Minireviews Open Access
Copyright ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Aug 16, 2021; 9(23): 6674-6685
Published online Aug 16, 2021. doi: 10.12998/wjcc.v9.i23.6674
Acute acalculous cholecystitis due to infectious causes
Ioulia Markaki, Department of Emergency, General Hospital of Kythira “Trifyllio”, Kythira 80200, Greece
Afroditi Konsoula, Department of Emergency, General Hospital of Mytilene "Vostaneio", Lesvos 81132, Greece
Lamprini Markaki, Department of Pediatrics, "Agia Sofia" Children's Hospital, Athens 11527, Greece
Nikolaos Spernovasilis, School of Medicine, University of Crete, Heraklion 71003, Greece
Marios Papadakis, Department of Surgery II, University of Witten-Herdecke, Wuppertal 40235, NRW, Germany
ORCID number: Ioulia Markaki (0000-0003-4861-336X); Afroditi Konsoula (0000-0002-1868-1559); Lamprini Markaki (0000-0003-3786-9706); Nikolaos Spernovasilis (0000-0002-6981-8535); Marios Papadakis (0000-0002-9020-874X).
Author contributions: Spernovasilis N and Papadakis M put forward the learning concept; Markaki I, Konsoula A, Spernovasilis N and Papadakis M designed the manuscript; Markaki I, Konsoula A and Markaki L did the literature search and drafted the manuscript; all authors reviewed and approved the final draft of the manuscript.
Conflict-of-interest statement: The authors declare no conflict of interest.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Marios Papadakis, MD, MSc, PhD, Research Scientist, Surgeon, Department of Surgery II, University of Witten-Herdecke, 40 Heusnerstrasse, Wuppertal 40235, NRW, Germany. marios_papadakis@yahoo.gr
Received: March 28, 2021
Peer-review started: March 28, 2021
First decision: April 28, 2021
Revised: May 8, 2021
Accepted: July 5, 2021
Article in press: July 5, 2021
Published online: August 16, 2021
Processing time: 130 Days and 5.4 Hours

Abstract

Acute acalculous cholecystitis (AAC) is an inflammation of the gallbladder not associated with the presence of gallstones. It usually occurs in critically ill patients but it has also been implicated as a cause of cholecystitis in previously healthy individuals. In this subgroup of patients, infectious causes comprise the primary etiology. We, herein, discuss the pathophysiological mechanisms involved in AAC, focusing on the infectious causes. AAC associated with critical medical conditions is caused by bile stasis and gallbladder ischemia. Several mechanisms are reported to be involved in AAC in patients without underlying critical illness including direct invasion of the gallbladder epithelial cells, gallbladder vasculitis, obstruction of the biliary tree, and sequestration. We emphasize that multiple pathogenic mechanisms may concurrently contribute to the development of AAC in varying degrees. Awareness of the implicated pathogens is essential since it will allow a more focused examination of the histopathological specimens. In conclusion, additional research and a high degree of clinical suspicion are needed to clarify the complex spectrum of mechanisms that are involved in the pathogenesis of AAC.

Key Words: Cholecystitis; Infectious causes; Vasculitis; Sequestration; Epstein-Barr virus

Core Tip: The most important mechanisms involved in acute acalculous cholecystitis in patients without underlying critical illness are direct invasion of the gallbladder epithelial cells, gallbladder vasculitis, obstruction of the biliary tree, and sequestration. Awareness of the implicated pathogens is essential since it will allow a more focused examination of the histopathological specimens.
INTRODUCTION

Acute acalculous cholecystitis (AAC) is an inflammation of the gallbladder not associated with the presence of gallstones. AAC accounts for approximately 5%-10% of all cases of acute cholecystitis in adults and 50%-70% of cases in the pediatric population[1]. AAC usually occurs in critically ill patients and is most frequently associated with trauma, surgery, shock, burns, sepsis, total parenteral nutrition (TPN) and mechanical ventilation[2]. Moreover, it is related to high mortality rates (30% in most studies) not only because it is an epiphenomenon of the critical illness, but also because it can progress to gangrene, perforation and empyema more frequently than calculous cholecystitis[2]. AAC has also been implicated as a cause of cholecystitis in previously healthy individuals. In this subgroup of patients, infectious causes comprise the primary etiology[1]. Since its first description by Duncan in 1884, numerous pathogens have been identified as causative agents. We, herein, discuss the pathophysiological procedures involved in AAC, focusing on the infectious causes.

PATHOGENESIS

AAC involves several pathological processes that seem to concurrently play a role in the manifestation of the disease. The pathogenesis of AAC, when it directly originates from infectious agents, falls into two main categories: (1) AAC associated with critical medical conditions; and (2) AAC in patients without underlying critical illness. We focus on the second group of patients and categorize the various pathophysiologic mechanisms identified in several reports in the literature concerning a wide range of pathogens. We briefly report the principal mechanisms that are implicated in the first category, as they have been extensively analyzed in previous articles.

ACUTE ACALCULOUS CHOLECYSTITIS ASSOCIATED WITH CRITICAL MEDICAL CONDITIONS
Bile stasis

Bile stasis has been identified to contribute to the pathogenesis of the disease. Prolonged fasting and TPN have both been linked to the formation of biliary sludge due to the absence of cholecystokinin stimulation of the gallbladder[3]. It is noteworthy to mention that according to a 10-year retrospective review, at least 4 wk of TPN were required for bile sludge formation in 50% of patients. By 6 wk, all patients had developed bile sludge[3]. In the pediatric population, congenital malformations (e.g., multiseptated gallbladder, choledochal cyst) interrupt normal bile flow[1]. Moreover, another factor that is related to the concentration of bile is volume depletion, which is commonly seen in critically ill patients[3]. Bile inspissation elevates intraluminal pressure and according to the principle of Laplace (tension = pressure × radius), the wall tension of the organ is increased. Therefore, arterial, lymphatic and venous flow to the gallbladder wall is impaired[4]. Opioid analgesics may further increase intraluminal pressure, because of the spasm of the sphincter of Oddi[3]. Mechanical ventilation with positive end-expiratory pressure (PEEP) is also implicated in the induction of bile stasis. PEEP of 7 to 10 cm H2O increases hepatic venous pressure, which leads to decreased portal perfusion[5]. In addition, bile stasis changes the chemical composition of the bile, directly causing injury to the gallbladder mucosa. For instance, lysophosphatidylcholine, which is found in the bile of patients with acute cholecystitis, has been shown to cause extensive mucosal damage in a dose-dependent manner[6].

