Delayed symptomatic haemorrhage from the remnants of a thalamic arteriovenous malformation after previous angiographic cure with radiotherapy

In 1995 a 16-year old girl was diagnosed with a large left thalamic AVM that was considered unsuitable for microsurgical resection and was treated with radiotherapy twice, which led to angiographic cure. She re-presented 19 years after initial treatment with a symptomatic acute thalamic haemorrhage....

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Published inActa neurochirurgica Vol. 159; no. 11; pp. 2123 - 2125
Main Authors Majewska, Paulina, Tsui, Alpha, Adamides, Alexios A.
Format Journal Article
LanguageEnglish
Published Vienna Springer Vienna 01.11.2017
Springer Nature B.V
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Abstract In 1995 a 16-year old girl was diagnosed with a large left thalamic AVM that was considered unsuitable for microsurgical resection and was treated with radiotherapy twice, which led to angiographic cure. She re-presented 19 years after initial treatment with a symptomatic acute thalamic haemorrhage. Her digital subtraction angiography was negative for arterio-venous shunting. MRI/MRA showed cystic change with adjacent contrast enhancement in the region of the previously irradiated arteriovenous malformation. The patient underwent an interhemispheric transcallosal resection of the left thalamic haemorrhagic lesion via a contralateral craniotomy. Intra-operatively there was a cystic cavity filled with blood products in association with thrombosed, calcified vessels as well as actively filling vessels. Histologically there were aggregated abnormal blood vessels with a dilated lumen and surrounded by brain parenchyma. Some of the vessel walls were thickened with fibrosis and some were arterialised with presence of elastin fibres. Potential mechanisms for the delayed haemorrhage are discussed.
AbstractList In 1995 a 16-year old girl was diagnosed with a large left thalamic AVM that was considered unsuitable for microsurgical resection and was treated with radiotherapy twice, which led to angiographic cure. She re-presented 19 years after initial treatment with a symptomatic acute thalamic haemorrhage. Her digital subtraction angiography was negative for arterio-venous shunting. MRI/MRA showed cystic change with adjacent contrast enhancement in the region of the previously irradiated arteriovenous malformation. The patient underwent an interhemispheric transcallosal resection of the left thalamic haemorrhagic lesion via a contralateral craniotomy. Intra-operatively there was a cystic cavity filled with blood products in association with thrombosed, calcified vessels as well as actively filling vessels. Histologically there were aggregated abnormal blood vessels with a dilated lumen and surrounded by brain parenchyma. Some of the vessel walls were thickened with fibrosis and some were arterialised with presence of elastin fibres. Potential mechanisms for the delayed haemorrhage are discussed.
In 1995 a 16-year old girl was diagnosed with a large left thalamic AVM that was considered unsuitable for microsurgical resection and was treated with radiotherapy twice, which led to angiographic cure. She re-presented 19 years after initial treatment with a symptomatic acute thalamic haemorrhage. Her digital subtraction angiography was negative for arterio-venous shunting. MRI/MRA showed cystic change with adjacent contrast enhancement in the region of the previously irradiated arteriovenous malformation. The patient underwent an interhemispheric transcallosal resection of the left thalamic haemorrhagic lesion via a contralateral craniotomy. Intra-operatively there was a cystic cavity filled with blood products in association with thrombosed, calcified vessels as well as actively filling vessels. Histologically there were aggregated abnormal blood vessels with a dilated lumen and surrounded by brain parenchyma. Some of the vessel walls were thickened with fibrosis and some were arterialised with presence of elastin fibres. Potential mechanisms for the delayed haemorrhage are discussed.
Author Majewska, Paulina
Tsui, Alpha
Adamides, Alexios A.
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  fullname: Majewska, Paulina
  organization: Imperial College London, Exhibition Road
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  givenname: Alpha
  surname: Tsui
  fullname: Tsui, Alpha
  organization: Department of Pathology, Royal Melbourne Hospital
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  givenname: Alexios A.
  surname: Adamides
  fullname: Adamides, Alexios A.
  email: alexios.adamides@mh.org.au
  organization: Department of Neurosurgery, Royal Melbourne Hospital, Department of Surgery, University of Melbourne
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Cites_doi 10.1007/s00701-014-2298-z
10.1159/000323543
10.3171/jns.1997.87.3.0352
10.1055/s-0028-1103265
10.1097/00006123-199610000-00016
10.3171/2016.4JNS152320
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Keywords Delayed haemorrhage
Angiographic cure
Arteriovenous malformation
Radiation
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Snippet In 1995 a 16-year old girl was diagnosed with a large left thalamic AVM that was considered unsuitable for microsurgical resection and was treated with...
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SubjectTerms Adolescent
Adult
Angiography
Angiography, Digital Subtraction
Blood vessels
Brain
Case Report - Vascular
Cerebral Angiography
Cerebral hemispheres
Cerebral Hemorrhage - etiology
Cerebral Hemorrhage - surgery
Disease Progression
Elastin
Female
Fibers
Fibrosis
Hemorrhage
Humans
Interventional Radiology
Intracranial Arteriovenous Malformations - complications
Intracranial Arteriovenous Malformations - diagnostic imaging
Intracranial Arteriovenous Malformations - radiotherapy
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Medicine
Medicine & Public Health
Minimally Invasive Surgery
Neurology
Neuroradiology
Neurosurgery
Neurosurgical Procedures
Parenchyma
Radiation therapy
Radiosurgery
Surgical Orthopedics
Thalamus
Thalamus - blood supply
Thalamus - surgery
Time Factors
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Title Delayed symptomatic haemorrhage from the remnants of a thalamic arteriovenous malformation after previous angiographic cure with radiotherapy
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