Clinical value of pathologic examination of non-neoplastic kidney in patients with upper urinary tract malignancies.

BACKGROUND/AIMS: While surgical resection remains the standard of care in the treatment of upper urinary tract malignancies, nephrectomy is a risk factor for the development of chronic kidney disease (CKD). The aim of this study was to determine whether histologic evaluation of non-neoplastic kidney could enable early identification of unrecognized kidney disease and could be of prognostic value in predicting postoperative renal outcomes.
METHODS: We retrospectively analyzed 51 patients with upper urinary tract malignancies who received uninephrectomy or uninephroureterectomy. A thorough pathologic evaluation of non-neoplastic kidney including special stains, immunofluorescence, and electron microscopic studies was performed. The degree of parenchymal changes was graded from 0 to 15.
RESULTS: Of 51 patients, only 13 showed normal kidney pathology. Fifteen patients showed glomerular abnormalities, 14 showed diabetic nephropathy, and 11 showed vascular nephropathy. There was one case each of reflux nephropathy and chronic pyelonephritis. The median histologic score was 5 points. Only 25.4% of patients had ≤ 3 points. Score more than 5 was observed in 47.1% of patients. Postoperative estimated glomerular filtration rate (eGFR) at 3 to 36 months were obtained from 90.2% of patients, and of those, 34.8% had de novo CKD. Since no one had CKD in partial nephrectomized patients, we determined risk factors for CKD in radical nephrectomized patients. Cox regression analysis revealed that postoperative AKI, preoperative eGFR, and histologic score of non-neoplastic kidney were the independent predictors for CKD.
CONCLUSIONS: We conclude that routine pathologic evaluation of non-neoplastic kidney provides valuable diagnostic and prognostic information.

INTRODUCTION

The incidence of kidney cancer has been dramatically increasing worldwide during the past decade. Renal cell carcinoma (RCC) accounts for 90% of kidney cancer and approximately 3% of all adult malignancies in the United States [1]. The Korea Central Cancer Registry reported that 3,989 patients were newly registered for RCC in 2011, accounting for 1.8% of all adult malignancies [2]. Due to recent advances in diagnostic imaging techniques, early detection of localized RCC has been increased and now comprises more than half of newly diagnosed RCCs [3]. Since oncologic outcomes are excellent for early stage tumors when treated with a nephrectomy, there has been an emerging interest in postoperative renal outcomes [4]. The risks of new onset chronic kidney disease (CKD) or accelerated CKD after radical nephrectomy have been shown to be as high as 65% [5]. In this regards, nephron-sparing surgeries have been proposed as the standard of care for small renal cortical tumors [6,7].

CKD is a public health problem and its prevalence is steadily rising [8]. CKD is associated with increased cardiovascular complications, lower survival, and a reduced quality of life [9,10]. The Third National Health and Nutrition Examination Survey reported the prevalence of CKD in the United States adult population to be 11% (19.2 million) [11]. It is well known that the cost of health services for patients with CKD is much higher than that for patients without CKD [12]. Therefore, early recognition of the patients at risk for CKD and prompt institution of treatment may be of considerable importance.

Given the fact that RCC and CKD share the risk factors such as hypertension (HTN), diabetes mellitus (DM), smoking, and advanced age [13], postoperative decline in renal functions might be more pronounced if unidentified intrinsic renal abnormalities were present at the time of nephrectomy. Furthermore, a solitary kidney is considered as a contraindication to percutaneous biopsy and the safety of this procedure in patients with partial nephrectomy has not been demonstrated [14]. Therefore, with thorough examination of non-neoplastic renal parenchyma, one can recognize the patients at risk for CKD and predict their clinical courses.

The aim of this study was to determine whether histologic evaluation of non-neoplastic kidney could enable early identification of unrecognized kidney disease and could be of prognostic value in predicting postoperative renal outcomes.

