Literature DB >> 34213590

An analysis of clinical characteristics and postoperative complications in children craniopharyngioma.

Deng Yaxian1, Yao Chunmei2, Xu Juanyu2, Wang Lei2, Gong Jian3, Zhao Chengsong4.   

Abstract

OBJECTIVE: Children treated for craniopharyngioma (CP) experience significant morbidity. We aimed to investigate the clinical characteristics and postoperative complications of pediatric CP and to determine risk factors for complications to provide a theoretical basis for postoperative treatment.
METHODS: In this retrospective analysis, we screened clinical data concerning children with CP who had undergone surgery at our hospital from December 2011 to June 2015. We statistically analyzed the relationship between age, sex, disease course, tumor location, extent of tumor resection, and neuroendocrine axis dysfunction.
RESULTS: Of 240 patients (males, n = 144; females, n = 96; mean age, 8.33 ± 4.64 years), the main clinical presentations were headache (n = 151, 62.92%), vomiting (n = 84, 35%), vision changes (n = 101, 42.08%), polydipsia and polyuria (n = 47, 19.58%), and growth retardation (n = 42, 17.5%). Hypothalamic-pituitary dysfunction was the most common postoperative complication. There were 216 (90.00%) and 181 (75.42%) patients with pituitary-thyroid and pituitary-adrenal axis injuries, respectively. Being a prepubescent girl was a risk factor for impaired pituitary-thyroid and pituitary-adrenal axis function (P < 0.05). No correlation was found between sex (male), age, disease course, tumor location, extent of tumor resection, and impaired pituitary-thyroid and pituitary-adrenal axis function (P > 0.05). Pituitary-gonad axis injury was observed in 91 (37.92%) patients. Saddle and suprasellar region tumors were risk factors for impaired pituitary-gonad axis function (P < 0.05). No statistically significant correlation was found between sex, disease course, extent of resection, and impaired pituitary-gonad axis function (P > 0.05).
CONCLUSIONS: Routine screening for complications during treatment is indicated for children with CP, to optimize the timing of interventions and reduce long-term morbidity.

Entities:  

Keywords:  Children; Clinical manifestation; Complication; Craniopharyngioma

Year:  2021        PMID: 34213590     DOI: 10.1007/s00381-021-05277-7

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


  3 in total

1.  Obesity in childhood craniopharyngioma: relation to post-operative hypothalamic damage shown by magnetic resonance imaging.

Authors:  C J de Vile; D B Grant; R D Hayward; B E Kendall; B G Neville; R Stanhope
Journal:  J Clin Endocrinol Metab       Date:  1996-07       Impact factor: 5.958

Review 2.  Pediatric craniopharyngiomas: classification and treatment according to the degree of hypothalamic involvement.

Authors:  Stéphanie Puget; Matthew Garnett; Alison Wray; Jacques Grill; Jean-Louis Habrand; Nathalie Bodaert; Michel Zerah; Mercia Bezerra; Dominique Renier; Alain Pierre-Kahn; Christian Sainte-Rose
Journal:  J Neurosurg       Date:  2007-01       Impact factor: 5.115

Review 3.  Diagnosis, treatment, clinical course, and prognosis of childhood-onset craniopharyngioma patients.

Authors:  Hermann L Müller
Journal:  Minerva Endocrinol       Date:  2017-02-09       Impact factor: 2.184

  3 in total

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