首页> 外文期刊>Polish Journal of Radiology >Radiological diagnostics in neonates with different types of congenital cystic adenomatoid malformation of the lungs (CCAM) treated in Polish Mother’s Memorial Hospital Research Institute (PMMHRI) in 1991-2005
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Radiological diagnostics in neonates with different types of congenital cystic adenomatoid malformation of the lungs (CCAM) treated in Polish Mother’s Memorial Hospital Research Institute (PMMHRI) in 1991-2005

机译:波兰母亲纪念医院研究所(PMMHRI)于1991-2005年对患有不同类型的先天性肺囊性腺瘤样畸形(CCAM)的新生儿进行放射学诊断

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Background: Congenital cystic adenomatoid malformation of the lungs (CCAM) is a rare congenital malformation of the respiratory tract. Authors present possibilities of the diagnostics of neonates with presumed CCAM based on radiological and morphological assessment of the respiratory tract. Clinical course of the CCAM may vary from uneventful to serious with different stage of the respiratory distress.The aim of the study was to establish diagnostic and clinical criteria of CCAM for neonates based on postnatal diagnostics in the reference centre. Material/ Methods: We studied 27 cases of neonates with different types of CCAM (type I, II, III) who had been diagnosed and/or treated in the Neonatal Department of PMMHRI in 01.01.1991-31.03.2005. The diagnosis was established based on clinical course of the malformation, chest x-ray and CT of the neonate’s lungs, autopsy and/or histopathology.Results: In the Neonatal Department of PMMHRI in 01.01.1991-31.03.2005 we observed 8 cases of CCAM type I (29,7%), 10 cases of CCAM type II (37%) and 9 cases of CCAM type III (33,3%). Diagnostic criteria were established based on radiological diagnostics of 17 cases and were confirmed by pathology. In 10 remaining cases of CCAM diagnosis was established by authopsy. Differential diagnosis included diaphragmatic hernia, bronchogenic cyst, enterogenic cyst, lung sequestrqtion, congenital lobar emphysema, hypoplasia or agenesis of the lungs, pneumonia/RDS. The guideline was established. Conclusions: 1. In case of CCAM suspicion monitoring in reference center is required 2. Surgical treatment should be applied based on the postnatal radiological diagnosis. 3. In case of CCAM in neonate complete differential diagnosis is required. 4. Asymptomatic course of CCAM or with a very few signs from respiratory tract can be difficult for identification both clinical and radiological.
机译:背景:先天性肺囊性腺瘤样畸形(CCAM)是一种罕见的先天性呼吸道畸形。作者介绍了基于呼吸道的放射学和形态学评估诊断为CCAM的新生儿的可能性。在不同的呼吸窘迫阶段,CCAM的临床过程可能从不平稳到严重不等。该研究的目的是基于参考中心的产后诊断建立新生儿CCAM的诊断和临床标准。材料/方法:我们研究了1991年1月1日至3月1日在PMMHRI新生儿科诊断和/或治疗的27例具有不同类型CCAM(I,II,III型)的新生儿。诊断是根据新生儿肺部畸形,胸部X线检查和CT的临床过程,尸检和/或组织病理学确定的。结果:1991年1月1日在PMMHRI新生儿科观察到8例I型CCAM(29.7%),II型CCAM 10例(37%)和III型CCAM 9例(33,3%)。根据17例放射学诊断结果建立诊断标准,并经病理证实。 authopsy确定了其余10例CCAM诊断。鉴别诊断包括diaphragm疝,支气管囊肿,肠源性囊肿,肺隔离症,先天性大叶肺气肿,肺发育不全或发育不全,肺炎/ RDS。指南已建立。结论:1.如果需要在参考中心进行CCAM怀疑检查,2.应根据产后放射学诊断进行手术治疗。 3.对于新生儿的CCAM,需要完全鉴别诊断。 4. CCAM的无症状病程或很少有呼吸道体征可能难以识别临床和影像学。

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