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Congenital Pulmonary Airway Malformation with Pulmonary Arteriovenous Malformation in Adulthood: A Case Report
Takehiro Suzuki1, Naohiro Kobayashi1, Yohei Yatagai2
1Department of General Thoracic Surgery, Tsukuba University Hospital, Tsukuba, Ibaraki, Japan.
Insights
This study reports a rare adult case of coexisting congenital pulmonary airway malformation (CPAM) and pulmonary arteriovenous malformation (PAVM). Surgical intervention was successful in managing the coexisting conditions and preventing complications.
Area of Science:
- Pulmonology
- Thoracic Surgery
- Medical Imaging
Background:
- Congenital pulmonary airway malformation (CPAM) is typically diagnosed in infancy or childhood.
- Pulmonary arteriovenous malformation (PAVM) is an abnormal vascular connection often linked to hereditary hemorrhagic telangiectasia.
- Coexistence of CPAM and PAVM is exceptionally rare in adults.
Observation:
- A 26-year-old woman presented with incidentally discovered lung abnormalities.
- Chest CT revealed multiple lung cysts (suspected CPAM Type 1) and two PAVMs in the left lower lobe.
- Pulmonary aspergillosis was diagnosed and treated, but one PAVM enlarged during treatment.
Findings:
- Surgical resection (left lower lobectomy) was performed due to uncontrolled infection and PAVM enlargement.
- Pathological diagnosis confirmed CPAM Type 1.
- The patient experienced no complications post-surgery.
Implications:
- Simultaneous CPAM and PAVM in adults is a rare clinical entity.
- Pulmonary infections associated with CPAM may contribute to PAVM development or enlargement.
- Surgical management should be considered for coexisting CPAM and PAVM to prevent serious complications.
Introduction:
Congenital pulmonary airway malformation (CPAM) is a congenital condition rarely detected in adults because most cases of CPAM are found through prenatal testing or through testing for recurrent pneumonia or lung abscesses in childhood. Pulmonary arteriovenous malformation (PAVM) is an abnormal vascular connection between the pulmonary arteries and veins, which is often related to hereditary hemorrhagic telangiectasia, but can also be induced by infections, trauma, or thoracic surgery. Herein, we report an adult case of coexisting CPAM and PAVM.
Case Presentation:
The patient was a 26-year-old woman. A medical checkup chest X-ray showed abnormalities. The patient had no past medical history, including of bleeding tendency or repeated pneumonia, and no familial history of CPAM and PAVM. A chest CT revealed multiple lung cysts (maximum diameter of 40 mm) in the left lower lobe of the lung, and congenital pulmonary cysts were suspected. The chest CT also showed two PAVMs (vessel diameters of 6 mm and 4 mm) in the same left lower lobe. Serum tests were positive for Aspergillus-specific antibodies and β-D-glucan, and pulmonary aspergillosis was diagnosed. An antifungal agent (itraconazole) was administered. However, consolidations had developed 9 months after, and the antifungal agent was changed to voriconazole. Then, the consolidations diminished slightly but nevertheless remained, and one of the PAVMs increased in diameter from 6 mm to 10 mm. A left lower lobectomy under thoracoscopy was performed owing to the uncontrolled infection and the risk of complications with PAVMs. The pathological diagnosis of the pulmonary cysts was CPAM type 1. The patient had no symptoms or complications after the surgery.
Conclusions:
Cases of CPAM with PAVM are rare, especially in adults. CPAM often leads to pulmonary infection, and the pulmonary infection is known to be one of the causes of PAVM. In our case, Aspergillus might have infected the pulmonary cysts and affected the enlargement of the vascular diameter of PAVM. If CPAM and PAVM are present simultaneously, surgical treatment should be considered to prevent complications associated with CPAM and PAVM.
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