Senta Kurschel
Senta Kurschel has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
Hans Georg Eder
Medical University
2 shared publicationsVerena Gellner
Department of Neurosurgery, Medical University, Auenbruggerplatz 29, 8036, Graz, Austria
2 shared publicationsJürgen Schleef
Karl-Franzens-University Graz
1 shared publicationK. A. Leber
Medical University
1 shared publicationM. Scarpatetti
Medical University
1 shared publicationMichael Mokry
Medical University
1 shared publication
Latest Publications
- 26 February 2008
- Published by Springer Nature in Child's Nervous System
- Vol. 24 (7) , 785-792
Lymphocytic hypophysitis in the pediatric population
- 26 February 2008
- Published by Springer Nature in Child's Nervous System
- Vol. 24 (7) , 785-792
Lymphocytic hypophysitis in the pediatric population
- 8 May 2007
- Published by Springer Nature in Child's Nervous System
- Vol. 23 (8) , 901-905
Chiari I malformation and intra-cranial hypertension:a case-based review
To present clinical and morphological findings before and after surgery in a child with Chairi I malformation (CMI) and intra-cranial hypertension (IH). The literature is reviewed and pathophysiologic factors are discussed. A 13-year-old obese boy with a 3-week history of headaches, neck pain, torticollis and progressive visual deterioration was admitted. Bi-lateral chronic papilloedema and decrease in visual acuity were found in the presence of a previously diagnosed CMI. Intra-cranial pressure monitoring demonstrating increased pressure levels was followed by a sub-occipital decompression, C1 laminectomy and duroplasty. Post-operatively, the boy improved markedly, the 6 months follow-up opthalmological examination demonstrated resolution of papilloedema, but consecutive bi-lateral optic nerve atrophy. IH with progressive visual deterioration represents one of the varying clinical presentations of CMI and may be classified as a secondary form of idiopathic IH. Neuro-ophthalmological examination in all patients with CMI is recommended to identify the real incidence of this presentation. Altered CSF dynamics, venous hypertension and obesity as co-factors may be causative pathophysiologic factors.
- 8 May 2007
- Published by Springer Nature in Child's Nervous System
- Vol. 23 (8) , 901-905
Chiari I malformation and intra-cranial hypertension:a case-based review
To present clinical and morphological findings before and after surgery in a child with Chairi I malformation (CMI) and intra-cranial hypertension (IH). The literature is reviewed and pathophysiologic factors are discussed. A 13-year-old obese boy with a 3-week history of headaches, neck pain, torticollis and progressive visual deterioration was admitted. Bi-lateral chronic papilloedema and decrease in visual acuity were found in the presence of a previously diagnosed CMI. Intra-cranial pressure monitoring demonstrating increased pressure levels was followed by a sub-occipital decompression, C1 laminectomy and duroplasty. Post-operatively, the boy improved markedly, the 6 months follow-up opthalmological examination demonstrated resolution of papilloedema, but consecutive bi-lateral optic nerve atrophy. IH with progressive visual deterioration represents one of the varying clinical presentations of CMI and may be classified as a secondary form of idiopathic IH. Neuro-ophthalmological examination in all patients with CMI is recommended to identify the real incidence of this presentation. Altered CSF dynamics, venous hypertension and obesity as co-factors may be causative pathophysiologic factors.
- 28 December 2004
- Published by Springer Nature in Acta Neurochirurgica
- Vol. 147 (3) , 321-325
Rare fatal vascular complication of transsphenoidal surgery
We report the case of a 61-year-old man, who underwent transsphenoidal surgery for a pituitary macroadenoma. The presence of tough fibrous septa dividing the tumour permitted only a partial resection. Progressive loss of consciousness soon after surgery occurred, an emergency CT scan showed no evidence of haemorrhage. Twenty hours later, MRI revealed compression of both internal carotid arteries with arrest of arterial flow resulting in stroke by an enlarged haemorrhagic mass consistent with a pituitary apoplexy. On the second postoperative day, the patient died as a result of this extensive stroke. The mechanisms of this rare complication after transsphenoidal surgery are theorized and the sensitivity of imaging methods is discussed.
- 28 December 2004
- Published by Springer Nature in Acta Neurochirurgica
- Vol. 147 (3) , 321-325
Rare fatal vascular complication of transsphenoidal surgery
We report the case of a 61-year-old man, who underwent transsphenoidal surgery for a pituitary macroadenoma. The presence of tough fibrous septa dividing the tumour permitted only a partial resection. Progressive loss of consciousness soon after surgery occurred, an emergency CT scan showed no evidence of haemorrhage. Twenty hours later, MRI revealed compression of both internal carotid arteries with arrest of arterial flow resulting in stroke by an enlarged haemorrhagic mass consistent with a pituitary apoplexy. On the second postoperative day, the patient died as a result of this extensive stroke. The mechanisms of this rare complication after transsphenoidal surgery are theorized and the sensitivity of imaging methods is discussed.
- 8 September 2004
- Published by Springer Nature in Child's Nervous System
- Vol. 21 (1) , 52-55
CSF shunts in children: endoscopically-assisted placement of the distal catheter
Ventriculoperitoneal shunting is the most common treatment for hydrocephalus. Repeated shunt revisions and other previous surgical procedures can complicate the placement of the distal catheter. Occasionally, when conventional sites like the abdominal cavity and the right atrium are used up or unavailable, a ventriculopleural shunt can be inserted.
- 8 September 2004
- Published by Springer Nature in Child's Nervous System
- Vol. 21 (1) , 52-55
CSF shunts in children: endoscopically-assisted placement of the distal catheter
Ventriculoperitoneal shunting is the most common treatment for hydrocephalus. Repeated shunt revisions and other previous surgical procedures can complicate the placement of the distal catheter. Occasionally, when conventional sites like the abdominal cavity and the right atrium are used up or unavailable, a ventriculopleural shunt can be inserted.