Gallbladder ischemia

A second critical mechanism is local ischemia. The gallbladder is quite susceptible to ischemic conditions since the main oxygenated blood supply is from the cystic artery, which is a terminal artery. Various diverse underlying diseases, like trauma, cardiovascular surgeries, septic shock, hypovolemic shock and burns that are identified as etiologic factors of AAC, share tissue hypoxia as the dominant pathophysiologic mechanism. The importance of ischemia in the development of the disease has been proven by Hakala et al[7]. They discovered that microangiographic findings of the gallbladder in acute calculous cholecystitis (ACC) differ from those in AAC. Briefly, microangiography revealed a poor and irregular capillary network in AAC, whereas in ACC a dense vessel network and dilated arterioles were demonstrated.

ACALCULOUS CHOLECYSTITIS IN PATIENTS WITHOUT UNDERLYING CRITICAL ILLNESS

Through an extensive review of cases of AAC in patients without underlying critical illness (Table 1), the main mechanisms that were found to be involved are: Direct invasion of the gallbladder epithelial cells, gallbladder vasculitis, and obstruction of the biliary tree. We will also briefly mention one proposed mechanism, that of sequestration. Epstein-Barr virus (EBV) will be discussed separately since it is the most common causative infectious agent of AAC. Lastly, we will present the available data in the medical literature regarding AAC due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Some of the pathogens mentioned in Table 1 will not be further discussed, as no pathophysiological mechanism was identified.

