Achalasia is a rare neuromuscular esophageal disorder in children. There are many surgical options to treatment including botulinum toxin (Botox) injections, oral pharmacologic therapies with nitrates and calcium channel blockers, pneumatic dilation (PD), and surgical myotomy (open surgery, endoscopy, laparoscopy and recently robotic approach). In pediatric age, usually, Heller's myotomy is the main choice. Laparoscopic approach is known and standardized. Few robotic have been published. We decided to report our first case to share our experience with scientific community.

Fusi, G., Molinaro, F., Ferrara, F., Bindi, E., Pellegrino, C., Calani, C., et al. (2019). Robot-assisted Heller myotomy for achalasia. JOURNAL OF PEDIATRIC SURGERY CASE REPORTS, 45, 1-2 [10.1016/j.epsc.2019.101204].

Robot-assisted Heller myotomy for achalasia

Fusi, Giulia;Molinaro, Francesco;Pellegrino, Chiara;CALANI, CHIARA;Messina, Mario;Angotti, Rossella
2019-01-01

Abstract

Achalasia is a rare neuromuscular esophageal disorder in children. There are many surgical options to treatment including botulinum toxin (Botox) injections, oral pharmacologic therapies with nitrates and calcium channel blockers, pneumatic dilation (PD), and surgical myotomy (open surgery, endoscopy, laparoscopy and recently robotic approach). In pediatric age, usually, Heller's myotomy is the main choice. Laparoscopic approach is known and standardized. Few robotic have been published. We decided to report our first case to share our experience with scientific community.
2019
Fusi, G., Molinaro, F., Ferrara, F., Bindi, E., Pellegrino, C., Calani, C., et al. (2019). Robot-assisted Heller myotomy for achalasia. JOURNAL OF PEDIATRIC SURGERY CASE REPORTS, 45, 1-2 [10.1016/j.epsc.2019.101204].
File in questo prodotto:
File Dimensione Formato  
1-s2.0-S221357661930079X-main-1.pdf

accesso aperto

Tipologia: PDF editoriale
Licenza: Creative commons
Dimensione 339.97 kB
Formato Adobe PDF
339.97 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/1072064