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| CASE SERIES |
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| Year : 2020 | Volume
: 66
| Issue : 2 | Page : 99-101 |
Fulminant amebic colitis: An unusual postoperative complication of intraabdominal malignancy
S Misra1, P Sakhuja1, AK Agarwal2, A Javed2
1 Department of Pathology, GB Pant Institute of Post Graduate Medical Education and Research, New Delhi, India
2 Department of Gastrointestinal Surgery, GB Pant Institute of Post Graduate Medical Education and Research, New Delhi, India
| Date of Submission | 29-Oct-2019 |
| Date of Decision | 23-Nov-2019 |
| Date of Acceptance | 21-Feb-2020 |
| Date of Web Publication | 01-Apr-2020 |
Correspondence Address:
P Sakhuja
Department of Pathology, GB Pant Institute of Post Graduate Medical Education and Research, New Delhi
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/jpgm.JPGM_605_19
Amebiasis caused by protozoa Entamoeba histolytica (EH) is the third leading parasitic cause of human mortality. Although amebiasis is endemic in India, only about 10% of the infected individuals manifest disease. Clinical spectrum of amebiasis ranges from asymptomatic colonization to amebic colitis to hemorrhagic and fulminant colitis. Factors causing an invasive infection are not completely understood. Pathogen virulence, host immunity, and ability of the pathogen to evade host immune response play vital role in determining the disease course. Host factors such as immunocompromised states may make an individual susceptible to develop symptomatic infection. Malignancies usually result in chronic debilitation which may make the individual prone to develop invasive amebiasis with rapid progression. We report two cases of invasive amebiasis which developed a fulminant course in the immediate postoperative period after abdominal surgeries for visceral malignancies.
Keywords: Entamoeba histolytica, fulminant colitis, gastrointestinal pathology, invasive amebiasis
How to cite this article:
Misra S, Sakhuja P, Agarwal A K, Javed A. Fulminant amebic colitis: An unusual postoperative complication of intraabdominal malignancy. J Postgrad Med 2020;66:99-101 |
How to cite this URL:
Misra S, Sakhuja P, Agarwal A K, Javed A. Fulminant amebic colitis: An unusual postoperative complication of intraabdominal malignancy. J Postgrad Med [serial online] 2020 [cited 2023 Mar 27];66:99-101. Available from: https://www.jpgmonline.com/text.asp?2020/66/2/99/280154 |
| :: Introduction | |  |
Amebiasis caused by Entamoeba histolytica (EH) is the third leading parasitic cause of human mortality after malaria and schistosomiasis, causing up to 100,000 deaths annually.[1] Amebiasis is endemic in India, affecting about 15% of the population.[2] However, only about 10% of the infected individuals manifest disease.[2] Clinical spectrum of amebiasis ranges from asymptomatic colonization to fulminant colitis.
Factors causing an invasive infection are not completely understood; ability of the parasite to lyse surface enterocytes is key feature. Studies on pathogenesis of invasive amebic colitis (IAC) focus on pathogen virulence, host immunity, and ability of the pathogen to evade host immune response.[3] There is an increased occurrence of IAC among HIV positive persons, institutionalized individuals, sexually active homosexual males, and organ transplant recipients indicating that immunocompromised states may make an individual susceptible to develop symptomatic infection.[4]
Although invasive amebiasis is quite common in endemic regions, fulminant progression is rare, carrying a grave prognosis with over 40% mortality.[2] Fulminant amebic colitis (FAC) presents as acute abdomen requiring prompt surgical intervention. Since FAC may not have the typical history of diarrhea with bloody mucous and mimics other conditions such as ischemic bowel disease, inflammatory bowel disease (IBD), and colonic malignancy, a high index of suspicion is needed for a correct preoperative diagnosis.[5] We report two cases of FAC developing post-surgery for abdominal malignancies.