Table 1 Reported cases of acute acalculous cholecystitis due to infectious causes.
Laboratory investigation
Infectious ACC
Ref.
Age (yr)
Sex
Immunocompromised
Pathogen
CCY
Stool culture
Blood culture
Bile culture
Serology
Histopathology1
Tissue PCR
IHC
Garrido-Benedicto et al[40], 199415M-Salmonella spp.-+NPNPNPNPNPNPPossible
Ruiz-Rebollo et al[41], 200827M-Salmonella enterica-+NPNPNPNPNPNPPossible
Khan et al[42], 200931M-Salmonella enterica-NP+NPNPNPNPNPPossible
Rajan et al[43], 201423F-Salmonella enterica+NP+NPNP+NPNPProbable
Lianos et al[44], 201932M-Salmonella enterica++NP+NPNPNPNPPossible
Mourani et al[9], 199468M-HAV+NPNPNP++NP+Proven
Suresh et al[45], 20092,5F-HAV-NPNPNP+NPNPNPPossible
Prashanth et al[46], 201212F-HAV-NPNPNP+NPNPNPPossible
Kaya et al[47], 201331F-HAV-NPNPNP+NPNPNPPossible
Hinnant et al[10], 198932MHIVCMV, Cryptosporidium spp.+NPNPNPNP+NPNPProven
Hinnant et al[10], 198944MHIVCMV, Cryptosporidium spp.++NPNPNP+NPNPProven
Riediger et al[11], 201360FRenal transplantationCMV+NPNPNP++NP+Proven
Agholi et al[12], 201625FCorticosteroid therapyCystoisospora belli++NPNPNP+NPNPProven
Agholi et al[12], 201635MHIVCystoisospora belli++NPNPNP++NPProven
Agholi et al[14], 201428FHIVSarcocystis spp. ++NPNPNP++NPProven
Zar et al[15], 200135MHIVCyclospora cayetanensis++NPNPNP+NP+Proven
Knapp et al[16], 199637MHIVEnterocytozoon bieneusi++NP+NP+NPNPProven
Shinha et al[17], 201538MHIVHistoplasma capsulatum+NPNP+NP+NPNPProven
Chen et al[18], 200836MHIVMycobacterium tuberculosis+NPNPNPNP+NPNPProven
Takeshita et al[20], 200664M-HBV+NPNPNP++NPNPProbable
Unal et al[48], 200949F-HBV-NPNP+NPNPNPNPPossible
Meier et al[22], 2005NANA-HCV+NPNPNPNP+NPNPProbable
Wright et al[49], 201933M-HCV+NPNPNP++NPNPProbable
Ono et al[23], 201854ΜLymphocytic leukemiaZika virus+NPNPNPNP++NPProven2
Guarner et al[24], 200129F-Leptospira+NPNPNP++NP+Proven
Guarner et al[24], 200160M-Leptospira+NPNPNP++NP+Proven
Walker et al[25], 198571F-Rickettsia rickettsii+NPNPNPNP+NP+Proven
Spernovasilis et al[50], 201754M-Rickettsia typhi-NPNPNP+NPNPNPPossible
Araki et al[28], 201770MImmunosuppressive agentsGiardia lamblia-+NPNPNPNPNPNPProven3
Colle et al[29], 200225F-Echinococcus granulosus+NPNPNP++NPNPProbable
Saha et al[51], 20057F-Plasmodium falciparum-NPNPNP+NPNPNPPossible4
Curley et al[33], 201126M-Plasmodium vivax-NPNPNPNPNPNPNPPossible4
Harris et al[32], 201359M-Plasmodium malariae-NPNPNPNPNPNPNPPossible4
Dinulos et al[35], 19944M-EBV-NPNPNP+NPNPNPPossible
Dinulos et al[35], 199416M-EBV+NPNPNP++NP-Probable
Lagona et al[52], 20074F-EBV-NPNPNP+NPNPNPPossible
Iaria et al[30], 200718F-EBV-NPNPNP+NPNPNPPossible
Prassouli et al[53], 200713F-EBV-NPNPNP+NPNPNPPossible
Attilakos et al[54], 20085M-EBV-NPNPNP+NPNPNPPossible
Gagneux-Brunon et al[55], 201418F-EBV-NPNPNP+NPNPNPPossible
Gagneux-Brunon et al[55], 201420F-EBV-NPNPNP+NPNPNPPossible
Agergaard et al[34], 201434F-EBV-NPNPNP+NPNPNPPossible
Alkhoury et al[56], 201415F-EBV-NPNPNP+NPNPNPPossible
Yesilbag et al[57], 201730F-EBV-NPNPNP+NPNPNPPossible
Ntelis et al[36], 201915F-EBV-NPNPNP+NPNPNPPossible
Alhassan et al[39], 202040F-SARS-CoV-2-NP-NPNPNPNPNPPossible
Andriopoulos et al[58], 200272M-Brucella melitensis+NP++++NPNPProbable
Hariz et al[59], 201962F-Brucella melitensis-NPNPNP+NPNPNPPossible
Figtree et al[60], 201038M-Coxiella burnetii+NPNPNP+++NPProven
Rolain et al[61], 201371M-Coxiella burnetii+NPNPNP++NP-Probable
Wu et al[62], 2003NANA-Dengue fever virus+NPNPNP++NPNPProbable
Marasinghe et al[63], 201029F-Dengue fever virus-NPNPNP+NPNPNPPossible
Hayakawa et al[64], 201172F-Orientia tsutsugamushi-NPNPNP+NPNPNPPossible
Mahapatra et al[65], 201957F-Ehrlichia chaffeensis+NPNPNP+++-Proven
Kurtovic et al[66], 200474FCVIDVZV-NPNPNP+NPNPNPPossible
Udayakumar et al[67], 200935F-Campylobacter jejuni++NPNPNPNPNPNPPossible
West et al[68], 199855F-Vibrio cholerae+NP++NP+NPNPProbable
Szvalb et al[69], 201939FAcute myelocytic leukemiaFusarium spp. -NP++NPNPNPNPPossible
1Histopathology is considered positive if inflammation is present or if the pathogen is identified.
2Zika virus was also identified using electron microscopy.
3Giardia was identified using bile duct brush cytology and biopsy of the hilar bile duct stricture.
4The parasites were detected through peripheral smear.
Proven: Cases in which cholecystectomy was performed, inflammation of the gallbladder was demonstrated, and the causative pathogen of acute acalculous cholecystitis (AAC) was identified using histopathology, polymerase chain reaction (PCR) on tissue specimen or immunohistochemistry (IHC); Probable: Cases in which the causative pathogen of AAC was identified using stool/blood/bile culture or serological methods, cholecystectomy was undertaken and inflammation of the gallbladder was demonstrated, but histopathology, PCR on tissue specimen or IHC were not performed or were negative for pathogens; Possible: Cases in which the causative pathogen of AAC was identified using stool/blood/bile culture or serological methods but cholecystectomy was not performed. CCY: Cholecystectomy; NP: Not performed; NA: Not available; CVID: Common variable immune deficiency; HAV: Hepatitis A virus; CMV: Cytomegalovirus; HIV: Human immunodeficiency virus; HBV: Hepatitis B virus; HCV: Hepatitis C virus; EBV: Epstein-Barr virus; VZV: Varicella zoster virus.
Direct invasion

A large number of pathogens have been shown to directly invade the gallbladder epithelium. Herein, we will include the cases in which the pathogen was identified by molecular techniques and/or histopathological examination of the gallbladder wall. Evidently, this was feasible only for cases where a cholecystectomy was performed. As on multiple occasions a more conservative approach was chosen, we cannot rule out the possibility that other pathogens may share the same pathophysiologic mechanism. Menendez et al[8] demonstrated that Salmonella enterica serovar Typhi has a unique tropism for gallbladder epithelial cells. By using microscopy, they were able to find a high concentration of bacteria both in the lumen and in the tissue. The bacterium was rarely seen within the lamina propria and was confined in the epithelial cells. Additionally, electron micrographs showed intracellular Salmonella undergoing cell division[8]. The routes by which Salmonella was able to access the gallbladder were through the bloodstream, the lymphatic system and by directly ascending from the gastrointestinal tract. Histopathology of the infected gallbladders revealed destruction of the epithelium and massive infiltration of neutrophils along with increased levels of proinflammatory cytokines. It should be emphasized that invasion-deficient bacteria were unable to produce the aforementioned changes, even though they were present in the gallbladder lumen.

Direct invasion was also proved by Mourani et al[9]. They were able to detect hepatitis A virus (HAV) antigen in most gallbladder epithelial cells using immunohistochemical staining. A cell-mediated immunologic response was proposed based on the high number of intraepithelial lymphocytes.

