Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Entire right lung"'
Autor:
Mehran Hiradfar, Saeedeh Majidi, Hosein Tajali, Reza Nazarzadeh, Ahmad Mohamadipour, Marjan Joudi
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 40, Iss, Pp 56-58 (2019)
Communicating bronchopulmonary foregut malformations (CBPFMs) or esophageal lung, are rare malformation which define by communication between respiratory system with esophagus or stomach. We presented a case whit esophageal lung, in whom the entire r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3480979ff4ae318d599e077db11f53c8
https://doi.org/10.1016/j.epsc.2018.10.019
https://doi.org/10.1016/j.epsc.2018.10.019
Autor:
Emiko Kusano, Shinji Sakaguchi, Daisuke Sato, Fumiaki Ishida, Keigo Takagi, Susumu Sakamoto, Yujiro Takai, Sakae Homma, Minaho Kobayashi, Kazutoshi Isobe, Kazutoshi Shibuya, Kyoko Gocho, Motohide Iwata, Keishi Sugino, Go Sano, Kyohei Kaburaki, Taito Miyazaki, Yoko Muramatsu
Publikováno v:
Internal Medicine. 48:459-463
We report a case of pulmonary Mycobacterium abscessus (M. abscessus) infection with destructive growth in the entire right lung. The patient was 56-year-old woman who had had pulmonary tuberculosis at the age of 40 and had been diagnosed as having pu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e43df84deac8df9460cdf4312414b6e
https://doi.org/10.2169/internalmedicine.48.1763
https://doi.org/10.2169/internalmedicine.48.1763
Publikováno v:
The Annals of Thoracic Surgery. 70:1400-1402
We present the case of a 1-month-old infant with right atrial isomerism and complex functionally univentricular heart disease, in whom totally anomalous pulmonary venous return drained below the diaphragm via two separate vertical veins. One of the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e0fcd59cb5ab7304df3a69e0d346bd9
https://doi.org/10.1016/s0003-4975(00)01706-9
https://doi.org/10.1016/s0003-4975(00)01706-9
Publikováno v:
Journal of thoracic imaging. 21(1)
Horseshoe lung is a rare congenital anomaly characterized by the presence of unilateral pulmonary hypoplasia and a midline isthmus bridging the right and the left lung. Almost all cases of horseshoe lung are associated with the scimitar syndrome. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::246aac2c1a777c69655b359473a0ec8a
https://pubmed.ncbi.nlm.nih.gov/16538166
https://pubmed.ncbi.nlm.nih.gov/16538166
Autor:
Armando R. Irizarry, Paul R. Facemire, Valerie A. Dutweiler, Janice E. Sojka, Clayton D. Chilcoat, Sophie Morisset, Stephen B. Adams, Walter E. Weirich
Publikováno v:
Journal of the American Veterinary Medical Association. 217(10)
A 7-year-old warmblood mare was referred because of a respiratory tract disorder; pulmonary granular cell tumor was diagnosed. Pulmonary granular cell tumor is a locally invasive but rare type of tumor with low metastatic potential. The entire right
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d84194c74ef6cc8eb1052f5c370fdfee
https://pubmed.ncbi.nlm.nih.gov/11128544
https://pubmed.ncbi.nlm.nih.gov/11128544
Publikováno v:
RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren. 128:271-274
Variations of the scimitar syndrome have been reported previously, the most common being the absence of systemic arterial supply to the right lung and varying degrees of lung hypoplasia. Anomalous scimitar-like veins draining the entire right lung an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d58a764aaa234021cab3e5739c2aa56
https://doi.org/10.1055/s-0029-1230841
https://doi.org/10.1055/s-0029-1230841
Autor:
Sv. Quist-Hanssen
Publikováno v:
Acta Paediatrica. 37:87-94
Summary The case history of a 7-week-old boy. From birth the child had repeated attacks of cyanosis and dyspnea, without stridor. Lung examination two days after birth disclosed atelectasis of the upper and middle lobe of the right lung, and later em
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b140294df60528f5cfcba7c30205c2b
https://doi.org/10.1111/j.1651-2227.1949.tb15556.x
https://doi.org/10.1111/j.1651-2227.1949.tb15556.x
Publikováno v:
Thorax. 32(5)
Two unusual cases of primary lymphocytic lymphosarcoma of the lung are presented. The first patient is a 5-year-old girl who showed a massive involvement of the entire right lung by tumour. She was treated by radiotherapy followed by cyclophosphamide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bc78841b2dde662301fc6f3f4f8cbc5
https://pubmed.ncbi.nlm.nih.gov/579482
https://pubmed.ncbi.nlm.nih.gov/579482
Publikováno v:
Archives of surgery (Chicago, Ill. : 1960). 86
The "scimitar syndrome" is a complex malformation of the heart, lungs, and blood vessels. The pathology of this disease was described in detail by Park19in 1912, but it was not until 1949 when Dotter et al.6made the first clinical diagnosis of this a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4181b4bce830dfb865b78cd32c6b54b
https://pubmed.ncbi.nlm.nih.gov/13976294
https://pubmed.ncbi.nlm.nih.gov/13976294
Autor:
Harry R. Morse, Sam Gladding
Publikováno v:
A.M.A. American journal of diseases of children. 89(3)
WITH THE increasing awareness of cardiovascular anomalies and the widening scope of surgical procedures to correct these abnormalities, it is imperative to report rare cases. The proper management of such cases demands a sharing of the experiences of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01843e9440a8fa827d977cf6573fa56a
https://pubmed.ncbi.nlm.nih.gov/14349368
https://pubmed.ncbi.nlm.nih.gov/14349368