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1.
Clin Nephrol Case Stud ; 5: 32-37, 2017.
Article in English | MEDLINE | ID: mdl-29043145

ABSTRACT

PURPOSE: We report the case of a 59-year-old man with chronic hepatitis B and C infection presenting with acute kidney injury and enterococcus faecalis-infective endocarditis (IE). An elevated proteinase-3 (PR3)-ANCA and pauci-immune glomerulonephritis (GN) on renal biopsy were discovered, corresponding to ANCA-mediated GN. We conducted a literature review to assess the role of ANCA in IE and treatment implications. METHODS: On systematic review of the literature, we found five previous cases whereby IE caused by streptococcus and bartonella species were related to ANCA vasculitis-associated GN. RESULTS: Most reports of IE-related GN are mediated by immune complex deposition and resolve following microbial clearance. Of the 5 cases of ANCA GN in the setting of IE, all had markedly elevated levels of PR3-ANCA with either a subacute or chronic course of infection. Patients were treated with a combination of steroids and cyclophosphamide (2/5), steroids and antibiotics alone (1/5), or with valvular replacement (2/5). Renal function was recovered in 4/5 patients. CONCLUSION: Infection is a major etiologic player in the formation of ANCA; however, the role of PR3-ANCA in IE remains unclear. Kidney biopsy is essential in differentiating IE-related GN due to infection and immune complex deposition versus ANCA-associated vasculitis. A paucity of reports on the development of GN in IE-associated ANCA vasculitis exists, highlighting the rarity of our case and lack of clear therapeutic strategies in a patient with active infection requiring immunosuppression. In this case, the patient's chronic hepatitis B and C coinfection presented a unique challenge.

2.
Can Urol Assoc J ; 9(3-4): 133-5, 2015.
Article in English | MEDLINE | ID: mdl-26085871

ABSTRACT

Testicular capillary hemangioma is a rare benign vascular tumour. We report a case of a 66-year-old man who underwent an uncomplicated radical orchiectomy for a painless left testicular mass. Pathology showed capillary hemangioma of the testis. There are only 22 cases reported in the English literature, including the presented case. Appropriate intra-operative recognition of this entity is vital to assess for potential testicular-sparing surgery.

3.
J Histochem Cytochem ; 63(1): 32-44, 2015 01.
Article in English | MEDLINE | ID: mdl-25319549

ABSTRACT

Schimke immuno-osseous dysplasia (SIOD) is a pleiotropic disorder caused by mutations in the SWI/SNF2-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a-like-1 (SMARCAL1) gene, with multiple clinical features, notably end-stage renal disease. Here we characterize the renal pathology in SIOD patients. Our analysis of SIOD patient renal biopsies demonstrates the tip and collapsing variants of focal segmental glomerulosclerosis (FSGS). Additionally, electron microscopy revealed numerous glomerular abnormalities most notably in the podocyte and Bowman's capsule. To better understand the role of SMARCAL1 in the pathogenesis of FSGS, we defined SMARCAL1 expression in the developing and mature kidney. In the developing fetal kidney, SMARCAL1 is expressed in the ureteric epithelium, stroma, metanephric mesenchyme, and in all stages of the developing nephron, including the maturing glomerulus. In postnatal kidneys, SMARCAL1 expression is localized to epithelial tubules of the nephron, collecting ducts, and glomerulus (podocytes and endothelial cells). Interestingly, not all cells within the same lineage expressed SMARCAL1. In renal biopsies from SIOD patients, TUNEL analysis detected marked increases in DNA fragmentation. Our results highlight the cells that may contribute to the renal pathogenesis in SIOD. Further, we suggest that disruptions in genomic integrity during fetal kidney development contribute to the pathogenesis of FSGS in SIOD patients.


