Peritonitis differential diagnosis: Difference between revisions

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==Differential Diagnosis==
==Differential Diagnosis==
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{| border="2" cellpadding="4" cellspacing="0" style="margin: 1em 1em 1em 0; background: #f9f9f9; border: 1px #aaa solid; border-collapse: collapse;
|+'''Differentiating Secondary peritonitis from other causes of peritonitis'''
! colspan="2" style="background: #4479BA; text-align: center;" | {{fontcolor|#FFF| '''Disease'''}}
! colspan="2" style="background: #4479BA; text-align: center;" | {{fontcolor|#FFF| '''Disease'''}}
!colspan="1" style="background: #4479BA; text-align: center;" | {{fontcolor|#FFF| '''Findings'''}}
! colspan="1" style="background: #4479BA; text-align: center;" | {{fontcolor|#FFF| '''Prominent clinical findings'''}}
! colspan="1" style="background: #4479BA; text-align: center;" | {{fontcolor|#FFF| '''Lab tests'''}}
! colspan="1" style="background: #4479BA; text-align: center;" | {{fontcolor|#FFF| '''Tratment'''}}
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| rowspan="3" |'''[[Primary peritonitis]]'''
| rowspan="3" |'''Primary peritonitis'''
|'''[[Primary peritonitis|Spontaneous bacterial peritonitis]]'''
|'''[[Primary peritonitis|Spontaneous bacterial peritonitis]]'''
|Absence of GI [[perforation]], most closely associated with [[cirrhosis]] and advanced liver disease. Presents with abrupt onset of [[fever]], [[abdominal pain]], [[distension]], and [[rebound tenderness]]. Most have clinical and biochemical manifestations of advanced [[cirrhosis]] or [[nephrosis]] like [[leukocytosis]],[[hypoalbuminemia]], a prolonged [[prothrombin]] time. SAAG >1.1 g/dL, ↑s.lactic acid level, or a ↓ascitic fluid pH (< 7.31) supports the diagnosis. Gram staining reveals bacteria in only 25% of cases . Diagnosed by analysis of the ascitic fluid which reveals [[WBC]] > 500/ML, and [[PMN]] >250cells/ml. Culture of ascitic fluid inoculated immediately into [[blood culture]] media at the bedside usually reveals a single [[enteric]] organism, most commonly ''[[Escherichia coli]]'', ''[[Klebsiella]]'', or [[streptococci]]. Once diagnosed,it is treated with [[Ceftriaxone]].
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* Absence of GI [[perforation]], most closely associated with [[cirrhosis]] and [[Liver disease|advanced liver disease]].  
* Presents with abrupt onset of [[fever]], [[abdominal pain]], [[distension]], and [[rebound tenderness]].  
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* Most have clinical and biochemical manifestations of advanced [[cirrhosis]] or [[nephrosis]] like [[leukocytosis]],[[hypoalbuminemia]],  
* a prolonged [[prothrombin]] time. SAAG >1.1 g/dL, increased serum [[lactic acid]] level, or a decreased [[Ascites|ascitic fluid]] pH (< 7.31) supports the diagnosis. [[Gram staining]] reveals bacteria in only 25% of cases.
* Diagnosed by analysis of the [[Ascitic|ascitic fluid]] which reveals [[WBC]] > 500/ML, and [[PMN]] >250cells/ml.  
* [[Culture medium|Culture]] of ascitic fluid inoculated immediately into [[blood culture]] media at the bedside usually reveals a single [[Enteric Bacilli|enteric organism]], most commonly ''[[Escherichia coli]]'', ''[[Klebsiella]]'', or [[streptococci]].  
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* Once diagnosed,it is treated with [[Ceftriaxone]].
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|'''[[Tuberculous peritonitis]]'''
|'''[[Tuberculous peritonitis]]'''
|Seen in 0.5% of new cases of [[tuberculosis]] particularly in young women in endemic areas as a primary infection. Presents with [[abdominal pain]] and [[distension]], [[fever]], [[night sweats]], [[weight loss]], and altered bowel habits. [[Ascites]] is present in about half of cases. Abdominal mass may be felt in a third of cases. The peritoneal fluid is characterized by a [[protein]] concentration > 3 g/dL with < 1.1 g/dL SAAG and [[lymphocyte]] predominance of [[WBC]]. Definitive diagnosis in 80% of cases is by culture. Most patients presenting acutely are diagnosed only by [[laparotomy]]. Combination antituberculosis chemotherapy is preferred in chronic cases.
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* Seen in 0.5% of new cases of [[tuberculosis]] particularly in young women in endemic areas as a primary infection.
* Presents with [[abdominal pain]] and [[distension]], [[fever]], [[night sweats]], [[weight loss]], and altered bowel habits.  
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* [[Ascites]] is present in about half of cases. [[Abdominal mass]] may be felt in a third of cases. The [[peritoneal fluid]] is characterized by a [[protein]] concentration > 3 g/dL with < 1.1 g/dL SAAG and [[Lymphocyte|lymphocyte predominance]] of [[WBC]].  
* Definitive diagnosis in 80% of cases is by culture. Most patients presenting acutely are diagnosed only by [[laparotomy]].
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* Combination [[Antituberculosis|antituberculosis chemotherapy]] is preferred in chronic cases.
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|'''[[CAPD peritonitis]]'''
|'''[[Continuous ambulatory peritoneal dialysis|Continuous Ambulatory Peritoneal Dialysis]]''' [[Continuous ambulatory peritoneal dialysis|('''CAPD peritonitis)''']]
