Hameed Shema, McHugh Kieran, Shah Neil, Arthurs Owen J
Departments of Radiology, Great Ormond Street Hospital for Children NHS Foundation Trust, and Institute of Child Health, University College of London, London, WC1N 3JH, UK.
Pediatr Radiol. 2014 Apr;44(4):392-7. doi: 10.1007/s00247-013-2828-5. Epub 2013 Nov 29.
Intramural duodenal haematomas (IDHs) are a rare complication of endoscopic biopsy but can cause significant morbidity and mortality, including duodenal obstruction, hospitalization and needing intravenous feeding. They are extremely uncommon in those with normal haematology.
To describe the occurrence of IDHs following endoscopic biopsy in our institution.
We identified three patients who developed a post biopsy IDH during an 18-month period (2010-2012) in a retrospective search of our hospital pathology and imaging databases.
All three children had complex medical problems and presented with gastrointestinal symptoms including severe abdominal pain, reflux, poor feeding and abnormal gut transit time. All underwent normal upper GI endoscopy with duodenal biopsy. Following endoscopy, they presented with intermittent GI obstruction with severe abdominal pain, distension and bilious vomiting or symptoms of pancreatitis, had imaging features of IDH and were managed conservatively making a full recovery. Initial haematology including platelet counts were normal, but two children were subsequently found to have platelet dysfunction and the third to have an unclassified coagulopathy.
IDHs may be the presenting factor in children with unsuspected bleeding problems. We present these findings to raise awareness of the imaging features and clinical impact of these cases because better understanding of these risk factors may help to avoid these complications in children in the future.
十二指肠壁内血肿(IDHs)是内镜活检的一种罕见并发症,但可导致严重的发病率和死亡率,包括十二指肠梗阻、住院治疗以及需要静脉营养支持。在血液学正常的人群中极为罕见。
描述我院内镜活检后IDHs的发生情况。
通过回顾性检索我院病理和影像数据库,我们确定了3例在18个月期间(2010 - 2012年)活检后发生IDH的患者。
所有3名儿童均有复杂的医疗问题,表现为胃肠道症状,包括严重腹痛、反流、喂养困难和肠道转运时间异常。所有患儿均接受了正常的上消化道内镜检查及十二指肠活检。内镜检查后,他们出现间歇性胃肠道梗阻,伴有严重腹痛、腹胀和胆汁性呕吐或胰腺炎症状,具有IDH的影像学特征,并经保守治疗后完全康复。最初的血液学检查包括血小板计数均正常,但随后发现2名儿童存在血小板功能障碍,第3名儿童存在未分类的凝血病。
IDHs可能是未被怀疑有出血问题儿童的首发因素。我们展示这些发现以提高对这些病例的影像学特征和临床影响的认识,因为更好地了解这些危险因素可能有助于未来避免儿童出现这些并发症。