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Query: UMLS:C0034186 (
pyelonephritis
)
6,144
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Xanthogranulomatous pyelonephritis
is a chronic renal inflammation characterized by destruction and replacement of its parenchyma with granulomatous tissue. This uncommon condition is rare in children. We report on a 5-month-old male infant with a left renal and hepatic mass detected by ultrasound. The case was preoperatively misdiagnosed as Wilms' tumor and total nephrectomy and biopsy from liver lesion were performed. The subsequent histopathological findings confirmed the diagnosis of xanthogranulomatous
pyelonephritis
for renal and liver lesions. Increasing awareness of this disease should lead to the diagnosis being suspected preoperatively even if it is with unconnected tissue lesions.
...
PMID:Xanthogranulomatous pyelonephritis with unconnected liver lesion. 2109 88
Xanthogranulomatous pyelonephritis
is an uncommon chronic destructive granulomatous process of renal parenchyma in association with long-term urinary tract obstruction and infection. It affects females more often than males, with a wide range of age, from newborn to elderly. Almost all patients are symptomatic and the most common symptoms are flank or abdominal pain, lower urinary tract symptoms, fever, palpable mass, gross hematuria, and weight loss. The common laboratory findings are leukocytosis and anemia. Urine cultures most often reveal Escherichia coli and Proteus mirabilis . Computed tomography is the mainstay of diagnostic imaging for xanthogranulomatous
pyelonephritis
. Imaging studies may demonstrate diffuse or focal form. Histologically, xanthogranulomatous
pyelonephritis
presents a granulomatous inflammatory infiltrate composed of neutrophils, lymphocytes, plasma cells, xanthomatous histiocytes, and multinucleated giant cells. The differential diagnosis includes clear cell renal cell carcinoma, papillary renal cell carcinoma, sarcomatoid renal cell carcinoma, leiomyosarcoma, malakoplakia, and megalocytic interstitial nephritis. Both antibiotics and surgery can be treatment options depending on the patient's disease status.
...
PMID:Xanthogranulomatous pyelonephritis. 2152 66
We report a case of a renal mass in a 4-month boy, which occured during the assessment of a pelvi-calyceal dilatation diagnosed at 23 weeks of gestational age. There was no history of urinary infection, fever or weight loss. Physical examination revealed a mass of the left flank with significant flank tenderness. Laboratory test showed a biological inflammatory syndrome and urine culture was negative. Investigations including ultrasound and computed tomography scan were suggestive of diffuse xanthogranulomatous
pyelonephritis
with a non-functioning left kidney. Left total nephrectomy was performed through a lumbar incision with an extraperitoneal approach. The kidney was enlarged with a dilated pelvis containing pus upstream of a proximal ureteral atretic segment. Pathological examination of the kidney confirmed the diagnosis of diffuse xanthogranulomatous
pyelonephritis
. The boy remains well at 1 year follow-up.
Xanthogranulomatous pyelonephritis
is very rare in infants. It is an uncommon severe progressive renal infection resulting in destruction of renal parenchyma, histologically replaced by xanthomatous cells and granulomatous reaction. Pathogenesis of xanthogranulomatous
pyelonephritis
remains unclear. But it is well known that urinary tract obstruction and renal lithiasis are determining factors. It can occur in variant clinical forms but its symptoms remain non-specific. Curative treatment consists in nephrectomy and definitive diagnosis is made on histological examination of the kidney. This diagnosis should be discussed when a renal mass occurs in a context of malformative uropathy and xanthogranulomatous
pyelonephritis
have to be included in the differential diagnosis of renal mass in infants and children.
...
PMID:[Diffuse xanthogranulomatous pyelonephritis in infant]. 2169 63
Xanthogranulomatous pyelonephritis
(XPN) is a rare inflammatory condition usually secondary to chronic obstruction caused by nephrolithiasis and resulting in infection and irreversible destruction of the renal parenchyma. Its standard therapy consists of total or partial nephrectomy. A case of stage III xanthogranulomatous
pyelonephritis
treated with antibiotherapy and percutaneous drainage is presented in this paper.
...
PMID:Stage III xanthogranulomatous pyelonephritis treated with antibiotherapy and percutaneous drainage. 2198 Jul 41
Xanthogranulomatous pyelonephritis
is a rare, chronic inflammatory lesion of the kidney associated with chronic infection and obstruction. It is uncommon in children and extremely rare in infants. Because of its rarity, the condition is often not considered in the differential diagnosis of a renal mass in children. We report a case of a 5-month-old boy presenting with fever and a left renal mass. The findings from radiologic investigations were suggestive of a renal mass and urine culture suggestive of urinary tract infection. Left radical nephrectomy was performed with difficulty because of the dense adhesions to the adjacent structures. Histopathologic examination confirmed the diagnosis of xanthogranulomatous
pyelonephritis
.
