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Non-syndromic keratocystic odontogenic tumor involving the maxillary sinus: case report

Tumor odontogênico queratocístico envolvendo o seio maxilar: relato de caso

Abstracts

INTRODUCTION: The odontogenic keratocyst tumor is rarely found in maxilla. CASE REPORT: This article describes a report of a case of a 60-year-old Caucasian female with an asymptomatic growth in the region of the posterior maxilla tumor diagnosed as odontogenic keratocyst. We discuss the diagnosis and workup for this type of injury.

odontogenic tumors; maxillary sinus; radiology; surgery


INTRODUÇÃO: O tumor odontogênico queratocístico é raramente encontrado em maxilla. RELATO DO CASO: Este artigo descreve o relato de um caso de uma paciente de 60 anos de idade, leucoderma, sexo feminino, com um crescimento assintomático na região de maxila posterior diagnosticada como tumor odontogênico queratocístico. Também é discutido o diagnóstico e a propedêutica para este tipo de lesão.

tumores odontogênicos; seio maxilar; radiologia; cirurgia


RELATO DO CASO

Non-syndromic keratocystic odontogenic tumor involving the maxillary sinus: case report

Tumor odontogênico queratocístico envolvendo o seio maxilar: relato de caso

Gustavo Davi RabeloI; João Cesar Guimarães HenriquesI; José Humberto MacedoII; Claudia Jordão SilvaIII; Sergio Vitorino CardosoIV; Adriano Mota LoyolaV; Antônio Francisco Durighetto JuniorVI

IMestre em Odontologia. Mestrado pela Faculdade de Odontologia da Universidade Federal de Uberlândia

IIEspecialista. Especialização em Cirurgia e Traumatologia Buco-Maxilo-Facial pela Faculdade de Odontologia da Universidade Federal de Uberlândia

IIIDoutora. Professora Adjunta, Departamento de Cirurgia e Traumatologia Buco-Maxilo-Facial da Faculdade de Odontologia da Universidade Federal de Uberlândia

IVDoutor. Professor Adjunto, Departamento de Patologia Oral da Faculdade de Odontologia da Universidade Federal de Uberlândia

VDoutor. Professor Titular, Departamento de Patologia Oral da Faculdade de Odontologia da Universidade Federal de Uberlândia

VIDoutor. Professor Titular, Departamento de Estomatologia da Faculdade de Odontologia da Universidade Federal de Uberlândia

Mail address Mail address: Gustavo Davi Rabelo Alameda Himalaia, 341 - Bairro Mansões Aeroporto Uberlândia / MG - Brazil - Zip code: 38406-389 Fax and Telephone: (+55 34) 3211-3690 E-mail: drgustavorabelo@yahoo.com.br

SUMMARY

INTRODUCTION: The odontogenic keratocyst tumor is rarely found in maxilla.

CASE REPORT: This article describes a report of a case of a 60-year-old Caucasian female with an asymptomatic growth in the region of the posterior maxilla tumor diagnosed as odontogenic keratocyst. We discuss the diagnosis and workup for this type of injury.

Keywords: odontogenic tumors, maxillary sinus, radiology, surgery.

RESUMO

INTRODUÇÃO: O tumor odontogênico queratocístico é raramente encontrado em maxilla.

RELATO DO CASO: Este artigo descreve o relato de um caso de uma paciente de 60 anos de idade, leucoderma, sexo feminino, com um crescimento assintomático na região de maxila posterior diagnosticada como tumor odontogênico queratocístico. Também é discutido o diagnóstico e a propedêutica para este tipo de lesão.

Palavras-chave: tumores odontogênicos, seio maxilar, radiologia, cirurgia.

INTRODUCTION

Odontogenic keratocyst is the traditional term used to describe a benign but locally aggressive odontogenic cystic lesion with distinctive clinical and histopathologic features (1). World Health Organization proposed the term "keratocystic odontogenic tumor" (KOT) to reflect the neoplastic nature of this lesion (2).

LITERATURE REVIEW

Keratocystic odontogenic tumors almost certainly arise from derivatives of the dental lamina, an embryonic structure that normally differentiates into tooth buds and enamel-producing cells during odontogenesis (3). This lesion shows features of both a cyst and a benign neoplasm (4). Albeit eventually associated to nevoid basal cell carcinoma syndrome, most of KOT occur as sporadic lesions.

Up to one-fourth from all of KOT affect the maxilla, but maxillary sinus involvement is very rare (5,6). In a retrospective study of 183 cases, the mandible was the site of occurrence of 70.5% of tumors and 16.4% occurred in the maxilla, however, 13.1% occurred in both (7).

