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craniopharyngioma/nauzea
Odkaz sa uloží do schránky
Strana 1 od 28 výsledky
[Craniopharyngioma in children: importance of a multidisciplinary approach and therapeutic strategies in the treatment of relapsing].
Články môžu prekladať iba registrovaní používatelia
Prihlásiť Registrácia
The craniopharyngioma is a benign intracranial nonglial tumor derived from a malformation of the embryonic tissue. Represents approximately 6-9% of brain tumors in children. It grows close to the optic nerve, hypothalamus and pituitary. The most frequent histological variety in children is
CRANIOPHARYNGIOMA - CLINICAL AND THERAPEUTIC OUTCOME DATA IN A MIXED COHORT OF ADULT AND PAEDIATRIC CASES.
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Prihlásiť Registrácia
Postoperative nausea and vomiting and pain after transsphenoidal surgery: a review of 877 patients.
Články môžu prekladať iba registrovaní používatelia
Prihlásiť Registrácia
Although postoperative nausea and vomiting and pain after supra- and infratentorial craniotomy have been evaluated in multiple studies, there are few data regarding pain or postoperative nausea and vomiting after transsphenoidal procedures. Therefore, we reviewed the perioperative records of 877
Craniopharyngioma presenting with severe hyponatremia, hyponatremia-induced myopathy, and panhypopituitarism: a case report.
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Prihlásiť Registrácia
BACKGROUND
Craniopharyngiomas are rare intracranial tumors commonly presenting with neurological symptoms. Reports of severe hyponatremia as a presenting manifestation of a craniopharyngioma and hyponatremia-induced myopathy are rare. We report the case of a patient with craniopharyngioma presenting
Acute presentation of craniopharyngioma in children and adults in a Danish national cohort.
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Prihlásiť Registrácia
We aimed to study the occurrence of acute-onset symptoms at initial presentation in a national Danish cohort of patients with childhood- or adult-onset craniopharyngioma, and to investigate potential risk factors for acute presentation. Medical records of 189 consecutive patients (39 children, 150
Endocrine sequelae of childhood craniopharyngioma.
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Prihlásiť Registrácia
The endocrine sequelae of 62 children with craniopharyngioma were studied retrospectively. These patients were followed for a median duration of 3 years (range 1 to 10 years). Eighteen patients had a long-term follow-up for more than 5 years (range 5 to 10 years). Complete surgical resection was
Cerebellopontine angle craniopharyngioma: case report and literature review.
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Prihlásiť Registrácia
The authors report an unusual case of adamantinomatous craniopharyngioma occurring in isolation in the cerebellopontine angle of a 12-year-old female. The patient presented with a 1-year history of nausea, vomiting, and headache. MRI revealed a left cerebellopontine angle tumor without connection to
Origin of craniopharyngiomas: implications for growth pattern, clinical characteristics, and outcomes of tumor recurrence.
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Prihlásiť Registrácia
OBJECT Craniopharyngiomas are associated with a high rate of recurrence. The surgical management of recurrent lesions has been among the most challenging neurosurgical procedures because of the craniopharyngioma's complex topographical relationship with surrounding structures. The aim of this study
Craniopharyngioma of the posterior fossa.
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Prihlásiť Registrácia
A case of craniopharyngioma originating in the very unusual location of the posterior fossa is presented. The patient, a 23-year-old man, was operated on at another hospital when he was 3 years old for craniopharyngioma in the suprasellar area. There was no complaint for several years after this
[Malignant changes in a craniopharyngioma].
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Prihlásiť Registrácia
The authors report a rare case of a 10-year-old girl with craniopharyngioma which showed malignant change after the first operation and irradiation. In June 1981, the patient complained of headache, nausea and vomiting. CT revealed obstructive hydrocephalus due to the calcified mass lesion which
Frontal dermoid cyst coexisting with suprasellar craniopharyngioma: a spectrum of ectodermally derived epithelial-lined cystic lesions?
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Prihlásiť Registrácia
There is a wide group of lesions that may exist in the sellar and suprasellar regions. Embryologically, there is varying evidence that many of these entities may in fact represent a continuum of pathology deriving from a common ectodermal origin. The authors report a case of a concomitant
Endocrine and growth features in childhood craniopharyngioma: a mono-institutional study.
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Prihlásiť Registrácia
OBJECTIVE
To evaluate growth and endocrine features in children with craniopharyngioma who were treated and followed up by a single institution between 1976 and 2004.
METHODS
The records of 32 children, 18 males and 14 females, were evaluated. The mean follow-up period was 6.3 years.
RESULTS
At
Giant cystic craniopharyngiomas with extension into the posterior fossa.
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Prihlásiť Registrácia
Between 1991 and 1998, 24 patients underwent surgery for a craniopharyngioma in our department. This group included two patients who had tumors with extensive growth along the midline, and along the posterior fossa in particular. In both cases suprasellar calcifications were typical features on
Collision Tumor in the Pituitary, Concurrent Pituitary Adenoma, and Craniopharyngioma
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Prihlásiť Registrácia
Collision tumors are two independent, distinct tumors occupying the same anatomical space. This case presents a pituitary adenoma-craniopharyngioma collision tumor presenting with hemianopsia. A 60-year-old with a past history of a nonsecretory pituitary adenoma presented with progressive headaches,
Long-term visual outcomes of craniopharyngioma in children.
Články môžu prekladať iba registrovaní používatelia
Prihlásiť Registrácia
Visual function is a critical factor in the diagnosis, monitoring, and prognosis of craniopharyngiomas in children. The aim of this study was to report the long-term visual outcomes in a cohort of pediatric patients with craniopharyngioma. The study design is a retrospective chart review of
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