Publication:
Clinical course of angiomyolipom in our cases

dc.contributor.buuauthorVURUŞKAN, HAKAN
dc.contributor.buuauthorÇalışkan, Zülküf
dc.contributor.buuauthorVuruşkan, Hakan
dc.contributor.buuauthorKordan, Yakup
dc.contributor.buuauthorSökmen, Ali
dc.contributor.buuauthorYavaşcaoğlu, İsmet
dc.contributor.buuauthorYAVAŞCAOĞLU, İSMET
dc.contributor.buuauthorOktay, Bülent
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Üroloji Anabilim Dalı.
dc.contributor.orcid0000-0002-9947-848X
dc.date.accessioned2024-10-22T12:17:13Z
dc.date.available2024-10-22T12:17:13Z
dc.date.issued2006-03-01
dc.description.abstractIntroduction: The aim of the study is to determine the factors that affect the clinical course of angiomyolipomas (AML)Materials and Methods: Between January 1992 and November 2003, 24 patients were diagnosed clinically and radiologically to have angiomyolipoma. They were followed prospectively for a mean of 4.6 years (range: 2-11 years). Patients were divided into 3 groups; Group 1: Patients with a solitary lesion, Group2: Patients with multiple lesions associated with tuberous sclerosis and Group 3: Patients with multiple lesions having no tuberous sclerosis. According to the size of the lesion (lesions <4 cm and lesions >4cm) patients were also subdivided into 2 groups. The lesions were followed regularly every 6 month with ultrasonography. These 3 groups were compared in terms of symptoms, size and the percentage of the growth of the lesion.Results: The median age of the patients was 43 (31-59). 13 patients in group 1, 1 patient in group 2 and 4 patients in group 3 had lesions <4 cm and 1 patient in group 1, 2 patients in group 2 and 3 patients in group 3 had lesions >4 cm. In 3 patients from group 2 and 2 patients from group 3 the lesions were bilateral. 7 cases out of 24 (29.1%) were diagnosed incidentally. Patients were found to have 8 different symptoms which were observed 37 times among all patients. The most common symptom, abdominal and flank pain, was observed in 54.1 % (13 patients) of patients. In patients with lesions <4 cm the prevalence of these symptoms were 16.2% (6), 2.7% (1), 5.4% (2) and in patients with lesions >4 cm were 8.1% (3), 37.8% ( 14), 29.7% (11) in group1, 2 and 3 respectively. Considering the growth of the lesions; in group 1with lesions <4 cm only 1 patient out of 13 showed 0.6 cm (18.1%) growth during follow-up. Similarly 1 patient of group1 with lesion >4 cm showed no increase in size of the lesion. In group 2 all patients showed an increase in size of the lesions, which was 1 cm (33.3%) in the group with the lesion <4 cm (1 patient) and 4.6 +/- 3.4 cm (41.8%) in the group with the lesion >4 cm (2 patients). Among group 3 patients with the lesions <4 cm, 3 of 4 showed a mean increase in the diameter of previous lesion of 0.9 +/- 4.2 cm (28.1%), while in 1 patient the lesion remained unchanged. Similarly in group 3 patients with the lesions >4 cm, 2 out of 3 showed a mean increase of 1.8 +/- 5.3 cm (33.3%), while 1 remained unchanged.Conclusion: In AML patients the most important factors which determine the lesion to grow and be symptomatic are the size, the number (multiplicity) of the lesions and the presence of tuberous sclerosis.
dc.identifier.endpage47
dc.identifier.issn2149-3235
dc.identifier.issue1
dc.identifier.startpage43
dc.identifier.urihttps://hdl.handle.net/11452/46853
dc.identifier.volume32
dc.identifier.wos000420432200007
dc.indexed.wosWOS.ESCI
dc.language.isoen
dc.publisherAves
dc.relation.journalTurkish Journal Of Urology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAngiomyolipoma
dc.subjectSymptom
dc.subjectSize of the lesion
dc.subjectTuberous sclerosis
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectUrology & nephrology
dc.titleClinical course of angiomyolipom in our cases
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublication2ca52f73-e8e4-425c-b8d2-b17047ba50a1
relation.isAuthorOfPublication457d116a-1243-4450-804b-3e670de18420
relation.isAuthorOfPublication.latestForDiscovery457d116a-1243-4450-804b-3e670de18420

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