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angiomyolipoma/рвота
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10 полученные результаты
[Bilateral angiomyolipomas of the kidney in Bourneville's tuberous sclerosis].
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We report on a 25-year-old patient diagnosed as having Bourneville tuberous sclerosis with a giant angiomyolipoma 16 X 12 cm. in diameter, and two small angiomyolipomas in the left kidney, multiple asymptomatic angiomas in the right kidney and two 1 cm. diameter angiomas in the liver. The presenting
Hepatic angiomyolipoma in a 26-year-old Caucasian woman with a history of tibial osteosarcoma.
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We report on a 26-year-old Caucasian woman who was referred to the Department of Surgery complaining of general malaise, feeling of fullness with occasional vomiting and intermittent jaundice. The patient had previously suffered from tibial osteosarcoma of the left leg which was resected 13 years
[Tuberous sclerosis associated with subependymal giant cell astrocytoma and renal angiomyolipoma: a case report].
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We presented a case of tuberous sclerosis (TS) associated with subependymal giant cell astrocytoma (SEGC) and renal angiomyolipoma (RAML). A 19-year-old female, who had been diagnosed as TS since she was 3 months old, was admitted with complaints of headache, vomiting, and abdominal pain. At 10
Epithelioid angiomyolipoma of the kidney: a case report.
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Renal angiomyolipoma is a distinctive benign neoplasm that occurs either sporadically or in patients with tuberous sclerosis complex. A 45-year-old woman was admitted with history offlank pain and vomiting. There were no signs suggestive of tuberous sclerosis either in the patient or her family. At
Rapture of renal angiomyolipoma during pregnancy: a case report.
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BACKGROUND
Rapture of a renal angiomyolipoma and massive retroperitoneal hemorrhage, during pregnancy is rare and occasionally fatal. The association of this complication with pregnancy has been reported sporadically in the literature.
METHODS
We report a case of a 28 years old woman, in 33 week of
[Acute abdomen due to spontaneous renal angiomyolipoma rupture].
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Renal Angiomyolipoma (AML) is a rare benign tumor As it is usually asymptomatic and small, AML sometimes may cause acute abdomen by spontaneous rupture and hemorrhage that may be life threatening in some cases for which surgical management is necessary. A 58-year-old female patient was admitted for
[Renal angiomyolipoma and fever: assessment with isotopic renogram and 67Ga scintigraphy].
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A 26 year-old woman with tuberous sclerosis who came to the Emergency Department with high fever, bilious vomit, right hemiabdomen pain and syncope during 2 weeks. Laboratory analyses show hemoglobin 6.7 g/dl, creatinine 1.5 mg/dl and leukocytes 30,000. Abdominal CT is performed because of suspicion
Transarterial embolization for renal angiomyolipomas: A single centre experience in 79 patients.
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Objective To evaluate the long-term efficacy and safety of selective arterial embolization (SAE) in the treatment of renal angiomyolipomas (AMLs). Methods This was a retrospective review of medical records and imaging findings from patients with renal AMLs who attended our clinic and received SAE
A case of multiple hepatic angiomyolipomas with high (18) F-fluorodeoxyglucose uptake.
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BACKGROUND
Hepatic angiomyolipoma is a rare benign mesenchymal tumor. We report an unusual case of a patient with multiple hepatic angiomyolipomas exhibiting high (18) F-fluorodeoxyglucose (FDG) uptake.
METHODS
A 29-year-old man with a medical history of tuberous sclerosis was admitted to our
Renal artery embolization: clinical indications and experience from over 100 cases.
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OBJECTIVE
To review current indications and techniques for renal artery embolization (RAE) and more specifically to review cases of RAE before nephrectomy for treating patients with a large renal mass.
METHODS
All RAEs done at our institution between May 1993 and December 2005 were reviewed.
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