METHODS

Participants and measurements

We studied a cohort of 49 patients with RCC and seven patients with urothelial cancer received uninephrectomy or uninephroureterectomy between January 2010 and January 2014 at Soon Chun Hyang University Hospital, Seoul, Korea. All nephrectomized patients due to upper urinary tract malignancies were included, with the exception of patients with end stage renal disease (ESRD, n = 4) and those with a transplanted kidney with RCC in the native kidney (n = 1). The study protocol was approved by the Institutional Review Board of the Soon Chun Hyang University Hospital.

Covariates and definitions

Baseline variables including demographic features (age and sex), medical history (DM, HTN, cardiovascular disease [CVD], and previous malignancies), smoking status, body mass index (BMI), and laboratory data (serum creatinine [sCr], proteinuria, hematuria, hepatitis B surface antigen, and hepatitis C antibody) were examined. Smoking status and medical history were extracted from electronic medical record database. History of DM and HTN was defined by clinical diagnosis. CVD was defined as the clinical diagnosis of heart failure, acute or chronic ischemic heart disease, and cerebrovascular disease. BMI was calculated by the baseline enrolled measurement using the formula weight in kilograms divided by the square of their height in meters. The definitions of CKD and acute kidney injury (AKI) were based on the Kidney Disease Improving Global Outcomes guidelines. CKD was defined as abnormalities of kidney function (estimated glomerular filtration rate [eGFR] < 60 mL/min/1.73 m2) over 3 months, and AKI was defined as an increase in sCr by 50% within 7 days, or an increase in sCr by 0.3 mg/dL within 2 days. The eGFR was calculated using the Chronic Kidney Disease Epidemiology Collaboration creatinine equation [15], as follows: 141 × min (sCr/κ,1)α × max (sCr/κ,1)–1.209 × 0.993Age [× 1.018 if female] [× 1.159 if black], where sCr is in mg/dL, κ is 0.7 for females and 0.9 for males, α is –0.329 for females and –0.411 for males, min is the minimum of sCr/κ or 1, and max is the maximum of sCr/κ or 1. Proteinuria or hematuria was defined as detection by dipstick.

Pathologic review

The routine pathologic evaluation of non-neoplastic tissues was performed. After nephrectomy, fractions of tumor and non-neoplastic cortical tissue samples from surgical specimens were collected. Representative non-neoplastic sections were examined at a significant distance from the tumor (at a minimum 2 cm away). Under light microscopy, slides were reviewed following staining with hematoxylin and eosin, as well as periodic acid-Schiff, Masson’s trichrome, and Jones methenamine silver. Immunofluorescent (IF) microscopy was performed on frozen tissue sections. Immunoglobulin G (IgG), IgA, IgM, complement component C3, and C1q were stained as usual. Routine electron microscopy (EM) was performed using 1-mm3 sections excised from fresh tissue, which was fixed with 2.5% glutaraldehyde solution. Pathologic review was performed by a renal pathologist (SYJ). We diagnosed hypertensive nephrosclerosis which has globally sclerotic glomeruli and patchy atrophic tubules of dependent nephron, surrounded by marked interstitial fibrosis and chronic inflammation with moderate to severe arteriosclerosis or arteriolosclerosis. Ischemic nephropathy was defined as lesions secondary to renal artery stenosis, tubular atrophy of distinctive "endocrinization" pattern affecting proximal tubules, accompanied by mild to moderate interstitial fibrosis, resulting in crowded glomeruli showing relative dilation of Bowman's space, variable degree of collapse of capillary loops, and wrinkling of capillary wall.

A complete histologic examination included an evaluation of the presence of glomerulosclerosis, interstitial fibrosis, tubular atrophy, and vascular pathology. All samples were graded according to a semi-quantitative scoring system [16]. This semi-quantitative scoring system ranged from a minimum of 0 to a maximum of 15 points.

