Usman Omer, Tariq Maham, Khan Muhammad W, Shahbaz Muhammad U, Mujahid Rehaab, Ijaz Osama, Hassan Muhammad A
Department of Internal Medicine, Texas Tech University Health Sciences Center, The Hospitals of Providence Transmountain Campus, El Paso, Texas, USA.
Department of Internal Medicine, Services Institute of Medical Sciences, Lahore, Pakistan.
Ann Med Surg (Lond). 2025 Jan 9;87(1):313-317. doi: 10.1097/MS9.0000000000002724. eCollection 2025 Jan.
Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder with an incidence of about 2-5:100 000. It is characterized by the triad of cutaneous hemangiomas, soft tissue or bone hypertrophy, and venous malformations. Gastrointestinal (GI) involvement in KTS, although uncommon, can lead to severe complications such as profuse GI bleeding. Our case highlights the challenges and management strategies of a patient with KTS.
A 5-year-old child presented with rectal bleeding since birth, accompanied by swelling and bluish discoloration on left flank, and multiple varicose veins on left leg. Examination revealed small hemangiomatous lesions scattered along the torso and trunk. Barium enema showed diffuse mucosal irregularity with polypoidal filling defects in the rectum and sigmoid colon. Doppler ultrasound revealed slow-flow vascular lesions in the left flank and leg without arteriovenous communication. Computed tomography (CT) scan showed diffuse cavernous hemangiomas in the descending colon, sigmoid colon, and rectum. Histopathology demonstrated numerous dilated, irregular vascular channels with calcification and hemosiderin-laden macrophages.
GI tract cavernous hemangiomas can cause chronic bleeding and anemia, necessitating careful evaluation. Imaging modalities like CT and Doppler ultrasound are crucial for assessing vascular lesions. Surgical interventions, including partial proctocolectomy and colorectal anastomosis, effectively control bleeding and improve outcomes. A multidisciplinary approach is essential for managing such cases.
This case underscores the importance of multidisciplinary management in KTS with GI bleeding. Effective diagnostic imaging and surgical treatment are key to managing severe complications and achieving successful outcomes. Long-term follow-up is crucial to monitor for recurrence and residual lesions.
克-特综合征(KTS)是一种罕见的先天性疾病,发病率约为2-5:100000。其特征为皮肤血管瘤、软组织或骨骼肥大以及静脉畸形三联征。KTS累及胃肠道虽不常见,但可导致严重并发症,如大量胃肠道出血。我们的病例突出了KTS患者面临的挑战及管理策略。
一名5岁儿童自出生以来出现直肠出血,伴有左侧腰腹部肿胀和青紫,以及左腿多处静脉曲张。检查发现沿躯干和躯体散在小的血管瘤样病变。钡剂灌肠显示直肠和乙状结肠弥漫性黏膜不规则,伴有息肉样充盈缺损。多普勒超声显示左侧腰腹部和腿部有缓慢血流的血管病变,无动静脉交通。计算机断层扫描(CT)显示降结肠、乙状结肠和直肠有弥漫性海绵状血管瘤。组织病理学显示大量扩张、不规则的血管通道,伴有钙化和含铁血黄素巨噬细胞。
胃肠道海绵状血管瘤可导致慢性出血和贫血,需要仔细评估。CT和多普勒超声等影像学检查对于评估血管病变至关重要。手术干预,包括部分直肠结肠切除术和结直肠吻合术,可有效控制出血并改善预后。多学科方法对于管理此类病例至关重要。
本病例强调了多学科管理在伴有胃肠道出血的KTS中的重要性。有效的诊断性影像学检查和手术治疗是管理严重并发症并取得成功预后的关键。长期随访对于监测复发和残留病变至关重要。