Intrachiasmatic abscess caused by IgG4-related hypophysitis

Introduction Autoimmune hypophysitis is a rare disease of the pituitary, which may affect vision by inflammation and compression of the optic chiasm. However, intrachiasmatic abscess formation has not been previously reported. Methods In this study, we report a case of a 29-year-old female with bite...

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Vydáno v:Acta neurochirurgica Ročník 159; číslo 11; s. 2229 - 2233
Hlavní autoři: Hadjigeorgiou, Georgios F., Lund, Eva Løbner, Poulsgaard, Lars, Feldt-Rasmussen, Ulla, Rasmussen, Åse Krogh, Wegener, Marianne, Fugleholm, Kåre
Médium: Journal Article
Jazyk:angličtina
Vydáno: Vienna Springer Vienna 01.11.2017
Springer Nature B.V
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ISSN:0001-6268, 0942-0940, 0942-0940
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Abstract Introduction Autoimmune hypophysitis is a rare disease of the pituitary, which may affect vision by inflammation and compression of the optic chiasm. However, intrachiasmatic abscess formation has not been previously reported. Methods In this study, we report a case of a 29-year-old female with bitemporal hemianopia due to a cystic intrasellar tumor. The patient underwent surgical decompression of the lesion, which was found to be an intrachiasmatic abscess. Results The histologic findings were consistent with IgG4 hypophysitis. Conclusion This rare clinical presentation suggests that in case of a disproportionate degree of visual impairment in relation to the size of the lesion, suspicion should lead to an intrachiasmatic lesion.
AbstractList Autoimmune hypophysitis is a rare disease of the pituitary, which may affect vision by inflammation and compression of the optic chiasm. However, intrachiasmatic abscess formation has not been previously reported. In this study, we report a case of a 29-year-old female with bitemporal hemianopia due to a cystic intrasellar tumor. The patient underwent surgical decompression of the lesion, which was found to be an intrachiasmatic abscess. The histologic findings were consistent with IgG4 hypophysitis. This rare clinical presentation suggests that in case of a disproportionate degree of visual impairment in relation to the size of the lesion, suspicion should lead to an intrachiasmatic lesion.
Autoimmune hypophysitis is a rare disease of the pituitary, which may affect vision by inflammation and compression of the optic chiasm. However, intrachiasmatic abscess formation has not been previously reported.INTRODUCTIONAutoimmune hypophysitis is a rare disease of the pituitary, which may affect vision by inflammation and compression of the optic chiasm. However, intrachiasmatic abscess formation has not been previously reported.In this study, we report a case of a 29-year-old female with bitemporal hemianopia due to a cystic intrasellar tumor. The patient underwent surgical decompression of the lesion, which was found to be an intrachiasmatic abscess.METHODSIn this study, we report a case of a 29-year-old female with bitemporal hemianopia due to a cystic intrasellar tumor. The patient underwent surgical decompression of the lesion, which was found to be an intrachiasmatic abscess.The histologic findings were consistent with IgG4 hypophysitis.RESULTSThe histologic findings were consistent with IgG4 hypophysitis.This rare clinical presentation suggests that in case of a disproportionate degree of visual impairment in relation to the size of the lesion, suspicion should lead to an intrachiasmatic lesion.CONCLUSIONThis rare clinical presentation suggests that in case of a disproportionate degree of visual impairment in relation to the size of the lesion, suspicion should lead to an intrachiasmatic lesion.
Autoimmune hypophysitis is a rare disease of the pituitary, which may affect vision by inflammation and compression of the optic chiasm. However, intrachiasmatic abscess formation has not been previously reported. In this study, we report a case of a 29-year-old female with bitemporal hemianopia due to a cystic intrasellar tumor. The patient underwent surgical decompression of the lesion, which was found to be an intrachiasmatic abscess. The histologic findings were consistent with IgG4 hypophysitis. This rare clinical presentation suggests that in case of a disproportionate degree of visual impairment in relation to the size of the lesion, suspicion should lead to an intrachiasmatic lesion.
