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Objectives: Lymphangiomatous lesions involving the gastrointestinal (GI) tract remain incompletely characterized, and their clinical and histopathologic features have not been systematically evaluated. The distinction between a primary lymphatic malformation (lymphangioma) and a dilation of existing lymphatics (lymphangiectasia) is of clinical significance, since lymphangiectasia may occur in the setting of lymphatic obstruction due to an unsampled malignancy. We describe clinical and morphologic features of lymphangiomas of the GI tract in adult and pediatric populations and contrast them with lymphangiectasia.

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Lymphocutaneous fistulas: pre-therapeutic evaluation by magnetic resonance lymphangiography.

Br J Radiol

August 2011

Department of Radiology, University Hospital of Freiburg, Hugstetter Strasse 55, D-79106, Freiburg, Germany.

Objective: Lymphocutaneous fistulas with intractable lymphatic leakage represent a serious clinical condition leading to a severe impairment of quality of life for the affected patients. To date, no adequate diagnostic imaging modality is in existence to allow selection of the correct treatment option. The aim of this study was to perform a pre-therapeutic evaluation of the lymphatic system in patients with lymphocutaneous fistulas by magnetic resonance lymphangiography (MRL).

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Article Synopsis
  • The study looked at how the lymphatic system works in patients with a condition called diffuse lymphangiomatosis using a special imaging technique called magnetic resonance imaging (MRI).
  • 15 patients were checked at different body parts like legs and belly to find and measure lymphangiomas, which are abnormal growths in the lymphatic system.
  • The results showed that most patients had lymphangiomas in their legs and belly, and using MRI helped doctors see these issues safely and accurately, which is important for planning the right treatment.
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Bone lymphangiomatosis: treatment with percutaneous cementoplasty.

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Departments of Diagnostic Radiology, University of Texas M. D. Anderson Cancer Center, Houston, TX 77030-4009, USA.

Study Design: Case report, minimally invasive technique.

Objectives: Disseminated lymphangiomatosis is a rare disorder that can produce clinical manifestation secondary to soft tissue, visceral and bone involvement. The overall prognosis of this disorder is usually poor, and the current treatment options for its sequelae are limited and only palliative.

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