Senning operation as a palliative therapy for a girl with complex heart defect and Eisenmenger syndrome (RCD code: II‑1A.4d)

Journal Title: Journal of Rare Cardiovascular Diseases - Year 2016, Vol 3, Issue 1

Abstract

Development of irreversible pulmonary hypertension in D-transposition of the great arteries (D-TGA) with ventricular septal defect (VSD) is a well-known phenomenon. Coexistence of left ventricular outflow tract obstruction (LVOTO) should theoretically protect the patient against pulmonary arterial hypertension (PAH). Application of the Blalock-Taussig shunt (B-TS) temporarily improves condition of the patient, but may contribute to irreversible PAH requiring palliative complex therapy. We present a case of a 18 year-old female with congenital complex heart defect: D-TGA with inflow VSD and subpulmonary stenosis, Eisenmenger syndrome, who was treated with several subsequent palliative cardiosurgical operations, including B-TS and Senning procedure and eventually, combined PAH-specific therapy, what resulted in stabilization of clinical status. JRCD 2016; 3 (1): 14–16

Authors and Affiliations

Jacek Kuźma, Andrzej Rudziński, Grzegorz Kopeć, Piotr Weryński, Dorota Palczewska, Daniel Porada, Marek Rączka, Maciej Pitak

Keywords

Related Articles

Left atrial myxoma as a cause of multiple cerebral microembolization (RCD code: VI‐1A.1)

We report a case of a 56-year-old female after breast cancer treatment, who was diagnosed with left atrial myxoma as a rare cause of cerebral and cerebellar stroke.JRCD 2017; 3 (5): 168–170

Giant cell aortitis of the ascending aorta without signs and symptoms of systemic vasculitis

We report a case of a patient with giant cell aortitis – a rare cause of aneurysm of the ascending aorta. Modern imaging techniques show promise in diagnosis, however the diagnosis only after hystopathotological examinat...

Pulmonary artery pressure matters – how to efficiently improve survival in pulmonary arterial hypertension (RCD code: II‐1A.1)

Pulmonary arterial hypertension is a disease characterized by poor prognosis despite treatment. Even in a modern era of pharmaco- therapy there is a strong need to further improve survival of patients. The current therap...

Mediastinal cyst: a case report (RCD code: VI)

We report a case of a 57‑year‑old female patient in whom a mediastinal tumor was found. Differential diagnosis included chiefly allergic alveolitis or an ectopic thymus. The exact nature of the lesion has not been fully...

Hereditary haemorrhagic telangiectasia in Benghazi, Libya; a population‑based study of incidence and prevalence (RCD code: I‑O)

Background: Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic disorder characterised by the formation of aberrant arteriovenous malformations (AVMs). Few studies have described the epidemiolog...

Download PDF file
  • EP ID EP244134
  • DOI 10.20418/jrcd.vol3no1.236
  • Views 89
  • Downloads 0

How To Cite

Jacek Kuźma, Andrzej Rudziński, Grzegorz Kopeć, Piotr Weryński, Dorota Palczewska, Daniel Porada, Marek Rączka, Maciej Pitak (2016). Senning operation as a palliative therapy for a girl with complex heart defect and Eisenmenger syndrome (RCD code: II‑1A.4d). Journal of Rare Cardiovascular Diseases, 3(1), 14-16. https://europub.co.uk/articles/-A-244134