منابع مشابه
[Gigantic cystic splenic lymphangioma. Report of one case].
Splenic lymphangiomas are benign primary simple or multiple tumors. They are incidentally diagnosed in children and people younger than 20 year-old. We report a 26-year-old female presenting with a history of five months of abdominal pain localized over the left upper hemi abdomen. A computed tomographic abdominal scan demonstrated a cystic tumor of 16 cm diameter originating from the spleen. H...
متن کاملUnusual imaging profile of a solitary splenic lymphangioma
Splenic lymphangioma is a rare, benign lesion of the spleen that is characterized microscopically by a proliferation of thin-walled vascular channels filled by proteinacious material. Based on microscopic features, three types of lymphangiomas are described as simple capillary, cavernous, and cystic; however, the distinction between these types is not uniformly accepted. The cystic type is the ...
متن کاملSplenic lymphangioma: a rare benign tumor of the spleen treated by laparoscopic surgery.
Spleen diseases are rare, being splenic abscesses, splenic cysts, benign tumors (hemangioma, lymphangioma and others), and malignant tumors (lymphomas, metastases and others)1. Primary benign tumors of the spleen are extremely rare and account for less than 0.007% of all tumors identified upon surgery and autopsy2. Splenic lymphangiomas (SL) are benign cystic tumors resulting from congenital ma...
متن کاملKlippel-Trenaunay syndrome presenting with acanthocytosis and splenic and retroperitoneal lymphangioma: a case report
INTRODUCTION Klippel-Trenaunay syndrome is a rare congenital mesodermal abnormality characterized by bone and soft tissue hypertrophy, extensive hemangioma and venous abnormalities. We report the case of a patient with two additional rare clinical manifestations in the background of Klippel-Trenaunay syndrome, namely, acanthocytosis and splenic and retroperitoneal lymphangioma. CASE PRESENTAT...
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ژورنال
عنوان ژورنال: International Journal of Surgery Case Reports
سال: 2019
ISSN: 2210-2612
DOI: 10.1016/j.ijscr.2019.07.078