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Solitary intracranial osteoma with attachment to the falx: a case report



Intracranial osteomas are uncommon lesions that usually arise from the inner table of the cranium. There are few reports in the literature of intracranial osteomas with meninges attachment and without direct relation with the skull bone; these osteomas were mostly attached with dura. We report a rare osteoma with falx attachment.


A 64-year-old woman presented with a 3-month history of intermittent tinnitus and dizziness. The scout film of petrous bone computed tomography scan revealed a high-density lesion in the frontal area. Magnetic resonance imaging showed a 2.5-cm mass attached to the surface of the falx in the right frontal parasagittal area. The patient underwent right frontal craniotomy, and a bony hard mass was found located in the right frontal parasagittal region extra-axially, with its medial surface attached to the falx. It could not be broken down by the cavitron ultrasonic surgical aspirator or even the cutting loop and was detached from the falx and removed in one piece. Histopathological examination showed a nodule with bony trabeculae and bone marrow tissue, compatible with osteoma. The postoperative course was uneventful, and the patient was discharged from the hospital with no neurological deficits one week after operation.


This is the first case report in the English literature of an intracranial osteoma arising from the falx. Because of their slow growth and their locations in silent brain areas, intracranial osteomas are usually diagnosed incidentally. Surgical resection is the primary treatment choice.


Osteomas are benign neoplasms consisting of mature normal osseous tissue. They commonly arise from the long bones of the extremities. In the head and neck region, they are usually found in the sinuses, facial bones, skull, and mandible [19]. Intracranial osteomas are rarely located intradurally without the involvement of bony structure [10]. The mechanism that triggers the formation of intracranial intradural osteomas without bony structure involvement remains unclear. We report the clinical presentation, pathologic picture, and intra-operative findings of an intradural osteoma with attachment to the falx.

Case presentation

A 64-year-old woman presented with a 3-month history of intermittent bilateral tinnitus, occasionally accompanied by dizziness. She had no history of major head injury or systemic infection. She visited an otology clinic where a temporal bone computed tomography (CT) scan of the petrous bone, semicircular canal, and hearing apparatus showed neither temporal bone lesions nor associated lesions in the ear; however, the scout film of the CT scan incidentally revealed a radiopaque nodule in the frontal area (Figure 1). Magnetic resonance imaging (MRI) revealed a 2.5-cm mass with minimal marginal enhancement in the right parasagittal region in axial and coronal contrast-enhanced T1-weighted images. The mass was hyperintense with a hypointense rim in T2-weighted images (Figure 2). The provisional diagnosis was a calcified meningioma originating from the falx. The patient was then referred to our neurosurgical department for surgical removal of the tumor. On admission, the physical and neurological findings were unremarkable. Her cognitive function was intact, and she had no sensorimotor deficit. Right frontal craniotomy was performed. After opening of the dura and retraction of the parasagittal gyri, a tumor was found attached to the falx in the mesial frontal lobe extra-axially. The tumor was as hard as bone and could not be broken by bipolar forceps, Cavitron ultrasonic surgical aspirators, or even cutting loops. The tumor had to be dissected apart from the falx surface in one piece (Figure 3).

Figure 1
figure 1

Scout film of the petrous bone computed tomography (CT) scan. It showed a dense radiopaque mass in the frontal area.

Figure 2
figure 2

Magnetic resonance imaging (MRI). Axial and coronal contrast-enhanced T1-weighted images with fat saturation show a 2.5-cm falx-based mass with minimal marginal enhancement in the right parasagittal region. The mass is hyperintense with a hypointense rim on T2-weighted images.

Figure 3
figure 3

Gross appearance of the osteoma. The medial surface (arrow) was attached on the falx.

Pathologic examination revealed lamellated bony trabeculae lined by osteoblasts, and the intertrabecular marrow spaces were occupied by loose fibrovascular tissue (Figure 4).

Figure 4
figure 4

Histopathology of the resected specimen. Lamellated bony trabeculae and the intertrabecular space occupied by loose fibrovascular tissue as observed during pathological examination (original magnification × 20).

The postoperative course was uneventful. The patient was discharged from the hospital with no neurological deficits after suture removal. During six months of post-operative follow-up, the frequency and degree of dizziness and tinnitus decreased progressively.