Statistical analysis

All statistical analyses were performed using SPSS version 18.0 (SPSS Inc., Chicago, IL, USA). Variables are presented as the medians with interquartile range or mean ± standard deviation. Fisher exact test and chi-square test were used for categorical covariates, and Student t test was used for continuous covariates. We also used logistic regression analyses to investigate independent risk factors for the occurrence of postoperative AKI. Multivariable Cox proportional hazards regression was used to determine the association of clinical characteristics and pathologic findings of non-neoplastic kidney with the development or acceleration of CKD. All p values less than 0.05 were considered to indicate statistical significance.

RESULTS

Baseline characteristics

Patient characteristics at the time of surgery are listed in Table 1. The median patient age was 63 years (53 to 73) and the median BMI was 24.3 kg/m2 (22.7 to 26.6). Twenty-six patients (51%) had HTN, 20 patients (39.2%) had DM, and nine patients (17.6%) had CVD. There were 13 patients (25.5%) with a history of malignancy. Of 51 patients, 22 (43.1%) were smokers or ex-smokers. Five patients (9.8%) had been diagnosed with hepatitis B and one patient (2%) with hepatitis C. Thirty-two patients were treated with radical nephrectomy, 12 patients with partial nephrectomy, and seven patients with nephroureterectomy. Initial urinalysis was performed in 50 patients (98%). Of those, 12 (23.5%) had proteinuria and 18 (35.3%) had hematuria. The median preoperative sCr was 0.81 mg/dL (0.71 to 1.01) and preoperative eGFR was 92.1 mL/min/1.73 m2 (72.8 to 104.8).

Table 1.

Baseline patient characteristics at the time of nephrectomy (n = 51)

Characteristic	Value
Age, yr	63 (53-73)
Male sex	38 (74-5)
Body mass index, kg/m2	24.3 (22.7-26.6)
Hypertension	26 (51)
Diabetes mellitus	20 (39.2)
Cardiovascular disease	9 (17.6)
Previous malignancy	13 (25.5)
Smoking history	22 (43.1)
Hepatitis B	5 (9.8)
Hepatitis C	1 (2)
Preoperative proteinuria	12 (23.5)
Preoperative hematuria	18 (35.3)
Preoperative creatinine, mg/dL	0.81 (0.71-1.01)
Preoperative eGFR, mL/min/1.73 m2	92.1 (72.8-104.8)

Values are presented as median (interquartile range) or number (%).

eGFR, estimated glomerular filtration rate.

Non-neoplastic pathologic findings

Pathologic reports of non-neoplastic kidney were obtained from 44 RCC patients treated with nephrectomy and seven urothelial cancer patients treated with nephroureterectomy. Of 51 patients, only 13 (25.5%) showed normal kidney pathology. Forty-two cases of pathologic diagnoses were obtained in 38 patients because four patients had dual diagnoses. Fifteen patients (29.4%) showed glomerular abnormality, 14 (27.5%) showed diabetic nephropathy (Fig. 1), and 11 showed (21.6%) vascular nephropathy. In glomerular abnormalities, there were nine cases (17.6%) of IgA nephropathy, five cases (9.8%) of C1q deposit (Fig. 2), and one case (2%) of membranous glomerulonephritis (Fig. 3). Vascular nephropathy included eight cases (15.7%) of hypertensive nephrosclerosis and three cases (5.9%) of ischemic nephropathy. There was one case each of reflux nephropathy and chronic pyelonephritis (2%) (Table 2).

Figure 1.

Nodular glomerulosclerosis and hyaline arteriolosclerosis in a case of diabetic nephropathy (periodic acid-Schiff, ×200).

Figure 2.

A case of C1q nephropathy. (A) Nearly normal appearing glomerulus with mesangial prominence (periodic acid-Schiff, ×400). (B) Positive immunofluorescence staining for C1q (×400). (C) Multiple mesangial electron dense deposits (arrows) on electron microscopy (×2,500).

Figure 3.

