Youn Joong Kee, Park Shin-Hoo, Han Ji-Won, Oh Chaeyoun, Kim Hyun-Young, Jung Sung-Eun
Department of Pediatric Surgery, Seoul National University College of Medicine, Seoul, Korea.
Medicine (Baltimore). 2017 Sep;96(37):e6974. doi: 10.1097/MD.0000000000006974.
Kaposiform hemangioendothelioma (KHE) is an aggressive vascular tumor, mainly occurring in infants and young children and previously reported cases were mainly cutaneous or visceral form. Intestinal kaposiform hemangioma was first reported in 2012. Intestinal type KHE showed better prognosis if the lesion was limited in the gastrointestinal tract and coagulopathy was not accompanied. Since the number of reported cases is small, further study for treatment options and prognosis need to be done.
We described the case of a 1-month-old female who had abdominal distention and bilious vomiting.
She was suspected as intestinal obstruction after diagnostic work up.
Surgical exploration was performed and jejunal obstruction with a mass was identified. Small bowel segmental resection and anastomosis was performed.
The patient discharged with symptom free. Through the pathological examination, the mass was identified as intestinal type KHE.
Intestinal KHE can cause bowel obstruction and be managed successfully with complete surgical resection. More cases should be reported and further evaluation for treatment options and prognosis evaluation is necessary.
卡波西样血管内皮瘤(KHE)是一种侵袭性血管肿瘤,主要发生于婴幼儿,既往报道的病例主要为皮肤型或内脏型。肠道卡波西样血管瘤于2012年首次报道。如果病变局限于胃肠道且不伴有凝血病,肠道型KHE的预后较好。由于报道的病例数量较少,需要进一步研究治疗方案和预后情况。
我们描述了一名1个月大的腹胀、胆汁性呕吐的女婴病例。
经过诊断检查,怀疑她患有肠梗阻。
进行了手术探查,发现空肠梗阻伴有肿块。实施了小肠节段性切除及吻合术。
患者无症状出院。经病理检查,肿块被确诊为肠道型KHE。
肠道KHE可导致肠梗阻,通过完整的手术切除可成功治疗。应报告更多病例,有必要进一步评估治疗方案和预后评估。