Publications by authors named "Chetna Rathi"

Duodenal anomalies represent a spectrum of congenital malformations that may present with similar clinical and radiological findings. We report a rare case of a congenital duodenal band mimicking duodenal atresia in a neonate. A primigravida woman in her 20s presented with polyhydramnios and suspected fetal duodenal atresia on antenatal ultrasound.

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Article Synopsis
  • * The classic features of KTS include port wine stains (capillary malformations), enlarged limbs or bones, and the presence of varicose veins.
  • * A case study highlights a 24-year-old male with KTS who experienced varicose veins since age five and had macrodactyly, also showing a connection to the vein of Servelle.
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Spontaneous rupture of the renal pelvis (SRRP) with urine extravasation is rare. This condition is primarily associated with an obstructing ureteric calculus. It creates a diagnostic dilemma, especially when the clinical diagnosis can be inconsistent.

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Mucormycosis is an invasive fungal infection. The prevalence is low for this disease, and the most common site of its occurrence in the gastrointestinal system is the stomach. The clinical signs and symptoms of gastric mucormycosis are vague such as pain in the abdomen, nausea, vomiting, haematemesis, etc.

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A meconium pseudocyst is formed following meconium peritonitis. At present, antenatal diagnosis and planned management of meconium pseudocyst have reduced the mortality rate significantly. We presented a case of a neonate with abdominal distension and non-passage of meconium who experienced respiratory distress and was taken for exploratory laparotomy at a tertiary care center due to suspected bowel perforation.

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