Evidence map›Paper›PMID 40109598›Full record

ArticleAnnals of medicine and surgery (2012)2025

Rectal bleeding due to cavernous hemangioma in Klippel-Trenuany syndrome: a rare presentation and review of management.

Omer Usman, Maham Tariq, Muhammad W Khan, Muhammad U Shahbaz, Rehaab Mujahid, Osama Ijaz, Muhammad A Hassan

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In one paragraph

Article in Annals of medicine and surgery (2012), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Omer UsmanDepartment of Internal Medicine, Texas Tech University Health Sciences Center, The Hospitals of Providence Transmountain Campus, El Paso, Texas, USA.
Maham TariqDepartment of Internal Medicine, Services Institute of Medical Sciences, Lahore, Pakistan.
Muhammad W KhanDepartment of Internal Medicine, Services Institute of Medical Sciences, Lahore, Pakistan.
Muhammad U ShahbazDepartment of Internal Medicine, Allama Iqbal Medical College, Lahore, Pakistan.
Rehaab MujahidDepartment of Internal Medicine, Shalamar Medical and Dental College, Lahore, Pakistan.
Osama IjazDepartment of Internal Medicine, Services Institute of Medical Sciences, Lahore, Pakistan.
Muhammad A HassanDepartment of Internal Medicine, Shifa College of Medicine, Islamabad, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and importance: 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. Case presentation: 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. Clinical discussion: 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. Conclusion: 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.

Indexed as

case reportcavernous hemangiomasgastrointestinal bleedingKlippel–Trenaunay syndromemultidisciplinary management

Identifiers

PMID40109598
PMCPMC11918785

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