A heterogeneous group of infectious causes leads to acute or chronic acalculous cholecystitis in immunocompromised patients: Cytomegalovirus (CMV)[10,11], Cryptosporidium spp.[10], Isospora belli[12,13], Sarcocystis spp.[14], Cyclospora cayetanensis[15], Enterocytozoon bieneusi[16], Histoplasma capsulatum[17], Mycobacterium tuberculosis[18]. In a retrospective study by French et al[19], it was established that AIDS-related biliary tract disease was most commonly related to CMV and Cryptosporidium spp. The most typical histopathological finding was ulceration and epithelial necrosis. CMV inclusion bodies were found in stromal cells in the base of the ulcers, in the mucosa adjacent to the ulcers and inside the endothelial cells, whereas Cryptosporidium spp. was located on the surface of nonulcerated mucosa[10]. It is thought that the presence of ulcers and the profound mucosal pathology that is observed in these patients is associated with secondary bacterial infection[19]. Agholi et al[12] and Benator et al[13] both reported cases of chronic acalculous cholecystitis associated with Isospora belli. Since these patients had positive stool samples for Isospora belli, the suspected mechanism is that the parasites migrated retrogradely to the gallbladder from a periampullary focus. All developmental stages of the parasite were seen in the cytoplasm of infected epithelial cells, yet none were identified in the lamina propria. Similarly, Sarcocystis spp.[14] and Cyclospora cayetanensis[15] also demonstrated the ability to replicate within the gallbladder epithelial cells.

Vasculitis

Vasculitis is a well-established mechanism through which gallbladder injury can occur. When the gallbladder vasculature is involved, local ischemia leads to cell death and gallbladder necrosis. Necrotizing vasculitis is observed in biopsy specimens of the gallbladder in chronic HBV infection. In a case report by Takeshita et al[20], a patient with hepatitis B-related polyarteritis nodosa (PAN) was presented. PAN represents one of the most typical extrahepatic complications of HBV. Histopathological examination of the gallbladder and liver revealed necrotizing vasculitis with fibrinoid necrosis in medium-sized vessels. Immunohistochemical analysis showed IgG and complement deposition in the inflamed vasculitis lesions. According to the aforementioned changes and the absence of circulating immune complexes, an antibody dependent cell-mediated cytotoxicity or complement-dependent cytotoxicity are regarded as possible mechanisms[20]. It is noteworthy that previous studies had identified immune complexes as one of the key aspects of hepatitis B-related PAN[21]. HCV-induced AAC has rarely been documented. In a case report by Meier et al[22], histologic evaluation was consistent with cryoglobulinemic vasculitis. Nonetheless, the pathogenesis of AAC in chronic HCV infection still remains obscure.

Similar to the other viruses mentioned above, Zika virus was found to cause microangiopathy of the gallbladder vessels in an immunocompromised patient[23]. Ono et al[23] used polymerase chain reaction to detect the virus in the gallbladder tissue and in the bile. Furthermore, through electron microscopy, they identified flavivirus-like particles both in intracellular and extracellular compartments of the vessel.

In leptospirosis, AAC has also been linked to the direct localization of these bacteria in the gallbladder that is accompanied by varying degrees of vasculitis[24]. Immunohistochemistry demonstrated areas of antigen staining in the vessel walls and occasionally in the submucosa. In one case, rare intact bacteria were found[24]. Leptospira infection seems to cause endothelial damage and leakage of vascular fluid leading to gallbladder wall edema. Interestingly, the mucosal epithelium was unremarkable.

Lastly, Rickettsia rickettsii was also found to induce vascular injury and nonocclusive thrombosis leading to AAC[25].

Obstruction

Obstruction of the biliary tract either by intrinsic factors or by extrinsic compression may lead to AAC. This mechanism is most frequently encountered in Ascaris lumbricoides infection. Hepatobiliary ascariasis is rare and is the result of high intestinal parasite load in the host[26]. The worms ascend through the ampulla of Vater, reach the bile duct (choledochal ascariasis) and block the cystic duct orifice. Occasionally, they can invade the gallbladder (gallbladder ascariasis)[27]. The anatomical variants of the biliary tree play a determining role in the migration of the worms inside the gallbladder[26]. In both cases, the intraluminal pressure and the gallbladder wall tension are increased causing ischemia.

Araki et al[28], presented a very unique case of AAC attributed to Giardia lamblia. During the patient’s workup, magnetic resonance cholangiopancreatography revealed a stricture of the hilar bile duct and cystic duct obstruction. A transpapillary bile duct brush cytology and biopsy of the stricture were performed, demonstrating active G. lamblia trophozoites. Subsequently, they proved that the parasite accessed the gallbladder through the ampulla of Vater by performing a duodenal biopsy, which was positive.

In addition, it is speculated that extrinsic cystic duct obstruction can arise from the formation of hydatid cysts during the course of echinococcal disease[29]. Furthermore, portal lymphadenitis from infectious causes, like EBV, has been proposed as a possible pathophysiological mechanism[5,30].

Sequestration

The phenomenon of sequestration has been proposed as a mechanism to explain the pathogenesis of AAC in the context of malaria infections[31]. During Plasmodium falciparum infection, protrusions (knobs) appear on the surface of infected erythrocytes, which cause the infected cells to adhere to each other and to the vessel walls. Once again, this leads to microcirculatory obstruction and ischemia. However, Plasmodium malariae[32] and Plasmodium vivax[33], which have also been documented to cause AAC, have not been shown to form knobs on the surface of erythrocytes.

EBV

EBV is documented as the most prevalent infectious cause of AAC in many reviews. However, the exact pathophysiological mechanism remains obscure, given that the disease is usually self-limited and a conservative treatment is followed. Direct invasion of the gallbladder epithelial cells is a proposed mechanism, as EBV infects oral epithelial cells[34]. In addition, as we mentioned above, other hepatotropic viruses, and specifically HAV, have been detected inside the gallbladder epithelial cells[9]. It should be mentioned that even when a cholecystectomy was performed, in situ hybridization of the tissue did not reveal the virus[35]. Moreover, Ntelis et al[36] speculated that vasculitis is the major underlying mechanism, but further investigation is required to support this hypothesis. Finally, compression of the cystic duct by an enlarged celiac lymph node could explain the development of AAC[30].