| :: Case Presentation | | |
Case 1
A 48-year-old male underwent pancreatico-duodenectomy for carcinoma head of pancreas. Antibiotic prophylaxis for anaerobic coverage (injectable metronidazole, 500 mg thrice daily) was given in the postoperative period. Patient developed high-grade fever 2 weeks post-surgery along with abdomen pain; he presented to the emergency with vomiting and abdominal distension on postoperative day 18. Computed tomography (CT) abdomen revealed dilated terminal ileum and colonic loops [Figure 1]a and patient was taken up for emergency laparotomy. Laboratory parameters revealed mild anemia, neutrophilic leukocytosis, and raised erythrocyte sedimentation rate (hemoglobin of 9 g/dl, TLC of 17,000/cu.mm with 80% neutrophils). Intraoperatively, there was hemorrhagic fluid in the peritoneal cavity. Ascending colon was gangrenous with perforations; anastomotic site of pancreatico-duodenectomy was healthy. A right hemicolectomy with ileostomy was performed. Grossly, the ileal mucosa was viable while cecum and ascending colon were gangrenous with serosal exudates [Figure 1]b. Microscopy of involved segments revealed transmural necrosis with numerous amebic trophozoites within the granulation tissue [Figure 2]a. Few mesenteric veins showed occlusion by fibrin thrombi and collections of amebic trophozoites [Figure 2]b. A diagnosis of FAC with venous thrombi was given. Patient was started on intravenous metronidazole (800 mg thrice daily) for 2 weeks. Patient's condition improved; he was taken out of ventilator support and extubated on day 7 of treatment. | Figure 1: (a) Computed tomography of abdomen showing dilated terminal ileum and colonic loops with evidence of mild colitis (yellow arrow); (b) Gross photograph of jumbled up mass of gangrenous colon with necrotic ulcers (white arrow)
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 | Figure 2: (a) Amebic trophozoites within granulation tissue, few showing erythro-phagocytosis; black arrow (HE, 400×); (b) Amebic trophozoites around mesenteric vessel; thin black arrow (PAS, 200×)
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Case 2
A 61-year-old female underwent radical cholecystectomy with distal gastrectomy for carcinoma gallbladder with duodenal involvement. Patient was started on injectable metronidazole (500 mg) for anaerobic coverage. On postoperative day 4, she developed septicemia. CT abdomen showed evidence of gangrenous changes in the right colon for which exploratory laparotomy was performed. Intraoperatively, the ascending colon was gangrenous; patient underwent a right hemicolectomy and ileostomy for the same. Microscopic examination revealed transmural hemorrhagic necrosis of the entire colonic segment [Figure 3]a. Aggregates of amebic trophozoites were noted within the necrotic mucosa and serosal exudates [Figure 3]b. A diagnosis of FAC was rendered. Patient was restarted on injectable metronidazole (800 mg thrice daily); however, she expired two days post colectomy. | Figure 3: (a) Transmural inflammation with dense active serositis; dotted line (HE, 40×); (b) Serosal aggregates of amebic trophozoites; black arrow (PAS, 100×); amebic trophozoites in inset (PAS, 400×)
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| :: Discussion | | |
FAC is life-threatening, resulting in massive bowel necrosis with perforation and peritonitis or toxic megacolon. A fatal outcome might occur due to both parasite and host-related factors. More virulent strains effectively evade host immunity by inhibiting T-regulatory cells and pro-inflammatory cytokines and produce greater amount of proteases to disrupt the protective intestinal mucous barrier.[3] Gut microbiota is altered (enriched in Prevotella copri) in individuals manifesting IAC with aggressive course.[6] Host-related factors include co-morbidities like IBD with corticosteroid therapy, HIV, co-infection with cytomegalovirus or clostridium difficile, prior surgeries, transplant, and use of immunomodulatory drugs. Infancy, age more than 60 years, male gender, pregnancy, diabetes mellitus, alcoholism, and immunosuppressed states are factors associated with higher mortality in FAC.[4] Clinical and biochemical parameters including signs of peritonitis, low leucocyte count (< 1.5 × 103/μl), hypokalemia, hyponatremia, and hypoalbuminemia have been indicated to be high-risk factors in one study, although only hypokalemia has been verified to be significant.[7] Conservative surgery and nonsurgical medical management have shown poor survival rates in FAC.
