Department of Paediatric Surgery, Bristol Children's Hospital, Bristol, United Kingdom.
Pediatr Blood Cancer. 2014 Feb;61(2):358-9. doi: 10.1002/pbc.24531. Epub 2013 Sep 9.
We report the case of a 27-month-old male with an unusual complication of aplastic anaemia and neutropenic enterocolitis. He suffered persistent neutropaenic sepsis and clinical deterioration forced the strategy of matched sibling haematopoietic stem cell transplantation. With engraftment and clinical recovery post-transplant, enteral feeding was re-established. Despite continued improvement the child began to vomit faeculent stomach content. Barium swallow showed gastro-colic and gastro-enteric fistulisation with contrast passing directly from stomach into descending colon and directly into jejunum. Laparotomy confirmed complex fistulae between the gastric body, the splenic flexure of the colon and the jejunum. The diagnosis and management of abdominal pathology secondary to severe pancytopaenia is challenging. Often the patient does not manifest the usual signs of acute abdominal pathology, making the decision to operate and the timing of surgery difficult. Counfounding this is the danger of performing surgery in a pancytopaenic patient. Our case illustrates these challenges and reports the unanticipated finding of a complex gastro-colic fistula.
我们报告了一例 27 个月大的男性患有再生障碍性贫血和中性粒细胞减少性肠炎的罕见并发症。他持续中性粒细胞减少性败血症,临床恶化迫使采用匹配的同胞造血干细胞移植策略。移植后,随着植入和临床恢复,重新开始肠内喂养。尽管持续改善,孩子开始呕吐粪便样胃内容物。钡餐显示胃-结肠和胃-肠瘘,造影剂直接从胃进入降结肠,并直接进入空肠。剖腹术证实胃体、结肠脾曲和空肠之间存在复杂瘘管。严重全血细胞减少继发的腹部病变的诊断和治疗具有挑战性。通常情况下,患者不会表现出急性腹部病变的常见体征,这使得手术决策和手术时机变得困难。使情况更加复杂的是在全血细胞减少症患者中进行手术的危险。我们的病例说明了这些挑战,并报告了一种复杂的胃结肠瘘的意外发现。