Prognoses of Multicystic Dysplastic Kidney Patients: A Single Center Experience

İsa Yılmaz; Harun Peru

Makale detayları

Prognoses of Multicystic Dysplastic Kidney Patients: A Single Center Experience

Yazarlar:

İsa Yılmaz | Harun Peru

Yayıncı:

Bolu Abant Izzet Baysal University

Ana Başlıklar:

Clinical Sciences

Dergi:

Abant Medical Journal Vol.13 Issue 1, pp.1-6

Belge Tipi:

Makale

Yayın Tarihi:

4/2024

Belge Dili:

İngilizce

Document ID (Org No.):

2001314373

pISSN:

1305-4392

Anahtar kelimeler:

Özet:

 Objective: In this study, it was aimed to evaluate the demographic characteristics and follow-up results of patients with multicystic dysplastic kidney MCDK in our pediatric nephrology clinic, based on the existing medical literature. Materials and Methods: A retrospective analysis was conducted on the medical records of patients who presented to the Pediatric Nephrology Clinic at Selçuk University Faculty of Medicine between January 2011 and January 2022. The data of 21 patients diagnosed with MCDK were recorded and analyzed. Results: Out of the total patients, 12 57 had left-sided MCDK, while 10 43 had right-sided MCDK. Three patients experienced urinary tract infections UTIs. Among the patients with right-sided MCDK, one had a concurrent right ureterocele, and five showed hydronephrosis in the contralateral kidney. No urinary anomalies except MCDK were observed in the remaining patients. None of the patients exhibited proteinuria nor hypertension. Vesicoureteral reflux VUR was not detected in the five patients who underwent voiding cystourethrography. In the follow-up of the patients, MCDK was involuted in a mean of 16.230,07 1-107 months. Conclusion: Multicystic dysplastic kidney in children has a good prognosis with conservative management. Periodic follow-up is important to prevent the potential development of hypertension or hyperfiltration injury.

 Objective: In this study, it was aimed to evaluate the demographic characteristics and follow-up results of patients with multicystic dysplastic kidney MCDK in our pediatric nephrology clinic, based on the existing medical literature. Materials and Methods: A retrospective analysis was conducted on the medical records of patients who presented to the Pediatric Nephrology Clinic at Selçuk University Faculty of Medicine between January 2011 and January 2022. The data of 21 patients diagnosed with MCDK were recorded and analyzed. Results: Out of the total patients, 12 57 had left-sided MCDK, while 10 43 had right-sided MCDK. Three patients experienced urinary tract infections UTIs. Among the patients with right-sided MCDK, one had a concurrent right ureterocele, and five showed hydronephrosis in the contralateral kidney. No urinary anomalies except MCDK were observed in the remaining patients. None of the patients exhibited proteinuria nor hypertension. Vesicoureteral reflux VUR was not detected in the five patients who underwent voiding cystourethrography. In the follow-up of the patients, MCDK was involuted in a mean of 16.230,07 1-107 months. Conclusion: Multicystic dysplastic kidney in children has a good prognosis with conservative management. Periodic follow-up is important to prevent the potential development of hypertension or hyperfiltration injury.

 Objective: In this study, it was aimed to evaluate the demographic characteristics and follow-up results of patients with multicystic dysplastic kidney MCDK in our pediatric nephrology clinic, based on the existing medical literature. Materials and Methods: A retrospective analysis was conducted on the medical records of patients who presented to the Pediatric Nephrology Clinic at Selçuk University Faculty of Medicine between January 2011 and January 2022. The data of 21 patients diagnosed with MCDK were recorded and analyzed. Results: Out of the total patients, 12 57 had left-sided MCDK, while 10 43 had right-sided MCDK. Three patients experienced urinary tract infections UTIs. Among the patients with right-sided MCDK, one had a concurrent right ureterocele, and five showed hydronephrosis in the contralateral kidney. No urinary anomalies except MCDK were observed in the remaining patients. None of the patients exhibited proteinuria nor hypertension. Vesicoureteral reflux VUR was not detected in the five patients who underwent voiding cystourethrography. In the follow-up of the patients, MCDK was involuted in a mean of 16.230,07 1-107 months. Conclusion: Multicystic dysplastic kidney in children has a good prognosis with conservative management. Periodic follow-up is important to prevent the potential development of hypertension or hyperfiltration injury.

 Amaç: Bu çalışmada çocuk nefroloji kliniğimizde multikistik displastik böbrek MKDB saptanan hastaların demografik özellikleri ve takip sonuçlarının literatür bilgileri eşliğinde değerlendirilmesi amaçlandı. Gereç ve Yöntemler: Ocak 2011- Ocak 2022 yılları arasında Selçuk Üniversitesi Tıp Fakültesi Çocuk Nefrolojisi kliniğine başvuran hastaların dosyaları retrospektif olarak incelendi. Multikistik displastik böbrek MKDB tanısı alan 21 hastanın bilgileri kaydedildi ve analiz edildi. Bulgular: Hastaların 12sinde 57 sol taraflı, 9unda 43 sağ taraflı MKDB mevcuttu. Üriner sistem enfeksiyonu ÜSE üç hastada görüldü. Sağ taraflı MKDBsi olan hastaların 1inde sağ üreterosel, 5inde karşı böbrekte hidronefroz mevcuttu. Diğer hastalarda MKDB dışında üriner anomali izlenmedi. Hastalarda proteinüri ve hipertansiyon tespit edilmedi. İşeme sistoüretrografi çekilen 5 hastada da vezikoüreteral reflü VUR tespit edilmedi. Hastaların izleminde MKDB ortalama 16,230,07 1-107 ayda involüsyona uğradı. Sonuç: Çocuklarda MKDB konservatif yönetim ile iyi prognoza sahiptir. Hipertansiyon veya hiperfiltrasyon hasarının potansiyel gelişimini önlemek için periyodik takip yapılması önemlidir.

Makale detayları

Prognoses of Multicystic Dysplastic Kidney Patients: A Single Center Experience

Yazarlar:

İsa Yılmaz | Harun Peru

Yayıncı:

Bolu Abant Izzet Baysal University

Ana Başlıklar:

Clinical Sciences

Dergi:

Abant Medical Journal Vol.13 Issue 1, pp.1-6

Belge Tipi:

Makale

Yayın Tarihi:

4/2024

Belge Dili:

İngilizce

Document ID (Org No.):

2001314373

pISSN:

1305-4392

Multicystic dysplastic kidney

Survival

ChildhoodMultikistik displastik böbrek

Sağkalım

Çocukluk çağı

Sayı

Makale detayları

Prognoses of Multicystic Dysplastic Kidney Patients: A Single Center Experience

Yazarlar: İsa Yılmaz | Harun Peru

Yayıncı: Bolu Abant Izzet Baysal University

Ana Başlıklar: Clinical Sciences

Dergi: Abant Medical Journal Vol.13 Issue 1, pp.1-6

Belge Tipi: Makale

Yayın Tarihi: 4/2024

Belge Dili: İngilizce

Document ID (Org No.): 2001314373

pISSN: 1305-4392

Multicystic dysplastic kidney

Survival

ChildhoodMultikistik displastik böbrek

Sağkalım

Çocukluk çağı

Sayı

Yazarlar:

İsa Yılmaz | Harun Peru

Yayıncı:

Bolu Abant Izzet Baysal University

Ana Başlıklar:

Clinical Sciences

Dergi:

Abant Medical Journal Vol.13 Issue 1, pp.1-6

Belge Tipi:

Makale

Yayın Tarihi:

4/2024

Belge Dili:

İngilizce

Document ID (Org No.):

2001314373

pISSN:

1305-4392