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Clinical and surgical aspects of congenital lobar over-inflation: a single center retrospective study.
Abdel-Bary, Mohamed; Abdel-Naser, Mohamed; Okasha, Ahmed; Zaki, Mohammed; Abdel-Baseer, Khaled.
Afiliación
  • Abdel-Bary M; Department of Cardiothoracic Surgery, Qena Faculty of Medicine, South Valley University, Safaga Road, Qena, 83523, Egypt. Dr_abdelbary@med.svu.edu.eg.
  • Abdel-Naser M; Department of Anaesthesia and ICU, Assiut Faculty of Medicine, Assiut University, Assiut, Egypt.
  • Okasha A; Department of Radiology, Qena Faculty of Medicine, South Valley University, Qena, Egypt.
  • Zaki M; Department of Radiology, Sohag Faculty of Medicine, Sohag University, Sohag, Egypt.
  • Abdel-Baseer K; Department of Pediatrics, Qena Faculty of Medicine, South Valley University, Qena, Egypt.
J Cardiothorac Surg ; 15(1): 102, 2020 May 19.
Article en En | MEDLINE | ID: mdl-32429981
ABSTRACT

BACKGROUND:

Congenital lobar overinflation (CLOI) is one of the most important causes of infantile respiratory distress (RD). We aim to evaluate our experience in CLOI management emphasizing on clinical features, diagnostic modalities, surgery and outcomes.

METHODS:

This is a retrospective study for all CLOI cases undergoing surgical management at Qena University Hospital. Demographic data, clinical data, radiographic findings, surgery and postoperative follow-up were reviewed.

RESULTS:

A total of 37 neonates and infants with CLOI were presented to our center between January 2015 and January 2019; their mean age was 111.43 ± 65.19 days and 22 were males. All cases presented with RD; and cyanosis in 19 cases. 15 cases presented with recurrent pneumonia and fever. Diminished breath sounds on the affected side and wheezes were the main clinical findings in 30 and 22 cases respectively. On CXR, emphysema was detected in all cases. A confirmatory CT chest was done for all cases. Left upper lobe was affected in 23 cases, right middle lobe in 7 and right upper lobe in 7 cases. Lobectomy was done in thirty-one cases; their mean age at surgery was 147.58 ± 81.49 days and 19 were males. Postoperative complications were noted in 5 cases and postoperative ventilation was required for 2 of them. No morbidity or mortality was reported. The follow-up duration ranged from 3 months to 1 year and all patients were doing well except one case that lost follow up after 3 months.

CONCLUSION:

CLOI is a rare bronchopulmonary malformation that requires a high index of clinical suspicion, especially in persistent and recurrent infantile RD. CT chest is the most useful diagnostic modality. Early management of CLOI improves outcome and avoid life-threatening complications. Surgical management is the treatment of choice in our center without recorded mortality.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfisema Pulmonar / Síndrome de Dificultad Respiratoria del Recién Nacido Límite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Cardiothorac Surg Año: 2020 Tipo del documento: Article País de afiliación: Egipto

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfisema Pulmonar / Síndrome de Dificultad Respiratoria del Recién Nacido Límite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Cardiothorac Surg Año: 2020 Tipo del documento: Article País de afiliación: Egipto