Renal hypoplastic dysplasia

Renal dysplasia is a disorganized development of the kidney because anomalous differentiation of the metanephrosis. Abnormalities of the collecting system are common. They include obstruction of the ureteropelvic junction, ureteral atresia and urethral obstruction. The case was a six months old female child with ultrasonografically detected right hydronephrosis and oligohydroamniosis at the 20 th week of gestation. She underwent an operation for bilateral hydroureteronephrosis at 1 month of age. There was no serious and related illness in family history and self-history. She underwent right nephrectomy at 6 months of age. The specimen included an atrophic nephrectomy material with lobulations and a dilated ureter. When sectioned, it was observed that the pericaliceal areas were dilated and the cortex-medulla border was obscured. On microscopic examination, the cortex was thin, contained rare small glomerules, primitive ducts and mononuclear cell infiltration were seen. A focus of cartilage was observed at the cortex-medulla junction. The case was diagnosed as renal hypoplastic dysplasia. During 4 months of follow-up, no complication was reported. This case is presented considering the uncommon occurence of renal dysplasia and its differential diagnosis from other congenital cystic renal malformations.

Dergi Adı Ondokuz Mayis Universitesi Tip Dergisi
Dergi Cilt Bilgisi 25
Dergi Sayısı 1
Sayfalar 25 - 29
Yayın Yılı 2008
Eser Adı
[dc.title]
Renal hypoplastic dysplasia
Yazar
[dc.contributor.author]
Numanoğlu-Yurdakan, Gamze
Yazar
[dc.contributor.author]
Kertiş, Gürkan
Yazar
[dc.contributor.author]
Bahadır, Burak
Yazar
[dc.contributor.author]
Numanoğlu, Kemal Varın
Yazar
[dc.contributor.author]
Özdamar, Şükü Oğuz
Yayın Yılı
[dc.date.issued]
2008
Yayın Türü
[dc.type]
article
Özet
[dc.description.abstract]
Renal dysplasia is a disorganized development of the kidney because anomalous differentiation of the metanephrosis. Abnormalities of the collecting system are common. They include obstruction of the ureteropelvic junction, ureteral atresia and urethral obstruction. The case was a six months old female child with ultrasonografically detected right hydronephrosis and oligohydroamniosis at the 20 th week of gestation. She underwent an operation for bilateral hydroureteronephrosis at 1 month of age. There was no serious and related illness in family history and self-history. She underwent right nephrectomy at 6 months of age. The specimen included an atrophic nephrectomy material with lobulations and a dilated ureter. When sectioned, it was observed that the pericaliceal areas were dilated and the cortex-medulla border was obscured. On microscopic examination, the cortex was thin, contained rare small glomerules, primitive ducts and mononuclear cell infiltration were seen. A focus of cartilage was observed at the cortex-medulla junction. The case was diagnosed as renal hypoplastic dysplasia. During 4 months of follow-up, no complication was reported. This case is presented considering the uncommon occurence of renal dysplasia and its differential diagnosis from other congenital cystic renal malformations.
Kayıt Giriş Tarihi
[dc.date.accessioned]
2019-12-23
Açık Erişim Tarihi
[dc.date.available]
2019-12-23
Yayın Dili
[dc.language.iso]
eng
Konu Başlıkları
[dc.subject]
Cystic renal malformation
Konu Başlıkları
[dc.subject]
Renal dysplasia
Konu Başlıkları
[dc.subject]
Urethral obstruction
Künye
[dc.identifier.citation]
Numanoǧlu Yurdakan, G., Kertiş, G., Bahadir, B., Numanoǧlu, K. V. ve Özdamar, Ş. O. (2008). Renal hypoplastic dysplasia. Ondokuz Mayis Universitesi Tip Dergisi, 25(1), 25–29. doi:10.5835/jecm.v25i1.1045
Haklar
[dc.rights]
info:eu-repo/semantics/closedAccess
ISSN
[dc.identifier.issn]
1300-2996
İlk Sayfa Sayısı
[dc.identifier.startpage]
25
Son Sayfa Sayısı
[dc.identifier.endpage]
29
Dergi Adı
[dc.relation.journal]
Ondokuz Mayis Universitesi Tip Dergisi
Dergi Sayısı
[dc.identifier.issue]
1
Dergi Cilt Bilgisi
[dc.identifier.volume]
25
Tek Biçim Adres
[dc.identifier.uri]
https://hdl.handle.net/20.500.12628/7388
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29
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08 Nisan 2024 07:40
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dysplasia months dilated obstruction underwent junction cortex-medulla observed nephrectomy pericaliceal microscopic cortex primitive glomerules border contained obscured examination mononuclear malformations cystic congenital diagnosis differential occurence uncommon considering presented reported complication follow-up During hypoplastic diagnosed sectioned
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