Clinical Characteristics and Postoperative Growth in Japanese Children with Craniopharyngioma.

IF 3 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Yuri Mukoyama, Shun Moriguchi, Fumihiko Takizawa, Atsushi Ogawa, Tetsushi Ogawa, Junko Ito, Susumu Yokoya, Noriaki Fukuhara, Mitsuo Yamaguchi-Okada, Hiroshi Nishioka, Shozo Yamada, Tsuyoshi Isojima
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Abstract

Objective: Craniopharyngioma (CP) has mostly nonspecific symptoms, leading to delayed diagnosis. Early indicators of CP in children are needed for early diagnosis and to detect postoperative growth patterns for their optimal care. This study aimed to investigate the clinical characteristics and postoperative growth patterns in Japanese children with CP.

Design: Retrospective analysis of medical records (2000-2022).

Methods: Seventy-three children (median age at diagnosis = 9.3 (0.9-18) years; 44 females) from Toranomon Hospital, Tokyo, Japan, who were diagnosed with CP and undergoing trans-sphenoidal or trans-cranial surgery, or both, were followed up for at least 3 years. We assessed clinical characteristics and changes in height and body mass index (BMI) standard deviation scores (SDSs).

Results: The SDSs for height and BMI were -1.7 (-4.0 to 1.3) and 0.21 (-2.3 to 2.2), respectively. Chief complaints at diagnosis were neurologic (n = 25, 34.2%), endocrine (n = 22, 30.1%), or ophthalmic (n = 22, 30.1%), while accompanying neurologic, endocrine, and ophthalmic symptoms were present in 34 (46.6%), 63 (86.3%), and 37 (50.7%) patients, respectively. One year after surgery, growth without growth hormone (GWGH) was detected in seven patients (13%), which could be categorized based on MRI-evident hypothalamic involvement (transient: n = 3, 5.6%; permanent: n = 4, 7.4%). Preoperative hydrocephalus (n = 21, 32.8%) was the only factor significantly associated with postoperative GWGH at 1 year (p = 0.037).

Conclusion: Children with CP have distinctive clinical characteristics and postoperative growth patterns. Identifying symptoms using school-based auxological measurements could help in early diagnosis.

日本颅咽管瘤患儿的临床特征和术后生长情况
目的:颅咽管瘤(CP)大多具有非特异性症状,导致诊断延迟。儿童颅咽管瘤需要早期指标以进行早期诊断,并检测术后生长模式,以获得最佳护理。本研究旨在调查日本 CP 儿童的临床特征和术后生长模式:设计:回顾性分析病历(2000-2022 年):对日本东京虎之门医院的 73 名儿童(诊断时的中位年龄 = 9.3 (0.9-18) 岁;44 名女性)进行了至少 3 年的随访。我们评估了临床特征以及身高和体重指数(BMI)标准偏差评分(SDS)的变化:身高和体重指数标准偏差分别为-1.7(-4.0至1.3)和0.21(-2.3至2.2)。确诊时的主诉为神经系统(25人,占34.2%)、内分泌(22人,占30.1%)或眼科(22人,占30.1%),而伴有神经系统、内分泌和眼科症状的患者分别为34人(46.6%)、63人(86.3%)和37人(50.7%)。术后一年,7 名患者(13%)被检测出生长激素缺乏(GWGH),可根据核磁共振成像显示的下丘脑受累情况进行分类(一过性:3 人,占 5.6%;永久性:4 人,占 7.4%)。术前脑积水(n = 21,32.8%)是与术后 1 年 GWGH 显著相关的唯一因素(p = 0.037):结论:CP 患儿具有独特的临床特征和术后生长模式。结论:CP 患儿具有独特的临床特征和术后生长模式,利用校内辅助测量来识别症状有助于早期诊断。
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来源期刊
Clinical Endocrinology
Clinical Endocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
3.10%
发文量
192
审稿时长
1 months
期刊介绍: Clinical Endocrinology publishes papers and reviews which focus on the clinical aspects of endocrinology, including the clinical application of molecular endocrinology. It does not publish papers relating directly to diabetes care and clinical management. It features reviews, original papers, commentaries, correspondence and Clinical Questions. Clinical Endocrinology is essential reading not only for those engaged in endocrinological research but also for those involved primarily in clinical practice.
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