(A) Few subepithelial spikes (arrow) and multiple intramembranous holes in a case of membranous glomerulonephritis (methenamine silver stain, ×600). (B) Weak granular staining for immunoglobulin G along the peripheral capillary wall (immunofluorescence, ×400). (C) Multiple small subepithelial and intramembranous electron dense deposits on electron microscopy (×3,000).

Table 2.

Pathologic review of non-neoplastic kidney in patients with nephrectomy

Pathologic diagnosis	No. of cases[a]
Normal	13 (25.5)
Glomerular abnormality	15 (29.4)
Immunoglobulin A nephropathy	9 (17.6)
C1q deposit	5 (9.8)
Membranous glomerulonephritis	1 (2.0)
Diabetic nephropathy	14 (27.5)
Vascular nephropathy	11 (21.6)
Hypertensive nephrosclerosis	8 (15.7)
Ischemic nephropathy	3 (5.9)
Reflux nephropathy	1 (2,0)
Chronic pyelonephritis	1 (2,0)

Values are presented as number (%).

The total number of findings exceed 100% because four patients had dual diagnoses.

Semi-quantitative evaluation of non-neoplastic kidney is shown in Table 3. Glomerulosclerosis was present in 94.1% of all patients, predominantly of grade 1 (56.9%). Severe glomerulosclerosis (> 20%) was present in 13.7% of cases. Interstitial fibrosis was present in 51%, predominantly of grade 1 (39.2%). Fifty-one percent of patients showed tubular atrophy and grade 1 was predominant (39.2%). Of note, fibrous intimal thickening was observed in most of the cases (94.1%), predominantly of grade 2 (49%). Hyaline arteriolar thickening was present in 78.4%. Grade 1 was predominant (49%) and grade 2 was the second (21.6%), followed by grade 3 (7.8%). After scoring each of the five components, we calculated the total score. The median total score was 5 points (3 to 7). Only 25.4% of patients had ≤ 3 points. Score more than 5 points was observed in 47.1% of patients.

Table 3.

Semi-quantitative evaluation of non-neoplastic kidney

Histologic scoring	All patients, %
Glomerular global sclerosis
0: none globally sclerosed	5.9
1: 1%-10% global glomerulosclerosis	56.9
2: 11%-20% global glomerulosclerosis	23.5
3: > 20% global glomerulosclerosis	13.7
Interstitial fibrosis
0: < 5% of renal tissue replaced by fibrous connective tissue absent	49
1: 6%-25% of renal tissue replaced by fibrous connective tissue	39.2
2: 26%-50% of renal tissue replaced by fibrous connective tissue	7.8
3: > 50% of renal tissue replaced by fibrous connective tissue	3.9
Tubular atrophy
0: absent	49
1: < 25% of tubule affected	39.2
2: 26%-50% of tubule affected	7.8
3: > 50% of tubule affected	3.9
Fibrous intimal thickening
0: absence of chronic vascular changes	5.9
1: < 25% narrowing of the vascular luminal area by fibrointimal thickening	39.2
2: similar changes with narrowing of the vascular luminal area from 26% to 50%	49
3: similar changes with more than 50% narrowing of the vascular luminal area	5.9
Hyaline arteriolar thickening
0: absence	21.6
1: replacement of degenerated smooth muscle cells by hyaline deposits present in onlyone arteriole, no circumferential involvement	49
2: similar changes in more than one arteriole, but no circumferential involvement	21.6
3: similar changes with circumferential involvement, independent of the number of arterioles involved	7.8

