Annular pancreas is a rare congenital malformation characterized by a band or ring of pancreatic tissue that completely or partially encases the second part of the duodenum, resulting in varying degrees of duodenal obstruction.^[1] The pancreatic tissue usually spans the second part of the duodenum, partly or completely, close to the papilla or ampulla of Vater, and rarely elsewhere.^[2] Symptoms and time of presentation usually depend upon the degree of obstruction caused by the pancreatic tissue or associated duodenal atresia/stenosis.^[3]

More importantly, life-threatening duodenal obstruction or atresia are associated with more than 40% of annular pancreas cases.^[4] Thus, if diagnosed antenatally, it represents a valuable predictor for future gastrointestinal emergencies and helpful in further management after birth.

A 33-year-old Indian primigravida with a history of hypothyroidism and Rh isoimmunization came for routine antenatal ultrasonography at 28 weeks and 4 days of gestation. Her triplet or triple test was negative. In her previous ultrasonography, done at 12 weeks, fetal growth parameters were lagging behind LMP [last menstrual period] by 10 days. The present ultrasound showed mild polyhydramnios with an amniotic fluid index of 28, a single umbilical artery, preaxial polydactyly, and fetal growth retardation. The stomach and duodenum were dilated leading to a double bubble sign with a hyperechogenic band surrounding the fetal duodenum (Fig.1). Differential diagnosis of duodenal obstruction either due to annular pancreas, duodenal atresia/stenosis, or malrotation were given. A maternal right ovarian cyst (8.1 x 5.4 cm) was also documented. The fetal amniotic karyotype was normal, 46 XX. Fetal ECHO was also normal. Fetal MRI performed demonstrated dilated stomach and the duodenum giving double bubble sign (Fig.2).

Due to gestational hypertension and absent end-diastolic flow in the uterine artery, elective lower segment uterine cesarean section was performed at 32week and 3days. A small for gestational age female baby was delivered. Cystectomy was also done as part of the procedure and the cyst was benign on histopathology. Ultrasonography done in the immediate postnatal period was consistent with antenatal ultrasonography (Fig.3). The upper gastrointestinal contrast study showed a non-passage of contrast beyond the second part of the duodenum (Fig.3). As annular pancreas rarely causes complete duodenal obstruction, therefore our provisional diagnosis was more inclined to the duodenal atresia rather than the annular pancreas.

A laparotomy was performed on the second day of the life and the annular pancreas was found causing the duodenal obstruction (Fig.4). A side-to-side duodeno-duodenal anastomosis was performed with an uneventful postoperative period.

As most of the cases of the annular pancreas are asymptomatic, no systematic antenatal or postnatal standard screening is practiced. Thus, the real incidence of the annular pancreas is not known. During embryogenesis, the pancreas develops from dorsal and ventral pancreatic buds between the fifth and seventh gestational weeks. In normal development, these two pancreatic buds rotate along with the rotation of the intestine. During that period, the duodenum rotates from left to right, the ventral pancreatic bud typically migrates posteriorly and inferiorly, merging with the more caudal portion of the pancreatic head and the uncinate process, and the dorsal bud develops into the body and tail of the pancreas.^[1] The annular pancreas is due to the failure of the ventral bud to rotate, resulting in the incarceration of the duodenum.^[5]

Antenatal diagnosis of the annular pancreas is suspected in case of significant duodenal obstruction leading to the double-bubble sign. The distended stomach and the duodenum are seen on the left and center, just to the right of the midline, of the fetal abdomen. Both these dilatations are seen in the pre-stenotic segment. Double-bubble sign is not specific for the annular pancreas and can be seen with various other conditions like duodenal atresia, tissue bands, and intestine duplications. The ultrasonographic findings of duodenal obstruction are usually detected during the second trimester, although two previous studies have described this finding in 1st trimester.^{[6], [7]} It is of utmost importance to identify the underlying cause of duodenal obstruction on antenatal scans, as it helps to define the prognosis and appropriate management after birth.

In our case, a hyperechoic band completely surrounding the duodenum was identified on antenatal as well as postnatal ultrasound scans. Like our case, hyperechoic bands around the duodenum with the double bubble sign secondary to the annular pancreas were reported by a few other authors.^{[3], [8], [9], [1]} But, we believe the presence of a hyperechoic band in conjunction with a double bubble sign is pathognomonic of the annular pancreas with duodenal obstruction. But this needs validation by further research. The prenatal diagnosis of the annular pancreas is extremely rare. It is also associated with other abnormalities, like polyhydramnios, Down syndrome, intestinal malrotation, gallbladder agenesis, and CHARGE syndrome.^{[8], [9], [1]} In our case, there was mild polyhydramnios, single umbilical artery, preaxial polydactyly, and annular pancreas. Therefore, associated anomalies of the annular pancreas must be looked for better management of newborn babies.

In conclusion, the presence of a hyperechoic band in conjunction with a double bubble sign may be pathognomonic of the annular pancreas and should be looked for. Also, there is a need for future studies to prove our hypothesis.