Abstract
Over a career, 76 patients with massive retroperitoneal necrosis associated with acute pancreatitis were initially treated conservatively. Seventy-one subsequently required operative debridement, between 18 days and 13 months after onset of the disease, including 3 who were explored within the first 2 weeks. In the absence of secondary infection, clinical evidence of toxemia was variable, sometimes relatively limited and occasionally minimal, even in association with large amounts of necrotic tissue. In almost all patients the necrotic tissue consisted chiefly of adipose tissue in the retroperitoneum, including the intramesenteric spaces. In 2 patients, the parapancreatic and retroperitoneal mass appeared to consist predominantly of old, partially liquefied blood clots. Liquefaction of necrotic tissue occasionally proceeded extremely slowly over a period of months. In no patient, up to a maximal lapse of 13 months, was liquefaction complete at the time of exploration. Of the 76 consecutive patients with massive retroperitoneal necrosis, managed by delayed and often frequent debridement, 2 patients (2.6%) died. An occasional patient had significant necrosis of the pancreas, per se; approximately 90% did not. Necrotic retroperitoneal adipose tissue or associated hematoma may prove quite toxic, but was sometimes well tolerated over a prolonged period. The advent of secondary infection leads rapidly to toxemia and, possibly, to an increased rate of liquefaction.
Similar content being viewed by others
References
Howard JM (1989) Delayed debridement (necrosectomy) and external drainage of massive pancreatic or peripancreatic necrosis. Surg Gynecol Obstet 168:25–29
McFadden DW, Reber HA (1994) Indications for surgery in severe acute pancreatitis. Int J Pancreatol 15:83–90
Buchler M, Uhl W, Isenmann R, Bittner R, Beger HG (1993) Necrotizing pancreatitis: Necrosectomy and closed continuous lavage of the lesser sac. In: Beger HG, Buchler M, Malfertheiner P (eds) Standards in pancreatic surgery, Springer, Berlin Heidelberg New York Tokyo, pp 191–202
Bradley EL III (1993) Open packing for infected pancreatic necrosis. In: Beger HG, Buchler M, Malfertheiner P (eds) Standards in pancreatic surgery. Springer, Berlin Heidelberg New York Tokyo, pp 220–232
Bassi C, Fontana R, Vesentini S, Cavallini G, Marchiori L, Falconi M, Corra S, Pederzoli P (1991) Antibacterial and mezlocillin-enhancing activity of pure human pancreatic fluid. Int J Pancreatol 10:293–297
Howard JM, Wagner SM (1989) Pancreatography after recovery from massive pancreatic necrosis. Ann Surg 209:31–35
Nordback I, Pessi T, Auvinen O, Autio V (1985) Determination of necrosis in necrotizing pancreatitis. Br J Surg 72:225–227
Nordback I, Lauslahti K (1986) Clinical pathology of acute necrotizing pancreatitis. J Clin Pathol 39:68–74
Leger L, Chiche B, Louvel A (1977) Necrosis in acute pancreatitis. Surgical and anatomopathological comparisons. Seven cases. Nouv Pres Med 6:337–340
Johnson LB, Rattner DW, Warshaw AL (1991) The effect of size of giant pancreatic pseudocysts on the outcome of internal drainage procedures. Surg Gynecol Obstet 174:171–174
Madry S, Fromm D (1994) Infected retroperitoneal fat necrosis associated with acute pancreatitis. J Am Coll Surg 178:277–282
Bradley EL III (1987) Management of infected pancreatic necrosis by open drainage. Ann Surg 206:542–550
Casey JE, Porter KA, Langevin RE, Banks PA (1993) Clinical features and natural history of central cavitary necrosis. Pancreas 8:141–145
Author information
Authors and Affiliations
About this article
Cite this article
Howard, J.M. Studies of acute pancreatitis with retroperitoneal necrosis: “The suet syndrome”. Improvements in patient survival. J Hep Bil Pancr Surg 3, 195–202 (1996). https://doi.org/10.1007/BF02391015
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF02391015