Literature DB >> 15995885

Long-term results of the surgical treatment of craniopharyngioma: the experience at the Policlinico Gemelli, Catholic University, Rome.

M Caldarelli1, L Massimi, G Tamburrini, M Cappa, C Di Rocco.   

Abstract

BACKGROUND: Craniopharyngioma (CP) is the most common intracranial non-glial tumour observed in pediatric age. Although histologically benign and amenable to surgical treatment, its location and relation with vital nervous and vascular structures makes the feasibility of a radical resection difficult even in the microneurosurgery era. Beside the difficulties experienced when performing tumour resection, post-operative complications, such as endocrinological imbalance, represent another point that makes CP total excision a challenge. In order to avoid such complications, some authors have suggested to renounce to radical resection and to rely on post-operative radiation therapy to minimise the risk of residual tumour progression.
METHODS: We report our experience with 52 children and adolescents operated on for CP at the Department of Pediatrics, Section of Pediatric Neurosurgery, Catholic University Medical School, Rome, between January 1985 and December 2002. The study included 14 children <5 years old (five less than 2 years of age), 25 between 6 and 10 years old, and 13 more than 10 years old. The most common presenting signs were related to endocrinological imbalance (35 cases), increased intracranial pressure (32 cases), and to a lesser extent, visual compromise (17 cases). Concerning location, CP was intrasellar in three cases; sellar/suprasellar with prominent prechiasmatic growth in 24 cases; retrochiasmatic/3rd ventricular in 14 cases, and giant (with an extension into the middle and/or posterior cranial fossae) in 11 cases. The tumour was managed by means of a single surgical approach in 47 cases and with a two-stage operation in the remaining five cases. In 11 cases of intrasellar or intra/suprasellar midline location, the first surgical approach was done through the transsphenoidal route (which represented the first step of a staged operation in five instances); in the remaining 41 patients, craniotomy was the first surgical procedure. Radical tumour resection was achieved in 40 cases, subtotal (only small tumour remnants adherent to the carotid arteries, 3rd ventricle floor or visual pathways) in nine, and only partial in the remaining three cases
RESULTS: Histology demonstrated the adamantinous variant in all cases. Two surgical deaths were recorded in this series (both following a transsphenoidal approach): one secondary to uncontrollable intra-operative bleeding from the carotid artery, and the other to fulminating bacterial meningoencephalitis. Morbidity included endocrinological disturbances, namely hypopituitarism and diabetes insipidus, in more than 80% of cases, worsening of pre-operative visual deficit in six cases, and transitory neurological deficits in five cases. One late death was recorded 2 years after surgery, secondary to electrolytic imbalance although favoured by a major head trauma with subacute subdural haematoma. Nine recurrences occurred 1-8 years after surgery (three true recurrences, and six re-growths of incompletely resected tumours) that required re-operation. Twelve patients underwent radiotherapy, six after an initially incomplete tumour resection and six following relapse. One patient presented with a malignant thalamic glioma 8 years after radiotherapy. At long-term follow-up, all survivors showed good clinical condition, even though approximately 60% relied on hormone replacement, and some patients presented obesity. Diabetes insipidus has subsided in about 80% of the cases; visual deficits improved or remained stable, whereas post-operative neurological deficits subsided in all but one patient.
CONCLUSION: In our experience, radical resection of CP represented the first and almost unique treatment modality. Although not insignificant, post-operative mortality and morbidity do not seem to represent a major contraindication in attempting a radical tumour resection whenever possible. On the other hand, extensive hypothalamic involvement should suggest a less aggressive attitude.

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Year:  2005        PMID: 15995885     DOI: 10.1007/s00381-005-1186-5

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  40 in total

1.  Ectopic recurrences of craniopharyngioma.

Authors:  Federica Novegno; Federico Di Rocco; Cesare Colosimo; Libero Lauriola; Massimo Caldarelli
Journal:  Childs Nerv Syst       Date:  2002-08-17       Impact factor: 1.475

2.  Surgery of large retrochiasmatic craniopharyngiomas in children.

Authors:  M Ammirati; M Samii; A Sephernia
Journal:  Childs Nerv Syst       Date:  1990-01       Impact factor: 1.475

3.  Long-term results of gamma knife surgery for craniopharyngioma.

Authors:  Tatsuya Kobayashi; Yoshihisa Kida; Toshinori Hasegawa
Journal:  Neurosurg Focus       Date:  2003-05-15       Impact factor: 4.047

4.  Intraventricular craniopharyngioma: a long-term follow-up of six cases.

Authors:  M J Davies; T T King; K A Metcalfe; J P Monson
Journal:  Br J Neurosurg       Date:  1997-12       Impact factor: 1.596

5.  Total removal of craniopharyngiomas. Approaches and long-term results in 144 patients.

Authors:  M G Yaşargil; M Curcic; M Kis; G Siegenthaler; P J Teddy; P Roth
Journal:  J Neurosurg       Date:  1990-07       Impact factor: 5.115

