期刊论文详细信息
BMC Pediatrics
A case of ultrasound-guided prenatal diagnosis of prune belly syndrome in Papua New Guinea – implications for management
Holger W Unger2  Sheryle Rogerson1  John Bolnga3  Moses Laman2  Peter Siba2  Alexandra J Umbers2  Nancy Hamura3  Regina Wangnapi2  Maria Ome2 
[1] Royal Women’s Hospital, Melbourne, VIC, 3052, Australia;Papua New Guinea Institute of Medical Research (PNG IMR), Vector Borne Disease Unit (VBU), P.O. Box 378, Madang 511, Papua New Guinea;Department of Obstetrics and Gynaecology, Modilon General Hospital, P.O. Box 2119, Madang, 511, Papua New Guinea
关键词: Ultrasound;    Prune belly syndrome;    Prenatal diagnosis;    Papua New Guinea;    Management;    Eagle-Barrett syndrome;    Congenital abnormality;   
Others  :  1144898
DOI  :  10.1186/1471-2431-13-70
 received in 2012-10-27, accepted in 2013-05-03,  发布年份 2013
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【 摘 要 】

Background

Prune belly syndrome is a rare congenital malformation of unknown aetiology and is characterised by abnormalities of the urinary tract, a deficiency of abdominal musculature and bilateral cryptorchidism in males. We report a case of prune belly syndrome from Papua New Guinea, which was suspected on pregnancy ultrasound scan and confirmed upon delivery.

Case presentation

A 26-year-old married woman, Gravida 3 Para 2, presented to antenatal clinic in Madang, Papua New Guinea, at 21+5 weeks’ gestation by dates. She was well with no past medical or family history of note. She gave consent to participate in a clinical trial on prevention of malaria in pregnancy and underwent repeated ultrasound examinations which revealed a live fetus with persistent megacystis and anhydramnios. Both mother and clinicians agreed on conservative management of the congenital abnormality. The mother spontaneously delivered a male fetus weighing 2010 grams at 34 weeks’ gestation with grossly abnormal genitalia including cryptorchidism, penile aplasia and an absent urethral meatus, absent abdominal muscles and hypoplastic lungs. The infant passed away two hours after delivery. This report discusses the implications of prenatal detection of severe congenital abnormalities in PNG.

Conclusion

This first, formally reported, case of prune belly syndrome from a resource-limited setting in the Oceania region highlights the importance of identifying and documenting congenital abnormalities. Women undergoing antenatal ultrasound examinations must be carefully counseled on the purpose and the limitations of the scan. The increasing use of obstetric ultrasound in PNG will inevitably result in a rise in prenatal detection of congenital abnormalities. This will need to be met with adequate training, referral mechanisms and better knowledge of women’s attitudes and beliefs on birth defects and ultrasound. National medicolegal guidance regarding induced abortion and resuscitation of a fetus with severe congenital abnormalities may be required.

