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10.1136/bcr-2013-010081 http://scihub22266oqcxt.onion/10.1136/bcr-2013-010081 C3736175!3736175!23904421     free     free     free       BMJ+Case+Rep 2013 ; 2013 (ä): ä Nephropedia Template TP {{tp|p=23904421|t=2013. CAPS: a rare acute abdomen |pdf=|usr=}}{{23904421}} gab.com Text CAPS: a rare acute abdomen JO: BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=23904421 #FOAvip An 11-year-old girl presented to the hospital with vomiting, left upper-quadrant pain and blood in the stool. An ultrasound scan showed no blood flow in the coeliac axis or the splenic artery. A contrast-enhanced CT scan then demonstrated no flow beyond the coeliac axis origin, a large clot in the distal superior mesenteric artery (SMA), a large splenic infarct and bilateral renal infarcts. Investigations revealed a positive lupus anticoagulant and she was given a presumptive diagnosis of catastrophic antiphospholipid syndrome (CAPS). She was anticoagulated and started on combination immunosuppressive therapy. Her surgical management was by SMA embolectomy, small bowel resection and proximal stoma formation. Stoma closure was performed at 3?months, and she was eventually established on full enteral feeds. Childhood CAPS is a rare condition with a very high mortality rate, and the successful outcome in this case reflects close multidisciplinary teamwork between medical and surgical specialties. Twit Text FOAVip CAPS: a rare acute abdomen ????BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=23904421 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=23904421 #FOAvip English Wikipedia <ref>{{Cite pmid|23904421}}</ref> CAPS: a rare acute abdomen #MMPMID23904421 Smith JP; Woodward M; Tunstall O; Ramanan A BMJ Case Rep 2013[]; 2013 (ä): ä PMID23904421show ga An 11-year-old girl presented to the hospital with vomiting, left upper-quadrant pain and blood in the stool. An ultrasound scan showed no blood flow in the coeliac axis or the splenic artery. A contrast-enhanced CT scan then demonstrated no flow beyond the coeliac axis origin, a large clot in the distal superior mesenteric artery (SMA), a large splenic infarct and bilateral renal infarcts. Investigations revealed a positive lupus anticoagulant and she was given a presumptive diagnosis of catastrophic antiphospholipid syndrome (CAPS). She was anticoagulated and started on combination immunosuppressive therapy. Her surgical management was by SMA embolectomy, small bowel resection and proximal stoma formation. Stoma closure was performed at 3?months, and she was eventually established on full enteral feeds. Childhood CAPS is a rare condition with a very high mortality rate, and the successful outcome in this case reflects close multidisciplinary teamwork between medical and surgical specialties. äCAPS: a rare acute abdomen (epmc).pdf DeepDyve Pubget Overpricing