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1.
Ultrastruct Pathol ; 36(2): 134-8, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22471437

ABSTRACT

A 41-year-old man was admitted for evaluation of nephrotic syndrome associated with microhematuria, hypertension, and moderate renal failure. In serum and urine samples, monoclonal IgG-lambda was detected. Bone marrow examination showed normal representation of all cell lines with normal range of plasma cells. Renal biopsy demonstrated diabetes-like nodular glomerulosclerosis. Immunofluorescence failed to demonstrate the presence of kappa or lambda light chains in the kidney. Electron microcopy showed granular electron-dense deposits along the glomerular basement membranes and in the mesangial nodules. The patient was diagnosed as having light-chain deposition disease (LCDD) without evidence of plasma cell dyscrasia. This report was designed to stress the significant challenges that remain in the diagnosis of LCDD-related glomerulopathy. The salient morphological features that help in making an accurate diagnosis are discussed.


Subject(s)
Immunoglobulin Light Chains/immunology , Kidney/pathology , Kidney/ultrastructure , Nephrotic Syndrome/pathology , Adult , Biopsy , Fluorescent Antibody Technique , Humans , Male , Microscopy, Electron, Transmission , Nephrotic Syndrome/immunology
2.
Ultrastruct Pathol ; 35(4): 176-82, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21657818

ABSTRACT

Obesity-related glomerulopathy (ORG) is a secondary form of focal segmental glomerulosclerosis (FSGS) occurring in obese patients with a body-mass index higher than 30 kg/m(2). It is typically manifested by nephrotic-range proteinuria without full nephrotic syndrome, and progressive renal insufficiency. Characteristic morphologic features include the consistent presence of glomerulomegaly, predominance of perihilar variant of FSGS, and the relatively mild fusion of visceral epithelial cell foot processes. The concept of podocyte depletion as a driver of the glomerular scarring in obesity-associated FSGS is well documented. The underlying mechanisms are likely to be related in part to the oxidative stress and the impairment of the integrity of the slit diaphragm and cell adhesion resulting mainly from angiotensin II and transforming growth factor-ß. These proapoptotic cytokines are upregulated in obesity in response to insulin resistance, compensatory hyperinsulinemia and glomerular hyperfiltration-hypertension mediated mechanical stress. This review is designed to discuss the clinicopathologic features of obesity-associated FSGS, with a focus on the podocyte injury, which is involved in the onset and progression of the glomerulosclerotic process. Ultrastructural glomerular lesions are documented.


Subject(s)
Glomerulosclerosis, Focal Segmental/pathology , Obesity/pathology , Disease Progression , Glomerulosclerosis, Focal Segmental/complications , Glomerulosclerosis, Focal Segmental/metabolism , Humans , Kidney Glomerulus/pathology , Microscopy, Electron, Transmission , Obesity/complications , Obesity/metabolism , Oxidative Stress , Podocytes/ultrastructure , Proteinuria , Renal Insufficiency
3.
Ultrastruct Pathol ; 35(1): 42-6, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21265634

ABSTRACT

Membranoproliferative glomerulonephritis with isolated C3 deposits (MPGNC3) is an uncommon condition characterized by overt glomerular C3 deposits in the absence of immunoglobulins and intramembranous dense deposits. Here the authors describe the clinical and morphological features of primary MPGNC3 in a 13-year-old boy and critically review the previously published cases. The patient presented with nephrotic syndrome and microscopic hematuria. Blood tests revealed very low circulating C3 levels. The renal biopsy exhibited subendothelial, subepithelial, and mesangial deposits, with C3 but not immunoglobulins seen on immunofluorescence. This case and the review of the literature indicate that the serum complement profile with decreased levels of C3 and normal levels of classical pathway components together with glomerular deposits containing exclusively complement C3 is highly suggestive of alternative pathway activation. The diagnosis of acquired and/or genetic complement abnormalities in some cases supports that complement dysregulation is implicated in the pathogenesis of MPGNC3. Such data show great promise to provide new therapy strategies based on modulation of the complement system activity.


