Jasić Mladen, Subat-Dezulović Mirna, Nikolić Harry, Jonjić Nives, Manestar Koraljka, Dezulović Matko
Pula General Hospital, Department of Pediatrics, Pula, Croatia.
Coll Antropol. 2011 Mar;35(1):197-201.
Henoch-Schönlein purpura (HSP) is the most common childhood systemic small-vessel vasculitis with skin, joint, gastrointestinal (GI) and renal involvement. Uncommon GI complications are intussusception, bowel perforation and rarely reported appendicitis. HSP-associated stenosing ureteritis represents a rare and potentially serious complication. We present a 5-year-old boy with severe and prolonged course of HSP and three very rare complications that occurred sequentially: appendicitis, intussusception and ureteritis. Only three days after admission, he developed clinical signs of acute appendicitis indicating surgical intervention. Histological analysis of excised appendix showed inflammation but without signs typical for vasculitis. Two weeks later, with the reccurence of HSP he again developed clinical picture of acute abdomen. Ultrasound and radiologic evaluation demonstrated ileo-ileal intussusception and the second laparotomy was undertaken. Histological analysis of the resected bowel tissue showed typical signs of leucocytoclastic vasculitis. In the fourth week of his illness, serial urinalysis showed nephritic urinary sediment indicative of renal involvement. Unexpectedly, control abdominal ultrasound demonstrated mild hydronephrosis of the left kidney, not seen on previous ultrasound evaluations. Undertaken excretory urography and computed tomography (CT) scan showed stenosis of upper/ midureter with mild dilation of upper part of the left ureter suggesting unilateral HSP-associated stenosing ureteritis. Eventually, the patient was discharged and closely followed-up for the next two years. He had no further reccurence of HSP, the urinalysis normalized after six months, while mild unilateral hydronephrosis remained unchanged. Our search of the literature did not show reports of HSP complicated by appendicitis, intussusception and ureteritis, and to our knowledge this is the first case with three different illness events that occured sequentially. We emphasize the necessity of repeated ultrasound evaluations in the course of HSR especially in cases with severe GI and renal invovement.
过敏性紫癜(HSP)是儿童期最常见的系统性小血管炎,可累及皮肤、关节、胃肠道(GI)和肾脏。罕见的胃肠道并发症有肠套叠、肠穿孔,阑尾炎的报道则更为少见。HSP相关的狭窄性输尿管炎是一种罕见且可能严重的并发症。我们报告一名5岁男孩,其HSP病程严重且迁延,并依次出现了三种非常罕见的并发症:阑尾炎、肠套叠和输尿管炎。入院仅三天后,他就出现了急性阑尾炎的临床症状,提示需要手术干预。切除阑尾的组织学分析显示有炎症,但无血管炎的典型征象。两周后,随着HSP复发,他再次出现急腹症的临床表现。超声和影像学评估显示为回肠-回肠型肠套叠,遂进行了第二次剖腹手术。切除肠组织的组织学分析显示有白细胞破碎性血管炎的典型征象。在患病的第四周,连续尿检显示有肾炎性尿沉渣,提示肾脏受累。出乎意料的是,腹部超声检查发现左肾轻度肾积水,之前的超声评估未发现此情况。进行的排泄性尿路造影和计算机断层扫描(CT)显示输尿管上/中段狭窄,左输尿管上段轻度扩张,提示单侧HSP相关的狭窄性输尿管炎。最终,患者出院,并在接下来的两年里接受密切随访。他的HSP未再复发,六个月后尿检恢复正常,而轻度单侧肾积水仍无变化。我们检索文献未发现HSP并发阑尾炎、肠套叠和输尿管炎的报道,据我们所知,这是首例依次出现三种不同疾病事件的病例。我们强调在HSP病程中,尤其是在严重胃肠道和肾脏受累的病例中,反复进行超声评估的必要性。