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Endoscopic endonasal resection of clival xanthoma: case report and literature review

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Abstract

Bone xanthoma is an extremely rare and benign tumor in terms of its nature and growth over time. We describe the first case coexisting with ventriculomegaly secondary to aqueduct stenosis (non-tumoral hydrocephalus), the second xanthoma of the clivus described to date. The patient was a 51-year-old woman with headaches and absence seizures. Axial T1-weighted MRI showed a well-demarcated, hypointense, osteolytic, 25 × 18 × 15 mm lesion with cortical erosion located at the right margin of the clivus. Sagittal T2-weighted MRI demonstrated a hypointense mass without associated edema. Sagittal gadolinium-enhanced T1-weighted MRI showed contrast uptake with a partially hypointense rim. The increased ventricular size without periventricular edema was associated with aqueduct stenosis, and there was no contiguity with the tumor. A neuronavigation image-guided transsphenoidal approach was chosen to perform a macroscopically complete resection. Intraoperative histopathological study showed a chordoma of the clivus. Exhaustive postsurgical study revealed the benign nature of a bone xanthoma. Given the finding of a clival lesion, the differential diagnosis is essentially with other malignant entities with a rapidly fatal outcome, such as metastases, or with a possible invasive evolution, such as clivus chordomas. This report describes the clinical, radiological, and pathological keys for such differentiation in order to avoid unnecessarily aggressive treatment with ablative surgery and radiotherapy.

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Abbreviations

CSF:

Cerebrospinal fluid

CT:

Computed tomography

GFAP:

Glial fibrillary acidic protein

MRI:

Magnetic resonance image

References

  1. Alden KJ, McCarthy EF, Weber KL (2008) Xanthoma of bone: a report of three cases and review of the literature. Iowa Orthop J 28:58–64

    PubMed Central  PubMed  Google Scholar 

  2. Asano K, Sato J, Matsuda N, Ohkuma H (2012) A rare case of primary bone xanthoma of the clivus. Brain Tumor Pathol 29:123–128

    Article  PubMed  Google Scholar 

  3. Elwood ET, Shahwan TG, Dajani N, Murray JD (2005) Isolated xanthoma of the frontal bone. J Craniofac Surg 16:391–394

    Article  PubMed  Google Scholar 

  4. Emery PJ, Gore M (1982) An extensive solitary xanthoma of the temporal bone, associated with hyperlipoproteinaemia. J Laryngol Otol 96:451–457

    Article  CAS  PubMed  Google Scholar 

  5. Ferlito A, Recher G, Bordin S (1983) Involvement of the temporal bone in hyperlipidemic xanthomatosis. Otolaryngol Head Neck Surg 91:100–104

    CAS  PubMed  Google Scholar 

  6. Fernandez-Miranda JC, Gardner PA, Snyderman CH, Devaney KO, Mendenhall WM, Suárez C, Rinaldo A, Ferlito A (2013) Clival chordomas: A pathological, surgical, and radiotherapeutic review. Head Neck. Jun 26. doi: 10.1002/hed.23415 [Epub ahead of print]

  7. Friedman O, Hockstein N, Willcox TO Jr, Keane WM (2000) Xanthoma of the temporal bone: a unique case of this rare condition. Ear Nose Throat J 79:433–436

    CAS  PubMed  Google Scholar 

  8. Huang CF, Cheng SN, Hung CH, Liu MY, Harn HJ, Yuh YS, Lee MY (2000) Xanthoma of bone in a normolipidemic child: report of one case. Acta Paediatr Taiwan 41:158–160

    CAS  PubMed  Google Scholar 

  9. Jackler RK, Brackmann DE (1987) Xanthoma of the temporal bone and skull base. Am J Otol 8:111–115

    CAS  PubMed  Google Scholar 

  10. Koch HJ Jr, Lewis JS (1956) Hyperlipidemic xanthomatosis with associated osseous granuloma; a clinical report. N Engl J Med 255:387–388

    Article  PubMed  Google Scholar 

  11. Koutourousiou M, Gardner PA, Tormenti MJ, Henry SL, Stefko ST, Kassam AB, Fernandez-Miranda JC, Snyderman CH (2012) Endoscopic endonasal approach for resection of cranial base chordomas: outcomes and learning curve. Neurosurgery 71(3):614–624

    Article  PubMed  Google Scholar 

  12. Kuroiwa T, Ohta T, Tsutsumi A (2000) Xanthoma of the temporal bone: case report. Neurosurgery 46:996–998

    CAS  PubMed  Google Scholar 

  13. Matoba M, Tonami H, Kuginuki M, Yamamoto I, Akai T, Iizuka H (2004) CT and MRI findings of xanthoma in the orbitofrontal region. Radiat Med 22:116–119

    PubMed  Google Scholar 

  14. Meyers SP, Hirsch WL Jr, Curtin HD, Barnes L, Sekhar LN, Sen C (1992) Chordomas of the skull base: MR features. AJNR Am J Neuroradiol 13:1627–1636

    CAS  PubMed  Google Scholar 

  15. Michele SM, Samuel CL (2003) Chordomas of the skull base: manifestations and management. Curr Opin Otolaryngol Head Neck Surg 11:324–327

    Article  Google Scholar 

  16. Muthusamy KA, Azmi K, Narayanan P, Rajagopalan R, Rahman NA, Waran V (2008) Bilateral temporal bone xanthoma. Case report. J Neurosurg 108:361–364

    Article  PubMed  Google Scholar 

  17. Tadmor R, Davis KR, Roberson G, New PF, Taveras JM (1977) Computed tomography in extra-dural epidermoid and xanthoma. Surg Neurol 7:371–375

    CAS  PubMed  Google Scholar 

  18. Turk C, Bilginer B, Benli K, Yavuz K, Saglam A, Ziyal IM (2010) Bilateral temporal bone xanthomas in type II hypercholesterolemia. Turk Neurosurg 20:533–535

    PubMed  Google Scholar 

  19. Yokoyama E, Ito J, Tokiguchi S, Tanaka R, Oyanagi K, Ikuta F (1990) A case of xanthoma of the skull. Jpn J Clin Radiol 35:1057–1060

    CAS  Google Scholar 

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Correspondence to Laura González-García.

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Comments

Oliver Bozinov, Zurich, Switzerland

Gonzalez-Garcia and colleagues present a very interesting case that has been mistakenly diagnosed first as a malignant tumor and turned out to be a very rare xanthoma of the clivus coexisting with ventriculomegaly secondary to aqueduct stenosis (non-tumoral hydrocephalus). This case report is nicely described and does have an impact on neurosurgical daily life. Most colleagues would assume a malignant case as well, but then again, sometimes a biopsy might be enough to treat such a lesion (at first) or strong intraoperative frozen section can be of a big help as well. Those cases have to be frequently mentioned/published to remind every colleague of possible differential diagnosis.

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González-García, L., Asenjo-García, B., Bautista-Ojeda, M.D. et al. Endoscopic endonasal resection of clival xanthoma: case report and literature review. Neurosurg Rev 38, 765–769 (2015). https://doi.org/10.1007/s10143-015-0630-6

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  • DOI: https://doi.org/10.1007/s10143-015-0630-6

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