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==Overview==
==Overview==
Typhlitis is most commonly seen in [[Neutropenic fever|neutropenic]] patients receiving [[chemotherapy]] for a cancer. It is also been seen in people with [[aplastic anemia]], [[lymphoma]], [[Acquired immunodeficiency syndrome|acquired immunodeficiency]] [[syndrome]], as well as people who have had a [[Kidney transplant|kidney transplan]]<nowiki/>t. Typhlitis is distinguished by [[edema]] and [[inflammation]] of the [[cecum]], [[ascending colon]], and, in some cases, [[terminal ileum]]. Transmural [[necrosis]], [[perforation]], and [[mortality]] can occur as a result of the [[inflammation]]. The exact cause of the condition is unknown, but it is most likely caused by a combination of [[ischemia]], infection (particularly with [[cytomegalovirus]]), [[mucosal]] [[hemorrhage]], and possibly [[neoplastic]] [[Infiltration (medical)|infiltration]]. [[Bowel]] rest, [[total parenteral nutrition]], antibiotics, and aggressive fluid and [[electrolyte]] replacement are all part of the treatment.  
Typhlitis is most commonly seen in [[Neutropenic fever|neutropenic]] patients receiving [[chemotherapy]] for a cancer. It is also been seen in people with [[aplastic anemia]], [[lymphoma]], [[Acquired immunodeficiency syndrome|acquired immunodeficiency]] [[syndrome]], as well as people who have had a [[Kidney transplant|kidney transplan]]<nowiki/>t. Typhlitis is distinguished by [[edema]] and [[inflammation]] of the [[cecum]], [[ascending colon]], and, in some cases, [[terminal ileum]]. Transmural [[necrosis]], [[perforation]], and [[mortality]] can occur as a result of the [[inflammation]]. The exact cause of the condition is unknown, but it is most likely caused by a combination of [[ischemia]], infection (particularly with [[cytomegalovirus]]), [[mucosal]] [[hemorrhage]], and possibly [[neoplastic]] [[Infiltration (medical)|infiltration]]. The treatment includes [[bowel]] rest, [[parenteral nutrition]], [[antibiotics]], and intensive fluid and [[electrolyte]] replacement.  
==Historical Perspective==
==Historical Perspective==
In 1970, Wagner et al found and described typhlitis as [[necrotizing]] [[colitis]] after [[autopsy]]<nowiki/>ing 191 [[leukemic]] children with terminal illness at the Texas Children's Hospital, Baylor College of Medicine, Houston, between 1958 and 1970.<ref>{{cite journal|doi=10.1002/1097-0142}}</ref>
In 1970, Wagner et al found and described typhlitis as [[necrotizing]] [[colitis]] after [[autopsy]]<nowiki/>ing 191 [[leukemic]] children with terminal illness at the Texas Children's Hospital, Baylor College of Medicine, Houston, between 1958 and 1970.<ref>{{cite journal|doi=10.1002/1097-0142}}</ref>
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==Pathophysiology==
==Pathophysiology==


