Suppr超能文献

巨大下丘脑错构瘤:病例报告及文献综述

Giant hypothalamic hamartoma: case report and literature review.

作者信息

Alves Cresio, Barbosa Veronica, Machado Marcos

机构信息

Pediatric Endocrinology Unit, Hospital Universitario Prof. Edgard Santos, Faculty of Medicine, Federal University of Bahia, Salvador, Bahia, Brazil.

出版信息

Childs Nerv Syst. 2013 Mar;29(3):513-6. doi: 10.1007/s00381-013-2022-y. Epub 2013 Jan 13.

Abstract

INTRODUCTION

Hypothalamic hamartomas are very rare (1:200,000) and range in size from 17.9 to 18 mm. When their dimensions exceed 30-40 mm, they are classified as giant hypothalamic hamartomas.

METHODS

We present a 14-month-old boy with central precocious puberty and gelastic seizures in whom a magnetic resonance imaging scan revealed a giant hypothalamic hamartoma measuring 50 × 50 × 40 mm.

RESULTS

In the 11 cases described so far, we found that in comparison to the average-size lesion, giant hypothalamic hamartomas had a lower frequency of precocious puberty, but a similar frequency of seizures. The mean age at diagnosis was younger, and males were more affected than females. Magnetic resonance imaging results were similar with the exception of mass effect.

CONCLUSIONS

Giant hypothalamic hamartomas had a higher tendency to adhere to surrounding structures. Their invasiveness and cystic degeneration were frequent findings among the 11 studies. Surgical removal was ineffective in controlling refractory epilepsy and caused postoperative morbidity in all patients.

摘要

引言

下丘脑错构瘤非常罕见(1:200,000),大小从17.9毫米到18毫米不等。当它们的尺寸超过30 - 40毫米时,就被归类为巨大下丘脑错构瘤。

方法

我们报告一名14个月大患有中枢性性早熟和痴笑性癫痫的男孩,其磁共振成像扫描显示一个大小为50×50×40毫米的巨大下丘脑错构瘤。

结果

在目前已报道的11例病例中,我们发现与平均大小的病变相比,巨大下丘脑错构瘤性早熟的发生率较低,但癫痫发作的发生率相似。诊断时的平均年龄更小,男性比女性受影响更严重。除占位效应外,磁共振成像结果相似。

结论

巨大下丘脑错构瘤更倾向于附着在周围结构上。在这11项研究中,它们的侵袭性和囊性变很常见。手术切除对控制难治性癫痫无效,且所有患者术后均出现并发症。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验