|Peritonitis is one of the major complications of [[peritoneal dialysis]] & 72.6% occurred within the first six months of peritoneal dialysis. Historically, [[coagulase-negative staphylococci]] were the most common cause of peritonitis in CAPD, presumably due to touch contamination or infection via the pericatheter route. Majority of peritonitis cases are caused by bacteria(50%-due to [[Gram-positive bacteria|gram positive]] organisms, 15% to [[gram negative]] organisms,20% were culture negative.2% of cases are caused by fungi, mostly [[Candida]] species. Polymicrobial infection in 4%.Exit-site infection was present in 13% and a peritoneal fluid leak in 3 % and M.tuberculosis 0.1%. Treatment for [[peritoneal dialysis]]-associated peritonitis consists of antimicrobial therapy, in some cases catheter removal is also warranted. Additional therapies for relapsing or recurrent peritonitis may include fibrinolytic agents and peritoneal lavage. Most episodes of peritoneal dialysis-associated peritonitis resolve with outpatient antibiotic treatment. Initial empiric antibiotic coverage for peritoneal dialysis-associated peritonitis consists of coverage for [[gram-positive]] organisms (by [[vancomycin]] or a first-generation [[cephalosporin]]) and [[gram-negative]] organisms (by a third-generation [[cephalosporin]] or an [[aminoglycoside]]). Subsequently, the regimen should be adjusted based on culture and sensitivity data. Cure rates are approximately 75%.
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* [[Peritonitis]] is one of the major complications of [[peritoneal dialysis]] & 72.6% occurred within the first six months of [[peritoneal dialysis]].  
* Historically, [[coagulase-negative staphylococci]] were the most common cause of peritonitis in [[Continuous ambulatory peritoneal dialysis|CAPD]], presumably due to touch contamination or infection via the pericatheter route.  
* Treatment for [[peritoneal dialysis]]-associated peritonitis consists of [[Antimicrobial drug|antimicrobial therapy]], in some cases catheter removal is also warranted.
* Additional therapies for [[Peritonitis|relapsing or recurrent peritonitis]] may include [[Fibrinolytic agent|fibrinolytic agents]] and [[peritoneal lavage]]. Most episodes of peritoneal dialysis-associated peritonitis resolve with outpatient [[Antibiotic|antibiotic treatment]].
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* Majority of [[peritonitis]] cases are caused by [[bacteria]] (50%-due to [[Gram-positive bacteria|gram positive]] organisms, 15% to [[gram negative]] organisms,20% were culture negative.2% of cases are caused by [[fungi]], mostly [[Candida]] species. Polymicrobial infection in 4%.Exit-site infection was present in 13% and a [[peritoneal fluid]] leak in 3 % and [[M.tuberculosis]] 0.1%.
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* [[Antibiotic|Initial empiric antibiotic coverage]] for peritoneal dialysis-associated peritonitis consists of coverage for [[gram-positive]] organisms (by [[vancomycin]] or a [[Cephalosporins|first-generation cephalosporin]]) and [[gram-negative]] organisms (by a [[cephalosporin|third-generation cephalosporin]] or an [[aminoglycoside]]). Subsequently, the regimen should be adjusted based on [[Culture medium|culture]] and [[sensitivity]] data. Cure rates are approximately 75%.
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| rowspan="2" |'''[[Acute bacterial secondary peritonitis|Secondary peritonitis]]'''
| rowspan="2" |'''[[Secondary peritonitis]]'''
|'''[[Acute bacterial secondary peritonitis]]'''
|'''Acute [[bacterial]] [[secondary peritonitis]]'''
|Occurs after perforating, penetrating, inflammatory, infectious, or [[ischemic]] injuries of the GI or GU tracts. Most often follows disruption of a hollow viscus→chemical peritonitis→bacterial peritonitis(polymicrobial, includes [[aerobic]] [[gram negative]] {[[E coli]], [[Klebsiella]], [[Enterobacter]], [[Proteus mirabilis]]} and gram positive { [[Enterococcus]], [[Streptococcus]]} and [[anaerobes]] {[[Bacteroides]], [[clostridia]]}). Presents with [[abdominal pain]], [[tenderness]], [[guarding]] or [[rigidity]], [[distension]], free peritoneal air, and diminished [[bowel sounds]]—signs that reflect irritation of the parietal peritoneum resulting [[ileus]]. Systemic findings include [[fever]], [[chills]] or [[rigors]], [[tachycardia]], [[sweating]], [[tachypnea]], [[restlessness]], [[dehydration]], [[oliguria]], [[disorientation]], and, ultimately, refractory [[shock]]. [[Peritoneal lavage]], [[Laparoscopy]] are the treatment of choice.
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* Occurs after perforating, penetrating, inflammatory, infectious, or [[ischemic]] injuries of the GI or GU tracts. Most often follows disruption of a hollow viscus→chemical peritonitis→bacterial peritonitis(polymicrobial, includes [[aerobic]] [[gram negative]] {[[E coli]], [[Klebsiella]], [[Enterobacter]], [[Proteus mirabilis]]} and gram positive { [[Enterococcus]], [[Streptococcus]]} and [[anaerobes]] {[[Bacteroides]], [[clostridia]]}).  
* Presents with [[abdominal pain]], [[tenderness]], [[guarding]] or rigidity, [[distension]], free peritoneal air, and diminished [[bowel sounds]]. Signs that reflect irritation of the parietal peritoneum resulting [[ileus]]. Systemic findings include [[fever]], [[chills]] or [[rigors]], [[tachycardia]], [[sweating]], [[tachypnea]], [[restlessness]], [[dehydration]], [[oliguria]], [[disorientation]], and, ultimately, refractory [[shock]].  
