Surgical management of myelocystocele: a single-center experience with long-term functional outcomes

Author:

Behbahani Mandana12,Shlobin Nathan A.12,Dziugan Klaudia12,Callas Hannah12,Meyer Theresa34,Yerkes Elizabeth34,Swaroop Vineeta T.56,DeCuypere Michael12,Lam Sandi12,McLone David12,Bowman Robin12

Affiliation:

1. Division of Pediatric Neurosurgery, Ann & Robert H. Lurie Children’s Hospital of Chicago;

2. Department of Neurological Surgery, Northwestern University Feinberg School of Medicine;

3. Division of Pediatric Urology, Ann & Robert H. Lurie Children’s Hospital of Chicago;

4. Department of Urology, Northwestern University Feinberg School of Medicine;

5. Division of Pediatric Orthopedics, Ann & Robert H. Lurie Children’s Hospital of Chicago; and

6. Department of Orthopedics, Northwestern University Feinberg School of Medicine, Chicago, Illinois

Abstract

OBJECTIVE Myelocystocele (MCC) is an uncommon form of skin-covered spinal dysraphism. The authors aimed to present long-term functional outcomes of patients treated for MCC with and without associated abnormalities of cloacal development (ACD). METHODS All patients with MCC and at least one tethered cord release (TCR) treated at a single institution between 1982 and 2019 were retrospectively reviewed. Demographic, operative, and functional outcome data were analyzed. RESULTS Of 51 children with MCC, 30 (58.8%) had MCC only and 21 (41.2%) had associated ACD (MCC/ACD). Thirty-two patients (62.7%) had undergone one TCR, while 19 patients (37.3%) had multiple TCRs. Urinary continence assessment was possible in 41 patients (80.4%), and bowel continence assessment was possible in 43 patients (84.3%) who were either older than 6 years or toilet trained. Although patients with MCC only were more likely to void volitionally (p = 0.0001), there was no difference in overall bladder continence based on the presence of ACD (p = 0.15) or the need for additional untethering procedures (p = 0.15). Those with MCC only were more likely to have overall bowel continence (p = 0.0001) and not require any management (p = 0.002), while those with MCC/ACD were more likely to have an ileostomy (p = 0.01). Of the 30 patients with MCC only, 29 (96.7%) were able to ambulate in the community. Of 21 patients with MCC/ACD, 14 (66.7%) were able to ambulate in the community, 5 (23.8%) were not ambulating, and 2 (9.5%) were therapeutic ambulators. A greater proportion of children in the MCC cohort were ambulating in the community (p = 0.01). There was no difference in community ambulation based on the number of TCRs (p > 0.99), but those with multiple TCRs were more likely to use braces (p = 0.01) and require lower-extremity orthopedic surgery (p = 0.01). CONCLUSIONS Patients born with an MCC, with or without an associated ACD, attained long-term favorable outcomes in bladder and bowel continence and ambulation.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

Reference29 articles.

1. Terminal myelocystocele;McLone DG,1985

2. Terminal myelocystoceles: a series of 17 cases;Gupta DK,2005

3. Terminal myelocystocele;Kumar R,2002

4. Skin-covered sacrococcygeal masses in infants and children;Lemire RJ,1971

5. Terminal myelocystocele—a case report;Sim KB,1996

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