Postoperative renal function outcome

Twenty-eight patients (54.9%) experienced postoperative AKI. Among these patients, 15 (53.6%) had HTN and 13 (46.4%) had DM. Five patients (17.9%) had a history of CVD. There was no correlation between the occurrence of postoperative AKI and clinical variables except older age (p = 0.026), male gender (p = 0.043), and radical nephrectomy (p = 0.002) compared to partial nephrectomy (Table 4). Logistic regression analysis was conducted with variables of age, gender, HTN, DM, smoking, surgical method, preoperative proteinuria, preoperative eGFR, presence of pathologic diagnosis of non-neoplastic tissue, and semi-quantitative histologic score (Table 5). It revealed that older age (p = 0.029) and radical nephrectomy (p = 0.012) were the independent risk factors for postoperative AKI. Data on eGFR at 3 to 36 months after surgery were obtained from 46 patients (90.2%); 16 patients (34.8%) had newly developed CKD stage 3 to 5 (eGFR < 60 mL/min/1.73 m2) after surgery. Four patients initially had CKD stage 3 at the time of nephrectomy. In three of four patients with pre-existing CKD, renal function was deteriorated by 27.5, 21.7, and 6.4 mL/min/1.73 m2 reduction of eGFR. Among the 19 patients who had de novo or accelerated CKD, 14 (73.7%) experienced postoperative AKI. The prevalence of CKD was significantly higher in patients with postoperative AKI than those without AKI (58.3% vs. 22.7%, p = 0.019), in patients with preoperative proteinuria than those without proteinuria (75% vs. 30.3%, p = 0.015), in patients who underwent radical nephrectomy versus partial nephrectomy (54.3% vs. 0%, p = 0.001), in patients with abnormal pathologic diagnosis than those without diagnosis (51.5% vs. 15.4%, p = 0.044), and in patients who have lower preoperative eGFR (p = 0.002) and higher semi-quantitative histologic score (p = 0.002). Clinical characteristics between the patients with or without CKD are compared in Table 6. Since no one has developed CKD in partial nephrectomized patients, we determined independent risk factors for CKD in radical nephrectomized patients. Cox regression analysis with variables of age, HTN, DM, smoking status, preoperative proteinuria, postoperative AKI, preoperative eGFR, presence of pathologic diagnosis of non-neoplastic kidney, and semi-quantitative histologic score was done. In this study, preoperative eGFR (hazard ratio [HR], 0.95; 95% confidence interval [CI], 0.92 to 0.98; p = 0.004), postoperative AKI (HR, 7.03; 95% CI, 2.01 to 24.61; p = 0.002), and semi-quantitative histologic score (HR, 1.23; 95% CI, 1.00 to 1.50; p = 0.047) were the independent predictors for CKD in radial nephrectomized patients. Characteristics of 19 patients who had de novo or accelerated CKD are shown in Table 7.

Table 4.

Univariate analysis for clinical variables affecting acute kidney injury

Variable	Acute kidney injury		p value
	Yes (n = 28)	No (n = 23)
Age, yr	65.7 ± 11.1	58.8 ± 10.1	0.026
Male sex	24 (85.7)	14 (60.9)	0.043
Body mass index, kg/m2	24.6 ± 3.1	24.4 ± 3.5	0.836
Hypertension	15 (53.6)	11.7 (47.8)	0.683
Diabetes mellitus	13 (46.4)	7 (30.4)	0.244
Cardiovascular disease	5 (17.9)	4 (17.4)	> 0.999
Smoking	12 (42.9)	10 (43.5)	0.964
Preoperative proteinuria	7 (25.0)	5 (22.7)	0.852
Radical nephrectomy	26 (92.9)	13 (56.5)	0.002
Preoperative eGFR, mL/min/1.73 m2	86.0 ± 20.0	95.9 ± 24.4	0.116
Pathologic abnormality	23 (82.1)	14 (60.9)	0.090
Histologic score	5.9 ± 3.4	5.0 ± 3.0	0.287

Values are presented as mean ± SD or number (%).

eGFR, estimated glomerular filtration rate.

Table 5.