Osteomas are recognized as benign bone neoplasms of uncertain etiology. In the head, osteomas often arise from the periosteum of the frontal or ethmoid sinuses and the mandible [19]. Less often, osteomas may originate from the cranial bone in the convexity or the inner layer of the dura mater [1114]. Osteomas attached to the meninges without relationship with the bone are even rarer. We reviewed related literature and summarized the data (Table 1). Fallon et al. [15] found intracranial meningeal osteomas in 5% of 200 adult autopsies. The tumors were usually located at the convexity dura and falx junction around the superior sagittal sinus. Solitary intracranial osteomas arising from the inner layer of the dura mater with no involvement of the cranium have been reported [11, 12, 14, 1618]. The tumors usually establish themselves with a wide base and grow inward as an expanding mass with a well-defined border [12]. The osteoma we report on here was a fungating nodule with a narrow neck attached to the falx.

Table 1 Patients with intracranial osteoma attached to the meninges without relationship with the bone reported in the literature

On the basis of their natural history, intracranial osteomas are more benign than osteomas of the frontal sinuses [19]. The tumor may cause pressure-related symptoms by compressing or displacing the underlying brain, and this depends on the location of the mass. When it appears in a silent area, it rarely causes sensorimotor deficit. Most commonly, such tumors are detected in patients presenting with headache or other non-specific complaints. The high frequency of head trauma history has been noted, and the possible importance of head trauma as a causative factor in cranial osteomas has been proposed [17, 20]. In our case, there was no history of major head trauma. This intracranial osteoma was found incidentally on the scout image during a temporal bone CT scan.

The pathogenesis of osteomas without bone involvement is still unknown. A dural osteoma can be confused with “meningeal ossification or meningeal calcification” originating from the dura or the falx because of the similarities in CT and MRI examinations and microscopic appearance [15]. This new bone might not represent a true neoplasm but possibly an osteogenic change in the cerebral meningeal tissue. However, meningeal ossifications are commonly multicentric and located on the dural-falx junction along the both sides of the superior sagittal sinus [21].

The factors leading to the genesis of intracranial meningeal osteomas are as yet unknown. New bone formation from the dura or falx has been postulated as one of the causes because the meninges may function as the periosteum of the inner table of the skull [10, 12, 15].


In our patient, the operative findings confirmed an intracranial bony hard mass arising from the falx. This intradural osteoma might have been the result of a focal falx osteogenic activity. To the best of our knowledge, this is the first report of an intracranial osteoma that originated from the falx in an otherwise normal patient.


The patient consented to the study and publication of this case report and images. A written consent is available for review.



Computed tomography


Magnetic resonance imaging.


  1. Armitage G: Osteoma of the frontal sinus: with particular reference to its intracranial complications and with report of a case. Br J Surg. 1931, 18: 565-580. 10.1002/bjs.1800187205.

    Article  Google Scholar 

  2. Bingas B: Tumours of the base of the skull. Handbook of Clinical Neurology. Edited by: Vinken PJ, Bruyn GW. 1974, New York, Amsterdam: Elsevier Publishing Co., Inc, 136-233.

    Google Scholar 

  3. Campbell EH, Gottschalk RB, Albany AB: Osteoma of frontal sinus and penetration of lateral ventricle with intermittent pneumocephalus. JAMA. 1938, 111: 239-241. 10.1001/jama.1938.72790290001007.

    Article  Google Scholar 

  4. Diaz F, Latchow R, Duvall AJ, Quick CA, Erickson DL: Mucoceles with intracranial and extracranial extensions. J Neurosurg. 1978, 48: 284-288. 10.3171/jns.1978.48.2.0284.

    Article  CAS  PubMed  Google Scholar 

  5. Suen JY, Meyers EH: Cancer of the Head and Neck. 1981, New York: Churchill, Livingstone

    Google Scholar 

  6. Lunardi P, Missori P, Di Lorenzo N, Fortuna A: Giant intracranial mucocele secondary to osteoma of the frontal sinuses: report of two cases and review of the literature. Surg Neurol. 1993, 39: 46-48. 10.1016/0090-3019(93)90109-E.

