Literature DB >> 28762040

Case update on cranial osteopetrosis: which is the role of the neurosurgeon?

Irene Stella1, Matthieu Vinchon2, Pierre Guerreschi3, Eva De Berranger4, Ikram Bouacha5.   

Abstract

PURPOSE: Osteopetrosis (OP) is a rare skeletal disease, which can affect the skull base and calvaria. A multidisciplinary approach is mandatory and patient may need neurosurgical care. Few observations have been published, and optimal management of OP is not established yet.
METHOD: We report a case of an infant with OP diagnosed at 5 months, who presented signs of intracranial hypertension associated with unilateral blindness. Bone marrow allograft was performed at 6 months of age. At neurosurgical first examination at 11 months, the child was hypotonic, with severe amblyopia; features of bicoronal synostosis were appreciated, with tense anterior fontanel bulging indicating synostotic oxycephaly. Head circumference had decreased from +3 SD to +1SD. Cerebral CT scan showed reduction of intracranial volume, inward thickening of the calvaria, bilateral stenosis of optic canal, ventricular dilatation, enlarged arachnoid spaces, and tonsillar herniation. We performed cranial vault expansion with frontal advancement and bi parietal decompression, thinning of the inner table, unroofing of the left orbit and optic canal in order to obtain optic nerve decompression.
RESULTS: Postoperative course was uneventful, and the patient was discharged on day 8. Vision was unchanged but rapid improvement of axial tonus was noted. The CT scan showed satisfactory calvarial expansion with regression of tonsillar herniation.
CONCLUSIONS: Neurosurgical evaluation and care are necessary in the context of a multidisciplinary approach to the patient affected by osteopetrosis. Cranial vault remodeling and expansion should be considered in patients with sign of intracranial hypertension. Timing of optic canal decompression is to be defined.

Entities:  

Keywords:  Albers-Schomberg; Craniostenosis; Hydrocephalus; Osteoclasts

Mesh:

Year:  2017        PMID: 28762040     DOI: 10.1007/s00381-017-3553-4

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  20 in total

1.  Bone marrow transplantation corrects osteopetrosis in the carbonic anhydrase II deficiency syndrome.

Authors:  C McMahon; A Will; P Hu; G N Shah; W S Sly; O P Smith
Journal:  Blood       Date:  2001-04-01       Impact factor: 22.113

Review 2.  Neurological aspects of osteopetrosis.

Authors:  C G Steward
Journal:  Neuropathol Appl Neurobiol       Date:  2003-04       Impact factor: 8.090

3.  An SNX10 mutation causes malignant osteopetrosis of infancy.

Authors:  Memet Aker; Alex Rouvinski; Saar Hashavia; Asaf Ta-Shma; Avraham Shaag; Shamir Zenvirt; Shoshana Israel; Michael Weintraub; Albert Taraboulos; Zvi Bar-Shavit; Orly Elpeleg
Journal:  J Med Genet       Date:  2012-04       Impact factor: 6.318

4.  Osteopetrosis: a single centre experience of stem cell tranisplantation and prenatal diagnosis.

Authors:  J Kapelushnik; C Shalev; I Yaniv; M Aker; R Carmi; Z Cohen; A Mozer; C Schulman; G Stein; R Or
Journal:  Bone Marrow Transplant       Date:  2001-01       Impact factor: 5.483

5.  [Surgical optic nerve decompression in marble bone disease (Albers-Schönberg disease)].

Authors:  E Schmöger; H J Gerhardt; R Burgold
Journal:  Klin Monbl Augenheilkd       Date:  1983-10       Impact factor: 0.700

6.  Bone marrow transplantation for autosomal recessive osteopetrosis. A report from the Working Party on Inborn Errors of the European Bone Marrow Transplantation Group.

Authors:  E J Gerritsen; J M Vossen; A Fasth; W Friedrich; G Morgan; A Padmos; A Vellodi; O Porras; A O'Meara; F Porta
Journal:  J Pediatr       Date:  1994-12       Impact factor: 4.406

Review 7.  Infantile malignant, autosomal recessive osteopetrosis: the rich and the poor.

Authors:  Anna Villa; Matteo M Guerrini; Barbara Cassani; Alessandra Pangrazio; Cristina Sobacchi
Journal:  Calcif Tissue Int       Date:  2008-12-12       Impact factor: 4.333

8.  Long-term outcome of haematopoietic stem cell transplantation in autosomal recessive osteopetrosis: an EBMT report.

Authors:  G J A Driessen; E J A Gerritsen; A Fischer; A Fasth; W C J Hop; P Veys; F Porta; A Cant; C G Steward; J M Vossen; D Uckan; W Friedrich
Journal:  Bone Marrow Transplant       Date:  2003-10       Impact factor: 5.483

9.  Surgical correction of craniosynostosis in malignant osteopetrosis.

Authors:  Michael Krimmel; Gerhard Niemann; Bernd Will; Siegmar Reinert
Journal:  J Craniofac Surg       Date:  2004-03       Impact factor: 1.046

10.  Infantile osteopetrosis, craniosynostosis, and Chiari malformation type I with novel OSTEM1 mutation.

Authors:  A H Mahmoud Adel; A Al Jabri Abdullah; Faqeih Eissa
Journal:  J Pediatr Neurosci       Date:  2013-01
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  2 in total

1.  Internal Acoustic Canal Stenosis Due to Hyperostosis.

Authors:  Amir Goodarzi; Atrin Toussi; Nicholas Garza; Mirna Lechpammer; Hilary Brodie; Rodney C Diaz; Kiarash Shahlaie
Journal:  J Neurol Surg B Skull Base       Date:  2019-04-22

Review 2.  Neonatal hydrocephalus: an atypical presentation of malignant infantile osteopetrosis.

Authors:  Angela Lee; Samuel Cortez; Peter Yang; Diane Aum; Prapti Singh; Catherine Gooch; Matthew Smyth
Journal:  Childs Nerv Syst       Date:  2021-09-14       Impact factor: 1.475

  2 in total

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