Les malformations pulmonaires kystiques : polymorphisme clinique et radiologique. À propos de 30 observations

Khémiri, M.; Khaldi, F.; Hamzaoui, A.; Chaouachi, B.; Hamzaoui, M.; Bêcher, S. Ben; Bellagha, I.; Barsaoui, S.

doi:10.1016/j.pneumo.2009.08.002

Cited by 8 publications

(11 citation statements)

References 38 publications

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“…It leads to a low rate of postoperative morbidity and mortality, shorter hospital stay, and mainly lowers the risk of recurrence [ 1 , 3 , 9 , 13 ]. It can lead to more or less severe respiratory failure [ 8 ], such as in our case.…”

Section: Discussionmentioning

confidence: 95%

“…The imagery is based primarily on CT scan, but the diagnosis remains difficult because of its scarcity [ 4 , 8 ]. It is necessary to resort to experienced radiologists to distinguish between CCAM and other pulmonary diseases (that is, pulmonary abscess, diaphragmatic hernia, and lung tumors) [ 3 , 4 ].…”

Section: Discussionmentioning

confidence: 99%

“…The elective and early surgical excision of CCAM would be justified to avoid complications and malignant transformation [1.3]. It was proposed from the age of 3 to 6 months [ 8 , 13 ].…”

Section: Discussionmentioning

confidence: 99%

“…Complicated forms are therapeutic emergencies: drainage in utero in macrocystic lesions, maternal corticosteroid in compressive microcystic forms, percutaneous sclerotherapy intrauterine, and early postnatal surgical resection [ 1 , 5 , 8 ]. To further reduce the risk of recurrence, some authors recommend not only the removal of the defect, but rather a lobectomy or pneumonectomy [ 11 , 13 ].…”

Section: Discussionmentioning

confidence: 99%

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Congenital cystic adenomatoid malformation – dangers of misdiagnosis: a case report

et al. 2017

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BackgroundCongenital cystic adenomatoid malformation is a rare pulmonary malformation, but is the most common lung malformation observed in children. In developing countries, such as Morocco, prenatal diagnosis is missing. Congenital cystic adenomatoid malformation may occur after birth in the presence of complications and needs a computed tomography scan for confirmation. However, our lack of awareness of this malformation has been responsible for a late and wrong diagnosis along with therapeutic errors. We report the first case in Morocco where diagnosis is confirmed by histology after death.Case presentationA 10-month-old Arab boy was prescribed various antibiotics (including anti-staphylococcal) and endured repeated chest drainages, leading to his death just after radiological diagnosis and instant surgery.ConclusionsThe goal of this case report is to firmly express the need for both pediatricians and radiologists to enlarge diagnosis investigations, especially of congenital or constitutional entities in children, as soon as recurrence of respiratory distress and pulmonary infections are manifested. We also emphasize this important entity because of its frequency, to avoid the eventual therapeutic errors.

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Section: Discussionmentioning

confidence: 95%

Section: Discussionmentioning

confidence: 99%

“…The elective and early surgical excision of CCAM would be justified to avoid complications and malignant transformation [1.3]. It was proposed from the age of 3 to 6 months [ 8 , 13 ].…”

Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

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Congenital cystic adenomatoid malformation – dangers of misdiagnosis: a case report

et al. 2017

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“…CPAM share similar embryologic and clinical characteristics with PS, CLE, and bronchogenic cyst (BC), the four major congenital cystic lesions that are an important cause of morbidity in neonates, infants, and children and presenting symptoms are primarily respiratory related [1,7]. In neonates and infants these congenital lesions cause respiratory distress whilst in children and young adults the presenting symptoms are primarily respiratory distress, recurrent attacks of respiratory embarrassment, pulmonary infection, which may be associated with haemoptysis, or rarely haemothorax [2,3,8]. Our case report is unique where a young adult presented with symptoms of sharp, episodic, retrosternal chest pains that were brought on with exercise.…”

Section: Resultsmentioning

confidence: 99%

An Adult With Episodic Retrosternal Chest Pain: An Unusual Presentation of Congenital Pulmonary Airway Malformation

Goldsmith

George

Aslam

et al. 2020

Preprint

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Background: Congenital pulmonary airway malformation (CPAM) with partial anomalous pulmonary venous connection presenting as episodic retrosternal chest pain on exertion in an adult has not been described. Case presentation: A 21-year-old female, non-smoker, presented with a 4-year history of sharp, episodic, retrosternal chest pains brought on with exercise. A contrast-enhanced computed tomography (CT) scan showed a grossly overinflated left lower lobe with partial anomalous pulmonary venous drainage into the left hemi-azygos vein. Lobectomy, the recommended treatment of choice, carried out thoracoscopically, was curative with satisfactory mid-term results. Histology confirmed type-II congenital pulmonary airway malformation.Conclusions: CPAM can present in young adults with unusual symptoms of chest pain on exertion. When suspected a contrast-enhanced CT scan is the gold standard for establishing the diagnosis. An anatomical lung resection is curative with satisfactory medium term results.

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Fetal

León

Gutiérrez

Ruiz

2010

Learning Pediatric Imaging

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Les malformations pulmonaires kystiques : polymorphisme clinique et radiologique. À propos de 30 observations

Cited by 8 publications

References 38 publications

Congenital cystic adenomatoid malformation – dangers of misdiagnosis: a case report

Congenital cystic adenomatoid malformation – dangers of misdiagnosis: a case report

An Adult With Episodic Retrosternal Chest Pain: An Unusual Presentation of Congenital Pulmonary Airway Malformation

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