Surgical insights and management in patients with the 22q11.2 deletion syndrome

被引:3
|
作者
McGovern, Patrick E. [1 ]
Crowley, T. Blaine [2 ]
Zackai, Elaine H. [2 ,3 ]
Burrows, Evanette [4 ]
McDonald-McGinn, Donna M. [2 ,3 ]
Nance, Michael L. [1 ,5 ]
机构
[1] Childrens Hosp Philadelphia, Div Gen Thorac & Fetal Surg, 3401 Civ Ctr Blvd, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Div Human Genet, 22q & You Ctr, 3401 Civ Ctr Blvd, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Pediat, Perelman Sch Med, 3401 Civ Ctr Blvd, Philadelphia, PA 19104 USA
[4] Childrens Hosp Philadelphia, Roberts Ctr Pediat Res, 2716 South St, Philadelphia, PA 19146 USA
[5] Univ Penn, Dept Surg, Perelman Sch Med, 3400 Spruce St 4, Philadelphia, PA 19104 USA
关键词
22q; General surgery; Genetics; Multidisciplinary care; TRACHEOESOPHAGEAL FISTULA; ESOPHAGEAL ATRESIA; CLINICAL-FEATURES; CHILDREN; DISEASE; GENETICS;
D O I
10.1007/s00383-022-05123-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose 22q11.2 deletion syndrome (22q11.2DS) can present with a variety challenges to patients and their caregivers, many of which require surgical evaluation and intervention. Surgical needs can also extend long into adulthood, prompting evaluation and intervention throughout development and beyond. Here, we identify common concerns and patient needs associated with the 22q11.2DS from a general surgery perspective, their management, and typical management based on our institution's experience with 1263 patients. Methods 1263 patients evaluated and treated at the 22q And You Center at the Children's Hospital of Philadelphia were enrolled and included in the study, from January 1992 to May 2017 Co-morbidities, procedures, and imaging studies performed were quantified and assessed via descriptive analysis. Results Gastroesophageal reflux disease (GERD) and feeding difficulties were the most common surgical issues identified, while gastrostomy tube placement, anorectal procedures, and hernia repairs were the most common surgical interventions performed by general surgeons. Conclusions General surgical procedures are commonly needed in this population and are part of the complex needs these patients and their surgeons may encounter in the setting of a 22q11.2DS diagnosis. These findings will help to inform a well-coordinated, multidisciplinary approach to care.
引用
收藏
页码:899 / 905
页数:7
相关论文
共 50 条
  • [1] Surgical insights and management in patients with the 22q11.2 deletion syndrome
    Patrick E. McGovern
    T. Blaine Crowley
    Elaine H. Zackai
    Evanette Burrows
    Donna M. McDonald-McGinn
    Michael L. Nance
    Pediatric Surgery International, 2022, 38 : 899 - 905
  • [2] Surgical Considerations in 22Q11.2 Deletion Syndrome
    Kirschner, Richard E.
    Baylis, Adriane L.
    CLINICS IN PLASTIC SURGERY, 2014, 41 (02) : 271 - +
  • [3] Aberrant Cortical Morphometry in the 22q11.2 Deletion Syndrome
    Schmitt, J. Eric
    Vandekar, Simon
    Yi, James
    Calkins, Monica E.
    Ruparel, Kosha
    Roalf, David R.
    Whinna, Daneen
    Souders, Margaret C.
    Satterwaite, Theodore D.
    Prabhakaran, Karthik
    McDonald-McGinn, Donna M.
    Zackai, Elaine H.
    Gur, Ruben C.
    Emanuel, Beverly S.
    Gur, Raquel E.
    BIOLOGICAL PSYCHIATRY, 2015, 78 (02) : 135 - 143
  • [4] A Comprehensive Craniofacial Study of 22q11.2 Deletion Syndrome
    Lewyllie, A.
    Roosenboom, J.
    Indencleef, K.
    Claes, P.
    Swillen, A.
    Devriendt, K.
    Carels, C.
    De Llano-Perula, M. Cadenas
    Willems, G.
    Hens, G.
    Verdonck, A.
    JOURNAL OF DENTAL RESEARCH, 2017, 96 (12) : 1386 - 1391
  • [5] Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome
    Demily, C.
    Rossi, M.
    Schneider, M.
    Edery, P.
    Leleu, A.
    d'Amato, T.
    Franck, N.
    Eliez, S.
    ENCEPHALE-REVUE DE PSYCHIATRIE CLINIQUE BIOLOGIQUE ET THERAPEUTIQUE, 2015, 41 (03): : 266 - 273
  • [6] Neurodevelopmental outcome in 22q11.2 deletion syndrome and management
    Swillen, Ann
    Moss, Edward
    Duijff, Sasja
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (10) : 2160 - 2166
  • [7] Clozapine Use in 22q11.2 Deletion Syndrome
    Colijn, Mark Ainsley
    JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2024, 44 (02) : 168 - 178
  • [8] Neuroradiographic findings in 22q11.2 deletion syndrome
    Bohm, Lauren A.
    Zhou, Tom C.
    Mingo, Tyler J.
    Dugan, Sarah L.
    Patterson, Richard J.
    Sidman, James D.
    Roby, Brianne B.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (08) : 2158 - 2165
  • [9] Neurological manifestation of 22q11.2 deletion syndrome
    Bayat, Michael
    Bayat, Allan
    NEUROLOGICAL SCIENCES, 2022, 43 (03) : 1695 - 1700
  • [10] Camptodactyly and the 22q11.2 deletion syndrome
    Couser, Natario L.
    Pande, Chetna K.
    Walsh, Jonathan M.
    Tepperberg, James
    Aylsworth, Arthur S.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (02) : 515 - 518