Hematochezia: An abnormal presenting symptom of an extensive vascular malformation in a 6-year-old boy.

JPGN reports Pub Date : 2025-05-20 eCollection Date: 2025-08-01 DOI:10.1002/jpr3.70032
Kathleen Ordas, Joy Brusenback, Sahana Ummadi, Shannon Tocchio, Razan Alkhouri, Soha Shah
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Abstract

Gastrointestinal (GI) bleeding can be a common symptom in the pediatric population. Vascular malformations, which cause symptoms based on their location and effect on surrounding structures, are an uncommon cause of GI bleeding. We present the case of a 6-year-old male with a 1-year history of hematochezia, constipation, and microcytic anemia. Physical exam demonstrated a firm, mobile, non-circumferential anal mass measuring 4 cm in diameter, and located predominantly at the right-anterior bowel wall. Initial imaging, including abdominal radiograph and abdominal ultrasound, was unremarkable. Colonoscopy was visually and histologically negative. Magnetic resonance imaging of the pelvis showed an extensive pelvic venous-lymphatic malformation in the left hemipelvis, with extension to the right hemipelvis and left lower extremity, displacement of the rectum and colon, and protrusion into the anal canal. He was started on Sirolimus with symptom improvement. This case discusses a rare presentation of a pediatric vascular malformation presenting with a protruding anal mass.

便血:6岁男孩广泛血管畸形的异常表现。
胃肠道(GI)出血可能是儿科人群的常见症状。血管畸形引起的症状取决于其位置和对周围结构的影响,是一种罕见的消化道出血原因。我们提出的情况下,6岁的男性与1年历史的便血,便秘,和小细胞性贫血。体格检查显示一个坚固的、可移动的、非圆周的肛门肿块,直径为4厘米,主要位于肠壁右前。最初的影像,包括腹部x光片和腹部超声,没有明显的变化。结肠镜检查视觉和组织学均为阴性。骨盆磁共振成像显示左侧半骨盆广泛的盆腔静脉淋巴畸形,延伸至右侧半骨盆和左下肢,直肠和结肠移位,并突出到肛管。他开始服用西罗莫司,症状有所改善。这个病例讨论了一个罕见的儿童血管畸形,表现为突出的肛门肿块。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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