Taha Abdulrahman, Algethami Nada E, AlQurashi Raghad, Alnemari Amal K
Pediatric Surgery, Raparin Teaching Hospital for Children, Erbil, IRQ.
Medicine, Taif University, Taif, SAU.
Cureus. 2021 Mar 5;13(3):e13714. doi: 10.7759/cureus.13714.
Spigelian hernia-undescended testes (SH-UDT) syndrome is a rare disorder, with only 57 cases reported in the literature. The presentation can be asymptomatic or symptomatic in the form of pain, tenderness, or a lump. We present a case of a 50-day-old boy with SH-UDT syndrome. The patient presented with signs and symptoms of acute intestinal obstruction. Exploration confirmed a Spigelian hernia containing small bowel loops and right undescended testis. Orchidopexy was done after ligation of the hernial sac. A follow-up visit after two years revealed right testicular atrophy.
半月线疝合并隐睾（SH-UDT）综合征是一种罕见疾病，文献中仅报道过57例。其表现可为无症状，或表现为疼痛、压痛或肿块等症状。我们报告一例50日龄患有SH-UDT综合征的男婴。该患者表现出急性肠梗阻的体征和症状。探查证实为一个包含小肠袢和右侧隐睾的半月线疝。在结扎疝囊后进行了睾丸固定术。两年后的随访显示右侧睾丸萎缩。
