Abstract:We report two cases in which necrotizing vasculitis with tenosynovitis arthralgia/arthritis syndrome developed after intestinal bypass surgery. Each of these patients had jejunoileostomies, and the excluded segment was placed in an ileal-colonic anastomosis. We speculate that since the attachment of the excluded segment to the large intestine predisposes it to increased bowel overgrowth of bacteria, these bacteria or their debris may have served as antigens for circulating immune complexes, which were detected… Show more
“…The patient's colitis-related fistulae associated with vasculitis and marked pustulation raises the possibility of bowel-associated pustular vasculitis. 8,9 This condition, characterized by a pustular, vasculitic rash and arthritis, is thought to be an immune complex-mediated reaction secondary to bacterial overgrowth within stagnant, blind-loops of bowel. However the conspicuous lack of response to broad spectrum antibiotics and absence of arthritis in our patient makes this diagnosis less likely.…”
Chronic granulomatous disease is an inherited disorder characterized by defective oxidative killing by neutrophils and other phagocytes. This results in susceptibility to persistent and life-threatening infections. We describe a 25-year-old man with chronic granulomatous disease who presented with an acute, febrile neutrophilic dermatosis. This indicates that normal neutrophil intracellular killing mechanisms are not essential in the pathogenesis of neutrophilic dermatoses.
“…The patient's colitis-related fistulae associated with vasculitis and marked pustulation raises the possibility of bowel-associated pustular vasculitis. 8,9 This condition, characterized by a pustular, vasculitic rash and arthritis, is thought to be an immune complex-mediated reaction secondary to bacterial overgrowth within stagnant, blind-loops of bowel. However the conspicuous lack of response to broad spectrum antibiotics and absence of arthritis in our patient makes this diagnosis less likely.…”
Chronic granulomatous disease is an inherited disorder characterized by defective oxidative killing by neutrophils and other phagocytes. This results in susceptibility to persistent and life-threatening infections. We describe a 25-year-old man with chronic granulomatous disease who presented with an acute, febrile neutrophilic dermatosis. This indicates that normal neutrophil intracellular killing mechanisms are not essential in the pathogenesis of neutrophilic dermatoses.
“…4,8,10 With rare exception, reanastomosis to reestablish bowel continuity has eliminated the syndrome. 9,10, [15][16][17] Although originally described after jejuno-iliac bypass, BADAS occurs more commonly after a jejuno-colic anastomosis 18 and has also been described in association with bilio-pancreatic diversion or bilio-intestinal bypass for morbid obesity, 19,20 Crohn disease, ileoanal pouch anastomosis, 21,22 ulcerative colitis, appendicitis, 23 diverticulitis, 11 and after Billroth II gastrectomy. 16,24 The standard surgical approach to carcinoma of the ampulla of Vater is the Whipple procedure, which involves en bloc resection of the gastric antrum and duodenum, a segment of the first portion of the jejunum, gallbladder, and distal common bile duct, the head and often the neck of the pancreas, and adjacent regional lymph nodes.…”
The development of bowel-bypass syndrome complicating the Whipple procedure for biliary tract carcinoma is described here for the first time. A 56-year-old HLA-B27 + man, treated with excision of adenocarcinoma of the ampulla of Vater, developed an undifferentiated spondyloarthropathy, initially unresponsive to nonsteroidal anti-inflammatory drugs and doxycycline, but eventually controlled with sulfasalazine and tapered corticosteroids. This condition represents another example of a rheumatic syndrome occurring after disruption of gastrointestinal tract continuity and likely development of small bowel bacterial overgrowth.
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