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The Rapunzel syndrome, found characteristically in girls with varying gastrointestinal symptoms, is a rare form of gastric trichobezoar extending throughout the bowel. The previously reported cases have different clinical and pathological features affecting the mortality. We describe a new case preoperatively diagnosed with none of the complications previously reported.

The younger the age at which the VP shunt was performed, the higher the incidence of CIM. Bilateral manifestations were higher than in the normal population. Increased intra-abdominal pressure by accumulation of fluid in combination with the high patency rate of processus vaginalis possibly plays a role in the development of CIM in VP shunt patients. Bilateral repair should be considered even when CIM is unilateral. Special care should be given to repair procedures since the recurrence rate is relatively high.

We report the case of a 3-month-old boy with a right-sided sliding appendiceal inguinal hernia that was diagnosed preoperatively with sonography. Surgery was performed, and intraoperative and histopathologic evaluations also revealed changes in the appendix that could have led to complications if left untreated. The infant's recovery was uneventful, and he was discharged on the second day after surgery. This condition is usually diagnosed intraoperatively, and to the best of our knowledge, this is only the second report in the English-language medical literature in which such a case was correctly diagnosed preoperatively with sonography. In our case, the early sonographic diagnosis led to early intervention and the avoidance of potential complications.