Pallister‐Killian syndrome is a multi‐system sporadic disorder with developmental delay. It is a rare chromosomal abnormality involving supernumerary isochormosome 12p. The disorder exhibits tissue specific mosaicism. The first prenatal diagnosis of PKS was reported in 1985 after ultrasound detection of fetal anomalies. Since this observation, there have been about 62 reports of fetuses with PKS. In this review, we cover the prenatal aspects of PKS.

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Spontaneous broad ligament hematomas are relatively rare in non- pregnant state. We hereby present a case report of a 73 year old post-menopausal female, who initially presented with complain of postmenopausal bleeding since 4 month. Patient had underwent a diagnostic endometrial curettage in an another hospital, prior to presenting to our institution. On imaging, she was found to have a right sided complex adenexal mass (about 5cm in size) suspicious of ovarian malignancy. Patient was taken up for exploratory laparotomy and per-operatively found to have a broad ligament hematoma, which was further confirmed on histopathological examination.