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At least 19 recordsLinked to original sources
PubMed1982

Ultrastructural demonstration of intracellular bacteria in xanthogranulomatous pyelonephritis.

Xanthogranulomatous pyelonephritis is considered to be an unusual cellular response to bacterial invasion. This assumption is based on circumstantial evidence and experimental studies. In our electron microscopic study of five cases of xanthogranulomatous pyelonephritis demonstrated a stratification of the cellular components, somewhat resembling that described in the experimental lesions. The center of the xanthogranulomas was occupied by purulent exudate. Bacteria were identified mainly in polymorphonuclear leukocytes and extracellularly in four cases in which central area were available for electron microscopic studies. Many bacteria were located in cytoplasmic vacuoles. more peripherally, histiocytes predominated, and their cytoplasm contained numerous lipid droplets with and without limiting membranes and phagolysosomes. The latter contained electron dense, granular, and membranous structures. The outermost layer of the lesion demonstrated macrophages with a decreased number of lipid droplets and larger intralysosomal particles. Lymphocytes, plasma cells, and fibroblasts represented an increasing proportion of the infiltrate in this layer. Our study suggests that xanthogranulomatous pyelonephritis is a bacteria induced process. Its histological appearance may be related to incomplete bacterial degradation and altered host response.

Adult↗
PubMed1989

Xanthogranulomatous pyelonephritis.

Xanthogranulomatous pyelonephritis is a rare chronic form of pyelonephritis with a clinical presentation often suggestive of a renal mass. We present 51 patients with histologically proven xanthogranulomatous pyelonephritis who were treated by nephrectomy. The results are discussed and compared with those from the literature.

Adolescent↗
PubMed1987

Ultrasonography and needle aspiration in diagnosis of xanthogranulomatous pyelonephritis.

Xanthogranulomatous pyelonephritis may present as a renal mass which can be difficult to differentiate from a hypovascular renal tumor by intravenous pyelography or selective renal angiography. Four patients are described in whom ultrasonography with or without fine-needle aspiration suggested or confirmed the diagnosis of xanthogranulomatous pyelonephritis.

Adult↗
PubMed1989

Evolving concepts in the diagnosis of xanthogranulomatous pyelonephritis.

Xanthogranulomatous pyelonephritis (XGP) is a rare inflammatory process of the kidney that results in focal or diffuse renal enlargement and nonexcretion. In the past, XGP often has been misdiagnosed as renal carcinoma. Newer investigative modalities and an increased awareness of XGP should make preoperative diagnosis possible. Thirty-two cases of XGP are presented, with emphasis on recent advances in radiographic approach to diagnosis.

Adult↗
PubMed1991

From the Archives of the AFIP. Xanthogranulomatous pyelonephritis.

Xanthogranulomatous pyelonephritis is a form of chronic infection of the kidney and surrounding tissues characterized by destruction and replacement of renal parenchyma by lipid-laden macrophages. Gross pathologic features include massive renal enlargement, lithiasis, peripelvic fibrosis, hydronephrosis, and lobulated yellow masses replacing renal parenchyma. Typically, the disease is diffuse and has characteristic imaging features. Less commonly, the process is focal and is difficult to differentiate from malignant disease on radiologic studies. Ultrasound demonstrates renal enlargement with multiple anechoic or hypoechoic masses replacing the normal corticomedullary differentiation and a contracted pelvis. Peripelvic fibrosis may obscure acoustic shadowing from a central staghorn calculus. On computed tomographic scans, a staghorn calculus may be seen in a contracted renal pelvis of an enlarged kidney, with characteristic low-attenuation, peripherally enhancing rounded masses. Extrarenal extension of the inflammatory process is frequently seen.

Adult↗
PubMed2002

Acute lumbago and sciatica as first symptoms of focal xanthogranulomatous pyelonephritis.

Xanthogranulomatous pyelonephritis (XGP) is a rare inflammatory disease of the kidney, presenting in a diffuse or focal form. The preoperative diagnosis of XGP is made only in 10% of the cases because neither the clinical nor the radiological presentation are specific and could be confused with renal tumors, thus deserving the name of 'great imitator'. We report a case of focal XGP in a middle-aged man presenting with acute lumbago and sciatica, an unusual clinical presentation.

Acute Disease↗
PubMed2002

[Xanthogranulomatous pyelonephritis].

