Mucormycosis of the neonatal gut is a rare disease, with uniformly fatal prognosis. It has occasionally been reported involving the stomach and ileum in immunocompromised hosts. However, mucormycosis of the colon is very rare. We report case of a preterm, low birth weight (LBW) neonate with clinical features of Necrotising enterocolitis found to have characteristic black-velvety colonic gangrene on exploratory laparotomy. The baby initially improved but succumbed to sepsis eventually. Tissue histology diagnosed mucormycosis of the colon. The diagnosis of colonic mucormycosis was unsuspected. This report is presented to create awareness about this rare entity so that it is suspected and diagnosed early.Keywords: Colon; Mucormycosis; Neonate; Low Birth Weight; Necrotising
EnterocolitisNeonatal gastrointestinal mucormycosis is a rare, opportunistic fungal infection, with dismal prognosis. Since, the diagnosis is based on histopathological examination of the resected segment (specimen) of stomach and/or bowel, it cannot be diagnosed preoperatively [1,2]. These cases are initially diagnosed as Necrotising enterocolitis (NEC), but later on are confirmed as gastrointestinal (colonic) mucormycosis. Hence, there is delay in specific treatment.
Case ReportEight-day-old male neonate was admitted in neonatal intensive care unit (NICU) for preterm care. He was born vaginally to an adolescent primigravida mother at 32 weeks gestational age. His birth weight was 1.2 Kg. The mother had received regular antenatal care and had no identifiable risk factors. Baby had not cried immediately following spontaneous vaginal delivery and had required bag and mask ventilation. There were no obvious congenital anomalies. He was on oral Sildenafil for management for pulmonary hypertension.On tenth day of life, he developed feeding intolerance and per rectal bleeding. A soft to firm lump of about 2×3 cm size was palpable in the right hypochondriac region. Nasogastric tube aspirate was bilious. Erect X-ray abdomen showed dilated stomach with paucity of gas in lower abdomen and pelvis (Figure 1). Dye study done for confirmation of diagnosis showed the same picture i.e. only gastric shadow could be visualized. Ultrasonography of the abdomen showed dilated, peristaltic bowel loops. Haematologic investigations showed raised WBC counts of 16,000/cmm and low Platelet count of 100,000/cmm. The differential diagnosis was malrotation with volvulus or Necrotising enterocolitis. In view of poor general condition, the child was explored under local anaesthesia. He had characteristic black-velvety gangrene confined to middle 8-10 cm of the mid-transverse colon without any frank / impending perforation. Initial 5-7 cm of midtransverse colon from the hepatic flexure was normal. Rest of the colon and small bowel was healthy looking. The non-viable colon was excised. After resection, the free ends were brought out as colostomy and mucus fistula through either end of the incision. Blood loss of about 20 cc was replaced on table. Postoperatively the acti...