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Cerebellar hemangioblastoma associated with diffuse neonatal hemangiomatosis in an infant

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Abstract

Introduction

Hemangioblastomas (HBLs) comprise approximately 2 % of all primary central nervous system (CNS) tumors. Although histological features of this rare tumor are generally benign, its outcome is often unfavorable due to high risk of recurrence and multifocal localization. HBLs can be detected as sporadic or associated with Von Hippel–Lindau disease. Diffuse neonatal hemangiomatosis (DNH) presents with multiple, progressive, rapidly growing cutaneous hemangiomas associated with widespread visceral hemangiomas in the liver, lungs, gastrointestinal tract, brain, and meninges. DNH with predominant CNS involvement is rarely reported. Herein, we present a neonatal case of cerebellar HBL associated with DNH.

Case report

A 5-day-old male baby was referred with complaints of multiple cutaneous lesions. Purple papules were noted on the trunk, extremities, and the head. Thoracic magnetic resonance imaging demonstrated multiple hyperintense lesions on the chest wall and apex of the right lung. On MRI, a 3 × 2-cm mass lesion in the right cerebellar hemisphere was detected. Total resection of the mass and ventriculoperitoneal shunting was performed. Histopathologic examination confirmed the diagnosis of HBL. Steroid therapy was administered for disseminated hemangiomatosis, and the lesions showed regression; the patient showed good clinical recovery. The parents refused further treatment, and he was out of our control when he was 9 months old.

Conclusion

According to our knowledge, the presented newborn is the second case of cerebellar HBL associated with diffuse skin and visceral hemangiomas in the English medical literature. Clinicians must be vigilant about the predictive value of visceral and/or cutaneous hemangioma for an associated intracranial HBL.

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References

  1. Acikalin MF, Oner U, Tel N, Pasaoglu O, Altinel F (2003) Supratentorial hemangioblastoma: a case report and review of the literature. Arch Pathol Lab Med 127:e382–e384

    PubMed  Google Scholar 

  2. Al-Kaabi A, Yanofsky R, Bunge M, Hyman J, Rafay MF (2009) Diffuse hemangiomatosis with predominant central nervous system involvement. Pediatr Neurol 40:54–57

    Article  PubMed  Google Scholar 

  3. Altinoz MA, Santaguida C, Guiot MC, Del Maestro R (2005) Spinal hemangioblastoma containing metastatic renal cell carcinoma in von Hippel-Lindau disease. Case report and review of the literature. J Neurosurg Spine 3:495–500

    Article  PubMed  Google Scholar 

  4. Conway JE, Chou D, Clatterbuck RE, Brem H, Long DM, Rigamonti D (2001) Hemangioblastomas of the central nervous system in von Hippel–Lindau syndrome and sporadic disease. Neurosurgery 48:55–63

    PubMed  CAS  Google Scholar 

  5. de la Monte SM, Horowitz SA (1989) Hemangioblastomas: clinical and histopathological factors correlated with recurrence. Neurosurgery 25:695–698

    Article  PubMed  Google Scholar 

  6. Ertas G, Altundag MB, Ucer AR, Cankal F, Altundag K (2005) Treatment of recurrent cerebellar hemangioblastoma with external radiotherapy in a patient with von Hippel- Lindau disease: a case report and review of the literature. J Neurooncol 73:273–275

    Article  PubMed  Google Scholar 

  7. Georg AE, Lunsford LD, Kondziolka D, Flickinger JC, Maitz A (1997) Hemangioblastoma of the posterior fossa. The role of multimodality treatment. Arq Neuropsiquiatr 55:278–286

    Article  PubMed  CAS  Google Scholar 

  8. Green JS, Bowmer MI, Johnson GJ (1986) Von Hippel–Lindau disease in a Newfoundland kindred. Can Med Assoc J 134:133–146

    CAS  Google Scholar 

  9. Ho VB, Smirniotopoulos JG, Murphy FM, Rushing EJ (1992) Radiologic–pathologic correlation: hemangioblastoma. AJNR Am J Neuroradiol 13:1343–1352

