Lymphangiomas are rare hamartomatous malformations of skin lymphatics and subcutaneous tissues, and can occur anywhere in the body. Approximately 50% of lymphangiomas are present at birth and up to 90% are visible by the age of 2 years [1]. Approximately 70%–80% occur in theneck [2] and the remaining20%–30%occur in the axillary region [3]. Rare locations include the mediastinum, extremities, trunk, retroperitoneal area, abdominal viscera, pelvis, and chest wall [4]. In the present case, previously undetected fetal lymphangiomas were discovered during delivery at Bankura Sammilani Medical College, Bankura, India. A24-year-oldwoman, gravida2,was referred to thehospital's tertiary center at 39 weeks of pregnancy owing to nonprogress of labor. Her first infant had been delivered vaginally 2.5 years previously. On admission, vaginal examination revealed 4-cm cervical dilation, 80% effacement of cervix, vertex presentation, and 0 station. Oxytocin infusion was started. After 4 hours, the head of the fetus was delivered; however, delivery of the shoulders proved difficult and shoulder dystocia was diagnosed. The McRoberts, Woods, and Zavanelli maneuvers were unsuccessful. At laparotomy, the anterolateral uterine segment was ruptured. The dead fetus was delivered abdominally with assistance from below and the rupture was repaired. A 10×10-cm swelling was found on the right side of the anterior chest of the fetus (Fig. 1) and nonpitting edemawas found on the right upper limb. The fetus weighed 4.5 kg. Multiple fluid-filled spaces were found via ultrasonogram. The presence of lymphangioma and hemangioma was suspected; this was supported by computed tomography scan and confirmed via histopathology. Lymphangiomas are classified into 3 groups: lymphangioma simplex, consisting of capillary-sized channels; cavernous lymphangioma, consisting of dilated lymphatic channels; and cystic lymphangioma (hygroma), comprising multiple cysts of varying sizes [3]. Although the incidence of cystic lymphangioma is estimated to be 1 per 6000 pregnancies, it is a relatively common anomaly (1 per 875) in spontaneously aborted fetuses [2]. Based on the autopsy findings, the lesions in thepresent casewere considered to be cystic lymphangiomas. Lymphangiomas result from a defect in the connection between the lymphatic channels and the venous system, or from abnormal development of the lymphatic vessels [5]. Burke et al. [6] described a similar case in which cystic lymphangioma caused a difficult breech delivery. The shoulders and head of the dead fetus were delivered after multiple perforations of the lesion with a curette. Prenatal diagnosis of lymphangioma helps to plan the mode of delivery and intrapartum/postpartum care, and may decrease the morbidity of both mother and infant. Intrapartum ultrasound, if available, may be useful in cases of significant, unexpected shoulder dystocia caused by fetal lymphangioma.