Subject(s)
Complement C3/metabolism , Glomerulonephritis, Membranoproliferative/metabolism , Glomerulonephritis, Membranoproliferative/pathology , Adolescent , Fluorescent Antibody Technique , Humans , Kidney Glomerulus/metabolism , Kidney Glomerulus/ultrastructure , Male , Microscopy, Electron, Transmission
4.
Ultrastruct Pathol ; 34(2): 49-61, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20192700

ABSTRACT

To evaluate the contribution of electron microscopy to the final diagnosis of glomerulopathies, the authors established a prospective study during the first semester of 2006. A total of 52 kidney biopsies were performed with 3 samples for light microscopy, immunofluorescence, and electron microscopy. Among these renal biopsies, only 20 were examined with electron microscopy because the diagnosis made on the basis of conventional methods had remained unclear or doubtful. In 18 cases, electron microscopy was undertaken for the investigation of primary kidney disease. The 2 remaining cases were transplant biopsies. In this series of 20 patients, there were 3 children with an average age of 9 years and 17 adults with an average age of 35.5 years. Fifteen patients (75%) were nephrotic. The study revealed that electron microscopy was essential for diagnosis in 8 cases (40%) and was helpful in 12 cases (60%). In conclusion, the results showed that the ultrastructural study provides essential or helpful information in many cases of glomerular diseases, and therefore electron microscopy should be considered an important tool of diagnostic renal pathology. As was recommended, it is important to reserve renal tissue for ultrastructural study unless electron microscopy can be routinely used in all biopsies. Thus, this technique could be performed wherever a renal biopsy has to be ultrastructurally evaluated.


Subject(s)
Glomerulonephritis/diagnosis , Kidney Glomerulus/ultrastructure , Microscopy, Electron, Transmission , Adolescent , Adult , Biopsy , Child , Child, Preschool , Female , Glomerulonephritis/pathology , Humans , Kidney Transplantation/pathology , Male , Microscopy, Fluorescence , Middle Aged , Prospective Studies , Young Adult
5.
Asian J Androl ; 10(4): 593-601, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18097508

ABSTRACT

AIM: to investigate the effects of crude garlic on adult male rat reproductive functions. METHODS: Thirty male rats were divided into five groups: group 1 (untreated) and groups 2, 3, 4 and 5 were fed for 30 days with 5%, 10%, 15% and 30% crude garlic, respectively. Testes and accessory organs were weighed and some markers were assessed. Light and electron microscopy observations were also performed. RESULTS: A significant decrease was observed in the body weight of groups 4 (14%; P < 0.01) and 5 (20%; P < 0.01); of the prostate weight in group 5 (29.1%; P < 0.05) and of seminal vesicle weight in groups 3 (14.4%; P < 0.01), 4 (18.3%; P < 0.01) and 5 (27.3%; P < 0.01). In contrast, testis and epididymis weights were unchanged. In epididymis tissue, the alpha glucosidase activity and the spermatozoa density were unchanged. The treatment resulted in a significant decrease in testosterone serum levels in groups 3 (77.3%; P < 0.01), 4 (77.3%; P < 0.01) and 5 (90.9%; P < 0.01), associated with a significant increase in LH serum levels (P < 0.01). Testicular histology showed a dose-dependent increase in the percentage of empty seminiferous tubules. Moreover, testicular function was affected; a significant decrease in phosphatase acid activity (P < 0.01) and testosterone (P < 0.05) contents were observed. CONCLUSION: Crude garlic consumption during 1 month reduced testosterone secretion and altered spermatogenesis at 10%, 15% and 30% doses.


Subject(s)
Garlic/adverse effects , Plant Preparations/pharmacology , Reproduction/physiology , Testis/drug effects , Animals , Dose-Response Relationship, Drug , Epididymis/drug effects , Epididymis/physiology , Leydig Cells/drug effects , Leydig Cells/physiology , Luteinizing Hormone/blood , Male , Prostate/drug effects , Prostate/physiology , Rats , Rats, Wistar , Reproduction/drug effects , Seminal Vesicles/drug effects , Seminal Vesicles/physiology , Sertoli Cells/drug effects , Sertoli Cells/physiology , Sperm Count , Spermatogenesis/drug effects , Spermatogenesis/physiology , Testis/cytology , Testis/metabolism , Testosterone/blood
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