Autosomal Dominant Polycystic Kidney Disease Patients Requiring Nephrectomy: Characteristics and Surgical Considerations

被引:0
作者
Chan, Joel Ern Zher [1 ,2 ]
Olakkengil, Kate S. [1 ,2 ]
Bhattacharjya, Shantanu [1 ,2 ]
Olakkengil, Santosh Antony [1 ,2 ]
机构
[1] Univ Adelaide, Adelaide Med Sch, Adelaide, SA, Australia
[2] Cent & Northern Adelaide Renal & Transplantat Serv, Adelaide, SA, Australia
关键词
autosomal dominant polycystic kidney disease; clinical characteristics; nephrectomy; renal cell carcinoma; RENAL-CELL CARCINOMA; DIAGNOSIS; PREVALENCE; TRANSPLANT;
D O I
10.1111/ans.70192
中图分类号
R61 [外科手术学];
学科分类号
摘要
BackgroundNephrectomies are major surgeries often required in ADPKD for symptom control, removal of septic/malignant foci, and to create space for renal transplantation. Whether ADPKD patients should proceed with nephrectomy/ies should be guided by patient characteristics, technical considerations and anticipated risks and benefits.MethodsA retrospective review of prospectively collected data for all patients who underwent nephrectomy/ies between 1 January 1995 and 31 December 2021, comparing ADPKD patients to patients with alternative primary nephrological conditions. Patient characteristics, technical aspects, and outcomes informing the risks and benefits of nephrectomies were examined. Statistical analyses included descriptive statistics, chi 2/Fisher's exact test and independent samples Mann-Whitney U test, as appropriate.ResultsAt the time of first nephrectomy, ADPKD patients were older and more likely to have end-stage renal failure, hypertension, gastro-oesophageal reflux disease, and hernia compared to non-ADPKD patients. They were more likely to require bilateral nephrectomies, open nephrectomies, and, where transplanted, receive donation after circulatory death. They were at higher risk of post-operative hypotension, anaemia, and more likely to require blood transfusions. Otherwise, nephrectomies achieved their indications in our ADPKD cohort with no apparent increase in adverse events. Renal cell carcinoma appears to be of higher incidence in our cohort, with a high proportion of multifocality and bilaterality, advanced staging at diagnosis and incidental diagnoses on histopathology.ConclusionOverall, in our ADPKD patients who received nephrectomy/ies, the procedure appeared to be safe and effective, with benefits outweighing risks. RCC exclusion is a prudent consideration especially for ADPKD patients on dialysis awaiting transplantation.
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页数:12
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共 35 条
[1]   Incidental occurrence of papillary renal cell carcinoma in the native kidney with autosomal dominant polycystic kidney disease after renal transplantation: A case report [J].
Abbas, Mahmoud ;
Paetzel, Melanie ;
Thurn, Angelika ;
Brinkmann, Olaf ;
Bettendorf, Olaf .
MOLECULAR AND CLINICAL ONCOLOGY, 2021, 15 (05)
[2]   Simultaneous bilateral laparoscopic nephrectomy with kidney transplantation in patients with ESRD due to ADPKD: A single-center experience [J].
Abrol, Nitin ;
Bentall, Andrew ;
Torres, Vicente E. ;
Prieto, Mikel .
AMERICAN JOURNAL OF TRANSPLANTATION, 2021, 21 (04) :1513-1524
[3]   Papillary (chromophil) renal cell carcinoma: Histomorphologic characteristics and evaluation of conventional pathologic prognostic parameters in 62 cases [J].
Amin, MB ;
Corless, CL ;
Renshaw, AA ;
Tickoo, SK ;
Kubus, J ;
Schultz, DS .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1997, 21 (06) :621-635
[4]   Outcome of Kidney Transplant in Patients with Polycystic Kidney Disease: A Single-Center Study in Tunisia [J].
Barbouch, Samia ;
Hajji, Meriam ;
Hedri, Hafedh ;
El Younsi, Fethi ;
Ben Hamida, Fathi ;
Bacha, Mohammed Mongi ;
Ounissi, Mondher ;
Abderrahim, Ezzedine ;
Ben Abdallah, Taieb .
EXPERIMENTAL AND CLINICAL TRANSPLANTATION, 2017, 15 :196-199
[5]   Allograft Vesicoureteral Reflux after Kidney Transplantation [J].
Brescacin, Alessandra ;
Iesari, Samuele ;
Guzzo, Sonia ;
Alfieri, Carlo Maria ;
Darisi, Ruggero ;
Perego, Marta ;
Puliatti, Carmelo ;
Ferraresso, Mariano ;
Favi, Evaldo .
MEDICINA-LITHUANIA, 2022, 58 (01)
[6]   Index cases of intracranial aneurysms in autosomal dominant polycystic kidney disease: longitudinal experience from a single renal transplantation centre [J].
Chan, Joel Ern Zher ;
Olakkengil, Kate S. ;
Bhattacharjya, Shantanu ;
Olakkengil, Santosh Antony .
ANZ JOURNAL OF SURGERY, 2025,
[7]   High prevalence of thromboembolic events in autosomal dominant polycystic kidney disease: a longitudinal study [J].
Chan, Joel Ern Zher ;
Bhattacharjya, Shantanu ;
Olakkengil, Santosh Antony .
JOURNAL OF NEPHROLOGY, 2024, 37 (08) :2399-2402
[8]   Recurrent thromboses and major vessel compressions in autosomal dominant polycystic kidney disease [J].
Chan, Joel Ern Zher ;
Kuah, Zhihong ;
Bhattacharjya, Shantanu ;
Olakkengil, Santosh Antony .
JOURNAL OF SURGICAL CASE REPORTS, 2022, 2022 (02)
[9]  
Chang Yu-Lung, 2007, J Chin Med Assoc, V70, P403, DOI 10.1016/S1726-4901(08)70029-7
[10]   Autosomal Dominant Polycystic Kidney Disease: Core Curriculum 2016 [J].
Chebib, Fouad T. ;
Torres, Vicente E. .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2016, 67 (05) :792-810