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DOI: 10.1055/s-0036-1596056
Osteochondroma Presenting as a Calcified Mass in the Sellar Region and Review of the Literature
Publication History
05 October 2015
26 August 2016
Publication Date:
30 November 2016 (online)
Abstract
Objective Osteochondroma (OC) is the most common benign bone neoplasm. It infrequently occurs in the cranial cavity as a calcified lesion and very rarely presents in the sellar region. The present study summarizes the knowledge about OCs of the sellar region.
Methods We searched the literature search for the clinical appearance of OCs and other calcified pathologies occurring in the sellar region.
Results A total of 21 English-language articles published from 1961 to 2015 documented cases of calcified lesions in the sellar region including cerebral aneurysm, chondroid chordoma, chondroma, craniopharyngioma, OC, odontome, osteoma, pituitary adenoma, pituitary stone, Rathke cleft cyst, retinoblastoma, schwannoma, and xanthogranuloma. Among them, six were OC cases: three in the parasellar region and three in the sellar-suprasellar region. Patients with sellar-suprasellar OCs presented with visual loss and hypopituitarism; patients with parasellar OCs did not show these symptoms. OCs appeared as irregular and multilobulated calcifications on X-ray and computed tomography. On magnetic resonance imaging, OCs showed variable intensity on T1-weighted sequences and consistently heterogenous intensity on T2. Four patients underwent transcranial tumor resection, and the transsphenoidal route was selected for one. Five of the six resulted in a partial resection or internal decompression with a satisfactory outcome.
Conclusions Calcified tumors occurring in the sellar region may be OCs, especially if they appear as irregular multilobulated calcification.
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References
- 1 Lee KJ, Goodrich I. Sellar lesions. Otolaryngol Head Neck Surg (1979) 1980; 88 (05) 536-543
- 2 Baena-Ocampo LdelC, Ramirez-Perez E, Linares-Gonzalez LM, Delgado-Chavez R. Epidemiology of bone tumors in Mexico City: retrospective clinicopathologic study of 566 patients at a referral institution. Ann Diagn Pathol 2009; 13 (01) 16-21
- 3 Bergovec M, Kubat O, Smerdelj M, Seiwerth S, Bonevski A, Orlic D. Epidemiology of musculoskeletal tumors in a national referral orthopedic department. A study of 3482 cases. Cancer Epidemiol 2015; 39 (03) 298-302
- 4 Haddad GF, Haddad FS, Zaatari G. Dural osteochondroma: case report, review of the literature and proposal of a new classification. Br J Neurosurg 1998; 12 (04) 380-384
- 5 Castillo M, Hudgins PA, Hoffman Jr JC. Lockjaw secondary to skull base osteochondroma: CT findings. J Comput Assist Tomogr 1989; 13 (02) 338-339
- 6 Agildere M, Senaati S, Eryilmaz M, Besim A. Parasellar osteochondroma. AJR Am J Roentgenol 1990; 155 (04) 900
- 7 Altinörs N, Bavbek M, Caner H, Ağildere M, Arikan U, Demirhan B. Interesting radiologic findings in suprasellar mass lesions. Report of three cases. Kobe J Med Sci 1998; 44 (02) 81-90
- 8 Bakdash H, Alksne JF, Rand RW. Osteochondroma of the base of the skull causing an isolated oculomotor nerve paralysis. Case report emphasizing microsurgical techniques. J Neurosurg 1969; 31 (02) 230-233
- 9 Inoue T, Takahashi N, Murakami K, Nishimura S, Kaimori M, Nishijima M. Osteochondroma of the sella turcica presenting with intratumoral hemorrhage. Neurol Med Chir (Tokyo) 2009; 49 (01) 37-41
- 10 Richards WW, Thompson MC. Suprasellar osteochondroma with chiasmal syndrome. Arch Ophthalmol 1961; 65: 437-441
- 11 Sato K, Kodera T, Kitai R, Kubota T. Osteochondroma of the skull base: MRI and histological correlation. Neuroradiology 1996; 38 (01) 41-43
- 12 Agarwal A, Agarwal K, Lee HK. Xanthogranuloma of the sellar region. A case report. Neuroradiol J 2012; 25 (02) 181-184
- 13 Aoki A, Mori K, Tajima A, Maeda M. Sellar chondroma—case report. Neurol Med Chir (Tokyo) 1999; 39 (12) 870-874
- 14 Bejjani GK, Donahue DJ, Selby D, Cogen PH, Packer R. Association of a suprasellar mass and intraocular retinoblastoma: a variant of pineal trilateral retinoblastoma?. Pediatr Neurosurg 1996; 25 (05) 269-275
- 15 Bakhtiar Y, Arita K, Hirano H. , et al. Prolactin-producing pituitary adenoma with abundant spherical amyloid deposition masquerading as extensive calcification. Neurol Med Chir (Tokyo) 2010; 50 (11) 1023-1026
- 16 Bokemeyer C, Frank B, Brandis A, Weinrich W. Giant aneurysm causing frontal lobe syndrome. J Neurol 1990; 237 (01) 47-50
- 17 Chen CY, Ying SH, Yao MS, Chiu WT, Chan WP. Sphenoid sinus osteoma at the sella turcica associated with empty sella: CT and MR imaging findings. AJNR Am J Neuroradiol 2008; 29 (03) 550-551
- 18 de Faria PR, Cardoso SV, Rocha A, Gomes DC, de Castro SC, Loyola AM. Intracranial compound odontome. J Craniomaxillofac Surg 2009; 37 (07) 376-379
- 19 Garnett MR, Puget S, Grill J, Sainte-Rose C. Craniopharyngioma. Orphanet J Rare Dis 2007; 2: 18
- 20 Hirosawa RM, Santos AB, França MM. , et al. Intrasellar chondroid chordoma: a case report. ISRN Endocrinol 2011; 2011: 259392
- 21 Kertmen H, Turkoglu E, Başkaya MK. A calcified sellar lesion. J Clin Neurosci 2010; 17 (07) 897-956
- 22 Müller HL. Craniopharyngioma. Endocr Rev 2014; 35 (03) 513-543
- 23 Ogawa Y, Tominaga T. A partially ossified solid and cystic Rathke cleft cyst. J Neurosurg 2010; 112 (06) 1324-1326
- 24 Sharifi G, Bakhtevari MH, Alghasi M. , et al. Hard calcified intrasellar schwannoma mimicking pituitary adenoma: a case report and review of the literature. Clin Neurol Neurosurg 2015; 137: 38-43
- 25 Tanriover N, Kucukyuruk B, Hatipoglu E, Comunoglu N. Pituitary stone: a case report and review of the literature. Turk Neurosurg 2014; 24 (06) 967-973