Xanthogranulomatous pyelonephritis is a rare disease probably caused by long-standing obstruction and secondary infection. We report a case in a 47-year-old woman with no previous history of renal stones. Preoperative diagnostic workout included ultrasonography, CT scan, and drainage. Nephrectomy was performed, and the patient's postoperative recovery was uneventful. The difficulties of correct preoperative diagnosis are discussed.

Diagnosis, Differential↗
PubMedDate not supplied

[10 cases of xanthogranulomatous pyelonephritis].

Xanthogranulomatous pyelonephritis (XGP) is a chronic inflammation of the kidney usually associated with renal stones, recurrent urinary tract infections or endocrine disorders. A correct preoperative diagnosis is rarely made, since no specific clinical or radiological pattern is known. Differential diagnosis must include renal tuberculosis and renal carcinoma. Ten cases of XGP are reported. Clinical findings, radiological and pathological features, biolaboratory abnormalities are discussed.

Adult↗
PubMed1988

[Diagnosis and therapy of xanthogranulomatous pyelonephritis].

Xanthogranulomatous pyelonephritis (XGP) is a rare, unilateral and multifocal inflammatory response of the kidney against bacterial toxins. In the Department of Urology of the University of Freiburg 6 patients with XGP were observed within 10 years. Despite modern diagnostic procedures differential diagnosis from kidney tumors and other parenchymal kidney diseases remains difficult. Recurrent urinary tract infections, fever, urolithiasis, obstruction and leucocytosis may be indicative of XGP. The diagnosis has to be confirmed by surgical intervention which preferably should preserve functioning renal tissue. The prognosis in general is quite good.

Adolescent↗
PubMedDate not supplied

Paediatric xanthogranulomatous pyelonephritis.

Xanthogranulomatous pyelonephritis (XGP) is a well recognised but rare type of chronic pyelonephritis classically occurring in middle-aged women. It is increasingly being recognised in children in whom it can be mistaken for Wilms' tumour. Awareness of the possibility of this condition occurring in children may allow early recognition and possible treatment. Two cases of XGP in children are described and the literature reviewed.

Child, Preschool↗
PubMed1976

Xanthogranulomatous pyelonephritis.

Xanthogranulomatous pyelonephritis is a stage in the progress of chronic pyelonephritis characterized by a combination of clinical and radiologic findings which suggest the diagnosis. Pathologically there are xanthogranulomatous deposits and large lipid-filled foam cells. These clinical-radiologic-pathologic features are demonstrated by means of a case report.

Adolescent↗
PubMed1989

[A case of emphysematous pyelonephritis combined with xanthogranulomatous pyelonephritis].

A case of emphysematous pyelonephritis, xanthogranulomatous pyelonephritis histologically, is reported. A 49-year-old female patient was referred to our department from the department of internal medicine because abdominal ultrasonography demonstrated left renal swelling with gas echo. Computed tomographic scan showed much emphysema in the left kidney. Although aggressive treatment with broad spectrum antibiotics and immunoglobulin had been performed, subfever and left lumbago continued. Thereafter, she underwent left nephrectomy, and histological findings revealed xanthogranulomatous pyelonephritis. In the Japanese literature 27 cases of emphysematous pyelonephritis have been reported. Many cases are in middle-aged females and 85% of these cases complicated with diabetes mellitus. E. coli and Klebsiella was the main causative organism. The mortality of this disease was 26%. This report is the first case combined with xanthogranulomatous pyelonephritis in Japan. We recommend adequate chemotherapy and timely surgical treatment for good results.

Diabetes Complications↗
PubMed1988

[A clinical study of xanthogranulomatous pyelonephritis with special emphasis on the differential preoperative diagnosis between xanthogranulomatous pyelonephritis and renal cell carcinoma].

An accurate preoperative diagnosis of xanthogranulomatous pyelonephritis is difficult because of its clinical and radiological similarities to renal cell carcinoma. We report two cases of xanthogranulomatous pyelonephritis. Furthermore, in an attempt to clarify the clinical distinction between this entity and renal cell carcinoma, we summarize the clinical characteristics of 143 cases with xanthogranulomatous pyelonephritis in the literature and 126 cases with renal cell carcinoma experienced in our clinic. According to the clinical reviews, several characteristics of xanthogranulomatous pyelonephritis were revealed. 1) Presence of history of pyelonephritis. 2) gamma-globulinemia in blood chemistry. 3) Non-visualizing kidney on the excretory urogram. 4) Hypovascular or avascular features and dilatation of renal capsular arteries on angiogram. 5) Heterogenous renal mass and thickness of Gerota's fascia on computed tomogram. 6) Positive uptake of renal mass in Ga-scintigram. When some of these features are found in the renal mass, the case could be of xanthogranulomatous pyelonephritis and therefore a kidney preserving operation should be considered.

