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Aneurysmal bone cyst of the maxilla rare presentation with radiological and pathological correlation

发表时间:2015-12-09  浏览次数:1301次

 Introduction

Aneurysmal bone cysts (ABC) are typically found in long bones and the spine, but rarely can be seen in the craniofacial region. The incidence is 2% and 1.3% in the craniofacial region and maxillary region, respectively. [1],[2] These benign, expansile bony tumors of unknown etiology are often referred to as aneurysmal bone tumors rather than cysts because of their aggressive behavior.

Case report

A 23-year-old man presented with a history of anosmia, the sensation of a blocked nose with mild pain that had been increasing over 6 months, and a gradual increase in bilateral exorbitism. The patient denies any history of fever, trauma, epistaxis, or oral bleeding. His physical examination was remarkable for a brownish bulge in the nasopharynx. The patient underwent computerized tomography (CT) and magnetic resonance imaging (MRI) examinations. Noncontrast computerized tomography (NCCT) of the nasopharynx region showed an expansile cystic lesion in the maxillary region bulging into the nasopharynx [Figure 1]. There was no cortical break [Figure 2] and [Figure 3]. Multiple fluid levels were seen within the lesion [Figure 4] and [Figure 5]. Cytology following fine-needle aspiration was performed, and a cytological diagnosis of ABC of the maxilla was given. The patient underwent enucleation of the mass. Histopathological examination further confirmed the diagnosis of a maxillary ABC, with cystic spaces filled with blood, and without an endothelial lining along with osteoclast giant cells [Figure 6a and b]. There were no surgical complications, and the patient was advised to follow-up in 3 months. His recovery has been uneventful.

Discussion

The maxilla is a rare site of ABC. It is neither an aneurysm nor a cyst. The World Health Organization (WHO) defines an ABC as an "expanding osteolytic lesion consisting of blood-filled spaces of variable size separated by connective tissue septa containing trabeculae of osteoid tissue and osteoclast giant cells." These are usually found within bones with high venous pressure and marrow content. Sixty-five percent are primary or simple, and 35% are secondary in nature as per Bonakdarpour et al.[3] Primary ABC has a high level of accuracy of diagnosis with radiological studies, diagnosis, but only 20% of secondary lesions can be diagnosed radiographically. It is usually found in individuals < 20 years old. There is no predilection for gender, but a 2:1 ratio in female to male has been recorded. ABC in the maxillary region may remain undiagnosed for a long period secondary to its gradual course as occurred in our case. A patient will generally report to the hospital after becoming symptomatic. The underlying pathology of giant cell tumor is well-known in secondary types of ABC. It is always diagnosed when the patient undergoes three dimensional imaging modalities such as CT and MRI. Radiographically, ABC gives the impression of a "blown out" or "ballooned" appearance of the underlying bone. CT and MRI demonstrate classic fluid-level images, but histological examination remains the hallmark for the diagnosis. The solid component of the lesion can be visualized on CT and MRI, which further indicates a secondary nature. Multiple areas of high intensity surrounded by hypointense rings are observed on T1-weighted and T2-weighted images. These represent the different ages of blood in the lesion. [4] There should be close collaboration between radiologist and pathologist when making the diagnosis, as a small specimen may miss the associated findings.Surgical excision with enucleation remains the best treatment. The path to surgery depends upon the extent of involvement and its nature. Other potential options for treatment include percutaneous sclerotherapy, therapeutic embolization, curettage, block resection and reconstruction, radiotherapy and systemic calcitonin therapy. [5] There have some cases of spontaneous healing. [6]In conclusion, ABC of hidden areas such as the maxilla as in our case poses a great diagnostic and management dilemma for the clinician. CT and MRI are quite helpful modalities in guiding the management path. This further helps in ruling out intracranial extension. The radiological modalities further help the anesthesiologist in guiding intubation and determining the level of risk during surgery.

References

1.Suzuki F, Fukuda S, Yagi K, Chida E, Inuyama Y. A rare aneurysmal bone cyst of the maxillary sinus: a case report. Auris Nasus Larynx 2001;28:S131-7.

2.Guzmán GP, Baeza OA, Araya OJ, Roa SJ, Brevis OL, Torres LP. Aneurysmal bone cyst of the maxilla. Report of one case. Rev Med Chil 2005;133:1355-60.

3.Bonakdarpour A, Levy WM, Aegerter E. Primary and secondary aneurysmal bone cyst: a radiological study of 75 cases. Radiology 1978;126:75-83.

4.Pahade J, Sekhar A, Shetty SK. Imaging of malignant skeletal tumors. In: Blake MA, Kalra MK, editors. Imaging in Oncology. New York: Springer-Verlag; 2008. p. 375.

5.Rai AT, Collins JJ. Percutaneous treatment of pediatric aneurysmal bone cyst at C1: a minimally invasive alternative: a case report. AJNR Am J Neuroradiol 2005;26:30-3.

6.Malghem J, Maldague B, Esselinckx W, Noel H, De Nayer P, Vincent A. Spontaneous healing of aneurysmal bone cysts. A report of three cases. J Bone Joint Surg Br 1989;71:645-50.

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