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  1. Article ; Online: Arteria coronaria derecha, un raro y riesgoso trayecto.

    Pumacayo-Cárdenas, Susan / Simborth-Luna, Javier / Pinto-Portugal, José

    Archivos de cardiologia de Mexico

    2023  Volume 93, Issue 2, Page(s) 237–239

    Title translation Right coronary artery, a rare and risky course.
    MeSH term(s) Humans ; Coronary Angiography ; Coronary Vessel Anomalies
    Language Spanish
    Publishing date 2023-04-05
    Publishing country Mexico
    Document type Journal Article
    ZDB-ID 2059019-2
    ISSN 1665-1731 ; 1665-1731
    ISSN (online) 1665-1731
    ISSN 1665-1731
    DOI 10.24875/ACM.22000073
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: An Unusual Equatorial Constriction of the Ventricular Cone.

    Pumacayo-Cárdenas, Susan / Quea-Pinto, Edgar / Jiménez-Santos, Moisés / Anderson, Robert H

    JACC. Case reports

    2022  Volume 4, Issue 18, Page(s) 1156–1159

    Abstract: A 25-year-old woman with a recent diagnosis of congenital heart disease and probable endocarditis was referred to our institution. During our evaluation we observed an unusual deformation of both ventricles. We discuss its possible origin as revealed by ... ...

    Abstract A 25-year-old woman with a recent diagnosis of congenital heart disease and probable endocarditis was referred to our institution. During our evaluation we observed an unusual deformation of both ventricles. We discuss its possible origin as revealed by printing of a three-dimensional model. (
    Language English
    Publishing date 2022-06-22
    Publishing country Netherlands
    Document type Case Reports
    ISSN 2666-0849
    ISSN (online) 2666-0849
    DOI 10.1016/j.jaccas.2021.12.029
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Anomalous origin of right pulmonary artery: diagnosis, treatment, and follow-up in an adult patient.

    Pumacayo-Cárdenas, Susan / Jimenez-Santos, Moises / Quea-Pinto, Edgar

    Cardiology in the young

    2020  Volume 30, Issue 8, Page(s) 1199–1201

    Abstract: Anomalous origin of a branch pulmonary artery from the aorta is a rare malformation, accounting for 0.12% of all congenital heart defects. We present the case of a 43-year-old man with an anomalous origin of the right pulmonary artery (AORPA) from the ... ...

    Abstract Anomalous origin of a branch pulmonary artery from the aorta is a rare malformation, accounting for 0.12% of all congenital heart defects. We present the case of a 43-year-old man with an anomalous origin of the right pulmonary artery (AORPA) from the ascending aorta. Reimplantation of the right pulmonary artery was carried out successfully, with favourable evolution in the medium-term follow-up. It is the first described case that receives corrective treatment in adulthood with a favourable evolution.
    MeSH term(s) Adult ; Aorta ; Follow-Up Studies ; Heart Defects, Congenital/diagnostic imaging ; Heart Defects, Congenital/surgery ; Humans ; Lung ; Male ; Pulmonary Artery/diagnostic imaging ; Pulmonary Artery/surgery
    Language English
    Publishing date 2020-07-06
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 1078466-4
    ISSN 1467-1107 ; 1047-9511
    ISSN (online) 1467-1107
    ISSN 1047-9511
    DOI 10.1017/S1047951120001729
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 4050: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (2.OG)
    ab Jg. 2022: Lesesaal (EG)

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  4. Article ; Online: Natural history of complex transposition of great arteries in an adult: a case report.

    Narcisse-Alvarez, Jahir Fresnel / Pumacayo-Cardenas, Susan Cristina / Espinola-Zavaleta, Nilda

    Cardiology in the young

    2019  Volume 29, Issue 5, Page(s) 720–724

    Abstract: Background: Transposition of the great arteries is the most common cyanotic cardiac lesion in newborns. Transposition of the great arteries without surgical correction is fatal during the first year of life. Contemporary outcome studies have shown that ... ...

    Abstract Background: Transposition of the great arteries is the most common cyanotic cardiac lesion in newborns. Transposition of the great arteries without surgical correction is fatal during the first year of life. Contemporary outcome studies have shown that survival rates after surgery are excellent and most patients live to adulthood.
    Case summary: Woman with complex transposition of the great arteries with atrial and ventricular septal defects and subvalvular and valvular pulmonary stenosis, who has survived until the age of 31 years without surgery. The diagnosis was made by echocardiography and cardiac magnetic resonance. She underwent successful corrective surgical treatment after this age, by means of a Jatene operation.
    Conclusion: In transposition of the great arteries patients, a high index of cases dies in the first month of life. Our case represents a natural history of the complex transposition of the great arteries. Non-invasive imaging studies are very useful for the diagnosis and follow-up of patients with transposition of the great arteries, especially echocardiography and cardiac magnetic resonance. In our case, the multimodality approach and the corrective surgery allowed her to survive.
    MeSH term(s) Adult ; Age of Onset ; Arterial Switch Operation ; Echocardiography ; Female ; Heart Septal Defects, Ventricular/diagnostic imaging ; Heart Septal Defects, Ventricular/surgery ; Humans ; Magnetic Resonance Imaging ; Pulmonary Valve Stenosis/diagnostic imaging ; Pulmonary Valve Stenosis/surgery ; Transposition of Great Vessels/diagnostic imaging ; Transposition of Great Vessels/surgery
    Language English
    Publishing date 2019-05-16
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 1078466-4
    ISSN 1467-1107 ; 1047-9511
    ISSN (online) 1467-1107
    ISSN 1047-9511
    DOI 10.1017/S1047951119000805
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 4050: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (2.OG)
    ab Jg. 2022: Lesesaal (EG)

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  5. Article ; Online: Infrecuente asociación de coronaria circunfleja anómala y coartación aórtica.

    Pumacayo-Cárdenas, Susan C / de la Mora-Cervantes, Regina

    Archivos de cardiologia de Mexico

    2019  Volume 89, Issue 2, Page(s) 183–184

    Title translation Uncommon association of anomalous circumflex coronary and aortic coarctation.
    Language English
    Publishing date 2019-08-01
    Publishing country Mexico
    Document type Journal Article
    ISSN 1665-1731
    ISSN (online) 1665-1731
    DOI 10.24875/ACM.M19000023
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Late Diagnosis of Complex Congenital Pulmonary Malformation: From Symptoms and Radiology to Histopathology.

    Pumacayo-Cárdenas, Susan / León-Bejarano, Ernesto / Recabarren-Lozada, Arturo

    Archivos de bronconeumologia

    2019  Volume 56, Issue 8, Page(s) 523

    Title translation Malformación pulmonar congénita compleja de diagnóstico tardío: de la clínica y radiología a la histopatología.
    MeSH term(s) Delayed Diagnosis ; Humans ; Lung/diagnostic imaging ; Radiography ; Radiology ; Respiratory System Abnormalities
    Language Spanish
    Publishing date 2019-08-19
    Document type Journal Article
    ZDB-ID 733126-5
    ISSN 1579-2129 ; 0300-2896
    ISSN (online) 1579-2129
    ISSN 0300-2896
    DOI 10.1016/j.arbres.2019.07.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.B 2655: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 2021: Bestellungen von Artikeln über das Online-Bestellformular
    ab Jg. 2022: Lesesaal (EG)

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