Neutropenic Enterocolitis: New Insights Into a Deadly Entity

Neutropenic enterocolitis (NE) is a deadly ileocecal-based disease seen in patients with a recent history of chemotherapy. As histology is not included in the current diagnostic criteria, the pathologic features of NE are poorly understood. We undertook a multi-institutional study of NE, and report...

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Veröffentlicht in:The American journal of surgical pathology 2015-12, Vol.39 (12), p.1635-1642
Hauptverfasser: Sachak, Taha, Arnold, Michael A, Naini, Bita V, Graham, Rondell P, Shah, Sejal S, Cruise, Michael, Park, Jason Y, Clark, Lindsey, Lamps, Laura, Frankel, Wendy L, Theodoropoulos, Nicole, Arnold, Christina A
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container_end_page 1642
container_issue 12
container_start_page 1635
container_title The American journal of surgical pathology
container_volume 39
creator Sachak, Taha
Arnold, Michael A
Naini, Bita V
Graham, Rondell P
Shah, Sejal S
Cruise, Michael
Park, Jason Y
Clark, Lindsey
Lamps, Laura
Frankel, Wendy L
Theodoropoulos, Nicole
Arnold, Christina A
description Neutropenic enterocolitis (NE) is a deadly ileocecal-based disease seen in patients with a recent history of chemotherapy. As histology is not included in the current diagnostic criteria, the pathologic features of NE are poorly understood. We undertook a multi-institutional study of NE, and report helpful clinical clues, such as immunosuppression (n=20/20), recent chemotherapy (n=17/18), neutropenia (n=16/18) gastrointestinal symptoms (n=19/19), abnormal imaging studies of the cecum/right colon (n=11/14), and positive microbiological studies (n=13/15). Fever (n=9/15) and sepsis (n=8/16) were also common. Pathologically, the cecum/right colon was always involved (n=17/17), but findings were identified in other bowel segments as well. NE lesions consisted of patchy necrosis (n=18/20), infiltrating organisms (n=17/20), hemorrhage (n=15/20), ulcer (n=15/19), edema (n=15/20), and depletion of inflammatory cells (n=15/20). Seventy-nine percent (n=15/19) of patients with histologically confirmed NE died47% (n=7/15) of these deaths were attributed to NE and the remainder to the patients’ underlying conditions. Importantly, we observed a clinical diagnostic discordancy rate of 35% (n=9/26)15% (n=3/20) of histologically confirmed NE were clinically unsuspected, and 26% (n=6/23) of clinically suspected NE represented a different disease process. Alternative diagnoses included unspecified colitis, infection, graft-versus-host disease, relapsed malignancy, mycophenolate injury, appendicitis, and ischemia. The causes of death in patients with NE mimics included unrecognized appendicitis and unrecognized graft-versus-host disease. To improve diagnostic accuracy, we propose that histology be required for a diagnosis of “definitive NE,” with other clinically suspicious cases reported as “suspicious for NE” until all other possible diagnoses have been reasonably excluded.
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As histology is not included in the current diagnostic criteria, the pathologic features of NE are poorly understood. We undertook a multi-institutional study of NE, and report helpful clinical clues, such as immunosuppression (n=20/20), recent chemotherapy (n=17/18), neutropenia (n=16/18) gastrointestinal symptoms (n=19/19), abnormal imaging studies of the cecum/right colon (n=11/14), and positive microbiological studies (n=13/15). Fever (n=9/15) and sepsis (n=8/16) were also common. Pathologically, the cecum/right colon was always involved (n=17/17), but findings were identified in other bowel segments as well. NE lesions consisted of patchy necrosis (n=18/20), infiltrating organisms (n=17/20), hemorrhage (n=15/20), ulcer (n=15/19), edema (n=15/20), and depletion of inflammatory cells (n=15/20). Seventy-nine percent (n=15/19) of patients with histologically confirmed NE died47% (n=7/15) of these deaths were attributed to NE and the remainder to the patients’ underlying conditions. Importantly, we observed a clinical diagnostic discordancy rate of 35% (n=9/26)15% (n=3/20) of histologically confirmed NE were clinically unsuspected, and 26% (n=6/23) of clinically suspected NE represented a different disease process. Alternative diagnoses included unspecified colitis, infection, graft-versus-host disease, relapsed malignancy, mycophenolate injury, appendicitis, and ischemia. The causes of death in patients with NE mimics included unrecognized appendicitis and unrecognized graft-versus-host disease. 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Importantly, we observed a clinical diagnostic discordancy rate of 35% (n=9/26)15% (n=3/20) of histologically confirmed NE were clinically unsuspected, and 26% (n=6/23) of clinically suspected NE represented a different disease process. Alternative diagnoses included unspecified colitis, infection, graft-versus-host disease, relapsed malignancy, mycophenolate injury, appendicitis, and ischemia. The causes of death in patients with NE mimics included unrecognized appendicitis and unrecognized graft-versus-host disease. 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As histology is not included in the current diagnostic criteria, the pathologic features of NE are poorly understood. We undertook a multi-institutional study of NE, and report helpful clinical clues, such as immunosuppression (n=20/20), recent chemotherapy (n=17/18), neutropenia (n=16/18) gastrointestinal symptoms (n=19/19), abnormal imaging studies of the cecum/right colon (n=11/14), and positive microbiological studies (n=13/15). Fever (n=9/15) and sepsis (n=8/16) were also common. Pathologically, the cecum/right colon was always involved (n=17/17), but findings were identified in other bowel segments as well. NE lesions consisted of patchy necrosis (n=18/20), infiltrating organisms (n=17/20), hemorrhage (n=15/20), ulcer (n=15/19), edema (n=15/20), and depletion of inflammatory cells (n=15/20). Seventy-nine percent (n=15/19) of patients with histologically confirmed NE died47% (n=7/15) of these deaths were attributed to NE and the remainder to the patients’ underlying conditions. 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subjects Adolescent
Adult
Aged
Aged, 80 and over
Biopsy
Child
Child, Preschool
Diagnosis, Differential
Diagnostic Errors
Enterocolitis, Neutropenic - etiology
Enterocolitis, Neutropenic - mortality
Enterocolitis, Neutropenic - pathology
Enterocolitis, Neutropenic - therapy
Female
Humans
Intestines - diagnostic imaging
Intestines - pathology
Intestines - surgery
Male
Middle Aged
Predictive Value of Tests
Prognosis
Risk Factors
Tomography, X-Ray Computed
United States
Young Adult
title Neutropenic Enterocolitis: New Insights Into a Deadly Entity
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