Radiologia Brasileira - Publicação Científica Oficial do Colégio Brasileiro de Radiologia

INTRODUCTION

Osteosarcoma accounts for approximately 20% of all primary bone malignancies. Of those, only 5–10% are located in the craniofacial bones accounts and most of those are found in the maxilla or mandible. Less than 1% are found in the cranial vault, and there have been only a few reported cases of osteosarcoma at the base of the skull, reflecting the low frequency of that location^(1–6). The osteoid and bone matrix of an osteosarcoma are composed of malignant connective tissue cells. Most osteosarcomas are of unknown cause and can therefore be designated idiopathic or primary^(1,2,4,6). Osteosarcomas related to known predisposing factors for malignancy, such as Paget’s disease, fibrous dysplasia, and external ionizing radiation, are referred to as secondary osteosarcomas^(1–7). The most common type of osteosarcoma is conventional osteosarcoma, the incidence of which is highest in patients in the second decade of life and the prevalence of which is slightly higher among males than among females^(1,2). In general, patients present with bone pain, occasionally accompanied by a mass or by soft tissue edema^(1,6). The distinct radiological aspects of conventional osteosarcoma are bone marrow lesions, cortical bone destruction, an aggressive periosteal reaction, a soft tissue mass, and a tumor matrix in the destructive lesion, as well as within the soft tissue mass. Although the tumors can present as purely sclerotic or purely osteolytic, most are a combination of the two. The borders are generally indistinct, with a broad zone of transition. The bone destruction is infiltrative, with a “moth-eaten” appearance, and only rarely geographic. The most common forms of periosteal reaction seen in osteosarcomas are the spiculated (sunburst) type and Codman’s triangle, the laminated (onion-skin) type being less common^(1,2,5–7).


CASE REPORT

A 14-year-old female patient presented with a headache and a mass that had been growing in the cranial vault for six months. The mass was hardened and was approximately 10 cm in diameter. An X-ray of the skull showed a discretely sclerotic lesion in the left parietal region, accompanied by an aggressive spiculated periosteal reaction (Figure 1). A computed tomography scan revealed a hyperintense mass in the left frontoparietal region, with intracranial and extracranial involvement (Figure 2). A contrast-enhanced magnetic resonance imaging scan showed an expansile lesion with intracranial and extracranial components, its epicenter being in the cranial vault. The lesion presented heterogeneous impregnation by the contrast medium, predominantly at its periphery (Figure 3). Evaluation of a biopsy sample identified malignant bone neoplasia that was classified as grade 3 (high grade) osteoblastic osteosarcoma. Therefore, the lesion was excised, with tumor-free margins, and part of the adjacent dura mater was resected because of suspicion of neoplastic involvement. The patient presented clinical improvement after the tumor resection and was discharged to outpatient follow-up.




DISCUSSION

Here, we report a case of primary osteosarcoma of the skull, an extremely rare neoplasm at that location. Approximately 100 cases have been described in the literature^(2,4,5). The prognosis is worse than is that of osteosarcoma involving the bones of the appendicular skeleton, osteosarcoma of the skull presenting a lower response to aggressive multimodal therapy, with a five-year survival rate below 10%^(1–6).

In a clinical context in which the patient presents bone pain associated with a soft tissue mass, with suspected aggressive lesion, the investigation should begin with conventional radiology, because it can demonstrate important aspects of osteosarcoma, such as a periosteal reaction and cortical bone destruction. Computed tomography should be performed in order to characterize the dissemination of the tumor into the medullary cavity, as well as to provide images of the calcified neoplastic component, as well as of the involvement of the soft tissue and cortical bone, which are fundamental to the surgical planning. Magnetic resonance imaging has become an effective modality for evaluating such tumors, particularly for mapping the intraosseous/intracranial spread of the tumor, involvement of the soft tissues, and involvement of the neurovascular bundle. On T1-weighted images, the solid, non-mineralized portions of osteosarcoma generally appear as areas of low-to-medium signal intensity. On T2-weighted images, the tumor shows high signal intensity^(1,6). The typical pattern of contrast uptake by the lesion is one of intense heterogeneous impregnation.

The imaging-based differential diagnoses of osteosarcoma include hemangioma, which is characterized by multilocular lytic foci or coarse vertical striations; giant cell tumor, which is typically well-circumscribed but can cause thinning of the cortical bone and usually manifests as a lytic lesion; atypical meningioma, in which there is cortical bone destruction and extradural involvement; and metastases from cancer of the thyroid or digestive tract, which can present as expansile lesions accompanied by bone destruction and invading the soft tissues. Despite their similarity to osteosarcoma, all of those diseases are more commonly found in patients who are considerably older^(3,5,7,8).

Because of the rarity of the osteosarcoma of the skull, it is difficult to make the definitive diagnosis on the basis of imaging data. However, the knowledge that it is a destructive lesion associated with a soft tissue mass and an aggressive periosteal reaction can facilitate the diagnosis⁽²⁾. The treatment involves complete surgical resection of the lesion, with tumor-free margins, as well as chemotherapy and radiotherapy^(1–7).


REFERENCES

1. Greenspan A. Radiologia ortopédica – uma abordagem prática. 5ª ed. Rio de Janeiro: Guanabara Koogan; 2012.

2. Mascarenhas L, Peteiro A, Ribeiro CA, et al. Skull osteosarcoma: illustrated review. Acta Neurochir (Wien). 2004;146:1235–9.

3. Fukunaga M. Low-grade central osteosarcoma of the skull. Pathol Res Pract. 2005;201:131–5.

4. Chander B, Ralte AM, Dahiya S, et al. Primary osteosarcoma of the skull. A report of 3 cases. J Neurosurg Sci. 2003;47:177–81.

5. Patel AJ, Rao VY, Fox BD, et al. Radiation-induced osteosarcomas of the calvarium and skull base. Cancer. 2011;117:2120–6.

6. Salvati M, Ciappetta P, Raco A. Osteosarcomas of the skull. Clinical remarks on 19 cases. Cancer. 1993;71:2210–6.

7. Reis C, Genden EM, Bederson JB, et al. A rare spontaneous osteosarcoma of the calvarium in a patient with long-standing fibrous dysplasia: CT and MR findings. Br J Radiol. 2008;81:e31–4.

8. Tokgoz N, Oner YA, Kaymaz M, et al. Primary intraosseous meningioma: CT and MRI appearance. AJNR Am J Neuroradiol. 2005;26:2053–6.










1. MD, Radiologist at Prodigy – Diagnóstico por Imagem, Brasília, DF, Brazil
2. MD, Radiologist, Head of the Radiology and Diagnostic Imaging Residency Program at the Hospital de Base do Distrito Federal (HBDF), Brasília, DF, Brazil
3. MD, Radiologist for Grupo Fleury – Hospital São Luiz, São Paulo, SP, Brazil
4. MD, Radiologist at Hospital Israelita Albert Einstein, Interventional Radiologist at the Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HC-FMUSP)/Instituto do Câncer do Estado de São Paulo (Icesp), São Paulo, SP, Brazil
5. MD, Radiologist at Exame – Imagem e Laboratório, Brasília, DF, Brazil

Mailing address:
Dr. Gabriel Lacerda Fernandes
SQSW 306, Bloco B, ap. 509, Setor Sudoeste
Brasília, DF, Brazil, 70673-432
E-mail: gabriellacerdafernandes@gmail.com

Received June 10, 2014.
Accepted after revision September 13, 2014.

Study conducted at the Hospital de Base do Distrito Federal (HBDF), Brasília, DF, Brazil.