    Article  CAS  PubMed  Google Scholar 

  7. Pool JL, Potanos JN, Keueger EG: Osteomas and mucocele of the frontal paranasal sinuses. J Neurosurg. 1962, 19: 130-135. 10.3171/jns.1962.19.2.0130.

    Article  CAS  PubMed  Google Scholar 

  8. Russell DS, Rubinstein LJ: Pathology of Tumours of the Nervous System. 1989, London: Edward Arnold

    Google Scholar 

  9. Spjut HJ, Dorfman HD, Fechner RE, Ackerman LV: Tumours of Bone and Cartilage. 1971, Washington DC: Armed Forces Institute of Pathology

    Google Scholar 

  10. Lee ST, Lui TN: Intracerebral osteoma: case report. Br J Neurosurg. 1997, 11: 250-252. 10.1080/02688699746357.

    Article  CAS  PubMed  Google Scholar 

  11. Cheon JE, Kim JE, Yang HJ: CT and pathologic findings of a case of subdural osteoma. Korean J Radiol. 2002, 3: 211-223. 10.3348/kjr.2002.3.3.211.

    Article  PubMed Central  PubMed  Google Scholar 

  12. Choudhury AR, Haleem A, Jjan GT: Solitary intradural intracranial osteoma. Brit J Neurosurg. 1995, 9: 557-559. 10.1080/02688699550041232.

    Article  CAS  Google Scholar 

  13. Rand CW: Osteoma of the skull. Report of two cases, one being associated with a large intracranial endothelioma. Arch Surg Chicago. 1923, 6: 573-586. 10.1001/archsurg.1923.01110180146005.

    Article  Google Scholar 

  14. Sugimoto K, Nakahara I, Nishikawa M, Tanaka M, Terashima T, Yanagihara H, Hayashi J: Osteoma originating in the dura: a case report. No Shinkei Geka. 2001, 29: 993-996. [In Japanese]

    CAS  PubMed  Google Scholar 

  15. Fallon MD, Ellerbrake D, Teitelbaum SL: Meningeal osteomas and chronic renal failure. Hum Pathol. 1982, 13: 449-453. 10.1016/S0046-8177(82)80027-0.

    Article  CAS  PubMed  Google Scholar 

  16. Aoki H, Nakase H, Sakaki T: Subdural osteoma. Acta Neurochir. 1998, 140: 727-728. 10.1007/s007010050171.

    Article  CAS  PubMed  Google Scholar 

  17. Dukes HT, Odom GL: Discrete intradural osteoma. Report of a case. J Neurosurg. 1962, 19: 251-253. 10.3171/jns.1962.19.3.0251.

    Article  CAS  PubMed  Google Scholar 

  18. Akiyama M, Tanaka T, Hasegawa Y, Chiba S, Abe T: Multiple intracranial subarachnoid osteomas. Acta Neurochir. 2005, 147: 1085-1089. 10.1007/s00701-005-0588-1.

    Article  CAS  PubMed  Google Scholar 

  19. Vaket A, Reuck JD, Thiery E, Eecken HV: Intracerebral osteoma: a clinicopathologic and neuropsychologic case study. Childs Brain. 1983, 10: 281-285.

    Google Scholar 

  20. Cushing H: Experiences with orbito-ethmoidal osteomata having intracranial complications. With the report of four cases. Surg Gynecol Obstet. 1927, 44: 721-742.

    Google Scholar 

  21. Jung TY, Jung S, Jin SG, Jin YH, Kim IY, Kang SS: Solitary intracranial subdural osteoma: intraoperative findings and primary anastomosis of an involved cortical vein. J Clin Neurosci. 2007, 14: 468-470. 10.1016/j.jocn.2005.11.021.

    Article  PubMed  Google Scholar 

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Correspondence to Tai-Ngar Lui.

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Authors' contributions

SMC participated in the preparation of the manuscript, literature search and drafted the manuscript. CCC participated in its design and coordination. CHT accomplished and analysed the CT scans and MRI. SMJ carried out the tissue preparation, (immuno)histology and edited the manuscript for its scientific content. TNL was responsible for the operations, follow-up of the patients and data preparation and conceived of the study. All authors read and approved the final manuscript.

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Chen, SM., Chuang, CC., Toh, CH. et al. Solitary intracranial osteoma with attachment to the falx: a case report. World J Surg Onc 11, 221 (2013).

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