Splenic infarction and infectious diseases in Korea.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
02 Dec 2020
Historique:
received: 21 07 2020
accepted: 22 11 2020
entrez: 3 12 2020
pubmed: 4 12 2020
medline: 15 12 2020
Statut: epublish

Résumé

The spleen contains immune cells and exhibits a pattern of infarction different from other organs; as such, splenic infarction (SI) may provide important clues to infection. However, the nature of the relationship between SI and infectious disease(s) is not well understood. Accordingly, this retrospective study investigated the relationship between SI and infection. Hospital records of patients with SI, who visited Inha University Hospital (Incheon, Republic of Korea) between January 2008 and December 2018, were reviewed. Patient data regarding clinical presentation, causative pathogens, risk factors, and radiological findings were collected and analyzed. Of 353 patients with SI, 101 with infectious conditions were enrolled in this study, and their data were analyzed to identify associations between SI and infection. Ten patients were diagnosed with infective endocarditis (IE), and 26 exhibited bacteremia without IE. Twenty-seven patients experienced systemic infection due to miscellaneous causes (negative result on conventional automated blood culture), including the following intracellular organisms: parasites (malaria [n = 12], babesiosis [n = 1]); bacteria (scrub typhus [n = 5]); viruses (Epstein-Barr [n = 1], cytomegalovirus [n = 1]); and unidentified pathogen[s] (n = 7). Splenomegaly was more common among patients with miscellaneous systemic infection; infarction involving other organs was rare. Thirty-eight patients had localized infections (e.g., respiratory, intra-abdominal, or skin and soft tissue infection), and most (35 of 38) had other risk factors for SI. In this study, various infectious conditions were found to be associated with SI, and intracellular organisms were the most common causative pathogens. Further studies are needed to examine other possible etiologies and the underlying pathophysiological mechanisms.

Sections du résumé

BACKGROUND BACKGROUND
The spleen contains immune cells and exhibits a pattern of infarction different from other organs; as such, splenic infarction (SI) may provide important clues to infection. However, the nature of the relationship between SI and infectious disease(s) is not well understood. Accordingly, this retrospective study investigated the relationship between SI and infection.
METHODS METHODS
Hospital records of patients with SI, who visited Inha University Hospital (Incheon, Republic of Korea) between January 2008 and December 2018, were reviewed. Patient data regarding clinical presentation, causative pathogens, risk factors, and radiological findings were collected and analyzed.
RESULTS RESULTS
Of 353 patients with SI, 101 with infectious conditions were enrolled in this study, and their data were analyzed to identify associations between SI and infection. Ten patients were diagnosed with infective endocarditis (IE), and 26 exhibited bacteremia without IE. Twenty-seven patients experienced systemic infection due to miscellaneous causes (negative result on conventional automated blood culture), including the following intracellular organisms: parasites (malaria [n = 12], babesiosis [n = 1]); bacteria (scrub typhus [n = 5]); viruses (Epstein-Barr [n = 1], cytomegalovirus [n = 1]); and unidentified pathogen[s] (n = 7). Splenomegaly was more common among patients with miscellaneous systemic infection; infarction involving other organs was rare. Thirty-eight patients had localized infections (e.g., respiratory, intra-abdominal, or skin and soft tissue infection), and most (35 of 38) had other risk factors for SI.
CONCLUSIONS CONCLUSIONS
In this study, various infectious conditions were found to be associated with SI, and intracellular organisms were the most common causative pathogens. Further studies are needed to examine other possible etiologies and the underlying pathophysiological mechanisms.

