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DOI 10.1007/s002470050348

Медицинская библиотека · Pediatric radiology · 1998

Spontaneous involution of pulmonary sequestration in children: a report of two cases and review of the literature.

García-Peña P, Lucaya J, Hendry G M, McAndrew P T, Duran C

Клинический случайСтатьяОбзорПеревод в очереди

Аннотация

BACKGROUND

Two cases of pulmonary sequestration which regressed spontaneously are presented.

OBJECTIVE

To demonstrate the value of imaging studies in the diagnosis and follow-up of some forms of congenital masses of the lung in asymptomatic patients.

MATERIAL AND

METHODS

We reviewed the clinical records and imaging studies of two asymptomatic children, one newborn and the other 3 months old, with thoracic masses which demonstrated variable degrees of spontaneous involution.

RESULTS

Abdominal ultrasound performed on the newborn with a palpable mass showed a triangular echogenic mass with a large central feeding vessel arising from the aorta. The mass had disappeared on follow-up US exam performed 6 years later. CT was performed in the 3-month-old patient with a persistent retrocardiac mass. A soft-tissue density mass in the left pulmonary base with a large feeding vessel arising from the aorta was visualised on contrast-enhanced CT. Five years later, a new CT scan showed significant shrinkage of the mass and no vessel.

CONCLUSION

Radiological techniques such as real-time US with Doppler imaging and contrast-enhanced CT may establish the diagnosis of pulmonary sequestration by demonstrating the mass and its systemic vessel, thereby eliminating the need for more aggressive imaging procedures. Partial or total disappearance of these masses represents a further example of involutive pathology and suggests that not all cases of pulmonary sequestration should be surgically treated.

Для цитирования: García-Peña P, Lucaya J, Hendry G M, McAndrew P T, Duran C. Spontaneous involution of pulmonary sequestration in children: a report of two cases and review of the literature.. Pediatric radiology. 1998. DOI: 10.1007/s002470050348.

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