SARS-COV-2

AAC has been reported in patients withs SARS-CoV-2, and it is usually associated with critical illness, mechanical ventilation and prolonged TPN[37,38]. However, it has been described a case of a patient with mild coronavirus disease 2019 (COVID-19) who, 14 days later, developed symptoms of AAC[39]. Blood and urine cultures were performed in order to identify other possible etiological pathogens but were negative. Thus, the authors argued that SARS-CoV-2 was the causative agent. The pathogenesis of AAC in the context of COVID-19 infection still remains vastly unknown. It has been well established that SARS-CoV-2 uses the angiotensin-converting enzyme 2 (ACE2) receptor to mediate cellular entry. Direct invasion of the biliary tree and the vascular endothelium of the gallbladder have both been proposed as possible pathophysiological mechanisms, as ACE2 receptor is highly expressed in these structures[38]. It should be noted that in one case where a percutaneous transhepatic gallbladder drainage was performed, SARS-CoV-2 RNA bile sample was negative[37].

CONCLUSION

AAC represents a diverse clinical entity, affecting both healthy and critically ill patients. We must emphasize that multiple pathogenic mechanisms may concurrently contribute to the development of AAC in varying degrees. Awareness of the implicated pathogens is essential since it will allow a more focused examination of the histopathological specimens. In conclusion, additional research and a high degree of clinical suspicion are needed to clarify the complex spectrum of mechanisms that are involved in the pathogenesis of AAC.