Radiographically, it appears as a well-defined lucency and is often multilocular. KOTs represent 5-15% of all odontogenic cysts and the recurrence rate for solitary KOT is 10-30% (8).

The aim of this paper was describe an intriguing case of a patient with a non-syndromic KOT involving maxillary sinus and discuss the pathogenesis of the disease, highlighting recent molecular data obtained from it.

CASE REPORT

A 60 year-old Caucasian female presented with an asymptomatic growth in the right posterior maxilla. It was present for sixteen years and the patient reported eventual gingival bleeding and mild pain. Past medical and familiar history was noncontributory. Oral examination revealed a firm swelling with normal overlying mucosa. Panoramic radiograph (Figure 1) evidenced a well defined 4cm round unilocular lesion effacing the right maxillary sinus. Also, sclerotic areas of mixed density were found in premolar and molar regions of the mandible in the right side, with a very suggestive aspect of benign fibro-osseous lesions (Figure 2). Axial and coronal computerized tomography images delineated a hypodense spherical lesion in the right maxilla with extension to the sinus, suggesting a cystic alteration (Figure 3). Aspiration with a 29-gauge needle obtained yellowish and viscous liquid, suggesting keratin content. Incisional biopsy was performed and histopathology confirmed the diagnosis of KOT (Figure 4). The lesion was then enucleated followed by vigorous curettage of the surgical margins. None treatment was proposed for the lesions in mandible, except for appropriate information to the patient about the nature of the lesion. Radiographic follow-up was warranted and the patient did not present recurrence four years after treatment.





DISCUSSION

Classic radiograph aspect comprises a radiolucent lesion with well defined borders. Most common sites of occurrence are mandibular third molar and ramus region, followed by anterior maxilla, maxillary third molar area, mandibular anterior, and mandibular premolar areas (5,9). Overall maxillary involvement has been observed in ranges from 16.4% (7) to 23.5% (5) of KOT and one percent of the lesions occur in the maxilla with sinus involvement (9). In the latter instance, an apparent radiopaque alteration may be found, differing from the classic description for this lesion. Such aspect has been reported by previous authors to resemble inflammatory antral pseudocyst, which is frequently associated to relevant symptoms, an important clue to differentiate it from other lesions. In addition, computerized tomography imaging of the present case depicted a thin rim of bone surrounding the lesion, as previously reported for KOT (10).

The radiopaque aspect is probably due to increased density of the cystic content in relation to the usual air filling of the sinus. Destruction of sinus floor and walls has also been described for other KOT involving the sinus (11,12), differently from the expansive growth seen the present case. Association in the same patient of KOT with the benign fibro-osseous lesions was probably a coincidence, since we were unable to find out other similar cases in the literature.

Molecular approaches of KOT has been the subject of several studies. Point mutations in the patched (PTCH) tumor suppressor gene have been reported for both the sporadic or nevoid basal cell carcinoma syndrome (13,14). Also, the most substantially over-expressed gene in this lesion is cytokeratin 6B, inferred as cytoskeletal response to increased proliferation of epithelial cells (15). Other over-expressed genes found include epidermal growth factor receptor 3 and glioma-associated oncogene homologue 1 (16). In addition, disruption of fragile histidine triad (FHIT) and p53 genes were detected in many KOT, suggesting participation in the pathogenesis of the lesion, probably due to alteration in proliferative and apoptotic pathways (17). However, specific role in KOT remains controversial (18).

Usual treatment of KOT consist in enucleation, marsupalization, or resection (19). Age of the patient, localization and size of the lesion must be considered in the treatment planning. Anyway, enucleation is the most performed treatment (20), as in the present case.

FINAL COMMENTS

In conclusion, a rare presentation of KOT is described, calling the attention of health care professionals for biologic, diagnostic and therapeutic features of this lesion.

Article received March 27, 2009.

Article approvad April 28, 2009.

Institution: Universidade Federal de Uberlândia. Uberlândia / MG - Brazil.

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  • Mail address:

    Gustavo Davi Rabelo
    Alameda Himalaia, 341 - Bairro Mansões Aeroporto
    Uberlândia / MG - Brazil - Zip code: 38406-389
    Fax and Telephone: (+55 34) 3211-3690
    E-mail:
  • Publication Dates

    • Publication in this collection
      05 Jan 2011
    • Date of issue
      Sept 2010

    History

    • Received
      27 Mar 2009
    • Accepted
      28 Apr 2009
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