Congenital Cystic Adenomatoid Malformation of the Lung—Type III
| Autor: | Amy N. Ratner, Garry Frisoli |
|---|---|
| Rok vydání: | 1999 |
| Předmět: |
Fetus
Pathology medicine.medical_specialty Lung Radiological and Ultrasound Technology business.industry Anatomy medicine.disease Pulmonary sequestration Lesion medicine.anatomical_structure medicine Congenital Cystic Adenomatoid Malformation Hamartoma Radiology Nuclear Medicine and imaging Diaphragmatic hernia Respiratory system medicine.symptom business |
| Zdroj: | Journal of Diagnostic Medical Sonography. 15:249-251 |
| ISSN: | 1552-5430 8756-4793 |
| DOI: | 10.1177/875647939901500605 |
| Popis: | Congenital cystic adenomatoid malformation of the lung (CCAML) is a hamartoma of the plung resulting from the overgrowth of terminal respiratory elements (adenomatoid). The lesion is almost always unilateral, with no lobe or gender preference. CCAML has been classified into three tpes, depending on the size of the cysts. Type I consists of one or several large cysts. ranging from 2 to 10 cm in diameter. Type II has multiple small cysts less than 1.5 cm in diameter. Type III is made up of a large solid mass affecting the entire lobe. The following case report is of a fetus diagnosed at 22 weeks with congenital cystic adenomatoid malformation of the lung type III. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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