1型先天性大囊性囊性腺瘤样畸形的自然消退:一个罕见的表现

MAMC Journal of Medical Sciences Pub Date : 2022-05-01 DOI:10.4103/mamcjms.mamcjms_79_21

Shishir Kumar, S. Panda, S. Neogi, S. Ratan

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引用次数: 0

摘要

摘要我们报告了一例6个月大的男孩，他因脓胸而出现呼吸窘迫，最初是通过肋间引流管治疗的。计算机断层扫描证实了1型先天性囊性腺瘤样畸形（CCAM）的诊断。随后，在手术干预之前，脓胸和CCAM得到了自发缓解。我们的病例说明先天性脑脊髓炎的产后自发消退，这是罕见的。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Spontaneous Resolution of Type 1 Macrocystic Congenital Cystic Adenomatoid Malformation: A Rare Presentation

Abstract We present a case of 6-month-old boy who presented with respiratory distress due to empyema, which was initially managed by the intercostal drain. Computed tomography scan confirmed the diagnosis of type 1 congenital cystic adenomatoid malformation (CCAM). Subsequently, there was the spontaneous resolution of empyema and CCAM prior to surgical intervention. Our case illustrates the postnatal spontaneous resolution of CCAM, which is rare.

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来源期刊

MAMC Journal of Medical Sciences

自引率

0.00%

发文量

审稿时长

20 weeks