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* [[Peritoneal lavage]], [[Laparoscopy]] are the treatment of choice.
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|'''[[Biliary peritonitis]]'''
|'''[[Biliary]] [[Secondary peritonitis|peritonitis]]'''
|Most often seen in cases of rupture of pathological [[gallbladder]] or [[bile duct]] or [[cholangitic abscess]] or secondary to obstruction of  the biliary tract.Seen in alcoholic patients with [[ascites]].
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* Most often seen in cases of rupture of pathological [[gallbladder]] or [[bile duct]] or [[Cholangitis|cholangitic abscess]] or secondary to obstruction of  the [[biliary tract]].
* Seen in alcoholic patients with [[ascites]].
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| colspan="2" |'''[[Tertiary peritonitis]]'''
| colspan="2" |'''[[Peritonitis|Tertiary peritonitis]]'''
|Persistence or recurrence of intraabdominal infection following apparently adequate therapy of primary or secondary peritontits.Enterococcus,Candida, Staphylococcus epidermidis, and Enterobacter being the most common organisms.Characterized by lack of response to appropriate surgical and antibiotic therapy due to disturbance in the hosts immune response. Associated with high mortality due to multi organ dysfunction. It presents in a similar way as other peritonitis but is recognized as an adverse outcome with poor prognosis.
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* Persistence or recurrence of [[Infection|intraabdominal infection]] following apparently adequate therapy of [[Peritonitis|primary or secondary peritonitis]].
* Associated with [[Mortality|high mortality]] due to multi organ dysfunction. It presents in a similar way as other [[peritonitis]] but is recognized as an adverse outcome with poor prognosis.
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* [[Enterococcus]], [[Candida]], [[Staphylococcus epidermidis]], and [[Enterobacter]] being the most common organisms.
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* Characterized by lack of response to appropriate surgical and [[antibiotic therapy]] due to disturbance in the hosts [[immune response]].
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| colspan="2" |'''[[Familial Mediterranean fever (periodic peritonitis, familial paroxysmal polyserositis)]]'''
| colspan="2" |'''[[Familial mediterranean fever|Familial Mediterranean fever (periodic peritonitis, familial paroxysmal polyserositis)]]'''
|Rare genetic condition which affects individuals of Mediterranean genetic background.Etiology is unclear.Presents with recurrent bouts of abdominal pain and tenderness along with pleuritic or joint pain. Fever and leukocytosis are common. Colchicine prevents but does not treat acute attacks.
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* Rare [[Genetic disorder|genetic condition]] which affects individuals of Mediterranean genetic background.  
* Etiology is unclear.
* Presents with recurrent bouts of [[abdominal pain]] and [[tenderness]] along with [[pleuritic]] or [[joint pain]]. [[Fever]] and [[leukocytosis]] are common.  
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* [[Colchicine]] prevents but does not treat acute attacks.
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| colspan="2" |'''[[Granulomatous peritonitis]]'''
| colspan="2" |'''[[Granulomatous peritonitis]]'''
|A rare condition caused by disposable surgical fabrics or food particles from a perforated ulcer, eliciting a vigorous granulomatous (delayed hypersensitivity) response in some patients 2-6 weeks after laparotomy. Presents with abdominal pain, fever, nausea and vomiting, ileus, and systemic complaints, mild and diffuse abdominal tenderness. Diagnosed by the demonstration of diagnostic Maltese cross pattern of starch particles.Treated with corticosteroids or anti-inflammatory agents. The disease is self-liniting.
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* A rare condition caused by disposable surgical fabrics or food particles from a [[perforated ulcer]], eliciting a vigorous [[granulomatous]] ([[Hypersensitivity|delayed hypersensitivity]]) response in some patients 2-6 weeks after [[laparotomy]].  
* Presents with [[abdominal pain]], [[fever]], [[nausea and vomiting]], [[ileus]], and systemic complaints, mild and diffuse [[abdominal tenderness]].  
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* Diagnosed by the demonstration of diagnostic Maltese cross pattern of starch particles.
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* The disease is self-limiting.
* Treated with [[corticosteroids]] or [[Anti inflammatory medications|anti-inflammatory agents]].
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| colspan="2" |'''[[Sclerosing encapsulating peritonitis]]'''
| colspan="2" |'''[[Sclerosing encapsulating peritonitis]]'''
|Seen in conditions associated with long term peritoneal dialysis, shunts like VP & PV, history of abdominal surgeries, liver transplantation. Symptoms include nausea, abdominal pain, diarrhea, anorexia, bloody ascites.
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* Seen in conditions associated with long term [[peritoneal dialysis]], shunts like [[Ventriculoperitoneal shunt|VP shunts]], history of [[Abdominal surgery|abdominal surgeries]], [[liver transplantation]].  