Carcinoma, Renal Cell↗
PubMed1999

Is the laparoscopic approach justified in patients with xanthogranulomatous pyelonephritis?

OBJECTIVES: Xanthogranulomatous pyelonephritis (XGP) is an atypical form of chronic renal infection. The treatment of choice is open nephrectomy, which is challenging, given the extent of the disease and the not uncommon involvement of the renal hilum and contiguous structures. We compared our experience with laparoscopic nephrectomy for histologically confirmed XGP with the open approach. METHODS: Review of all nephrectomy specimens at Washington University School of Medicine from July 1990 to March 1998 disclosed 9 patients with a pathologic diagnosis of unilateral XGP, of whom 5 patients underwent laparoscopic nephrectomy and 4 underwent open nephrectomy. XGP was suspected preoperatively in 56% of the patients. RESULTS: For the laparoscopic group, the average operating room time was 360 minutes, average blood loss was 260 mL, and complications occurred in 60% of patients (1 conversion to open, 1 ileus, 1 pulmonary embolus). For the open group, the average operating room time was 154 minutes, average blood loss was 438 mL, and there were no complications. Both groups were similar regarding time to oral intake, analgesia requirement, hospital stay, and time to complete recovery. CONCLUSIONS: Our early experience demonstrates that the benefits of laparoscopic nephrectomy, at present, do not extend to patients with XGP. Conventional open surgery is quicker, associated with fewer complications, and results in a similar use of analgesics, hospital stay, and recovery time.

Aged↗
PubMed1985

Xanthogranulomatous pyelonephritis in children.

Xanthogranulomatous pyelonephritis usually occurs in women 50 to 60 years old, and has the distinct clinical presentation suggestive of a renal mass. Since 1963 an increasing number of children with xanthogranulomatous pyelonephritis have been reported in the literature, with data suggesting that the characteristics of the disease are different from those in adults. We compared our children with xanthogranulomatous pyelonephritis to adults who had been described in the literature and to our cases of chronic pyelonephritis to determine whether xanthogranulomatous pyelonephritis in children is an entity as clearly different from chronic pyelonephritis as it is in adults. Twenty-one cases were eliminated from the study because of incomplete charts. We found 39 cases in which nephrectomy had been done for an anatomical diagnosis of chronic or xanthogranulomatous (8) pyelonephritis. Average age at presentation, duration of clinical course and sex distribution were similar in both groups. The left kidney was involved more often in both groups. Severe malnutrition, urolithiasis, reno-cutaneous fistula and negative urine cultures were more frequent in cases of xanthogranulomatous pyelonephritis, while obstructive nonlithiasic uropathy occurred more often in cases of chronic pyelonephritis. Microorganisms were similar in both groups and Escherichia coli was isolated most frequently. All cases of xanthogranulomatous pyelonephritis were of the diffuse type with areas corresponding to all histological stages. Our study suggests that perhaps in children xanthogranulomatous pyelonephritis occurs the same as chronic pyelonephritis, and is determined possibly by an affected immune response secondary to malnutrition and by the presence of urolithiasis.

Age Factors↗
PubMed1993

Clinicopathological features of xanthogranulomatous pyelonephritis in infancy.

Xanthogranulomatous pyelonephritis (XGP) is an unusual chronic inflammatory condition which most often affects women in their 5th to 7th decades and is rare in infants. Predisposing factors include infection, calculi and obstructive uropathy. We have reviewed the surgical files of 4 cases seen over a 28 yr period from 1964-91. All of the 3 partial and one total nephrectomy specimens demonstrated typical features of XGP with renal parenchyma effaced by a mixed acute and chronic inflammatory infiltrate which included prominent aggregates of foamy histiocytes containing eosinophilic inclusions. No Michaelis-Gutmann bodies were seen. This study shows the association of XGP with chronic infection, anatomical malformation and reflux in infancy, and raises the possibility of a temporary altered immune response in its pathogenesis.

Female↗