Caracterización ecográfica y anatomopatológica de pacientes con artrogriposis múltiple congénita. Serie de casos

Q4 Medicine
D. K. Sandoval-Martínez, Luz Ángela Gutiérrez-Sánchez, M. Z. Jaimes-Sanabria
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引用次数: 0

Abstract

OBJECTIVE: To describe a series of cases of multiple congenital arthrogryposes reported in fetal and newborn autopsies, performed in the pathology department of a high complexity hospital, between September 2016 and April 2019. MATERIALS AND METHODS : A retrospective descriptive study of a series of cases of autopsies, with anatomopathological findings of multiple congenital arthrogryposes, performed on fetuses and newborns, during the established time lapse. RESULTS: The analysis included 8 cases with an anatomopathological diagnose of multiple congenital arthrogryposes, six of them with PCR positive for ZIKA. Among the ultrasound reports, altered limb movement and abnormal central nervous system development (corpus callosum and cerebellum), were the main findings; which were confirmed by the anatomopathological study. Regarding perinatal results, 7/8 cases died during the first hour of life. CONCLUSION: In case of suspicion or confirmation of multiple congenital arthrogry- poses by ultrasound, infectious processes should be ruled out; also, a clinical genetics consult should be sought to exclude associated alterations. en el sistema nervioso central. Letra A. Hiperdensidades a nivel talámico, caso 1 semana 26; letra B. Hiperdensidades en cerebelo, caso 6, semana 32; letra C Aspecto macroscópico de corte coronal en el que se reconocen (en los círculos rojos) lesiones amarillentas concordantes con hiperecogenicidades ecográficas, caso letra D. Histología de las calcificaciones (+) corticales en cortes del encéfalo, caso teñidos eosina letra Corte de la región periventricular en la que se observan manguitos perivasculares señala reactividad glial subependimaria, con hematoxilina eosina manguitos perivasculares reactividad glial subependimaria, caso eosina
先天性多发性骨关节炎患者的超声和解剖病理学特征。案例系列
目的:对2016年9月至2019年4月在一家高复杂性医院病理部进行的胎儿和新生儿尸检中报告的一系列先天性多发性关节挛缩病例进行分析。材料和方法:回顾性描述性研究的一系列病例尸检,与解剖病理发现的多种先天性关节挛缩,执行胎儿和新生儿,在既定的时间推移。结果:分析8例经解剖病理诊断为多发性先天性关节挛缩的患者,其中6例寨卡病毒PCR阳性。超声报告以肢体运动改变和中枢神经系统(胼胝体和小脑)发育异常为主要表现;解剖病理研究证实了这一点。关于围产期结果,7/8例在出生后一小时内死亡。结论:超声检查怀疑或确认多发先天性关节痉挛时,应排除感染过程;此外,临床遗传学咨询应寻求排除相关的改变。enel sistema nervioso central。Letra a . Hiperdensidades a nivel talámico, caso 1 semana 26;[a] [b] [a] [b] [b] [b] [c] [6];letra C Aspecto macroscópico de corte corononal en que que se reconocen (en los círculos rojos) lesiones amarillentas concorantes con hipercogenicidades ecográficas, caso letra D. Histología de las钙化(+)皮质en cortes en cortes del encacfalo, caso teñidos eosina letra corte la región心室周围en la que se observan manguitos血管周围señala反应性神经胶质下,con hematoxilina eosina manguitos血管周围反应性神经胶质下,caso eosina manguitos血管周围反应性神经胶质下,caso eosina
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来源期刊
Ginecologia y obstetricia de Mexico
Ginecologia y obstetricia de Mexico Medicine-Obstetrics and Gynecology
CiteScore
0.20
自引率
0.00%
发文量
107
期刊介绍: Indizada en: Artemisa, Embase Cd/Obstetrics and Gynecology, Embase. Co/Pediatrics, Excerfta Médica, Índice Médico Latinoamericano, Lulacs, Medline, Science Citation Index, Ulrich, Ebsco.
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