【 授权许可】

   
2013 Ome et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Frölich F: Der Mangel der Muskeln, insbesondere der Seitenbauchmuskeln. Würzburg: Dissertation; 1839.
  • [2]Eagle JF Jr, Barrett GS: Congenital deficiency of abdominal musculature with associated genitourinary abnormalities: A syndrome. Report of 9 cases. Pediatrics 1950, 6(5):721-736.
  • [3]Obrinsky W: Agenesis of abdominal muscles with associated malformation of the genitourinary tract; a clinical syndrome. Am J Dis Child 1949, 77(3):362-373.
  • [4]Routh JC, Huang L, Retik AB, Nelson CP: Contemporary epidemiology and characterization of newborn males with prune belly syndrome. Urology 2010, 76(1):44-48.
  • [5]Baird PA, MacDonald EC: An epidemiologic study of congenital malformations of the anterior abdominal wall in more than half a million consecutive live births. Am J Hum Genet 1981, 33(3):470-478.
  • [6]Reinberg Y, Shapiro E, Manivel JC, Manley CB, Pettinato G, Gonzalez R: Prune belly syndrome in females: a triad of abdominal musculature deficiency and anomalies of the urinary and genital systems. J Pediatr 1991, 118(3):395-398.
  • [7]Tonni G, Ida V, Alessandro V, Bonasoni MP: Prune-belly syndrome: case series and review of the literature regarding early prenatal diagnosis, epidemiology, genetic factors, treatment, and prognosis. Fetal Pediatr Pathol 2012, 31(1):13-24.
  • [8]Zugor V, Schott GE, Labanaris AP: The Prune Belly syndrome: urological aspects and long-term outcomes of a rare disease. Pediatr Rep 2012, 4(2):e20.
  • [9]Osborne NG, Bonilla-Musoles F, Machado LE, Raga F, Bonilla F Jr, Ruiz F, Perez Guardia CM, Ahluwalia B: Fetal megacystis: differential diagnosis. J Ultrasound Med 2011, 30(6):833-841.
  • [10]Granberg CF, Harrison SM, Dajusta D, Zhang S, Hajarnis S, Igarashi P, Baker LA: Genetic basis of prune belly syndrome: screening for HNF1beta gene. J Urol 2012, 187(1):272-278.
  • [11]Stephens FD, Gupta D: Pathogenesis of the prune belly syndrome. J Urol 1994, 152(6 Pt 2):2328-2331.
  • [12]Schott G, Herrlinger A, Willital G: The prune-belly syndrome. Urologe A 1982, 21(6):322-326.
  • [13]Yamamoto H, Nishikawa S, Hayashi T, Sagae S, Kudo R: Antenatal diagnosis of prune belly syndrome at 11 weeks of gestation. J Obstet Gynaecol Res 2001, 27(1):37-40.
  • [14]Jimmy S, Kemiki AD, Vince JD: Neonatal outcome at Modilon Hospital, Madang: a 5-year review. P N G Med J 2003, 46(1–2):8-15.
  • [15]Poki HO, Shun A, Cooper MG, Paiva H: Gastroschisis management: an experience in Angau Memorial Hospital. P N G Med J 2003, 46(1–2):41-45.
  • [16]Kaptigau WM, Ke L, Rosenfeld JV: Big heads in Port Moresby General Hospital: an audit of hydrocephalus cases seen from 2003 to 2004. P N G Med J 2007, 50(1–2):44-49.
  • [17]Culverwell AD, Tapping CR: Congenital talipes equinovarus in Papua New Guinea: a difficult yet potentially manageable situation. Int Orthop 2009, 33(2):521-526.
  • [18]Amoa AB, Wapi J, Klufio CA: Longitudinal fetal biometry of normal pregnant Melanesian Papua New Guineans to construct standards of reference for Papua New Guinea. P N G Med J 1993, 36(3):219-227.
  • [19]Tobian AA, Tarongka N, Baisor M, Bockarie M, Kazura JW, King CL: Sensitivity and specificity of ultrasound detection and risk factors for filarial-associated hydroceles. Am J Trop Med Hyg 2003, 68(6):638-642.
  • [20]Mueller I, Rogerson S, Mola GD, Reeder JC: A review of the current state of malaria among pregnant women in Papua New Guinea. P N G Med J 2008, 51(1–2):12-16.
  • [21]Intermittent Preventive Treatment With Azithromycin-containing Regimens in Pregnant Women in Papua New Guinea (IPTp in PNG). http://clinicaltrials-lhc.nlm.nih.gov/ct2/show/NCT01136850 webcite
  • [22]Loughna P, Chitty LTE, Chudleigh T: Fetal size and dating: charts recommended for clinical obstetric practice. Ultrasound 2009, 17(3):161-167.
  • [23]Kofinas AD, Espeland MA, Penry M, Swain M, Hatjis CG: Uteroplacental Doppler flow velocity waveform indices in normal pregnancy: a statistical exercise and the development of appropriate reference values. Am J Perinatol 1992, 9(2):94-101.
  • [24]Acharya G, Wilsgaard T, Berntsen GK, Maltau JM, Kiserud T: Reference ranges for serial measurements of blood velocity and pulsatility index at the intra-abdominal portion, and fetal and placental ends of the umbilical artery. Ultrasound Obstet Gynecol 2005, 26(2):162-169.
  • [25]Acharya G, Wilsgaard T, Berntsen GK, Maltau JM, Kiserud T: Reference ranges for serial measurements of umbilical artery Doppler indices in the second half of pregnancy. Am J Obstet Gynecol 2005, 192(3):937-944.
  • [26]Olofsson P, Olofsson H, Molin J, Marsal K: Low umbilical artery vascular flow resistance and fetal outcome. Acta Obstet Gynecol Scand 2004, 83(5):440-442.
  • [27]World Health Organisation: Birth defects. http://apps.who.int/gb/ebwha/pdf_files/WHA63/A63_10-en.pdf webcite
  • [28]International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR): Annual Report 2011 with data for 2009. Rome: ICBDSR; 2011.
  • [29]FIGO Committee for the Ethical Aspects of Human Reproduction and Women's Health: Ethical issues in the management of severe congenital anomalies. Int J Gynaecol Obstet 2013, 120(3):307-308.
  • [30]Heuser CC, Eller AG, Byrne JL: Survey of physicians' approach to severe fetal anomalies. J Med Ethics 2012, 38(7):391-395.
  • [31]Chervenak F, McCullough LB: Responsibly counselling women about the clinical management of pregnancies complicated by severe fetal anomalies. J Med Ethics 2012, 38(7):397-398.
  • [32]Iserson KV, Chiasson PM: The ethics of applying new medical technologies. Semin Laparosc Surg 2002, 9(4):222-229.
  • [33]McGoldrick IA: Termination of pregnancy in Papua New Guinea: the traditional and contemporary position. P N G Med J 1981, 24(2):113-120.
  • [34]Response from the Faculty of Public Health to the Nuffield Council on Bioethics consultation on Ethics of Prolonging Life in Fetuses and the Newborn (June 2005). http://www.fph.org.uk/consultations webcite
  • [35]Rijken MJ, Gilder ME, Thwin MM, Ladda Kajeechewa HM, Wiladphaingern J, Lwin KM, Jones C, Nosten F, McGready R: Refugee and migrant women's views of antenatal ultrasound on the Thai Burmese border: a mixed methods study. PLoS One 2012, 7(4):e34018.
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