Nisheena et al.[8] reported a definite preoperative diagnosis of FAC in only 1 out of 6 cases, while in the study by Chaturvedi et al.,[5] 5 out of 30 cases were diagnosed before surgery. Gross findings include mucosal ulceration, bowel necrosis, and serosal exudates; classic flask shape ulcers are usually not identified. Mesenteric vessel thromboses were noted in 3 cases by Chaturvedi et al.[5] FAC is rare and may not present with classic symptoms of IAC; thus, definite preoperative diagnosis is seldom made.[9] The presence of abundant eosinophilic necrosis with nuclear debris and paucity of inflammatory cells should raise suspicion for amebiasis and prompt the pathologist to hunt for amebic trophozoites. Special stains like Periodic acid Schiff (PAS) or phosphotungstic acid hematoxylin (PTAH) and multiple deeper serial cuts may be employed, if necessary. Histological evidence of transmural invasion of EH trophozoites, abundant tissue necrosis, intestinal perforation, and mesenteric vessel thrombi are associated with increased mortality; these features were seen in both of our cases.
Complex host-pathogen interactions lead to the varied clinical spectrum of amebiasis. The cause for the development of fulminant progression is attributed to both amebic virulence factors and impaired host immune response. Malignancy leads to chronic debilitation and lowered immunity. Major intraabdominal surgery for visceral malignancy can further diminish immune functioning, making the individual susceptible to develop IAC with rapid progression. Incidence of FAC is higher in endemic countries due to high frequency of asymptomatic intestinal carriage; latent infections are also known to become invasive in a setting of impaired host immunity.[5] Both case 1 and 2 developed FAC in the immediate postoperative period. Therefore, it is possible that in both cases, the symptoms of amebiasis were masked by that of the malignancies or they had a quiescent infection which got activated with the additional stress of surgery leading to a fulminant course. Although prophylactic antibiotic coverage in the form of injectable metronidazole was given to both patients in the initial postoperative period, yet they developed FAC. In endemic regions, it might be important to workup patients preoperatively for amebiasis (both amebic serology and stool microscopy) to avoid fatality in such cases. Clinical studies are needed to establish the correct dose of anti-amebic cover (in addition to the routine antibiotic prophylaxis before major intraabdominal surgery) in susceptible individuals.
Declaration of patient consent
The authors certify that appropriate patient consent was obtained.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
| :: References | | |
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| 4. | Nagata N, Shimbo T, Akiyama J, Nakashima R, Nishimura S, Yada T, et al. Risk factors for intestinal invasive amebiasis in Japan, 2003-2009. Emerg Infect Dis 2012;18:717-24. |
| 5. | Chaturvedi R, Gupte PA, Joshi AS. Fulminant amoebic colitis: A clinicopathological study of 30 cases. Postgrad Med J 2015;91:200-5. |
| 6. | Gilchrist CA, Petri SE, Schneider BN, Reichman DJ, Jiang N, Begum S, et al. Role of the gut microbiota of children in diarrhea due to the protozoan parasite entamoeba histolytica. J Infect Dis 2016;213:1579-85. |
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| 8. | Nisheena R, Ananthamurthy A, Inchara YK. Fulminant amebic colitis: A study of six cases. Indian J Pathol Microbiol 2009;52:370-3. [ PUBMED] [Full text] |
| 9. | Takahashi T, Gamboa-Dominguez A, Gomez-Mendez TJ, Remes JM, Rembis V, Martinez-Gonzalez D, et al. Fulminant amebic colitis: Analysis of 55 cases. Dis Colon Rectum 1997;40:1362-7. |
[Figure 1], [Figure 2], [Figure 3]
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