Subscribe to RSS
![](/products/assets/desktop/img/oa-logo.png)
DOI: 10.1055/s-0042-1758211
Rare Presentation of Morganella morganii Microorganism as Epidural and Subdural Empyema
Apresentação rara de Morganella morganii Microrganismo como Empiema Epidural e SubduralAbstract
Background Morganella morganii is a gram-negative bacterium that rarely infects the central nervous system (CNS). Few reports described such an infection in the CNS. We present a case of extremely invasive M. morganii infection in the CNS. In addition, we performed a literature review of M. morganii infection in the CNS.
Case report A 53-year-old male was admitted to the hospital due to fever, general weakness, and left-sided facial muscle twitching. He had a history of diabetes mellitus, hypertension, brain tumor, and epilepsy. Multiple left frontal scalp ulcers were revealed. In addition, a computed tomography (CT) scan and magnetic resonance imaging (MRI) revealed a left side epidural abscess and subdural empyema. Moreover, the patient had left frontal bone osteomyelitis. The next day, the patient underwent craniectomy, was transferred to the intensive care unit and started an empirical antibiotic course. Morganella morganii was identified from the infected scalp ulcers. On the 13th day, the patient passed away due to uncontrolled status epilepticus.
Conclusion M. morganii can cause isolated or multiple types of CNS infections, including brain abscess, meningitis, and subdural empyema. The mortality rate may differ according to age and to the use of surgical evacuation.
#
Resumo
Introdução Morganella morganii é uma bactéria gram-negativa que raramente infecta o sistema nervoso central (SNC). Poucos relatos descreveram tal infecção no SNC. Apresentamos um caso de infecção extremamente invasiva por M. morganii no SNC. Além disso, realizamos uma revisão da literatura sobre a infecção por M. morganii no SNC.
Relato de caso Um homem de 53 anos foi admitido no hospital devido a febre, fraqueza geral e espasmos da musculatura facial do lado esquerdo. Ele tinha história de diabetes mellitus, hipertensão, tumor cerebral e epilepsia. Múltiplas úlceras no couro cabeludo frontal esquerdo foram reveladas. Além disso, uma tomografia computadorizada (TC) e uma ressonância magnética (RM) revelaram um abscesso epidural do lado esquerdo e empiema subdural. Além disso, o paciente apresentava osteomielite do osso frontal esquerdo. No dia seguinte, o paciente foi submetido à craniectomia, foi transferido para a unidade de terapia intensiva e iniciou curso empírico de antibiótico. Morganella morganii foi identificada a partir das úlceras do couro cabeludo infectadas. No 13° dia, o paciente faleceu devido a estado de mal epiléptico não controlado.
Conclusão M. morganii pode causar tipos isolados ou múltiplos de infecções do SNC, incluindo abscesso cerebral, meningite e empiema subdural. A taxa de mortalidade pode diferir de acordo com a idade e com o uso da evacuação cirúrgica.
#
Palavras-chave
Empiema Subdural - Morganella morganii - Infecção cerebral - Úlcera do couro cabeludoIntroduction
Morganella morganii is a gram-negative aerobic bacilli that belongs to the Enterobacteriaceae family and is part of the normal gut microbiota.[1] [2] [3] Morganella morganii infection can cause urinary tract infection, blood sepsis, soft tissue, wound, and hepatobiliary tract infection.[1] [2] Central nervous system (CNS) infection with M. morganii is rarely encountered and reported in the literature, including brain abscess, meningitis, and subdural empyema.[3] In the present case report, we present a case of aggressive M. morganii CNS infection using case report (CARE) guidelines.[4] Moreover, we performed a literature review by searching for articles related to CNS infection by M. morganii in the PubMed and Scopus databases.
