| Literature DB >> 35865513 |
Francesca Palmisani1, Wilfried Krois1, Janina Patsch2, Martin Metzelder1, Carlos A Reck-Burneo1.
Abstract
Introduction Anorectal malformations (ARM) affect 1 in 5,000 newborns with a wide range of defects. In the absence of a visible fistula, the diagnosis and classification of ARM require an augmented pressure distal colostogram. This procedure can be done after a diverting colostomy has been performed and implies exposing the child to radiation. We hypothesized that high-resolution transperineal ultrasound could correctly diagnose the type of ARM, thus sparing radiation exposure. Case Description Four full-term male newborns with ARM and no visible anal opening were referred to our center for further management. A diverting descendostomy was performed in the first 48 hours of life in all cases. Prior to the reconstructive surgery, we performed a high-resolution transperineal ultrasound with 3D tomographic reconstruction of the perineal region to assess the urethra, the rectum, and a possible fistula. Findings were compared with a conventional augmented pressure distal colostogram. The image acquisition was fast and did not cause any additional distress to the children. Conclusion In all cases the results of the distal colostogram nicely correlated with the high-resolution transperineal ultrasound with 3D tomographic reconstruction. In the future, we envision a time when it can potentially replace the distal colostogram in preoperative assessment of ARM with no distress and exposure to radiation. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. ( https://creativecommons.org/licenses/by/4.0/ ).Entities:
Keywords: anorectal malformations; diagnostics; reconstructive surgery; ultrasound
Year: 2022 PMID: 35865513 PMCID: PMC9296266 DOI: 10.1055/s-0042-1750027
Source DB: PubMed Journal: European J Pediatr Surg Rep ISSN: 2194-7619
Clinical data of the reported cases
| Patient 1 | Patient 2 | Patient 3 | Patient 4 | |
|---|---|---|---|---|
| Gestational age of birth (weeks) | 36 6/7 | 38 2/7 | 39 0/7 | 38 5/7 |
| Weight at birth | 2910 g | 3180 g | 3240 g | 2990 g |
| Visual appearance at birth | ARM with no visible fistula | ARM with no visible fistula | ARM with no visible fistula | ARM with no visible fistula |
| Meconium in the urine | No | No | Yes | Yes |
| Comorbidities | Hypospadia, hydronephrosis I right kidney with multiple dysplastic cysts, small VSD, ASD II | Hydronephrosis I-II left kidney | Hydronephrosis I-II right kidney | None |
| Age at colostomy (days) | 2 | 2 | 2 | 1 |
| Age at colostogram date (days) | 16 | 8 | 6 | 8 |
| Age at perineal US (days) | 16 | 8 | 6 | 8 |
| Diagnosis according to colostogram and perineal US | ARM with recto-bulbar fistula | ARM with recto-prostatic fistula | ARM with recto-bulbar fistula | ARM with recto-prostatic fistula |
| Age at PSARP (days) | 58 | 50 | 45 | 87 |
| Follow-up (weeks postop) | 55 | 55 | 25 | 10 |
Fig. 1High resolution perineal ultrasound images: position of the linear transducer with PIUR tUS Infinity System add on mediansagittal at the center of the perineal body, patient supine held in lithotomy position, foley cathter in the mucous fistula. ( A ); recto-bulbar fistula ( B ); recto-prostatic fistula ( C ).
Fig. 23D reconstruction process: on the left side respectively two coronal ( A, B ) and two sagittal cuts ( C, D ) created from the ultrasound acquisition, which are used to automatically reconstruct the structure, shown on the right side ( E ).
Fig. 3Comparison between distal colostogram ( A, C ) and the automatically 3D reconstructed structures, including bladder, urethra, and recto-urethral fistula, acquired from the linear ultrasound imaging ( B, D ) from the same patient. A and B show a recto-bulbar fistula, C and D a recto-prostatic fistula. The star indicates the rectum, the diamond shape of the bladder, and the arrow points to the recto-urethral fistula.