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Background: Generalized lymphatic anomaly (GLA) is a rare congenital lymphatic malformation (LM) characterized by multiple infiltrating lymphangiomas in various tissues. Owing to its rarity, information on this disease is obtained mainly through case reports, leading to delayed diagnosis. In this study, we reported a case of generalized lymphatic anomaly in a pediatric patient manifesting as hemorrhagic pleural effusion.

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Introduction: While laparoscopic splenectomy (LS) has been widely used in benign splenic tumor, more concerns have been raised for postoperatively short-term and long-term complications. Laparoscopic partial splenectomy (LPS) is a surgical option, to preserve splenic function, and reduce postoperative complications. The aim of our study was to retrospectively identify the safety and feasibility of LPS compared with LS in patients with splenic benign tumor.

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Article Synopsis
  • Lymphangiomas are non-cancerous tumors from lymphatic tissue, mostly seen in kids under 2 years old, while adult cases are rare.
  • A 64-year-old woman was found to have a cyst in her abdomen during a check-up, and tests revealed it was a type of lymphangioma.
  • These tumors can invade other tissues, but most don’t cause symptoms, and the best way to treat them is by surgically removing them completely.
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Microcystic lymphangioma is a rare but benign lesion that should be differentiated from a neoplasm.

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Introduction: Lymphangiomatosis is a rare abnormal proliferation of lymphatic vessels involving multiple organs like the brain, lung, heart, spleen, liver, and bones. Lymphangiomas constitute 5.6% of all benign tumors in infancy and adulthood.

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