*The exact [[pathogenesis]] of [[neutropenic]] [[enterocolitis]] is not fully understood.
*The precise [[pathophysiology]] of [[Neutropenic sepsis|neutropenic]] [[enterocolitis]] is unknown.
*[[Intestinal]] [[mucosal]] damage, [[Neutropenia|neutropenia,]] and the [[immunocompromised]] status of the afflicted patients appear to be the key factors in disease initiation.
*The primary variables in illness beginning appear to be [[intestinal]] [[mucosal]] injury, [[Neutropenia causes|neutropenia]], and the [[immunocompromised]] status of the patients.  
*[[Intestinal|Intestinal edema]], engorged [[veins]], and a disturbed [[mucosal]] surface result from these early circumstances, making the [[mucosa]] more prone to [[bacterial]] intramural invasion.
*These early circumstances cause intestinal edema, engorged veins, and a disrupted mucosal surface, making the mucosa more susceptible to bacterial intramural invasion.
*The [[intestinal]] [[motility]] is affected by the distension and [[necrosis]] caused directly by [[chemotherapeutic agents]].
*The [[distension]] and [[necrosis]] generated by [[Chemotherapy agents|chemotherapy]] drugs directly influence [[intestinal]] motility.  
*Superimposed [[infections]] caused by [[bacteria]],[[fungi]] and [[viruses]] can also disrupts the already damaged [[mucosa]] leading further [[intestinal]] [[edema]],distension and [[necrosis]] of [[intestinal]] layer which lead to [[intestinal]] [[perforation]].<ref name="pmid19646645">{{cite journal| author=Cloutier RL| title=Neutropenic enterocolitis. | journal=Emerg Med Clin North Am | year= 2009 | volume= 27 | issue= 3 | pages= 415-22 | pmid=19646645 | doi=10.1016/j.emc.2009.04.002 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19646645  }}</ref>
*Superimposed [[infections]] caused by [[bacteria]],[[fungi]] and [[viruses]] can also disrupts the already damaged [[mucosa]] leading further [[intestinal]] [[edema]],distension and [[necrosis]] of [[intestinal]] layer which lead to [[intestinal]] [[perforation]].<ref name="pmid19646645">{{cite journal| author=Cloutier RL| title=Neutropenic enterocolitis. | journal=Emerg Med Clin North Am | year= 2009 | volume= 27 | issue= 3 | pages= 415-22 | pmid=19646645 | doi=10.1016/j.emc.2009.04.002 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19646645  }}</ref>
*[[Gram-negative]] rods, [[gram-positive cocci]], [[enterococci]], [[fungi]], and [[viruses]] have all been blamed for the outbreak.<ref name="pmid28104979">{{cite journal| author=Rodrigues FG, Dasilva G, Wexner SD| title=Neutropenic enterocolitis. | journal=World J Gastroenterol | year= 2017 | volume= 23 | issue= 1 | pages= 42-47 | pmid=28104979 | doi=10.3748/wjg.v23.i1.42 | pmc=5221285 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28104979  }}</ref><ref name="pmid31869058">{{cite journal| author=| title=StatPearls | journal= | year= 2021 | volume=  | issue=  | pages=  | pmid=31869058 | doi= | pmc= | url= }}</ref>
*[[Gram-negative]] rods, [[gram-positive cocci]], [[enterococci]], [[fungi]], and [[viruses]] have all been blamed for the outbreak.<ref name="pmid28104979">{{cite journal| author=Rodrigues FG, Dasilva G, Wexner SD| title=Neutropenic enterocolitis. | journal=World J Gastroenterol | year= 2017 | volume= 23 | issue= 1 | pages= 42-47 | pmid=28104979 | doi=10.3748/wjg.v23.i1.42 | pmc=5221285 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28104979  }}</ref><ref name="pmid31869058">{{cite journal| author=| title=StatPearls | journal= | year= 2021 | volume=  | issue=  | pages=  | pmid=31869058 | doi= | pmc= | url= }}</ref>

Revision as of 23:52, 28 June 2021

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: neutropenic colitis; neutropenic enterocolitis; cecitis

Overview

Typhlitis is most commonly seen in neutropenic patients receiving chemotherapy for a cancer. It is also been seen in people with aplastic anemia, lymphoma, acquired immunodeficiency syndrome, as well as people who have had a kidney transplant. Typhlitis is distinguished by edema and inflammation of the cecum, ascending colon, and, in some cases, terminal ileum. Transmural necrosis, perforation, and mortality can occur as a result of the inflammation. The exact cause of the condition is unknown, but it is most likely caused by a combination of ischemia, infection (particularly with cytomegalovirus), mucosal hemorrhage, and possibly neoplastic infiltration. The treatment includes bowel rest, parenteral nutrition, antibiotics, and intensive fluid and electrolyte replacement.

Historical Perspective

In 1970, Wagner et al found and described typhlitis as necrotizing colitis after autopsying 191 leukemic children with terminal illness at the Texas Children's Hospital, Baylor College of Medicine, Houston, between 1958 and 1970.[1]

Classification

There is no established system for the classification of Typhlitis.

Pathophysiology

Causes by Organ System

Cardiovascular No underlying causes
Chemical/Poisoning No underlying causes
Dental No underlying causes
Dermatologic No underlying causes
Drug Side Effect Doxorubicin Hydrochloride, Sulfasalazine
Ear Nose Throat No underlying causes
Endocrine No underlying causes
Environmental No underlying causes
Gastroenterologic No underlying causes
Genetic No underlying causes
Hematologic No underlying causes
Iatrogenic No underlying causes
Infectious Disease No underlying causes
Musculoskeletal/Orthopedic No underlying causes
Neurologic No underlying causes
Nutritional/Metabolic No underlying causes
Obstetric/Gynecologic No underlying causes
Oncologic No underlying causes
Ophthalmologic No underlying causes
Overdose/Toxicity No underlying causes
Psychiatric No underlying causes
Pulmonary No underlying causes
Renal/Electrolyte No underlying causes
Rheumatology/Immunology/Allergy No underlying causes
Sexual No underlying causes
Trauma No underlying causes
Urologic No underlying causes
Miscellaneous No underlying causes

Causes in Alphabetical Order

Differentiating Typhlitis from other Diseases

Typhlitis must be distinguished from other diseases characterized by fever, abdominal pain, and diarrhea. Before diagnosing this condition, some diseases with similar clinical manifestations should be ruled out.