* Symptoms include [[nausea]], [[abdominal pain]], [[diarrhea]], [[anorexia]], bloody [[ascites]].
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| colspan="2" |'''[[Intraperitoneal abscesses]]'''
| colspan="2" |'''[[Abscess|Intraperitoneal abscesses]]'''
|Most common etiologies being Gastrointestinal perforations, postoperative complications, and penetrating injuries. Signs and symptoms depend on the location of the abscess within the peritoneal cavity and the extent of involvement of the surrounding structures.Diagnosis is suspected in any patient with a predisposing condition.In a third of cases it occurs as a sequela of generalized peritonitis.The pathogenic organisms are similar to those responsible for peritonitis, but anaerobic organisms occupy an important role.Diagnosed best by CT scan of the abdomen. Treatment consists of prompt and complete CT or US guided drainage of the abscess, control of the primary cause, and adjunctive use of effective antibiotics. Open drainage is reserved for abscesses for which percutaneous drainage is inappropriate or unsuccessful.The mortality rate of serious intra-abdominal abscesses is about 30%.
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* Most common etiologies being [[Perforation|Gastrointestinal perforations]], postoperative complications, and penetrating injuries.  
* Signs and symptoms depend on the location of the [[abscess]] within the [[peritoneal cavity]] and the extent of involvement of the surrounding structures.
* Diagnosis is suspected in any patient with a predisposing condition. In a third of cases it occurs as a sequela of [[Peritonitis|generalized peritonitis]].  
* The pathogenic organisms are similar to those responsible for [[peritonitis]], but [[anaerobic]] organisms occupy an important role.
* The [[mortality rate]] of serious [[Abscesses|intra-abdominal abscesses]] is about 30%.
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* Diagnosed best by [[CT-scans|CT]] scan of the abdomen.
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* Treatment consists of prompt and complete [[CT]] or [[Ultrasound|US]] guided drainage of the [[abscess]], control of the primary cause, and adjunctive use of effective [[Antibiotics|antibiotics.]] Open drainage is reserved for [[abscesses]] for which percutaneous drainage is inappropriate or unsuccessful.
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| colspan="2" |'''[[Peritoneal mesothelioma]]'''
| colspan="2" |'''[[Peritoneal mesothelioma]]'''
|Arises from the mesothelium lining the peritoneal cavity. Its incidence is approximately 300-500 new cases being diagnosed in the United States each year.  As with pleural mesothelioma, there is an association with an asbestos exposure.Most commonly affects men at the age of 50-69 years. Patients most often present with abdominal pain and later increased abdominal girth and ascites along with anorexia, weight loss and abdominal pain.CT with intravenous contrast typically demonstrates the thickening of the peritoneum.Laparoscopy with tissue biopsy or CT guided tissue biopsy with immunohistochemical staining for calretinin, cytokeratin 5/6, mesothelin, and Wilms tumor 1 antigen remain the gold standard for diagnosis. Mean time from diagnosis to death is less than 1 year without treatment.  At laparotomy the goal is cytoreduction with excision.Debulking surgery and intraperitoneal chemotherapy improves survival in some cases.
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* Arises from the [[mesothelium]] lining the [[peritoneal cavity]].  
* Its incidence is approximately 300-500 new cases being diagnosed in the United States each year.  As with [[pleural mesothelioma]], there is an association with an [[Asbestos|asbestos exposure]].
* Most commonly affects men at the age of 50-69 years. Patients most often present with [[abdominal pain]] and later increased abdominal girth and [[ascites]] along with [[anorexia]], [[weight loss]] and [[abdominal pain]].  
* Mean time from diagnosis to death is less than 1 year without treatment. 
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* [[Computed tomography|CT]] with [[Contrast|intravenous contrast]] typically demonstrates the thickening of the [[peritoneum]]. [[Laparoscopy]] with tissue biopsy or CT guided tissue biopsy with [[immunohistochemical staining]] for [[calretinin]], [[cytokeratin|cytokeratin 5/6]], [[mesothelin]], and [[WT1|Wilms tumor 1 antigen]] remain the [[Gold standard (test)|gold standard]] for diagnosis.
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* At [[laparotomy]] the goal is cytoreduction with [[excision]]. Debulking surgery and intraperitoneal [[chemotherapy]] improves survival in some cases.
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| colspan="2" |'''[[peritoneal carcinomatosis]]'''
| colspan="2" |'''[[peritoneal carcinomatosis]]'''
|Associated with a history of ovarian or GI tract malignancy.Symptoms include ascites,abdominal pain,nausea,vomiting.
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* Associated with a history of [[ovarian]] or [[Malignancy|GI tract malignancy]].
* Symptoms include [[ascites]], [[abdominal pain]], [[nausea]], [[vomiting]].
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Latest revision as of 12:48, 1 May 2017

