Results on purified protein derivative test were negative. The patient required initiation of continuous bladder irrigation (CBI) and packed red blood cell transfusion. On hospital day 5, the patient was taken for cystoscopy, clot evacuation, and ureteroscopy. Diffuse clot was irrigated from the bladder. Multiple bullous lesions in the bladder were biopsied and fulgurated. Retrograde

pyelogram revealed moderate right hydroureteronephrosis with filling defects in the ureter and pelvis. Ureteroscopy revealed inflamed renal pelvis mucosa; however, visualization Inhibitors,research,lifescience,medical was limited secondary to large clots filling portions of the collecting system. Washings were sent for cytology, AFB, and culture. Multiple biopsies were taken, and a double-J GSK126 chemical structure ureteral stent was placed. Pathologic analysis revealed urothelial tissue with hemorrhage and focal chronic inflammation. The patient had an uneventful postoperative course, was draining clear urine, and was discharged home. Hematologic consultation revealed no Inhibitors,research,lifescience,medical coagulation disorders. One week later the patient was readmitted to the hospital with recurrent gross hematuria. Renal MRI/magnetic resonance angiography showed improved right hydroureteronephrosis

and no vascular malformation or fistula. The patient’s bleeding persisted despite Inhibitors,research,lifescience,medical CBI and repeated transfusion therapy, and he was taken for laparoscopic right nephroureterectomy on hospital day 4. Postoperative oozing continued from the bladder cuff site, requiring transurethral fulguration Inhibitors,research,lifescience,medical on postoperative day 2. On postoperative day 4, decreasing hematocrit prompted a computed tomography scan that revealed retroperitoneal hematoma and significant blood in the subcutaneous tissues; thus, re-exploration through the kidney extraction site was performed and was negative for active bleeding. Pathologic evaluation of the right kidney and ureter revealed kidney and ureter with marked luminal hemorrhage in the ureter. The sections showed extramedullary hematopoiesis (EMH) in the

Inhibitors,research,lifescience,medical renal parenchyma extending into the perirenal fat (Figure 2A–C). The infiltrate was composed predominantly of left-shifted myeloid and monocytic precursors (highlighted by immunohistochemical stains for myeloperoxidase much and lysozyme) and dysplastic megakaryocytes and normoblasts. Few scattered lymphoblasts (CD34+, CD117+) were present within the infiltrate, without evidence of discrete aggregates. Admixed within the infiltrate were polytypic plasma cells and lymphocytes. These findings are characteristic of the involvement of the renal parenchyma and the ureter by CMML. A follow-up bone marrow biopsy showed a hypercellular marrow for age with myeloid hyperplasia and erythroid and megakaryocytic hypoplasia with megakaryocytic dysplasia. The abovementioned bone marrow findings-increased WBC count (17.