The urachus is a natural embryonic remnant. In adults, it is a fibrous cord potentially located in the midline region between the peritoneum and the transversalis fascia, developing from the bladder dome to the navel (
1). In the first trimester of gestation, the urachus is responsible for removing the neonate's nitrogenous waste via the placenta and the umbilical cord (
2), but its function in adults is unclear. The urachus opening after birth causes anomalies. Four types of congenital urachal anomalies include patent urachus (~50% of all anomalies), umbilical-urachal sinus (~15%), vesicourachal diverticulum (~3% to 5%), and urachal cyst (~30%), which may be seen in children or adults. These anomalies may mostly close after birth but open again following some pathological conditions (
3). Urachal anomalies occur at an incidence of 1 in 5,000 births; of this number, about 2% can be found in adults. It is two-fold more common in males than in females (
4). The clinical symptoms are nonspecific and vary between children and adults. The most common symptoms in adults are hematuria, dysuria, and pain. Of course, it is possible to be asymptomatic or associated with dermatitis or abscess of the periumbilical. Most patients with urachal anomalies are asymptomatic unless associated with infection (
5). Ultrasonography (US) and a computerized tomography (CT) scan are effective tools for diagnosis. Timely and correct diagnosis of urachal anomalies is vital because they are prone to infection and malignancy (
6). The two complications after these anomalies are calculi and cancer (
7). According to our best search of the English literature, urachus calculi are a rare anomaly, with only eleven cases reported in adults to date.