  1. Clostridium difficile infection[5]
  2. Cytomegalovirus colitis[6]
  3. Norovirus infection[7]
  4. Graft versus host disease[8]
  5. Acute appendicitis[9]
  6. Ischemic colitis[10]

Epidemiology and Demographics

Risk Factors

Common risk factors in the development of Typhlitis include hematological, solid tumors, neutropenic and Immunocompromised individuals.[14]

Screening

There is insufficient evidence to recommend routine screening for neutropenic enterocolitis.

Natural History, Complications, and Prognosis

Diagnosis

Neutropenic enterocolitis

Neutropenic enterocolitis is typically diagnosed based on a combination of clinical and radiological findings.

Diagnostic Study of Choice

There are no established criteria for the diagnosis of typhlitis.

History and Symptoms

The most common symptoms of typhlitis include fever, abdominal pain, and diarrhea. In severe cases, diarrhea can be bloody. Abdominal distension and paralytic ileus may also occur in patients.

Physical Examination

Common physical examination of patients with neutropenic enterocolitis is usually remarkable for Abdominal discomfort which can be diffuse or localized, with the right lower quadrant being the most common location. A rigid abdomen could be an indication of bowel perforation.[17]

Laboratory Findings

Laboratory findings consistent with the diagnosis of typhlitis include neutropenia with absolute neutrophil count <500 cells/microL, thrombocytopenia ranged from 4000/pl to 120,000/pl.[18]

Electrocardiogram

There are no ECG findings associated with typhlitis

Echocardiography

There are no echocardiography associated with neutropenic colitis.

X-ray

An x-ray may be helpful in the diagnosis of Typhlitis but nonspecific. Findings on an x-ray suggestive of Neutropenic enterocolitis include inflated cecum with dilated small bowel loops, can detect free air.[19]

CT Abdomen


Other Imaging Findings/Ultrasound Abdomen

Ultrasound (US) may be helpful in the diagnosis of neutropenic enterocolitis. Findings on an ultrasound suggestive of neutropenic enterocolitis include circumferential wall thickening and prominent submucosa .[21]

Life Threatening Causes

Life-threatening causes include conditions such as pneumatosis, pneumoperitoneum, and pericolic fluid collections is important because they indicate a need for urgent surgical management

Treatment

Medical Therapy

Surgery

Primary Prevention

Effective measures for the primary prevention of Neutropenic enterocolitis include early detection and treatment can help to avoid problems and improve outcomes in patients who have undergone intensive chemotherapy or a stem cell transplant.

Secondary Prevention

Effective measures for the secondary prevention include early surgical evaluation in the management of this condition, as it can be life-saving for some patients who present with a complicated neutropenic enterocolitis

