نتایج جستجو برای: cystic adenomatoid malformation

تعداد نتایج: 62304  

2018
Juneyoug Koh Euiseok Jung Se Jin Jang Dong Kwan Kim Byong Sop Lee Ki-Soo Kim Ellen Ai-Rhan Kim

Congenital pulmonary airway malformation (CPAM), previously known as congenital cystic adenomatoid malformation, is a rare developmental lung abnormality associated with rhabdomyosarcoma, pleuropulmonary blastoma, and mucinous adenocarcinoma of the lung. We report an unusual case of a 10-day-old male newborn with a left lower lobe pulmonary cyst who underwent lobectomy, which revealed type II C...

Journal: :Journal of perinatal medicine 2009
Lucia Aite Antonio Zaccara Alessandro Trucchi Christiana Brizzi Antonella Nahom Barbara Iacobelli Irma Capolupo Pietro Bagolan

AIM To assess reasons for higher levels of anxiety generated by prenatal counselling of a condition with good outcome such as cystic adenomatoid malformation (CCAM) of the lung compared to a life-threatening malformation such as congenital diaphragmatic hernia (CDH). MATERIALS AND METHODS The Spielberger State-Trait Anxiety Inventory (STAI-S) was used to measure anxiety in two groups of mothe...

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 ...

2013
Yong Jin Kim Do Young Kim Jung Woong Seo Song Am Lee Jae Joon Hwang Hee Joung Kim Kye Young Lee

We present a case of congenital cystic adenomatoid malformation (CCAM) in a 25-year-old male who was presented with chronic cough. Chest radiography revealed an abnormal mass-like shadow in the right lower pulmonary zone. A contrast enhanced computed tomography showed an 11 cm solid, cystic mixed mass on the right lower lobe. A right lower lobectomy was performed by video-assisted thoracoscopic...

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 ...

Journal: :The Journal of the Japanese Association for Chest Surgery 2016

2017
Mingxia Shi Firas Al-Delfi Majd Al Shaarani Kurt Knowles James Cotelingam

Adenomatoid tumor of the ovary is rare, and so are collision tumors in this location. The most common histological combination of ovarian collision tumors is the coexistence of mature cystic teratoma with ovarian cystadenoma or cystadenocarcinoma. Presented herein is a rare case of ovarian adenomatoid tumor found incidentally and coexisting with mature cystic teratoma. A 44-year-old woman prese...

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