Footnotes

Manuscript source: Invited manuscript

Specialty type: Infectious diseases

Country/Territory of origin: Germany

Peer-review report’s scientific quality classification

Grade A (Excellent): 0

Grade B (Very good): B

Grade C (Good): 0

Grade D (Fair): 0

Grade E (Poor): 0

P-Reviewer: Massaro MG S-Editor: Wu YXJ L-Editor: A P-Editor: Li JH

References
1.  Poddighe D, Sazonov V. Acute acalculous cholecystitis in children. World J Gastroenterol. 2018;24:4870-4879.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 44]  [Cited by in F6Publishing: 52]  [Article Influence: 8.7]  [Reference Citation Analysis (0)]
2.  Huffman JL, Schenker S. Acute acalculous cholecystitis: a review. Clin Gastroenterol Hepatol. 2010;8:15-22.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 196]  [Cited by in F6Publishing: 164]  [Article Influence: 11.7]  [Reference Citation Analysis (0)]
3.  Barie PS, Eachempati SR. Acute acalculous cholecystitis. Gastroenterol Clin North Am. 2010;39:343-357.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 170]  [Cited by in F6Publishing: 141]  [Article Influence: 10.1]  [Reference Citation Analysis (1)]
4.  McChesney JA, Northup PG, Bickston SJ. Acute acalculous cholecystitis associated with systemic sepsis and visceral arterial hypoperfusion: a case series and review of pathophysiology. Dig Dis Sci. 2003;48:1960-1967.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 59]  [Cited by in F6Publishing: 60]  [Article Influence: 2.9]  [Reference Citation Analysis (0)]
5.  Barie PS, Eachempati SR. Acute acalculous cholecystitis. Curr Gastroenterol Rep. 2003;5:302-309.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 107]  [Cited by in F6Publishing: 89]  [Article Influence: 4.2]  [Reference Citation Analysis (0)]
6.  Neiderhiser DH. Acute acalculous cholecystitis induced by lysophosphatidylcholine. Am J Pathol. 1986;124:559-563.  [PubMed]  [DOI]  [Cited in This Article: ]
7.  Hakala T, Nuutinen PJ, Ruokonen ET, Alhava E. Microangiopathy in acute acalculous cholecystitis. Br J Surg. 1997;84:1249-1252.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 10]  [Cited by in F6Publishing: 10]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
8.  Menendez A, Arena ET, Guttman JA, Thorson L, Vallance BA, Vogl W, Finlay BB. Salmonella infection of gallbladder epithelial cells drives local inflammation and injury in a model of acute typhoid fever. J Infect Dis. 2009;200:1703-1713.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 77]  [Cited by in F6Publishing: 81]  [Article Influence: 5.4]  [Reference Citation Analysis (0)]
9.  Mourani S, Dobbs SM, Genta RM, Tandon AK, Yoffe B. Hepatitis A virus-associated cholecystitis. Ann Intern Med. 1994;120:398-400.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 48]  [Cited by in F6Publishing: 48]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
10.  Hinnant K, Schwartz A, Rotterdam H, Rudski C. Cytomegaloviral and cryptosporidial cholecystitis in two patients with AIDS. Am J Surg Pathol. 1989;13:57-60.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 19]  [Cited by in F6Publishing: 18]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
11.  Riediger C, Beimler J, Weitz J, Zeier M, Sauer P. Cytomegalovirus infection of the major duodenal papilla in a renal allograft recipient with severe biliary obstruction and acalculous cholecystitis. Transpl Infect Dis. 2013;15:E129-E133.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 7]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
12.  Agholi M, Aliabadi E, Hatam GR.   Cystoisosporiasis-related human acalculous cholecystitis: the need for increased awareness. Pol J Pathol 2016 67: 270-276.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 10]  [Cited by in F6Publishing: 10]  [Article Influence: 1.4]  [Reference Citation Analysis (1)]
13.  Benator DA, French AL, Beaudet LM, Levy CS, Orenstein JM. Isospora belli infection associated with acalculous cholecystitis in a patient with AIDS. Ann Intern Med. 1994;121:663-664.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 58]  [Cited by in F6Publishing: 56]  [Article Influence: 1.9]  [Reference Citation Analysis (0)]
14.  Agholi M, Heidarian HR, Moghadami M, Hatam GR. First detection of acalculous cholecystitis associated with Sarcocystis infection in a patient with AIDS. Acta Parasitol. 2014;59:310-315.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 10]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
15.  Zar FA, El-Bayoumi E, Yungbluth MM. Histologic proof of acalculous cholecystitis due to Cyclospora cayetanensis. Clin Infect Dis. 2001;33:E140-E141.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 49]  [Cited by in F6Publishing: 51]  [Article Influence: 2.2]  [Reference Citation Analysis (0)]
16.  Knapp PE, Saltzman JR, Fairchild P. Acalculous cholecystitis associated with microsporidial infection in a patient with AIDS. Clin Infect Dis. 1996;22:195-196.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
17.  Shinha T, Zabarsky G. Acalculous Cholecystitis Due to Histoplasma capsulatum in a Patient With HIV Infection. ACG Case Rep J. 2015;2:245-246.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 4]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
18.  Chen PL, Lee HC, Shan YS, Ko NY, Lee NY, Chang CM, Wu CJ, Lee CC, Ko WC. Respiratory failure and acalculous cholecystitis in a patient with AIDS and disseminated tuberculosis: masking effect of fluoroquinolone monotherapy and immune restoration syndrome. Int J Infect Dis. 2009;13:e165-e168.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 1]  [Article Influence: 0.1]  [Reference Citation Analysis (0)]
19.  French AL, Beaudet LM, Benator DA, Levy CS, Kass M, Orenstein JM. Cholecystectomy in patients with AIDS: clinicopathologic correlations in 107 cases. Clin Infect Dis. 1995;21:852-858.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 78]  [Cited by in F6Publishing: 79]  [Article Influence: 2.7]  [Reference Citation Analysis (0)]
20.  Takeshita S, Nakamura H, Kawakami A, Fukushima T, Gotoh T, Ichikawa T, Tsujino A, Ida H, Toriyama K, Hayashi T, Eguchi K. Hepatitis B-related polyarteritis nodosa presenting necrotizing vasculitis in the hepatobiliary system successfully treated with lamivudine, plasmapheresis and glucocorticoid. Intern Med. 2006;45:145-149.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 16]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
21.  Janssen HL, van Zonneveld M, van Nunen AB, Niesters HG, Schalm SW, de Man RA. Polyarteritis nodosa associated with hepatitis B virus infection. The role of antiviral treatment and mutations in the hepatitis B virus genome. Eur J Gastroenterol Hepatol. 2004;16:801-807.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 31]  [Cited by in F6Publishing: 32]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
22.  Meier M, Holl-Ulrich K, Perras B. A rare manifestation of cryoglobulinemic vasculitis: acalculous cholecystitis. Clin Gastroenterol Hepatol. 2005;3:xxvi.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 4]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
23.  Ono SK, Bassit L, Van Vaisberg V, Avancini Ferreira Alves V, Caldini EG, Herman BD, Shabman R, Fedorova NB, Paranaguá-Vezozzo D, Sampaio CT, Lages RB, Terrabuio D, Andraus W, Schinazi RF, Carrilho FJ. Acute acalculous cholecystitis during zika virus infection in an immunocompromised patient. Hepatology. 2018;67:2051-2054.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 3]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