Introduction Autoimmune hypophysitis is a rare disease of the pituitary, which may affect vision by inflammation and compression of the optic chiasm. However, intrachiasmatic abscess formation has not been previously reported. Methods In this study, we report a case of a 29-year-old female with bitemporal hemianopia due to a cystic intrasellar tumor. The patient underwent surgical decompression of the lesion, which was found to be an intrachiasmatic abscess. Results The histologic findings were consistent with IgG4 hypophysitis. Conclusion This rare clinical presentation suggests that in case of a disproportionate degree of visual impairment in relation to the size of the lesion, suspicion should lead to an intrachiasmatic lesion.
Author Poulsgaard, Lars
Feldt-Rasmussen, Ulla
Hadjigeorgiou, Georgios F.
Lund, Eva Løbner
Fugleholm, Kåre
Rasmussen, Åse Krogh
Wegener, Marianne
Author_xml – sequence: 1
  givenname: Georgios F.
  surname: Hadjigeorgiou
  fullname: Hadjigeorgiou, Georgios F.
  email: georgehadji@gmail.com
  organization: Department of Neurosurgery, Academic Hospital Munich-Bogenhausen, Technical University of Munich
– sequence: 2
  givenname: Eva Løbner
  surname: Lund
  fullname: Lund, Eva Løbner
  organization: Department of Pathology, University Hospital of Copenhagen
– sequence: 3
  givenname: Lars
  surname: Poulsgaard
  fullname: Poulsgaard, Lars
  organization: Department of Neurosurgery, University Hospital of Copenhagen
– sequence: 4
  givenname: Ulla
  surname: Feldt-Rasmussen
  fullname: Feldt-Rasmussen, Ulla
  organization: Department of Endocrinology, University Hospital of Copenhagen
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  givenname: Åse Krogh
  surname: Rasmussen
  fullname: Rasmussen, Åse Krogh
  organization: Department of Endocrinology, University Hospital of Copenhagen
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  givenname: Marianne
  surname: Wegener
  fullname: Wegener, Marianne
  organization: Department of Neuro-opthalmology, University Hospital of Copenhagen
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  givenname: Kåre
  surname: Fugleholm
  fullname: Fugleholm, Kåre
  organization: Department of Neurosurgery, University Hospital of Copenhagen
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28799078$$D View this record in MEDLINE/PubMed
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Keywords IgG4
Intrachiasmatic
Abscess
Hypophysitis
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Snippet Introduction Autoimmune hypophysitis is a rare disease of the pituitary, which may affect vision by inflammation and compression of the optic chiasm. However,...
Autoimmune hypophysitis is a rare disease of the pituitary, which may affect vision by inflammation and compression of the optic chiasm. However,...
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SubjectTerms Adult
Autoimmune Hypophysitis - complications
Autoimmune Hypophysitis - diagnostic imaging
Autoimmune Hypophysitis - pathology
Autoimmune Hypophysitis - surgery
Brain Abscess - complications
Brain Abscess - diagnostic imaging
Brain Abscess - pathology
Brain Abscess - surgery
Case Report - Brain Tumors
Case reports
Compression
Decompression
Decompression, Surgical
Female
Hemianopsia - etiology
Humans
Immunoglobulin G
Interventional Radiology
Magnetic Resonance Imaging
Medicine
Medicine & Public Health
Minimally Invasive Surgery
Neurology
Neuroradiology
Neurosurgery
Neurosurgical Procedures
Optic chiasm
Optic Chiasm - diagnostic imaging
Optic Chiasm - surgery
Pituitary
Rare diseases
Surgical Orthopedics
Vision
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Title Intrachiasmatic abscess caused by IgG4-related hypophysitis
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https://www.ncbi.nlm.nih.gov/pubmed/28799078
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