6.  Outcome of craniopharyngioma in children: long-term complications and quality of life.

Authors:  Andrea Poretti; Michael A Grotzer; Karin Ribi; Eugen Schönle; Eugen Boltshauser
Journal:  Dev Med Child Neurol       Date:  2004-04       Impact factor: 5.449

7.  Endocrine and neurologic outcome in childhood craniopharyngioma: Review of effect of treatment in 42 patients.

Authors:  M J Thomsett; F A Conte; S L Kaplan; M M Grumbach
Journal:  J Pediatr       Date:  1980-11       Impact factor: 4.406

8.  Surgical management of craniopharyngiomas. A review of 74 cases.

Authors:  D S Baskin; C B Wilson
Journal:  J Neurosurg       Date:  1986-07       Impact factor: 5.115

9.  The psychosocial impacts on families of low-incidence, complex conditions in children: the case of craniopharyngioma.

Authors:  Alun C Jackson; Menka Tsantefski; Helen Goodman; Belinda Johnson; Jeffery Rosenfeld
Journal:  Soc Work Health Care       Date:  2003

10.  Craniopharyngiomas in children.

Authors:  P W Carmel; J L Antunes; C H Chang
Journal:  Neurosurgery       Date:  1982-09       Impact factor: 4.654

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  32 in total

1.  Management of pediatric craniopharyngioma: 10-year experience from high-flow center.

Authors:  Abd El Rahman Enayet; Mostafa M E Atteya; Hala Taha; Mohamed Saad Zaghloul; Amal Refaat; Eslam Maher; Amal Abdelaziz; Mohamed A El Beltagy
Journal:  Childs Nerv Syst       Date:  2020-07-26       Impact factor: 1.475

2.  Sixty years single institutional experience with pediatric craniopharyngioma: between the past and the future.

Authors:  Mohammed A Fouda; R Michael Scott; Karen J Marcus; Nicole Ullrich; Peter E Manley; Mark W Kieran; Liliana C Goumnerova
Journal:  Childs Nerv Syst       Date:  2019-07-10       Impact factor: 1.475

Review 3.  Risk-adapted, long-term management in childhood-onset craniopharyngioma.

Authors:  Hermann L Müller
Journal:  Pituitary       Date:  2017-04       Impact factor: 4.107

4.  Gonadotropin-dependent precocious puberty: neoplastic causes and endocrine considerations.

Authors:  Matthew D Stephen; Peter E Zage; Steven G Waguespack
Journal:  Int J Pediatr Endocrinol       Date:  2011-03-06

5.  Incidence, predictors and early post-operative course of diabetes insipidus in paediatric craniopharygioma: a comparison with adults.

Authors:  Ravindran Pratheesh; Diane Margaret A Swallow; Simon Rajaratnam; K S Jacob; Geeta Chacko; Mathew Joseph; Ari G Chacko
Journal:  Childs Nerv Syst       Date:  2013-02-06       Impact factor: 1.475

6.  Acute presentation of craniopharyngioma in children and adults in a Danish national cohort.

Authors:  E H Nielsen; J O Jørgensen; P Bjerre; M Andersen; C Andersen; U Feldt-Rasmussen; L Poulsgaard; L Ø Kristensen; J Astrup; J Jørgensen; P Laurberg
Journal:  Pituitary       Date:  2013-12       Impact factor: 4.107

7.  Trends in treatment and outcomes of pediatric craniopharyngioma, 1975-2011.

Authors:  Michal Cohen; Ute Bartels; Helen Branson; Abhaya V Kulkarni; Jill Hamilton
Journal:  Neuro Oncol       Date:  2013-03-13       Impact factor: 12.300

8.  Practical approach to childhood craniopharyngioma: a role of an endocrinologist and a general paediatrician.

Authors:  Maria A Kalina; Eliza Skala-Zamorowska; Barbara Kalina-Faska; Ewa Malecka-Tendera; Marek Mandera
Journal:  Childs Nerv Syst       Date:  2009-06-17       Impact factor: 1.475

9.  Limited utility despite accuracy of the national SEER dataset for the study of craniopharyngioma.

Authors:  Todd C Hankinson; Emma C Fields; Michelle R Torok; Brenda L Beaty; Michael H Handler; Nicholas K Foreman; Brent R O'neill; Arthur K Liu
Journal:  J Neurooncol       Date:  2012-08-23       Impact factor: 4.130

10.  Investigating the Role of Hypothalamic Tumor Involvement in Sleep and Cognitive Outcomes Among Children Treated for Craniopharyngioma.

Authors:  Lisa M Jacola; Heather M Conklin; Matthew A Scoggins; Jason M Ashford; Thomas E Merchant; Belinda N Mandrell; Robert J Ogg; Elizabeth Curtis; Merrill S Wise; Daniel J Indelicato; Valerie M Crabtree
Journal:  J Pediatr Psychol       Date:  2016-05-16
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