Multivariate logistic regression analysis for clinical variables affecting acute kidney injury

Variable	OR (95% CI)	p value
Age	1.11 (1.01-1.22)	0.029
Sex, male vs. female	0.15 (0.02-1.28)	0.083
Hypertension, yes vs. no	0.27 (0.04-1.99)	0.199
Diabetes mellitus, yes vs. no	1.44 (0.22-9.36)	0.704
Smoking, yes vs. no	0.69 (0.11-4.19)	0.687
Surgical method, radical vs. partial nephrectomy	15.31 (1.84-127.23)	0.012
Preoperative proteinuria, yes vs. no	0.38 (0.04-3.89)	0.412
Preoperative eGFR	1.00 (0.96-1.04)	0.971
Pathologic abnormality, yes vs. no	1.86 (0.27-12.57)	0.527
Histologic score	1.06 (0.76-1.46)	0.735

OR, odds ratio; CI, confidence interval; eGFR, estimated glomerular filtration rate.

Table 6.

Univariate analysis for clinical variables affecting chronic kidney disease

Variable	Chronic kidney disease		p value
	Yes (n = 19[a])	No (n = 27)
Age, yr	65.2 ± 12.0	59.5 ± 10.1	0.089
Male sex	16 (84.2)	19 (70.4)	0.320
Body mass index, kg/m2	24.3 ± 3.4	24.2 ± 3.0	0.897
Hypertension	12 (63.2)	12 (44.4)	0.245
Diabetes mellitus	8 (42.1)	10 (37)	0.767
Cardiovascular disease	4 (21.1)	4 (14.8)	0.700
Smoking	10 (52.6)	12 (44.4)	0.756
Preoperative proteinuria	9 (47.4)	3 (11.5)	0.015
Radical nephrectomy	19 (100.0)	16 (59.3)	0.001
Postoperative AKI	14 (73.7)	10 (37)	0.019
Preoperative eGFR, mL/min/1.73 m2	78.2 ± 19.8	99.3 ± 21.6	0.002
Pathologic abnormality	17 (89.5)	16 (59.3)	0.044
Histologic score	7.1 ± 3.6	4.0 ± 2.0	0.002

Values are presented as mean ± SD or number (%).

AKI, acute kidney injury; eGFR, estimated glomerular filtration rate.

Including 16 patients with de novo chronic kidney disease (CKD) and three patients with accelerated CKD.

Table 7.

Characteristics of patients who had de novo or accelerated chronic kidney disease

No.	Sex/Age, yr	DM/HTN	BMI, kg/m2	Baseline Cr (mg/dL)/eGFR (mL/min/1.73 m2)	Final Cr (mg/dL)/eGFR (mL/min/1.73 m2)	Time to development of eGFR < 60 mL/min/1.73 m2, day	Pathologic diagnosis
1	M/78	+/+	26.4	0.77/103.9	1.79/35.3	1	Normal
2	M/46	-/-	23.6	0.96/89.6	1.59/50.9	18	C1q deposit
3	M/59	+/+	24.5	1.55/49	2.99/21.5	0[a]	C1q deposit, DN
4	M/43	-/-	19.5	0.77/117.2	2.57/29.1	366	HN
5	M/84	+/-	19.3	1.1/67.8	3.22/19.6	1	IN
6	F/66	+/-	26.6	0.7/89	0.99/58.7	549	C1q deposit
7	M/66	-/-	27.9	0.86/94.6	1.28/57.1	199	C1q deposit
8	F/68	+/+	24.1	1.01/57.9	1.46/36.2	0[a]	DN
9	F/73	+/+	22.3	0.64/96.7	0.98/59.1	30	DN
10	M/64	-/+	22.0	1.0/80	1.96/34.6	1	Reflux nephropathy
11	M/73	+/+	27.3	1.1/69.7	2.36/26	1	IN
12	M/61	+/+	21.3	1.2/65.4	1.61/44.8	189	DN
13	M/58	-/-	31.9	0.9/92.1	1.46/51.5	22	Normal
14	F/83	+/+	23.3	0.8/72.9	1.68/28.5	1	HN
15	M/79	+/-	23.8	1.82/34.6	2.15/28.2	0[a]	Chronic pyelonephritis
16	M/75	+/+	29.0	1.03/70.7	1.53/43.8	1	MGN
17	M/71	+/-	19.1	0.73/93.3	1.75/37.8	3	C1q deposit
18	M/48	-/-	24.2	0.95/94.3	1.44/56.6	1	DN
19	M/61	-/-	22.7	1.05/76.2	1.72/41.7	1	DN

All patients received radical nephrectomy.

