Fetal lung interstitial tumor: The first Japanese case report and a comparison with fetal lung tissue and congenital cystic adenomatoid malformation/congenital pulmonary airway malformation type 3

2013 ◽  
Vol 63 (10) ◽  
pp. 506-509 ◽  
Author(s):  
Mariko Yoshida ◽  
Mio Tanaka ◽  
Kiyoshi Gomi ◽  
Tadashi Iwanaka ◽  
Louis P. Dehner ◽  
...  
Keyword(s):  
Case Report ◽  
Lung Tissue ◽  
Fetal Lung ◽  
Congenital Cystic Adenomatoid Malformation ◽  
Congenital Pulmonary Airway Malformation ◽  
Japanese Case ◽  
Cystic Adenomatoid Malformation ◽  
Pulmonary Airway ◽  
Type 3

Prenatal Diagnosis of Fetal Trisomy 5 Mosaicism with Congenital Pulmonary Airway Malformation Type 3: A Case Report

2020 ◽  
pp. 1-7
Author(s):  
Maria Paola Bonasoni ◽  
Giuseppina Comitini ◽  
Gabriele Tonni ◽  
Silvia Asioli ◽  
Veronica Barbieri ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Congenital Pulmonary Airway Malformation ◽  
Pulmonary Airway ◽  
Type 3

Congenital Pulmonary Airway Malformation (Congenital Cystic Adenomatoid Malformation) with Multiple Extrapulmonary Anomalies: Autopsy Report of a Fetus at 19 Weeks of Gestation

2004 ◽  
Vol 7 (6) ◽  
pp. 661-666 ◽  
Author(s):  
Truc T. Pham ◽  
Kurt Benirschke ◽  
Eliezer Masliah ◽  
J. Thomas Stocker ◽  
Eunhee S. Yi
Keyword(s):  
Surfactant Protein ◽  
Maternal Serum ◽  
Congenital Cystic Adenomatoid Malformation ◽  
Normal Female ◽  
Cytokeratin 20 ◽  
Congenital Pulmonary Airway Malformation ◽  
Thyroid Transcription Factor 1 ◽  
Cystic Adenomatoid Malformation ◽  
Estimated Risk ◽  
Pulmonary Airway

Congenital pulmonary airway malformation, or congenital cystic adenomatoid malformation, is postulated to be a disorder of pulmonary airway morphogenesis and encompasses 5 different types with distinct levels or stages of tracheobronchial development. We present a unique case of type 2 congenital pulmonary airway malformation with a previously undocumented combination of multiple extrapulmonary anomalies, featuring ipsilateral multicystic renal dysgenesis, contralateral renal agenesis, and ovarian germ cell hypoplasia, diagnosed in a 19-week gestational age fetus by autopsy. Epithelial cells comprising the pulmonary lesions were positive for thyroid transcription factor-1, surfactant protein-B, and cytokeratin-7 but negative for cytokeratin-20 immunostainings, with the pattern seen in normal terminal bronchioles. Chromosomal analysis showed a normal female karyotype, despite a high estimated risk for Down syndrome suggested by the low maternal serum α-fetoprotein level.

scholarly journals It is not pneumothorax: Multicystic lung lesion in a six-year-old child

2016 ◽  
Vol 26 (2) ◽  
pp. 121-124
Author(s):  
Eman Sobh ◽  
Amira Bahour ◽  
Shady Elia Anis
Keyword(s):  
Surgical Resection ◽  
Lung Development ◽  
Lung Lesion ◽  
Congenital Cystic Adenomatoid Malformation ◽  
Congenital Pulmonary Airway Malformation ◽  
Cystic Lung ◽  
Cystic Adenomatoid Malformation ◽  
Pulmonary Airway ◽  
Cystic Lung Lesion

Congenital cystic adenomatoid malformation (CCAM) – recently reported as congenital pulmonary airway malformation – is a rare abnormality of lung development. We present a case of a six-year-old child having a cystic lung lesion that proved to be CCAM after surgical resection. The child is performing well on follow-up.

Pleuropulmonary Blastoma Developing in a Case of Misinterpreted Congenital Pulmonary Airway Malformation: a Case Report

2018 ◽  
Vol 37 (5) ◽  
pp. 377-386 ◽  
Author(s):  
Moupali Ghosh ◽  
Nelofar Islam ◽  
Arindam Ghosh ◽  
Priyanka Maity Chaudhuri ◽  
Koushik Saha ◽  
...  
Keyword(s):  
Case Report ◽  
Pleuropulmonary Blastoma ◽  
Congenital Pulmonary Airway Malformation ◽  
Pulmonary Airway
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