Subject(s)
Arteriosclerosis/metabolism , Arteriosclerosis/pathology , DNA Helicases/metabolism , Gene Expression Regulation , Immunologic Deficiency Syndromes/metabolism , Immunologic Deficiency Syndromes/pathology , Kidney/metabolism , Kidney/pathology , Nephrotic Syndrome/metabolism , Nephrotic Syndrome/pathology , Osteochondrodysplasias/metabolism , Osteochondrodysplasias/pathology , Pulmonary Embolism/metabolism , Pulmonary Embolism/pathology , Animals , Arteriosclerosis/complications , Arteriosclerosis/genetics , Child , Child, Preschool , DNA Fragmentation , Female , Glomerulosclerosis, Focal Segmental/complications , Humans , Immunologic Deficiency Syndromes/complications , Immunologic Deficiency Syndromes/genetics , Kidney/embryology , Kidney/ultrastructure , Male , Mice , Nephrotic Syndrome/complications , Nephrotic Syndrome/genetics , Osteochondrodysplasias/complications , Osteochondrodysplasias/genetics , Primary Immunodeficiency Diseases , Pulmonary Embolism/complications , Pulmonary Embolism/genetics
4.
Ital J Pediatr ; 37: 17, 2011 Apr 15.
Article in English | MEDLINE | ID: mdl-21496243

ABSTRACT

Drug-induced acute interstitial nephritis (AIN) represents a growing cause of renal failure in current medical practice. While antimicrobials and non-steroidal anti-inflammatory drugs are typically associated with drug-induced AIN, few reports have been made on the involvement of other analgesics. We report our experience in managing a 17-year-old female with AIN and subsequent renal injury following an acetaminophen overdose in conjunction with acute alcohol intoxication. It is well established that acetaminophen metabolism, particularly at high doses, produces reactive metabolites that may induce renal and hepatic toxicity. It is also plausible however, that such reactive species could instead alter renal peptide immunogenicity, thereby inducing AIN. In the following report, we review a possible mechanism for the acetaminophen-induced AIN observed in our patient and also discuss the potential involvement of acute alcohol ingestion in disease onset. The objective of our report is to increase awareness of healthcare professionals to the potential involvement of these commonly used agents in AIN pathogenesis.


Subject(s)
Acetaminophen/adverse effects , Alcoholic Intoxication/complications , Analgesics, Non-Narcotic/adverse effects , Ethanol/adverse effects , Nephritis, Interstitial/chemically induced , Acute Disease , Adolescent , Alcoholic Intoxication/blood , Alcoholic Intoxication/therapy , Female , Fluid Therapy/methods , Follow-Up Studies , Humans , Nephritis, Interstitial/therapy , Treatment Outcome
5.
Med Mycol ; 43(5): 413-6, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16178369

ABSTRACT

The precise ecological niche of Blastomyces dermatitidis is unknown. The related dimorphic fungus, Paracoccidioides brasiliensis, has been isolated from South American ground-dwelling insectivorous armadillos. We attempted to isolate Blastomyces from shrews, North American ground-dwelling insectivores that have been shown to harbor Histoplasma capsulatum in endemic areas. Forty-seven masked shrews (Sorex cinereus) and 13 northern short-tailed shrews (Blarina brevicauda) were collected in endemic areas of northern Wisconsin and Michigan using pitfall traps. Specimens were collected between 1998 and summer 2002, stored frozen, then necropsied. Cultures of nasopharynx, lungs, liver, spleen and large and small bowel were placed on yeast extract phosphate agar with one or two drops of ammonium hydroxide. Cultures for Blastomyces were negative from all 60 shrews and two deer mice (Peromyscus maniculatus) and three southern red-backed voles (Clethrionomys gapperi), which were trapped inadvertently. Histological examination of 36 of these specimens revealed no Blastomyces yeast forms. Northern Wisconsin shrews do not appear to be carriers of B. dermatitidis.


Subject(s)
Blastomyces/isolation & purification , Blastomycosis/microbiology , Lung Diseases, Fungal/veterinary , Animals , Blastomyces/classification , Blastomycosis/epidemiology , Blastomycosis/veterinary , Lung Diseases, Fungal/epidemiology , Shrews , Wisconsin/epidemiology
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