DM, diabetes mellitus; HTN, hypertension; BMI, body mass index; Cr, creatinine; eGFR, estimated glomerular filtration rate; DN, diabetic nephropathy; HN, hypertensive nephrosclerosis; IN, ischemic nephropathy; MGN, membranous glomerulonephritis.

These patients had pre-existing chronic kidney disease.

DISCUSSION

In this study, pathologic examination of non-neoplastic kidney revealed that 74.5% of patients underwent nephrectomy showed definitive morphological abnormalities. The most frequent pathologic finding was glomerular abnormality followed by diabetic and vascular nephropathies. Since almost 40% to 50% of our study population had HTN and DM and the median age was 63 years, diabetic nephropathy and vascular diseases would be expected to be present. However, the frequency of glomerular abnormalities was much higher than the previous studies. Two separate analyses demonstrated the presence of abnormal pathologic findings in 61.8% [17] and 15% [18] of the kidneys where the non-neoplastic portions from tumor nephrectomy specimens were reviewed. In both studies, the most common findings were diabetic nephropathy and vascular-related changes. There were only two cases of IgA nephropathy out of 110 cases reviewed [17] and one case each of proliferative glomerulonephritis and membranous nephropathy out of 381 cases reviewed [18]. We believe that the higher diagnostic rate of glomerular abnormality in our study is related to our methodology. Unlike the previous reports [17-19] that performed special studies only in selected cases, all non-neoplastic tissue samples were routinely subjected to IF and EM, which detect unsuspected immune deposits, glomerular architecture changes, and other pathologic processes in this study. To our knowledge, our analysis is the first to include all special stains, IF, and EM studies in pathologic evaluation of non-neoplastic kidney.

IgA nephropathy is considered the most common glomerular disease worldwide [20], and had a diagnosis rate of 17.6% in our study. During the follow-up period of 3 to 36 months, all patients were asymptomatic and their renal functions were preserved. IgA nephropathy is characterized by a highly variable course ranging from a totally benign condition to rapidly progressive renal failure [21]. Although our patients with silent IgA nephropathy showed preserved renal function during the study period, following such patients prospectively over many years may be important because chronic, slowly progressive renal failure develops in some patients with this disease [21]. Five cases revealed to have C1q deposit. Four of five patients diagnosed with C1q deposit showed normal renal function prior to nephrectomy, but following surgery, all progressed to CKD. One patient diagnosed with C1q deposit who had pre-existing CKD had an acceleration of CKD progression. There is a possibility of C1q nephropathy of those five patients diagnosed with C1q deposit, which is known to have heterogeneous histologic findings, as well as diverse clinical presentations varying from asymptomatic to ESRD [22]. Membranous glomerulonephritis is the most common cause of nephrotic syndrome in adults [23]. Most patients with membranous glomerulonephritis present as nephrotic syndrome and the remainder are diagnosed following an evaluation for asymptomatic proteinuria [23]. Our patient who was diagnosed with membranous glomerulonephritis had normal urinalysis initially, but this patient had de novo CKD after nephrectomy. It is worth mentioning that all the patients diagnosed with glomerular abnormalities in our study had no known kidney disease at the time of nephrectomy. The detection of unknown kidney disease in non-neoplastic kidney tissues, although they are early lesions, may be of considerable importance to alert the physician for ongoing risk factors or causes of CKD, especially given that the solitary kidney is considered as a contraindication to percutaneous biopsy.