References

  1. . doi:10.1002/1097-0142. Missing or empty |title= (help)
  2. Cloutier RL (2009). "Neutropenic enterocolitis". Emerg Med Clin North Am. 27 (3): 415–22. doi:10.1016/j.emc.2009.04.002. PMID 19646645.
  3. Rodrigues FG, Dasilva G, Wexner SD (2017). "Neutropenic enterocolitis". World J Gastroenterol. 23 (1): 42–47. doi:10.3748/wjg.v23.i1.42. PMC 5221285. PMID 28104979.
  4. "StatPearls".   ( ). 2021:  . PMID 31869058.
  5. Czepiel J, Dróżdż M, Pituch H, Kuijper EJ, Perucki W, Mielimonka A; et al. (2019). "Clostridium difficile infection: review". Eur J Clin Microbiol Infect Dis. 38 (7): 1211–1221. doi:10.1007/s10096-019-03539-6. PMC 6570665 Check |pmc= value (help). PMID 30945014.
  6. Pillet S, Pozzetto B, Roblin X (2016). "Cytomegalovirus and ulcerative colitis: Place of antiviral therapy". World J Gastroenterol. 22 (6): 2030–45. doi:10.3748/wjg.v22.i6.2030. PMC 4726676. PMID 26877608.
  7. "StatPearls". 2021. PMID 31335045.
  8. Ramachandran V, Kolli SS, Strowd LC (2019). "Review of Graft-Versus-Host Disease". Dermatol Clin. 37 (4): 569–582. doi:10.1016/j.det.2019.05.014. PMID 31466596.
  9. Bhangu A, Søreide K, Di Saverio S, Assarsson JH, Drake FT (2015). "Acute appendicitis: modern understanding of pathogenesis, diagnosis, and management". Lancet. 386 (10000): 1278–1287. doi:10.1016/S0140-6736(15)00275-5. PMID 26460662.
  10. Theodoropoulou A, Koutroubakis IE (2008). "Ischemic colitis: clinical practice in diagnosis and treatment". World J Gastroenterol. 14 (48): 7302–8. doi:10.3748/wjg.14.7302. PMC 2778113. PMID 19109863.
  11. Gorschlüter M, Mey U, Strehl J, Ziske C, Schepke M, Schmidt-Wolf IG; et al. (2005). "Neutropenic enterocolitis in adults: systematic analysis of evidence quality". Eur J Haematol. 75 (1): 1–13. doi:10.1111/j.1600-0609.2005.00442.x. PMID 15946304.
  12. Aksoy DY, Tanriover MD, Uzun O, Zarakolu P, Ercis S, Ergüven S; et al. (2007). "Diarrhea in neutropenic patients: a prospective cohort study with emphasis on neutropenic enterocolitis". Ann Oncol. 18 (1): 183–189. doi:10.1093/annonc/mdl337. PMID 17023562.
  13. Nesher L, Rolston KV (2013). "Neutropenic enterocolitis, a growing concern in the era of widespread use of aggressive chemotherapy". Clin Infect Dis. 56 (5): 711–7. doi:10.1093/cid/cis998. PMID 23196957.
  14. Biasoli, I; Nucci, M; Spector, N; Portugal, R; Domingues, A; Pulcheri, W (1997). "Risk factors for typhlitis". Oncology Reports. doi:10.3892/or.4.5.1029. ISSN 1021-335X.
  15. Gorschlüter M, Mey U, Strehl J, Ziske C, Schepke M, Schmidt-Wolf IG; et al. (2005). "Neutropenic enterocolitis in adults: systematic analysis of evidence quality". Eur J Haematol. 75 (1): 1–13. doi:10.1111/j.1600-0609.2005.00442.x. PMID 15946304.
  16. Wade DS, Nava HR, Douglass HO (1992). "Neutropenic enterocolitis. Clinical diagnosis and treatment". Cancer. 69 (1): 17–23. doi:10.1002/1097-0142(19920101)69:1<17::aid-cncr2820690106>3.0.co;2-x. PMID 1727660.
  17. Nesher, L.; Rolston, K. V. I. (2012). "Neutropenic Enterocolitis, a Growing Concern in the Era of Widespread Use of Aggressive Chemotherapy". Clinical Infectious Diseases. 56 (5): 711–717. doi:10.1093/cid/cis998. ISSN 1058-4838.
  18. . doi:10.1002/1097-0142. Missing or empty |title= (help)
  19. Wade DS, Nava HR, Douglass HO (1992). "Neutropenic enterocolitis. Clinical diagnosis and treatment". Cancer. 69 (1): 17–23. doi:10.1002/1097-0142(19920101)69:1<17::aid-cncr2820690106>3.0.co;2-x. PMID 1727660.
  20. Kirkpatrick, Iain D. C.; Greenberg, Howard M. (2003). "Gastrointestinal Complications in the Neutropenic Patient: Characterization and Differentiation with Abdominal CT". Radiology. 226 (3): 668–674. doi:10.1148/radiol.2263011932. ISSN 0033-8419.
  21. Tamburrini, Stefania; Setola, Francesca Rosa; Belfiore, Maria Paola; Saturnino, Pietro Paolo; Della Casa, Maria Gabriella; Sarti, Giuseppe; Abete, Roberta; Marano, Ines (2018). "Ultrasound diagnosis of typhlitis". Journal of Ultrasound. 22 (1): 103–106. doi:10.1007/s40477-018-0333-2. ISSN 1876-7931.
  22. Freifeld AG, Bow EJ, Sepkowitz KA, Boeckh MJ, Ito JI, Mullen CA; et al. (2011). "Clinical practice guideline for the use of antimicrobial agents in neutropenic patients with cancer: 2010 update by the infectious diseases society of america". Clin Infect Dis. 52 (4): e56–93. doi:10.1093/cid/cir073. PMID 21258094.
  23. Salazar R, Solá C, Maroto P, Tabernero JM, Brunet J, Verger G; et al. (1999). "Infectious complications in 126 patients treated with high-dose chemotherapy and autologous peripheral blood stem cell transplantation". Bone Marrow Transplant. 23 (1): 27–33. doi:10.1038/sj.bmt.1701520. PMID 10037047.
  24. Shamberger RC, Weinstein HJ, Delorey MJ, Levey RH (1986). "The medical and surgical management of typhlitis in children with acute nonlymphocytic (myelogenous) leukemia". Cancer. 57 (3): 603–9. doi:10.1002/1097-0142(19860201)57:3<603::aid-cncr2820570335>3.0.co;2-k. PMID 3484659.