نتایج جستجو برای: cystic adenomatoid malformation of lung

تعداد نتایج: 21224878  

Journal: :American journal of respiratory cell and molecular biology 2008
Sílvia Gonzaga Tiago Henriques-Coelho Marcus Davey Philip W Zoltick Adelino F Leite-Moreira Jorge Correia-Pinto Alan W Flake

Fibroblast growth factor-10 (FGF10) is a mesenchymal growth factor, involved in epithelial and mesenchymal interactions during lung branching morphogenesis. In the present work, FGF10 overexpression was transiently induced in a temporally and spatially restricted manner, during the pseudoglandular or canalicular stages of rat lung development, by trans-uterine ultrasound-guided intraparenchymal...

Journal: :International Journal of Reproduction, Contraception, Obstetrics and Gynecology 2017

2011
J. Toelen M. Carlon F. Claus R. Gijsbers I. Sandaite K. Dierickx R. Devlieger K. Devriendt A. Debeer M. Proesmans Z. Debyser A.J. Deprest

The widespread use of prenatal ultrasound has made the fetus a patient. A number of conditions diagnosed as such may require therapy prior to birth. Herein we describe past, current and potential future procedures designed to treat pulmonary conditions in the antenatal period. When congenital cystic adenomatoid malformation (CCAM) is -associated with fetal hydrops, treatment is required. Prior ...

Journal: :Respiratory care 2012
Ryan J McDonough Alexander S Niven Keith A Havenstrite

Congenital parenchymal lung malformations have an estimated incidence at 1:25,000-1:35,000 births. We present a case of this rare congenital abnormality in a 38 year-old male, review the current literature with discussion of proposed causes, malignant potential, and management strategies. A 38-year-old white male presented with a 4-day history of chronic stable hemoptysis. Social history was n...

2012
Hyun Jung Kwak Ji-Yong Moon Sa-Il Kim Tae Hyung Kim Jang Won Sohn Sang-Heon Kim Dong Ho Shin Sung Soo Park Won Sang Chung Ho Joo Yoon

UNLABELLED Congenital cystic adenomatoid malformation (CCAM) is an uncommon, nonhereditary anomaly caused by arrest of lung. Patients with CCAM may present with respiratory distress as newborns, or may remain asymptomatic until later in life. CCAM type I is rarely found in association with bronchial atresia (BA) in adults; we present such a case. CASE A 54-year-old female presented with chron...

Journal: :International journal of clinical and experimental pathology 2013
Mitsuaki Ishida Tomoyuki Igarashi Koji Teramoto Jun Hanaoka Muneo Iwai Keiko Yoshida Akiko Kagotani Noriaki Tezuka Hidetoshi Okabe

Congenital cystic adenomatoid malformation (CCAM) of the lung is a rare hamartomatous cystic lesion, characterized by the presence of large cysts, which are histopathologically lined by pseudostratified ciliated cells. It has been recognized that rare cases of type 1 CCAM show malignant transformation, usually bronchioloalveolar carcinoma (BAC) or adenocarcinoma. Herein, we describe a case of B...

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