Identifiants

pubmed: 33267828
doi: 10.1186/s12879-020-05645-9
pii: 10.1186/s12879-020-05645-9
pmc: PMC7708890
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

915

Références

Curr Rheumatol Rep. 2018 Aug 20;20(10):62
pubmed: 30123926
J Glob Infect Dis. 2014 Apr;6(2):86-8
pubmed: 24926171
Circulation. 1999 Jul 27;100(4):e20-8
pubmed: 10421626
Blood. 2003 Jun 15;101(12):4823-7
pubmed: 12609841
Clin Infect Dis. 2000 Apr;30(4):633-8
pubmed: 10770721
Am Surg. 1998 Feb;64(2):182-8
pubmed: 9486895
J Lab Clin Med. 1998 Jan;131(1):77-83
pubmed: 9452130
Surgery. 1986 Oct;100(4):743-50
pubmed: 3764696
Lancet. 2002 Mar 2;359(9308):753-9
pubmed: 11888586
Dig Surg. 2000;17(4):354-7
pubmed: 11053942
Thromb Haemost. 1995 Feb;73(2):223-30
pubmed: 7792734
Blood. 2004 Feb 15;103(4):1342-7
pubmed: 14576054
Infect Immun. 2015 Dec;83(12):4772-80
pubmed: 26416903
Medicine (Baltimore). 2015 Sep;94(36):e1363
pubmed: 26356690
Pediatr Infect Dis J. 2013 Apr;32(4):415-6
pubmed: 23271442
J Clin Virol. 2005 Mar;32(3):245-7
pubmed: 15722031
Neth J Med. 2012 Apr;70(3):114-20
pubmed: 22516575
Eur J Clin Microbiol Infect Dis. 2002 Jan;21(1):63-4
pubmed: 11913506
Lancet. 2002 May 25;359(9320):1819-27
pubmed: 12044378
Infect Immun. 2002 Feb;70(2):631-41
pubmed: 11796592
Prog Cardiovasc Dis. 1979 Nov-Dec;22(3):169-80
pubmed: 388518
Semin Thromb Hemost. 2013 Jul;39(5):559-66
pubmed: 23625756
Trans R Soc Trop Med Hyg. 2014 Aug;108(8):455-60
pubmed: 24942899
Infect Dis (Lond). 2020 Mar;52(3):177-185
pubmed: 31718355
Glycobiology. 2016 Nov;26(11):1222-1234
pubmed: 27037304
J Pharmacol Exp Ther. 2002 Mar;300(3):729-35
pubmed: 11861775
J Gastrointest Surg. 2016 Mar;20(3):656-61
pubmed: 26160320
Malar J. 2017 Jan 28;16(1):51
pubmed: 28129766
Radiology. 1984 Jun;151(3):723-9
pubmed: 6718733
Clin Infect Dis. 2008 Jan 1;46(1):e8-11
pubmed: 18171204
Ann Med. 2018 Sep;50(6):494-500
pubmed: 29929401
PLoS Pathog. 2014 Dec 04;10(12):e1004540
pubmed: 25474103
Infection. 2013 Aug;41(4):867-73
pubmed: 23696110

Auteurs

Jae Hyoung Im (JH)

Division of Infectious Diseases, Department of Internal Medicine, Inha University School of Medicine, Incheon, 22212, Republic of Korea.

Moon-Hyun Chung (MH)

Department of Internal Medicine, Seogwipo Medical Center, Jeju-do, Republic of Korea.

Hye-Jin Lee (HJ)

Translation Research Center, Inha University School of Medicine, Incheon, Republic of Korea.

Hea Yoon Kwon (HY)

Division of Infectious Diseases, Department of Internal Medicine, Inha University School of Medicine, Incheon, 22212, Republic of Korea.

Ji Hyeon Baek (JH)

Division of Infectious Diseases, Department of Internal Medicine, Inha University School of Medicine, Incheon, 22212, Republic of Korea.

Ji-Hun Jang (JH)

Department of Hospital Medicine, Inha University School of Medicine, Incheon, 22212, Republic of Korea. haijinn@naver.com.

Jin-Soo Lee (JS)

Division of Infectious Diseases, Department of Internal Medicine, Inha University School of Medicine, Incheon, 22212, Republic of Korea. ljinsoo16@gmail.com.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH