| Autor: |
Pradeep, Immanuel, Kumar, Naina, Kalyani, Poojitha, Nigam, Jitendra Singh, Somalwar, Shrinivas Bheemrao, Srirambhatla, Annapurna, Rath, Ashutosh |
| Zdroj: |
Pediatric & Developmental Pathology; Jan2024, Vol. 27 Issue 1, p77-82, 6p |
| Abstrakt: |
Urorectal septum malformation sequence (URSMS) is an uncommon disease characterized by a failure of the anorectal septum to divide the cloaca and fuse with the cloacal membrane. Complete URSMS is usually lethal in newborn due to severe renal dysfunction and pulmonary hypoplasia. Partial URSMS is compatible with life with a single perineal opening draining a common cloaca with an imperforate anus which amenable to surgical management. Antenatal diagnosis of URSMS is challenging because of multisystem, complex abnormalities involving gastrointestinal, urogenital tract, cardiovascular, and musculoskeletal systems. In this case report, we describe a 15-week male fetus with partial URSMS having a spectrum of multisystem structural anomalies associated with fetal neuroblastoma in retroperitoneal location and adrenal neuroblastoma in situ. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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