Lymphangioma of the upper extremity is rare; its treatment is unstandardized. We reviewed five female and one male patient with cavernous lymphangioma of the hand and forearm. Each of them underwent at least one surgical procedure. Five patients had satisfactory results with cosmesis and hand function. Satisfactory results are expected in those treated initially in early childhood, as most lymphangiomas tend to increase gradually in size and infiltrate previously uninvolved normal tissues.
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Int J Surg Case Rep
January 2025
Department of General Surgery, Trauma and Burns Center, Ben Arous, University of Tunis El Manar, Tunisia.
Int J Surg Case Rep
December 2024
Student Research Committee, M.D, Shiraz University of Medical Sciences, Shiraz, Iran.
Introduction: Lymphangioma is a benign neoplasm that involves the lymphatic vessels in multiple anatomical regions, including the pancreas, where it is exceptionally rare, with a prevalence of only 0.2 %. These tumors, often found in children, are uncommon in adults and may present with symptoms like abdominal pain, distention, and nausea.
View Article and Find Full Text PDFInt J Surg Case Rep
November 2024
Department of Surgery, Rafidia Hospital, Ministry of Health, Nablus, Palestine. Electronic address:
Introduction And Importance: Lymphangiomas are rare benign lymphatic malformations, typically affecting the head, neck, or axillary regions, with abdominal cystic lymphatic malformations (CLM) being particularly uncommon in adults. Abdominal CLM account for less than 5 % of all lymphangiomas and 7 % of all abdominal cystic lesions in adults with a prevalence of approximately 1 in 250,000. These lesions are commonly found by accident during imaging investigations and are asymptomatic.
View Article and Find Full Text PDFJ Cutan Pathol
October 2024
Dermatology and Venereology Department, Faculty of Medicine, Assiut University, Assiut, Egypt.
Generalized lymphatic anomaly (GLA), previously known as lymphangiomatosis, is a rare developmental disease characterized by abnormal proliferation of lymphatic vascular structures that may involve the dermis, soft tissue, bone, and visceral parenchyma. Being an uncommon condition and the lack of specific symptoms often result in a delayed diagnosis or even misdiagnosis, which, in addition to its progressive nature, can lead to dysfunction of vital organs, and ultimately, a poor prognosis. In this report, we present a unique case of GLA in an upper Egyptian female child.
View Article and Find Full Text PDFRev Esp Enferm Dig
October 2024
Gastroenterology and Hepatology, Hospital Universitario de Toledo, España.
The increasing number of endoscopic explorations help recognize rare lesions of the gastrointestinal tract, such as lymphangiomas, rare benign vascular tumours in adults. Patients with lymphangioma are generally asymptomatic but if complications arise, the approach is endoscopic or surgical. Endoscopic ultrasound aids in distinguishing this tumour from other subepithelial lesions.
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