24.  Guarner J, Shieh WJ, Morgan J, Bragg SL, Bajani MD, Tappero JW, Zaki SR. Leptospirosis mimicking acute cholecystitis among athletes participating in a triathlon. Hum Pathol. 2001;32:750-752.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 33]  [Cited by in F6Publishing: 32]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
25.  Walker DH, Lesesne HR, Varma VA, Thacker WC. Rocky Mountain spotted fever mimicking acute cholecystitis. Arch Intern Med. 1985;145:2194-2196.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
26.  Wani I. Gallbladder ascariasis. Turk J Gastroenterol. 2011;22:178-182.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 7]  [Cited by in F6Publishing: 7]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
27.  Khuroo MS, Rather AA, Khuroo NS, Khuroo MS. Hepatobiliary and pancreatic ascariasis. World J Gastroenterol. 2016;22:7507-7517.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 62]  [Cited by in F6Publishing: 57]  [Article Influence: 7.1]  [Reference Citation Analysis (1)]
28.  Araki H, Shimizu S, Hayashi K, Yamada T, Kusakabe A, Kanie H, Mizuno Y, Kojima I, Saitou A, Nagao K, Suzuki Y, Toyohara T, Suzuki T, Uchida E, Uno K, Nakazawa T. Acute Acalculous Cholecystitis Caused by Giardia lamblia. Intern Med. 2017;56:1657-1662.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 7]  [Cited by in F6Publishing: 7]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
29.  Colle I, Van Vlierberghe H, Brenard R, Troisi R, de Hemptinne B, Navez B, De Coninck S, De Vos M. Biliary complications of large Echinococcus granulosus cysts: report of 2 cases and review of the literature. Acta Clin Belg. 2002;57:349-354.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 5]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
30.  Iaria C, Arena L, Di Maio G, Fracassi MG, Leonardi MS, Famulari C, Cascio A. Acute acalculous cholecystitis during the course of primary Epstein-Barr virus infection: a new case and a review of the literature. Int J Infect Dis. 2008;12:391-395.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 47]  [Cited by in F6Publishing: 52]  [Article Influence: 3.3]  [Reference Citation Analysis (0)]
31.  Yombi JC, Meuris CM, Van Gompel AM, Ben Younes M, Vandercam BC. Acalculous cholecystitis in a patient with Plasmodium falciparum infection: a case report and literature review. J Travel Med. 2006;13:178-180.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 12]  [Cited by in F6Publishing: 13]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
32.  Harris EF, Younger E, Llewelyn MB. Acalculous cholecystitis occurring in the context of Plasmodium malariae infection: a case report. J Med Case Rep. 2013;7:197.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 3]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
33.  Curley JM, Mody RM, Gasser RA Jr. Malaria caused by Plasmodium vivax complicated by acalculous cholecystitis. Am J Trop Med Hyg. 2011;85:42-49.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 8]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
34.  Agergaard J, Larsen CS. Acute acalculous cholecystitis in a patient with primary Epstein-Barr virus infection: a case report and literature review. Int J Infect Dis. 2015;35:67-72.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 22]  [Cited by in F6Publishing: 22]  [Article Influence: 2.4]  [Reference Citation Analysis (0)]
35.  Dinulos J, Mitchell DK, Egerton J, Pickering LK. Hydrops of the gallbladder associated with Epstein-Barr virus infection: a report of two cases and review of the literature. Pediatr Infect Dis J. 1994;13:924-929.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 33]  [Cited by in F6Publishing: 33]  [Article Influence: 1.1]  [Reference Citation Analysis (0)]
36.  Ntelis K, Mazarakis D, Sapountzis A, Zissi D, Sparangi S, Xidia N, Velissaris D. Acute Acalculous Cholecystitis Associated with Epstein-Barr Infection: A Case Report and Review of the Literature. Case Rep Med. 2020;2020:9029601.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 5]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
37.  Mattone E, Sofia M, Schembari E, Palumbo V, Bonaccorso R, Randazzo V, La Greca G, Iacobello C, Russello D, Latteri S. Acute acalculous cholecystitis on a COVID-19 patient: a case report. Ann Med Surg (Lond). 2020;58:73-75.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 28]  [Cited by in F6Publishing: 26]  [Article Influence: 6.5]  [Reference Citation Analysis (0)]
38.  Roy J, Sahu N, Golamari R, Vunnam R. Acute Acalculous Cholecystitis in a Patient With COVID-19 and a LVAD. J Card Fail. 2020;26:639.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 7]  [Article Influence: 1.8]  [Reference Citation Analysis (0)]
39.  Alhassan SM, Iqbal P, Fikrey L, Mohamed Ibrahim MI, Qamar MS, Chaponda M, Munir W. Post COVID 19 acute acalculous cholecystitis raising the possibility of underlying dysregulated immune response, a case report. Ann Med Surg (Lond). 2020;60:434-437.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 17]  [Cited by in F6Publishing: 24]  [Article Influence: 6.0]  [Reference Citation Analysis (0)]
40.  Garrido-Benedicto P, González-Reimers E, Santolaria-Fernández F, Rodríguez-Moreno F. Acute acalculous cholecystitis due to Salmonella. Dig Dis Sci. 1994;39:442-443.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 2]  [Article Influence: 0.1]  [Reference Citation Analysis (0)]
41.  Ruiz-Rebollo ML, Sánchez-Antolín G, García-Pajares F, Vallecillo-Sande MA, Fernández-Orcajo P, Velicia-Llames R, Caro-Patón A. Acalculous cholecystitis due to Salmonella enteritidis. World J Gastroenterol. 2008;14:6408-6409.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 15]  [Cited by in F6Publishing: 10]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
42.  khan FY, Elouzi EB, Asif M. Acute acalculous cholecystitis complicating typhoid fever in an adult patient: a case report and review of the literature. Travel Med Infect Dis. 2009;7:203-206.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 18]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
43.  Rajan N, Motoroko I, Udayasiri D, McKenzie JL, Tan JS, Tramontana AR. A case report of typhoidal acute acalculous cholecystitis. Case Rep Infect Dis. 2014;2014:171496.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 3]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
44.  Lianos GD, Drosou P, Souvatzoglou R, Karampa A, Vangelis G, Angelakis E, Pappas V, Lekkas E. Acute Acalculous Cholecystitis with Empyema due to Salmonellosis. Case Rep Gastrointest Med. 2019;2019:5185314.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 2]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
45.  Suresh DR, Srikrishna R, Nanda SK, Annam V, Sunil K, Arjun B. Acalculous gallbladder distension in a young child due to HAV infection: Diagnostic dilemma. Indian J Clin Biochem. 2009;24:316-318.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 7]  [Cited by in F6Publishing: 8]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
46.  Prashanth GP, Angadi BH, Joshi SN, Bagalkot PS, Maralihalli MB. Unusual cause of abdominal pain in pediatric emergency medicine. Pediatr Emerg Care. 2012;28:560-561.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 12]  [Cited by in F6Publishing: 13]  [Article Influence: 1.1]  [Reference Citation Analysis (0)]