Our findings showing that the higher histologic scores of non-neoplastic portions could be an independent risk factor for CKD after nephrectomy further support the clinical significance of pathologic evaluation of non-neoplastic kidney. We used a simple semi-quantitative histological scoring system that has been validated in the previous studies to predict graft function after cardiac death kidney transplantations [16,24,25]. The degree of glomerulosclerosis, interstitial fibrosis, tubular atrophy, arteriolosclerosis, and arteriolar hyalinosis was graded from 0 to 3. Surprisingly, this study showed that optimal scores (≤ 3 points) were observed in only 25.4% of patients and that 13.7%, 3.9%, 3.9%, 5.9%, and 7.8% of total patients had global glomerulosclerosis, interstitial fibrosis, tubular atrophy, fibrous intimal thickening, and hyaline arteriolar thickening of grade 3. For each 1 point increase in histologic scores, the risk of CKD increased 23%. These findings are in keeping with previous reports that have demonstrated that postoperative sCr levels increased significantly in patients with severe parenchymal changes. In a study of 110 tumor nephrectomy specimens, patients with > 20% of global glomerulosclerosis and advanced diffuse diabetic glomerulosclerosis showed a greater decline in sCr levels at 6-month follow-up period [17]. Among 156 patients who were followed-up for at least 12 months after tumor nephrectomy, postoperative sCr levels increased significantly in patients with severe arteriosclerosis or arteriolosclerosis, > 5% global glomerulosclerosis, or > 10% interstitial fibrosis or tubular atrophy [18]. In this regard, we feel that recent update of the protocol for examination of tumor nephrectomy and nephroureterectomy specimens by the College of American Pathologists to require routine evaluation of non-neoplastic renal parenchyma is reasonable and appropriate.

Multiple studies have shown that radical nephrectomy, compared with partial nephrectomy, could lead to a substantial decline in renal function. In a study involving 1,151 patients who underwent radical nephrectomy or partial nephrectomy, radical nephrectomy nearly doubled the risk of adverse renal outcomes including ESRD, urgent dialysis, CKD, or rapidly progressive CKD when compared with partial nephrectomy [4]. Current recommendation from the American Urological Association [6] and the European Association of Urology [7] suggested partial nephrectomy as the standard of care for type 1a (T1a) RCC (tumor diameter ≤ 4 cm) and as a viable option for T1b RCC (tumor diameter ≤ 7 cm). In accordant with these findings, our study also showed higher event of adverse postoperative renal outcomes including AKI and CKD in radical nephrectomy. None of the partial nephrectomized patients had de novo CKD in the present study. Our findings showing that a lower preoperative eGFR and the presence of AKI were the independent risk factors for the development of postoperative CKD were consistent with the previous studies [13,26].

Limitation of this study is a small sample size with short follow-up period. Further prospective studies with long-term follow-up should be performed to prove the beneficial effect of pathologic evaluation of non-neoplastic kidney in terms of early recognition of the patients at risk for CKD and timely institution of early measures to preserve their renal function.

In conclusion, our data clearly demonstrated that a thorough pathologic evaluation of non-neoplastic kidney provides valuable diagnostic and prognostic information. Therefore, routine pathologic examination of non-neoplastic parenchyma in resected tumor specimens using special stains, IF, and EM studies is recommended in the clinical practice.

1. The incidence of kidney cancer has been dramatically increasing worldwide, and nephrectomy remains the standard of care in the treatment of upper urinary tract malignancies, which is a risk factor of chronic kidney disease.

2. As a solitary kidney is considered as a contraindication to percutaneous biopsy and the safety of this procedure in patients with partial nephrectomy has not been demonstrated, thorough histologic evaluation of non-neoplastic kidney enables early identif ication of unrecognized kidney disease and provides valuable prognostic information. Therefore, routine pathologic examination of non-neoplastic parenchyma in resected tumor specimens is recommended in the clinical practice.