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变形综合征:一个困难的诊断与管理方案。

Proteus Syndrome: a difficult diagnosis and management plan.

作者信息

Popescu M D, Burnei G, Draghici L, Draghici I

机构信息

"Carol Davila" University of Medicine and Pharmacy, Bucharest ; Department of Pediatric Surgery, "Maria Sklodowska Curie" Clinical Emergency Hospital for Children, Bucharest.

"Carol Davila" University of Medicine and Pharmacy, Bucharest ; Department of General Surgery, "Sf. Ioan" Clinical Emergency Hospital, Bucharest.

出版信息

J Med Life. 2014 Oct-Dec;7(4):563-6.

Abstract

RATIONALE

Proteus Syndrome (PS) is an extremely rare congenital pathology that causes overgrowth of multiple tissues, in particular bone and fat, following a mosaic pattern. The estimated incidence is of less than 1 per 1,000.000 live births and represents a significant challenge to the pediatric and orthopedic surgeons in order to establish a diagnosis and to elaborate a management plan.

OBJECTIVES

We had the opportunity of treating many children who were afflicted by overgrowth syndromes and have been previously misdiagnosed as Proteus Syndrome in our department of pediatric and orthopedic surgery of "Maria Sklodowska Curie" Clinical Emergency Hospital for Children. This study helped us develop a diagnostic for these patients and report the first case of a confirmed PS in Romania.

METHODS AND RESULTS

We report the case of a 5-year-old white male who is in the attention of the clinic since birth. He presented with multiple overgrowth bone segments, fatty subcutaneous or intraabdominal tumors and other connective tissues abnormalities. All the tests performed confirmed the diagnosis of PS at the age of 4 and the management is still to be decided.

DISCUSSIONS

We followed the latest diagnostic indications and the patient fulfilled the general and specific criteria. The treatment is still in progress and it represents a challenge for the multidisciplinary medical team.

摘要

理论依据

变形综合征(PS)是一种极为罕见的先天性疾病,会导致多种组织过度生长,尤其是骨骼和脂肪,呈嵌合模式。估计发病率低于每100万活产儿1例,这对儿科和骨科外科医生来说是一个重大挑战,难以进行诊断并制定治疗方案。

目的

我们有机会治疗了许多患有过度生长综合征的儿童,这些儿童先前在“玛丽亚·斯克沃多夫斯卡·居里”儿童临床急救医院的儿科和骨科手术科室被误诊为变形综合征。这项研究帮助我们为这些患者制定了诊断方法,并报告了罗马尼亚首例确诊的PS病例。

方法与结果

我们报告了一名5岁白人男性的病例,自出生起就受到临床关注。他出现了多个骨骼过度生长节段、皮下或腹腔内脂肪肿瘤以及其他结缔组织异常。所有检查在其4岁时确诊为PS,治疗方案仍有待确定。

讨论

我们遵循了最新的诊断指征,该患者符合一般和特定标准。治疗仍在进行中,这对多学科医疗团队来说是一项挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c5c/4316140/14657c279fd5/JMedLife-07-563-g001.jpg

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