Peritonitis Main Page

Patient Information

Overview

Causes

Classification

Spontaneous Bacterial Peritonitis
Secondary Peritonitis

Differential Diagnosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Shivani Chaparala M.B.B.S [2]

Overview

Differential Diagnosis

Differentiating Secondary peritonitis from other causes of peritonitis
Disease Prominent clinical findings Lab tests Tratment
Primary peritonitis Spontaneous bacterial peritonitis
Tuberculous peritonitis
Continuous Ambulatory Peritoneal Dialysis (CAPD peritonitis)
Secondary peritonitis Acute bacterial secondary peritonitis
Biliary peritonitis
Tertiary peritonitis
Familial Mediterranean fever (periodic peritonitis, familial paroxysmal polyserositis)
  • Colchicine prevents but does not treat acute attacks.
Granulomatous peritonitis
  • Diagnosed by the demonstration of diagnostic Maltese cross pattern of starch particles.
Sclerosing encapsulating peritonitis
Intraperitoneal abscesses
  • Diagnosed best by CT scan of the abdomen.
  • Treatment consists of prompt and complete CT or US guided drainage of the abscess, control of the primary cause, and adjunctive use of effective antibiotics. Open drainage is reserved for abscesses for which percutaneous drainage is inappropriate or unsuccessful.
Peritoneal mesothelioma
peritoneal carcinomatosis

References

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