Chronic Low Back Pain due to Retroperitoneal Cystic Lymphangioma
نویسندگان
چکیده مقاله:
Abdominal cystic lymphangioma is a rare benign neoplasm. Less than 1% of lymphangiomas is in the retroperitoneum. Lymphangioma is mostly asymptomatic. Chronic symptoms were reported in retroperitoneal type more than others. Acute symptoms due to complications like infection, cyst rupture or hemorrhage may occur. We report an 18-years-old girl with low back pain from 6 months ago with huge pelvic mass and diagnosis of retroperitoneal cystic lymphangioma.
منابع مشابه
chronic low back pain due to retroperitoneal cystic lymphangioma
abdominal cystic lymphangioma is a rare benign neoplasm. less than 1% of lymphangiomas is in the retroperitoneum. lymphangioma is mostly asymptomatic. chronic symptoms were reported in retroperitoneal type more than others. acute symptoms due to complications like infection, cyst rupture or hemorrhage may occur. we report an 18-years-old girl with low back pain from 6 months ago with huge pelvi...
متن کاملChronic Low Back Pain due to Retroperitoneal Cystic Lymphangioma.
Abdominal cystic lymphangioma is a rare benign neoplasm. Less than 1% of lymphangiomas is in the retroperitoneum. Lymphangioma is mostly asymptomatic. Chronic symptoms were reported in retroperitoneal type more than others. Acute symptoms due to complications like infection, cyst rupture or hemorrhage may occur. We report an 18-years-old girl with low back pain from 6 months ago with huge pelvi...
متن کاملA Huge Cystic Retroperitoneal Lymphangioma Presenting with Back Pain
Retroperitoneal lymphangioma is a rare location and type of benign abdominal tumors. The clinical presentation of this rare disease is nonspecific, ranging from abdominal distention to sepsis. Here we present a 73-year-old female patient with 3-month history of back pain. USG and CT revealed a huge cystic mass which was surgically excised and appeared to be lymphangioma on histopathology.
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A case of a large retroperitoneal tumor in a previously asymptomatic twenty-two-year-old white female is presented. A review of the literature confirms the rarity of this tumor. Its histologic and embryologic derivation as well as its subtle and bizarre method of presentation are discussed. The cause of such lesions is debatable, but primary cure can be accomplished by meticulous excision of th...
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عنوان ژورنال
دوره 2 شماره 1
صفحات 72- 74
تاریخ انتشار 2014-03-01
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