نتایج جستجو برای: cystic adenomatoid malformation of lung

تعداد نتایج: 21224878  

Journal: :European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery 2006
Indalecio Cano Juan L Antón-Pacheco Araceli García Steve Rothenberg

OBJECTIVE Congenital lung malformations are often discovered on routine prenatal sonography or postnatal imaging. Lesions such as congenital cystic adenomatoid malformation or pulmonary sequestration may be asymptomatic at birth, and their management is controversial. Thoracoscopy in children has been mainly used for lung biopsy and for the treatment of empyema and recurrent pneumothorax. Very ...

2016
Francesco Molinaro Rossella Angotti Alfredo Garzi Vincenzo Giuseppe Di Crescenzo Antonio Cortese Mario Messina

Congenital cystic lung lesions are a rare but clinically significant group of anomalies, including congenital cystic adenomatoid malformation (CCAM), pulmonary sequestration, congenital lobar emphysema (CLE) and bronchogenic cysts. Despite the knowledge of these lesions increasing in the last years, some aspects are still debated and controversial. The diagnosis is certainly one aspect which un...

2012
Ho Sung Lee Jae Sung Choi Ki Hyun Seo Ju Ock Na Yong Hoon Kim Mi Hye Oh Sung Shick Jou

Congenital cystic adenomatoid malformation of the lung is a rare disease that shows multiple cystic lesions in pulmonary tissues in the development process. It was first described by Chin et al.1 in 1949 and its incidence is known to be 1:25,000 to 1:35,0002. With the development of prenatal diagnosis, this disease can be diagnosed in 60% and detected within 2 years because of such symptoms as ...

Farzaneh Jalali, Sepideh Siadati,

CCAM is a rare conolition in the neonatal Period. Two babies were admitted to Mofid hospital with cyanosis and respiratory distress. Pneumectomy was done for both of them for space occupaying lesion. Pathology examination of first case showed area of cuboidal epithelium lined tubes and spaces resembling fetal bronchioles, which are torn in folds. In second case, pathologic examination revealed...

Journal: :The Malaysian journal of pathology 2000
H K Darnal H Ibrahim S S Mutum

An eight-week-old infant presented with dyspnoea two months after an uneventful normal vaginal delivery. Radiologically, a sharply outlined radiolucent area surrounded by atelectasis was seen in the upper lobe of the left lung. A left upper lobectomy was performed with the clinical impression of congenital pulmonary emphysema. The resected specimen displayed multiple cysts 2 to 6 mm in diameter...

2013
Ji-Hye Seok Eun-Ju Kim Jong-Seouk Ban Sang-Gon Lee Ji-Hyang Lee Da-Mi Seo Kwang-Seok Shim

There are many methods for achieving one-lung ventilation (OLV) during thoracic surgery in neonates and the accuracy of OLV may affect postoperative outcome. The authors have performed OLV using a 5 Fr Arndt endobronchial blocker (AEB, Cook Inc., Bloomington, IN, USA) on a neonate diagnosed with congenital cystic adenomatoid malformation and respiratory distress syndrome (RDS) associated with m...

Journal: :Journal of clinical ultrasound : JCU 1982
M H Jaffe E R Bank T M Silver R A Bowerman

Pulmonary sequestration is a congenital anomaly in which aberrant, nonfunctioning lung tissue receives its entire blood supply from the systemic circulation. Early diagnosis may be difficult because the radiographic and clinical presentation may be mimicked by other lesions, such as cystic adenomatoid malformation, congenital bronchogenic cyst, pleural effusion, congenital diaphragmatic hernia,...

Journal: :The Journal of the Japanese Association for Chest Surgery 2012

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