...
PMID:Xanthogranulomatous pyelonephritis-mimicking renal mass in 5-month-old child. 2234 9
Xanthogranulomatous pyelonephritis
is a severe, atypical form of chronic renal parenchymal infection, which mimics neoplasia and other inflammatory renal parenchymal diseases. Although xanthogranulomatous
pyelonephritis
has characteristic findings on sonography and CT scan, a clinical diagnosis is seldom possible. Correct diagnosis is made on exploration, by the presence of dense adhesions to the surrounding tissue and presence of pus in the kidney, which is confirmed histopathologically by the presence of lipid laden foamy macrophages, accompanied by both chronic and acute phase inflammatory cells.
...
PMID:Xanthogranulomatous pyelonephritis in early infancy. 2260 3
Xanthogranulomatous pyelonephritis
(XGPN) is a rare, severe and atypical form of chronic
pyelonephritis
. It is characterised by destruction of the renal parenchyma and replacement with a chronic inflammatory infiltrate and lipid-laden macrophages resulting in a non-functional kidney. The authors report a case of a 5-year-old boy presented with a history of abdominal pain, malaise, anorexia and weight loss for 2 months. Physical examination revealed a large flank mass and the child was directed to the oncology unit on suspicion of renal tumour. Based on clinical examination and imaging, the presumptive diagnosis of XGPN of the left kidney was made. A left transperitoneal nephrectomy was performed and the histology confirmed the diagnosis. Although rare, XGPN is a clinically important entity that should be considered in the differential diagnosis of an atypical-appearance renal mass in paediatric age.
...
PMID:Xanthogranulomatous pyelonephritis presenting as a pseudotumour in a 5-year-old boy. 2323 19
Xanthogranulomatous pyelonephritis
(XGP) is a rare entity and constitutes less than 1% of chronic
pyelonephritis
. A 71-year-old male was introduced to our department with general malaise and abnormal findings of computed tomography (CT). Abnormal findings of complete blood count and laboratory examination included an elevated WBC count and C-reactive protein. Urinalysis showed combined hematuria and pyuria, and Escherichia coli was detected in urine culture. Abdominal CT revealed left hydronephrosis with staghorn renal calculi and thin cortex of the left kidney. Because of poor condition, the patient underwent construction of the left nephrostomy. After that, the remission of the inflammation was achieved. Several months after the construction, frequent obstructions of nephrostomy catheter because of turbid urine and intermittent fever elevation were observed. The patient and his family desired left nephrectomy despite his poor condition in general. Surgical dissection was very difficult due to fixed mass. Not long after that the patient died due to sepsis and cardiovascular failure. Microscopic findings of the left kidney revealed infiltration of lymphocytes and lipid-laden macrophages (xanthoma cells) corresponding to XGP.
...
PMID:Case of the diffuse form of xanthogranulomatous pyelonephritis. 2336 80
Xanthogranulomatous pyelonephritis
is a rare type of renal infection characterised by granulomatous inflammation with giant cells and foamy histiocytes.The peak incidence is in the sixth to seventh decade with a female to male ratio of 2:1. It is rare in children. A case of xanthogranulomatous
pyelonephritis
in a 11-year-old male child who presented with a history of high grade fever and chills for 15 days, right flank pain and progressive pyuria for two months is reported. He had a prior history of surgery for vesical calculus and anterior urethral calculus for which he underwent open cystolithotomy and urethrolithotomy four years back. Although Gram-negative bacilli were isolated from thick pus aspirated from the right renal pelvis under ultrasound guidance, urine and blood culture were sterile. Following a renal biopsy diagnosed as chronic
pyelonephritis
the patient underwent subscapsular right. nephrectomy.
...
PMID:Xanthogranulomatous pyelonephritis in a male child--a case report with a brief review of literature. 2373 10
Xanthogranulomatous pyelonephritis
(XGP) is an uncommon form of chronic
pyelonephritis
and a well recognized entity. It is rarely seen in children and neonates. The preoperative diagnosis is difficult and the etiology is still obscure. The condition is mostly diagnosed on nephrectomy specimen. The focal form mimicking neoplastic condition is rare. A case of XGP is reported here in an 8 month old child in which case nephrectomy was done with the clinical diagnosis of malignant renal tumor. Various modalities of preoperative diagnosis of this entity with conservative approach are also discussed.
...
PMID:Xanthogranulomatous pyelonephritis masquerading as a tumor in an infant. 2509 28
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