Literature DB >> 3335915

Optic nerve decompression in osteopetrosis.

O Al-Mefty1, J L Fox, N Al-Rodhan, J H Dew.   

Abstract

Osteopetrosis is a rare disorder characterized by generalized increased skeletal density with abnormalities of bone modeling. The skull base is usually involved. Loss of vision with optic nerve atrophy is the most common neurological finding and is traditionally believed to be the result of optic nerve compression within the compromised optic canal. However, retinal degeneration has recently been described and is hypothesized to be the etiology of the visual loss (thus challenging the value of surgical decompression). The authors report their experience with six children suffering from osteopetrosis and severe visual loss. All six patients underwent bilateral microsurgical optic nerve decompression through a supraorbital craniotomy. Improvement in visual acuity occurred postoperatively in five patients, and none had complications. Two technical points are emphasized: 1) optic nerve decompression should be wide and include not only unroofing of the canal but also drilling along both sides of the optic nerve, and 2) the thick, irregular, and highly domed orbital roof should be smoothed down by high-speed drilling to facilitate surgical exposure with minimal retraction of the frontal lobe.

Entities:  

Mesh:

Year:  1988        PMID: 3335915     DOI: 10.3171/jns.1988.68.1.0080

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  8 in total

Review 1.  Autosomal recessive osteopetrosis: diagnosis, management, and outcome.

Authors:  C J Wilson; A Vellodi
Journal:  Arch Dis Child       Date:  2000-11       Impact factor: 3.791

2.  A case of osteopetrosis with acute optic neuropathy.

Authors:  Hirotsugu Tsuchida; Mineo Takagi; Atsushi Miki; Tomoaki Usui; Shigeru Hasegawa; Haruki Abe
Journal:  Jpn J Ophthalmol       Date:  2008-03-28       Impact factor: 2.447

Review 3.  Endoscopic third ventriculostomy for hydrocephalus in osteopetrosis: a case report and review of the literature.

Authors:  Nobuyuki Akutsu; Junji Koyama; Atsufumi Kawamura; Tatsuya Nagashima; Masaaki Taniguchi; Eiji Kohmura
Journal:  Childs Nerv Syst       Date:  2018-01-11       Impact factor: 1.475

4.  Progressive skeletal defects caused by Kindlin3 deficiency, a model of autosomal recessive osteopetrosis in humans.

Authors:  Tejasvi Dudiki; Daniel W Nascimento; Lauren S Childs; Swetha Kareti; Charlie Androjna; Irina Zhevlakova; Tatiana V Byzova
Journal:  Bone       Date:  2022-03-25       Impact factor: 4.626

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

Authors:  Irene Stella; Matthieu Vinchon; Pierre Guerreschi; Eva De Berranger; Ikram Bouacha
Journal:  Childs Nerv Syst       Date:  2017-07-31       Impact factor: 1.475

Review 6.  Allogeneic stem cell transplantation for the treatment of diseases associated with a deficiency in bone marrow products.

Authors:  Reuven Or; Memet Aker; Michael Yechiel Shapira; Igor Resnick; Menachem Bitan; Simcha Samuel; Shimon Slavin
Journal:  Springer Semin Immunopathol       Date:  2004-09-30

7.  An unusual cause of optic atrophy in a child.

Authors:  Nishant Kumar; Anirudh Singh; Rohit Saxena; Vimla Menon; Sanjay Sharma
Journal:  Indian J Ophthalmol       Date:  2014-04       Impact factor: 1.848

8.  Osteopetrosis and Chiari type I malformation: a rare association.

Authors:  Mehmet Ali Ekici; Ulaş Cıkla; Andrew Bauer; Mustafa K Başkaya
Journal:  J Surg Case Rep       Date:  2015-10-26
  8 in total

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