47.  Kaya S, Eskazan AE, Ay N, Baysal B, Bahadir MV, Onur A, Duymus R. Acute Acalculous Cholecystitis due to Viral Hepatitis A. Case Rep Infect Dis. 2013;2013:407182.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 8]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
48.  Unal H, Korkmaz M, Kirbas I, Selcuk H, Yilmaz U. Acute acalculous cholecystitis associated with acute hepatitis B virus infection. Int J Infect Dis. 2009;13:e310-e312.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 12]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
49.  Wright WF, Palisoc K, Pinto CN, Lease JA, Baghli S. Hepatitis C Virus-Associated Acalculous Cholecystitis and Review of the Literature. Clin Med Res. 2020;18:33-36.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 10]  [Cited by in F6Publishing: 8]  [Article Influence: 2.0]  [Reference Citation Analysis (0)]
50.  Spernovasilis N, Tsioutis C, Zafeiri M, Hamilos G, Gikas A. Severe Murine Typhus Presenting with Acalculous Cholecystitis: A Case Report and Literature Review. Case Rep Med. 2017;2017:3769074.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 4]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
51.  Saha A, Batra P, Vilhekar KY, Chaturvedi P. Acute acalculous cholecystitis in a child with Plasmodium falciparum malaria. Ann Trop Paediatr. 2005;25:141-142.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 12]  [Cited by in F6Publishing: 13]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
52.  Lagona E, Sharifi F, Voutsioti A, Mavri A, Markouri M, Attilakos A. Epstein-Barr virus infectious mononucleosis associated with acute acalculous cholecystitis. Infection. 2007;35:118-119.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 34]  [Cited by in F6Publishing: 36]  [Article Influence: 2.1]  [Reference Citation Analysis (0)]
53.  Prassouli A, Panagiotou J, Vakaki M, Giannatou I, Atilakos A, Garoufi A, Papaevangelou V. Acute acalculous cholecystitis as the initial presentation of primary Epstein-Barr virus infection. J Pediatr Surg. 2007;42:E11-E13.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 29]  [Cited by in F6Publishing: 29]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
54.  Attilakos A, Prassouli A, Hadjigeorgiou G, Lagona E, Kitsiou-Tzeli S, Galla A, Stasinopoulou A, Karpathios T. Acute acalculous cholecystitis in children with Epstein-Barr virus infection: a role for Gilbert's syndrome? Int J Infect Dis. 2009;13:e161-e164.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 27]  [Cited by in F6Publishing: 26]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
55.  Gagneux-Brunon A, Suy F, Pouvaret A, Pillet S, Tarantino E, Bouchet D, Fresard A, Cazorla C, Guglielminotti C, Lucht F, Botelho-Nevers E. Acute acalculous cholecystitis, a rare complication of Epstein-Barr virus primary infection: report of two cases and review. J Clin Virol. 2014;61:173-175.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 18]  [Cited by in F6Publishing: 17]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
56.  Alkhoury F, Diaz D, Hidalgo J. Acute acalculous cholecystitis (AAC) in the pediatric population associated with Epstein-Barr Virus (EBV) infection. Case report and review of the literature. Int J Surg Case Rep. 2015;11:50-52.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 21]  [Cited by in F6Publishing: 19]  [Article Influence: 1.9]  [Reference Citation Analysis (0)]
57.  Yesilbag Z, Karadeniz A, Kaya FO. Acute Acalculous Cholecystitis: A Rare Presentation of Primary Epstein-Barr Virus Infection in Adults-Case Report and Review of the Literature. Case Rep Infect Dis. 2017;2017:5790102.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 10]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
58.  Andriopoulos P, Tsironi M, Asimakopoulos G. Acute abdomen due to Brucella melitensis. Scand J Infect Dis. 2003;35:204-205.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 12]  [Cited by in F6Publishing: 12]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
59.  Hariz A, Beji I, Hamdi MS, Cherif E. Brucellosis, an uncommon cause of acute acalculous cholecystitis: two new cases and concise review. BMJ Case Rep. 2019;12.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 4]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
60.  Figtree M, Miyakis S, Stenos J, Graves S, Botham S, Ferson M, Krilis S. Q fever cholecystitis in an unvaccinated butcher diagnosed by gallbladder polymerase chain reaction. Vector Borne Zoonotic Dis. 2010;10:421-423.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 6]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
61.  Rolain JM, Lepidi H, Harlé JR, Allegre T, Dorval ED, Khayat Z, Raoult D. Acute acalculous cholecystitis associated with Q fever: report of seven cases and review of the literature. Eur J Clin Microbiol Infect Dis. 2003;22:222-227.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 31]  [Cited by in F6Publishing: 31]  [Article Influence: 1.5]  [Reference Citation Analysis (0)]
62.  Wu KL, Changchien CS, Kuo CM, Chuah SK, Lu SN, Eng HL, Kuo CH. Dengue fever with acute acalculous cholecystitis. Am J Trop Med Hyg. 2003;68:657-660.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 34]  [Cited by in F6Publishing: 34]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
63.  Marasinghe JP, Sriyasinghe RY, Wijewantha VI, Gunaratne KA, Wijeyaratne CN. Acute acalculous cholecystitis due to dengue hemorrhagic fever during pregnancy. J Obstet Gynaecol Res. 2011;37:1489-1492.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 4]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
64.  Hayakawa K, Oki M, Moriya Y, Mizuma A, Ohnuki Y, Yanagi H, Fukuda R, Ozawa H, Takizawa S, Takagi A. A case of scrub typhus with acalculous cholecystitis, aseptic meningitis and mononeuritis multiplex. J Med Microbiol. 2012;61:291-294.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 17]  [Cited by in F6Publishing: 17]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
65.  Mahapatra R, Cohen D, Viccellio AW, Sasson A, Bandovic J, Spitzer ED, Lier A, Marcos LA. Acute acalculous cholecystitis as a manifestation of ehrlichiosis. Ticks Tick Borne Dis. 2019;10:1033-1034.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 2]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
66.  Kurtovic J, Webster GJ, Singh-Grewal I, Bullpitt P, Haindl W, Wakefield D, Riordan SM. Acalculous cholecystitis, multifocal gastrointestinal infarction and pancreatitis resulting from Varicella-zoster virus. Intern Med J. 2005;35:69-70.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 7]  [Cited by in F6Publishing: 7]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
67.  Udayakumar D, Sanaullah M. Campylobacter cholecystitis. Int J Med Sci. 2009;6:374-375.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 9]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
68.  West BC, Silberman R, Otterson WN. Acalculous cholecystitis and septicemia caused by non-O1 Vibrio cholerae: first reported case and review of biliary infections with Vibrio cholerae. Diagn Microbiol Infect Dis. 1998;30:187-191.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 29]  [Cited by in F6Publishing: 29]  [Article Influence: 1.1]  [Reference Citation Analysis (0)]
69.  Szvalb AD, Kontoyiannis DP. Acute acalculous cholecystitis due to Fusarium species and review of the literature on fungal cholecystitis. Mycoses. 2019;62:847-853.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 5]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]