Imaging findings of a twin male neonate with megacystis microcolon intestinal hypoperistalsis syndrome

Radiology Case Reports

Jack Hua, MD¹  Christopher Arcement, MD²  Jennifer Lim, BS³ 

[1] Corresponding author.;Children's Hospital New Orleans, 200 Henry Clay Avenue, New Orleans, LA 70118, USA;Tulane University Medical Center, 1430 Tulane Avenue, New Orleans, LA 70112, USA;

关键词: Pediatrics;    Megacystis microcolon intestinal hypoperistalsis syndrome;    Gastrointestinal;    Genitourinary;    Neonatal;    Perinatal;   

DOI  :  

来源: DOAJ

【 摘 要 】

Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital defect of the bowel and bladder that is especially rare in males. We present a case of MMIHS in a male nonidentical twin neonate who presented with abdominal distention, urinary retention, and hypoplastic bowel. The voiding cystourethrogram included in this report displays rare image of MMIHS in a male urogenital system. The constellation of clinical and imaging findings presented in this case are characteristic of MMIHS and may aid the early diagnosis of male neonates affected by this disease.

【 授权许可】

Unknown