    PubMed  CAS  Google Scholar 

  10. Ho V, Krol A, Bhargava R, Osiovich H (2000) Diffuse neonatal haemangiomatosis. J Paediatr Child Health 36:286–289

    Article  PubMed  CAS  Google Scholar 

  11. Hussein MR (2007) Central nervous system capillary haemangioblastoma: the pathologist's viewpoint. Int J Exp Pathol 88:311–324

    Article  PubMed  CAS  Google Scholar 

  12. Jääskeläinen JE, Niemelä M (2006) Hemangioblastoma and von Hippel-Lindau disease. In: Tonn JC, Westphal M, Rutka JT, Grossman SA (eds) Neuro-oncology of CNS tumors. Springer, Berlin, pp 235–242

    Chapter  Google Scholar 

  13. Lamiell JM, Salazar FG, Hsia YE (1989) Von Hippel-Lindau disease affecting 43 members of a single kindred. Medicine 68:1–29

    Article  PubMed  CAS  Google Scholar 

  14. Lopriore E, Markhorst DG (1999) Diffuse neonatal haemangiomatosis: new views on diagnostic criteria and prognosis. Acta Paediatr 88:93–97

    Article  PubMed  CAS  Google Scholar 

  15. Neumann HP, Eggert HR, Scheremet R et al (1992) Central nervous system lesions in von Hippel-Lindau syndrome. J Neurol Neurosurg Psychiatry 55:898–901

    Article  PubMed  CAS  Google Scholar 

  16. Obrador S, Martin-Rodriquez JG (1977) Biological factors involved in the clinical features and surgical management of cerebellar hemangioblastomas. Surg Neurol 7:79–85

    PubMed  CAS  Google Scholar 

  17. Patrice SJ, Sneed PK, Flickinger JC et al (1996) Radiosurgery for hemangioblastoma: results of a multiinstitutional experience. Int J Radiat Oncol Biol Phys 35:493–499

    Article  PubMed  CAS  Google Scholar 

  18. Sundaram C, Rammurti S, Reddy JJ, Prasad SS, Purohit AK (2003) Hemangioblastoma: a study of radiopathologic correlation. Neurol India 51:373–375

    PubMed  CAS  Google Scholar 

  19. Tekkök IH, Sav A (2006) Supratentorial cystic hemangioblastoma with infratentorial extension—a unique location and a rare infant case. Childs Nerv Syst 22:1177–1181

    Article  PubMed  Google Scholar 

  20. Wang C, Zhang J, Liu A, Sun B (2001) Surgical management of medullary hemangioblastoma. Report of 47 cases. Surg Neurol 56:218–226, Discussion, 226–227

    Article  PubMed  CAS  Google Scholar 

  21. Wananukul S, Voramethkul W, Nuchprayoon I, Seksarn P (2006) Diffuse neonatal hemangiomatosis: report of 5 cases. J Med Assoc Thai 89:1297–1303

    PubMed  Google Scholar 

  22. Young RS, Zalneraitis EL, Bauman ML (1981) Disseminated neonatal hemangiomatosis: successful hepatic resection with subsequent development of hydrocephalus. J Pediatr Surg 16:752–753

    Article  PubMed  CAS  Google Scholar 

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Conflict of interest

The authors do not report any conflict of interest concerning the materials or methods used in this study or the findings specified in this paper.

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Correspondence to Ekrem Unal.

Additional information

This case report was presented as a poster presentation at 14th International Symposium on Pediatric Neuro-Oncology, 20–23 June 2010, Vienna, Austria.

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Patiroglu, T., Sarici, D., Unal, E. et al. Cerebellar hemangioblastoma associated with diffuse neonatal hemangiomatosis in an infant. Childs Nerv Syst 28, 1801–1805 (2012). https://doi.org/10.1007/s00381-012-1858-x

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