Renal Hamartoma (Angiomyolipoma): Report of Three Oases

Rusche, Carl

doi:10.1016/s0022-5347(17)68425-8

Cited by 51 publications

(6 citation statements)

References 3 publications

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“…Four cases, who consequently underwent nephrectomy, had renal benign tumors, that is, hamartoma. 4,5,8,9 Five cases were complicated by structural and/or infectious diseases of the urinary tract; that is, pyelonephritis, abscess, or vesicoureteral reflux. 6,7,[9][10][11][12] The other six cases had no other underlying condition.…”

Section: Discussionmentioning

confidence: 99%

Spontaneous Rupture of the Renal Pelvis During Pregnancy: A Case Report and Review of the Literature

Shoji¹,

Okuma²,

Fujita³

et al. 2002

Am J Perinatol

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We report a case with spontaneous rupture of the renal pelvis during pregnancy. A 34-year-old Japanese woman was referred at 20 weeks' gestation because of sudden severe right flank pain. She had severe colic pain radiating to the right lower abdomen with percussion tenderness at the right costovertebral angle and was initially suspected to have renal/ureteral calculi. Ultrasonography and intravenous pyelography showed urine extravasating from the renal pelvis, indicating rupture of the right renal pelvis. Immediately following the insertion of a double-J indwelling catheter, her symptoms and perirenal extravasation ceased. She had no further urological problems during pregnancy and a male infant was delivered at 41 weeks' gestation. Cases with spontaneous rupture of the renal pelvis in pregnancy are reviewed.

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Section: Discussionmentioning

confidence: 99%

Spontaneous Rupture of the Renal Pelvis During Pregnancy: A Case Report and Review of the Literature

Shoji¹,

Okuma²,

Fujita³

et al. 2002

Am J Perinatol

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“…22,23 Rusche et al 24 were the first to describe a surgical series in which haemorrhage was a complication of renal AML; however, since that time a number of surgical and angiographic series describing the haemorrhagic complication of AML have been reported and were reviewed by Nelson et al 25 Oesterling et al 26 were the first to describe that the risk of future haemorrhage was related to the size of the AML and proposed a 4 cm threshold for intervention; the conclusion that the risk of future haemorrhage is related to AML size has been validated in numerous other studies. 25 Risk of haemorrhage in AML is also related to the presence and size of intra-tumoural aneurysms; the latter having the strongest association with future risk of rupture ( Fig 6).…”

Section: Intra-tumoural Aneurysms and Size Are Risk Factors For Rupturementioning

confidence: 99%

Ten uncommon and unusual variants of renal angiomyolipoma (AML): radiologic–pathologic correlation

et al. 2015

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“…14 We were interested in determining how many of our patients with the renal tumor had various other findings of the tuberous sclerosis complex. In only three patients in our series (a11 children with severe disease of the rentral nervous system) was the condition suspected (Table 4).…”

Section: Keiationship To Tuberous Sclerosismentioning

confidence: 99%

Renal angiomyolipoma. A clinicopathologic study of 32 cases

Farrow

Harrison

Utz

et al. 1968

Cancer

155

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T h e data from 32 cases of angiomyolipoma (renal hamartoma) are presented: 23 of the tumors were removed a t surgery and nine a t autopsy. T h e histopathologic findings are reviewed and the spectrum of gross renal involvement is emphasized. O n the basis of the duration of symptoms and findings a n d the subsequent course of patients subjected to surgical resection, the clinical behavior of the tumor is assessed. Of particular interest is the relationship of this tumor to the tuberous sclerosis complex. Data presented indicate that many of the patients have various components of the syndrome, which in some patients have familial manifestations. I t is inferred from this study that the tuberous sclerosis complex may vary in expression from a solitary renal tumor to the fully developed clinical syndrome. HE ANGIOMYOLIPOMA OR RENAL HAMAR-T toma is a n uncommon tumor: only about 150 cases appear in the literature.16 Although the pathologic features have been well described,8.9, 1 3~1 5 the neoplastic features and biologic behavior should be re-evaluated and the clinicopathologic aspects, particularly the relationship to tuberous sclerosis, brought into sharper focus.This report is based on the study of 32 cases of renal angiomyolipoma seen at the Mayo Clinic during a 50-year period; 23 of the tumors were seen at surgical exploration and nine at autopsy. Four of these cases have been previously reported.10, 15 The gross specimen was available and examined in all but three cases. T h e original histopathologic slides and the new slides made from samplings of tissue from several areas of each tumor were examined. Clinical and follow-up information was obtained from the records and from questionnaires sent to the patient or the family. PATHOLOGIC FEATURESThese turn or s were char act e r i s t i c a 11 y located within the parenchyma of the kidney. From the Mayo Clinic and Mayo Foundation: Section of Surgical Pathology (Drs. Farrow and Harrison),

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Renal Hamartoma (Angiomyolipoma): Report of Three Oases

Cited by 51 publications

References 3 publications

Spontaneous Rupture of the Renal Pelvis During Pregnancy: A Case Report and Review of the Literature

Spontaneous Rupture of the Renal Pelvis During Pregnancy: A Case Report and Review of the Literature

Ten uncommon and unusual variants of renal angiomyolipoma (AML): radiologic–pathologic correlation

Renal angiomyolipoma. A clinicopathologic study of 32 cases

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