history

In July 1995, a 25-year-old female complaining of a mild facial swelling on the left side was seen in Kawaguchi-Kogyo General Hospital. The swelling had been present for few years, and the patient also had a heavy feeling. The patient had no previous history of rhinosinusitis, craniofacial trauma or nasal surgery. Computed tomographic (CT) scans (Fig. 1, Fig. 2) and magnetic resonance (MR) images (Fig. 3, Fig. 4) showed a cystic lesion and dense bone changes in the maxillary bone.

An inferior

Discussion

Although, in the present case, the FD affected the maxillary bone itself and not the maxillary sinus, CT scans and MR images showed that the cystic lesion almost entirely occupied the maxillary sinus. Therefore, we considered this case as one FD in the maxillary sinus.

FD of the maxillary bone, which is the most commonly affected craniofacial bone, usually manifests as a painless facial deformity. However, the disease may also show symptoms like loosening of teeth and deformity of the alveolar

References (13)

  • B.J. Ferguson

    Fibrous dysplasia of the paranasal sinuses

    Am. J. Otolaryngol.

    (1994)
  • K. Ikeda et al.

    Endonasal endoscopic management in fibrous dysplasia of the paranasal sinuses

    Am. J. Otolaryngol.

    (1997)
  • D.J. Commins et al.

    Fibrous dysplasia and ossifying fibroma of the paranasal sinuses

    J. Laryngol. Otol.

    (1998)
  • D.M.L. Williams et al.

    Fibrous dysplasia

    J. Laryngol. Otol.

    (1975)
  • J.W. Fries

    The roentgen features of fibrous dysplasia of the skull and facial bones. A critical analysis of thirty-nine pathologically proved cases

    Am. J. Roentgenol.

    (1957)
  • D.B. Mendelsohn et al.

    Computer tomography of craniofacial fibrous dysplasia

    J. Comput. Assist. Tomogr.

    (1984)
There are more references available in the full text version of this article.

Cited by (8)

View all citing articles on Scopus
View full text