ABSTRACT
We report a case of pure red cell aplasia due to parvovirus B19 infection in a renal transplant recipient. The patient was a 32-year-old male with end stage renal disease due to chronic glomerulonephritis, who had been undergoing regular hemodialysis. He received a living nonrelated renal transplant and immumosuppressive therapy including prednisolone, tacrolimus, and mycophenolate mofetil. One week after kidney transplantation, severe anemia was persisted despite recombinant human erythropoietin administration and packed red blood cell transfusion. His bone marrow aspiration smear demonstrated erythroid hypoplasia and giant pronormoblasts with prominent intranuclear inclusions. Both serum and bone marrow were positive for parvovirus B19 DNA polymerase chain reaction and anti-parvovirus B19 IgM. He was treated with intravenous immunoglobulin and conversion of tacrolimus to cyclosporine. His hemoglobin level was completely recovered three months later.
Subject(s)
Adult , Humans , Male , Anemia , Bone Marrow , Cyclosporine , DNA , Erythroblasts , Erythrocyte Transfusion , Erythropoietin , Glomerulonephritis , Immunoglobulin M , Immunoglobulins , Intranuclear Inclusion Bodies , Kidney Failure, Chronic , Kidney Transplantation , Parvovirus , Polymerase Chain Reaction , Prednisolone , Red-Cell Aplasia, Pure , Renal Dialysis , Tacrolimus , TransplantationABSTRACT
A nephrocolic fistula is uncommon complication resulting from chronic inflammatory processes in the kidney. We report here a case of nephrocolic fistula associated with staghorn calculi. A 61-year-old female with known renal stones for three years was admitted to our hospital because of left flank pain and gross hematuria. Abdominal CT scan showed pyonephrosis with staghorn calculi in the left kidney. We performed percutaneous nephrostomy because of pelvocaliceal dilatation and high fever. Leakage of contrast dye was also detected in antegrade pyelogram, and drainage of fecal contents from nephrostomy was noted, suggesting fistulous formation between left kidney and colon. Clinical and laboratory findings of the patient deteriorated rapidly in spite of conservative management including antibiotics administration, so we performed nephrectomy with excision of the fistulous tract and partial colectomy. However, she showed delirium and had several attacks of generalized seizure, and she died of sepsis and multiple organ failure on the 33rd hospital day. In conclusion, when a nephrocolic fistula develops in patient with renal stone, prompt investigation and appropriate surgical treatment should be considered to improve the clinical outcome.
Subject(s)
Female , Humans , Middle Aged , Anti-Bacterial Agents , Calculi , Colectomy , Colon , Delirium , Dilatation , Drainage , Fever , Fistula , Flank Pain , Hematuria , Kidney , Multiple Organ Failure , Nephrectomy , Nephrostomy, Percutaneous , Pyonephrosis , Seizures , Sepsis , Tomography, X-Ray ComputedABSTRACT
Hypertension and atherosclerosis are the most important factors contributing to the development of aortic dissection. Primary aldosteronism is a rare cause of hypertension. The concurrence of aortic dissection is very rare in primary aldosteronism. However, when aortic dissection is found as a life-threatening complication of primary aldosteronism, then the diagnosis of primary aldosteronism is important because the therapeutic intervention can be curative. Only 3 cases of primary aldosteronism with aortic dissection have been reported in the literature. We report here on a case of primary aldosteronism with aortic dissection, which was treated by laparoscopic adrenalectomy. We lowered the blood pressure with antihypertensive drugs and potassium replacement was done to treat the aortic dissection. After stabilization of aortic dissection, we removed his left adrenal mass by laparoscopic adrenalectomy. Postoperatively, the patient's blood pressure has been within normal limits and the serum potassium increased to a normal level without supplementation. The aortic dissection has remained in a stable state
Subject(s)
Adrenalectomy , Antihypertensive Agents , Atherosclerosis , Blood Pressure , Diagnosis , Hyperaldosteronism , Hypertension , PotassiumABSTRACT
Hypertension and atherosclerosis are the most important factors contributing to the development of aortic dissection. Primary aldosteronism is a rare cause of hypertension. The concurrence of aortic dissection is very rare in primary aldosteronism. However, when aortic dissection is found as a life-threatening complication of primary aldosteronism, then the diagnosis of primary aldosteronism is important because the therapeutic intervention can be curative. Only 3 cases of primary aldosteronism with aortic dissection have been reported in the literature. We report here on a case of primary aldosteronism with aortic dissection, which was treated by laparoscopic adrenalectomy. We lowered the blood pressure with antihypertensive drugs and potassium replacement was done to treat the aortic dissection. After stabilization of aortic dissection, we removed his left adrenal mass by laparoscopic adrenalectomy. Postoperatively, the patient's blood pressure has been within normal limits and the serum potassium increased to a normal level without supplementation. The aortic dissection has remained in a stable state
Subject(s)
Adrenalectomy , Antihypertensive Agents , Atherosclerosis , Blood Pressure , Diagnosis , Hyperaldosteronism , Hypertension , PotassiumABSTRACT
A 74-years-old female with leprosy was hospitalized because of nausea, vomiting, and oliguria after ingestion of rifampin 600 mg once for one day. At this time, after taking the second dose of rifampin, she presented with anemia, hepatic dysfunction and oliguric renal failure. Renal biopsy specimen showed acute interstitial nephritis and tubular necrosis without immunoglobulin deposition on immunofluorescence examination. Peripheral blood smear showed fragmented red blood cells (RBCs) and direct Coombs' test was positive. Indirect antiglobulin test with patient's serum using RBCs sensitized in vitro with rifampin showed positive finding. The renal failure and systemic symptoms were improved after discontinuation of rifampin, high dose prednisolone administration and several sessions of hemodialysis.