Successful Surgery of Severely Comorbid Cystic Pulmonary Hypoplasia
Background. Cystic pulmonary hypoplasia is a malformation of terminal bronchial tree as a cystic dilatation of various size at the level of subsegmental bronchi or bronchioles, which accounts for 60–80% of the overall malformation incidence.Materials and methods. We present a descriptive case of gen...
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| Format: | Article |
| Language: | English |
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Bashkir State Medical University
2020-12-01
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| Series: | Креативная хирургия и онкология |
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| Online Access: | https://www.surgonco.ru/jour/article/view/532 |
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| author | O. V. Galimov V. O. Khanov G. S. Mukhamadyanov A. E. Sekundov R. G. Mazitov M. A. Karimov |
| author_facet | O. V. Galimov V. O. Khanov G. S. Mukhamadyanov A. E. Sekundov R. G. Mazitov M. A. Karimov |
| author_sort | O. V. Galimov |
| collection | DOAJ |
| description | Background. Cystic pulmonary hypoplasia is a malformation of terminal bronchial tree as a cystic dilatation of various size at the level of subsegmental bronchi or bronchioles, which accounts for 60–80% of the overall malformation incidence.Materials and methods. We present a descriptive case of general clinical picture, diagnostic radiological examination and choosing a strategy for surgical diagnosis and treatment of cystic pulmonary hypoplasia. Patient K., 57 yo, was admitted to the Republican Clinical Tuberculosis Dispensary with fibroatelectasis of the right lung lower lobe and underlying subcompensated diabetes type II, inspected by a phthisiatrician, thoracic surgeon and referred for surgical treatment.Results and discussion. A careful history inspection and Xray data in most cases suffice to successfully diagnose the congenital type of cystic pulmonary defects. Treatment in such patients is personalised, with preference towards surgical intervention. A correct diagnosis is usually conditioned by a detailed and careful examination of the lung morbid morphology during surgery.Conclusion. Modern instrumental methods, with multispiral computed tomography in particular, are key to correctly diagnose a malformation. Relevant case reports are of interest and importance to advance research into causative factors of the disease. |
| first_indexed | 2024-04-10T00:58:12Z |
| format | Article |
| id | doaj.art-3da45f0048294f358845cad5abc98adc |
| institution | Directory Open Access Journal |
| issn | 2307-0501 2076-3093 |
| language | English |
| last_indexed | 2024-04-10T00:58:12Z |
| publishDate | 2020-12-01 |
| publisher | Bashkir State Medical University |
| record_format | Article |
| series | Креативная хирургия и онкология |
| spelling | doaj.art-3da45f0048294f358845cad5abc98adc2023-03-13T10:01:09ZengBashkir State Medical UniversityКреативная хирургия и онкология2307-05012076-30932020-12-0110429129510.24060/2076-3093-2020-10-4-291-295403Successful Surgery of Severely Comorbid Cystic Pulmonary HypoplasiaO. V. Galimov0V. O. Khanov1G. S. Mukhamadyanov2A. E. Sekundov3R. G. Mazitov4M. A. Karimov5Башкирский государственный медицинский университетБашкирский государственный медицинский университетРеспубликанский клинический противотуберкулезный диспансерБашкирский государственный медицинский университетБашкирский государственный медицинский университетБашкирский государственный медицинский университетBackground. Cystic pulmonary hypoplasia is a malformation of terminal bronchial tree as a cystic dilatation of various size at the level of subsegmental bronchi or bronchioles, which accounts for 60–80% of the overall malformation incidence.Materials and methods. We present a descriptive case of general clinical picture, diagnostic radiological examination and choosing a strategy for surgical diagnosis and treatment of cystic pulmonary hypoplasia. Patient K., 57 yo, was admitted to the Republican Clinical Tuberculosis Dispensary with fibroatelectasis of the right lung lower lobe and underlying subcompensated diabetes type II, inspected by a phthisiatrician, thoracic surgeon and referred for surgical treatment.Results and discussion. A careful history inspection and Xray data in most cases suffice to successfully diagnose the congenital type of cystic pulmonary defects. Treatment in such patients is personalised, with preference towards surgical intervention. A correct diagnosis is usually conditioned by a detailed and careful examination of the lung morbid morphology during surgery.Conclusion. Modern instrumental methods, with multispiral computed tomography in particular, are key to correctly diagnose a malformation. Relevant case reports are of interest and importance to advance research into causative factors of the disease.https://www.surgonco.ru/jour/article/view/532кистозная гипоплазия легкогополикистоз легкихсотовое легкоеврожденные аномалиибронхоэктазиякомпьютерная томографияторакотомия |
| spellingShingle | O. V. Galimov V. O. Khanov G. S. Mukhamadyanov A. E. Sekundov R. G. Mazitov M. A. Karimov Successful Surgery of Severely Comorbid Cystic Pulmonary Hypoplasia Креативная хирургия и онкология кистозная гипоплазия легкого поликистоз легких сотовое легкое врожденные аномалии бронхоэктазия компьютерная томография торакотомия |
| title | Successful Surgery of Severely Comorbid Cystic Pulmonary Hypoplasia |
| title_full | Successful Surgery of Severely Comorbid Cystic Pulmonary Hypoplasia |
| title_fullStr | Successful Surgery of Severely Comorbid Cystic Pulmonary Hypoplasia |
| title_full_unstemmed | Successful Surgery of Severely Comorbid Cystic Pulmonary Hypoplasia |
| title_short | Successful Surgery of Severely Comorbid Cystic Pulmonary Hypoplasia |
| title_sort | successful surgery of severely comorbid cystic pulmonary hypoplasia |
| topic | кистозная гипоплазия легкого поликистоз легких сотовое легкое врожденные аномалии бронхоэктазия компьютерная томография торакотомия |
| url | https://www.surgonco.ru/jour/article/view/532 |
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