#
Case Presentation
A 53-year-old male patient with multiple comorbidities, including diabetes mellitus and hypertension, was admitted to our hospital as an emergency case of a 1-week history of intermittent fever, general weakness, and left-sided facial muscle twitching. He had a history of left side temporoparietal brain tumor excision (astrocytoma) 20 years ago. He was found to be neglected by the family as all his relatives live far away from him. Besides, he had been diagnosed with right side acute subdural hematoma (SDH) and was treated surgically 8 months before, and he had been diagnosed with epilepsy 8 years before, which was managed with phenytoin as a single antiepileptic medication. Physical examination revealed high-grade fever (38.3 C°) and other vital signs were within normal ranges. Multiple left frontal scalp ulcers and necrosis were detected ([Figure 1]). The patient's Glasgow coma scale was 11 as he could open his eyes spontaneously (4), as well as producing sounds when in pain (2) and flexion to pain (5). Pupils were normal sized and reactive to light. Power examinations showed right-side weakness. Blood laboratory exams showed elevation in white blood cell (WBC) count (13.4 * × 109/L), mainly neutrophils (81%), C-reactive protein (140 mg/L), erythrocyte sedimentation rate (ESR) (62 mm/hr). Other lab results were within normal ranges. Both CT scan and MRI images revealed left side epidural abscess, subdural empyema, cerebral atrophy, and cerebritis in the frontal area ([Figure 2]). The patient was prepared for surgery and, on the next day, he underwent left decompressive craniectomy surgery and evacuation of the epidural abscess, the subdural empyema, and the infected part of the skull. The artificial dura of the previous tumor excision was also removed. Pus biopsy was taken and sent to the microbiology lab.
![](https://www.thieme-connect.de/media/10.1055-s-00028832/202303/thumbnails/10-1055-s-0042-1758211-i2200018-1.jpg)
![Zoom Image](/products/assets/desktop/css/img/icon-figure-zoom.png)
![](https://www.thieme-connect.de/media/10.1055-s-00028832/202303/thumbnails/10-1055-s-0042-1758211-i2200018-2.jpg)
![Zoom Image](/products/assets/desktop/css/img/icon-figure-zoom.png)
MacConkey agar or blood agar were used for bacteria while sabouraud dextrose agar was used to detect any fungal growth. Although no growth was detected from the pus culture, the scalp ulcer culture was positive for M. morganii. The antibiotic susceptibility test showed resistance against fluoroquinolones, cefixime, and ampicillin with sulbactam. On the other hand, it was sensitive to aminoglycosides and other cephalosporins. The patient was kept on phenytoin for seizure control and treated with vancomycin, ceftriaxone, and metronidazole at the initial period, then the antibiotics regimen changed to gentamicin and ceftriaxone IV according to the susceptibility to antibiotics.
The patient was observed in the intensive care unit for 13 days, then he passed away due to uncontrolled status epilepticus.
#
Discussion
Morganella morganii is a rare causative agent of intracranial infections. Previous studies have reported brain abscesses, meningitis, and subdural empyema with this infection.[5] [6] In the present case report, we reported the first case of extremely invasive M. morganii CNS infection involving the scalp, the skull, and the epidural and subdural spaces.
Risk factors and the source of the infection in the brain are unclear due to the scarcity of cases reported in the literature. However, iatrogenic, otogenic, wound infections, and urinary tract infection (UTI) as possible sources of infection have been reported previously.[1] [2] [5] In our case, tumor excision surgery was performed on the same side of the infection but was performed 20 years ago which was an unusual risk factor.
In the previously reported studies, the age of the patients ranged from 1 day to 78 years old ([Tables 1] and [2]). There were more male cases than female cases (nine male cases, seven female cases, and one unreported case). The mortality rate of the reported studies in the literature, including our case, was 27.8%. The most common presentation was meningitis, with 10 cases; 5 cases were isolated meningitis,[7] [8] [9] [10] [11] 2 were combined with brain abscesses,[3] [12] 1 was combined with subdural empyema,[13] 1 was combined with encephalitis,[14] and 1 was combined with sepsis.[15] The second most common presentation was brain abscess, with seven cases; five cases were isolated brain abscesses,[5] [16] [17] [18] two cases were combined with meningitis,[3] [12] and one case was combined with subdural empyema.[19] Eight cases were < 2 years old ([Table 1]). A total of 47% of the cases were infants with a history of trauma,[6] [13] preterm infants,[15] born from mothers with chorioamnionitis,[11] and delivered by vacuum-assisted vaginal delivery.[20] No significant prior history or possible risk factors were identified in the remaining infant cases.[9] [17] [18] Surprisingly, none of the infants had died.
Name |
Age (gender) |
Description of the infection |
Treatment |
Outcome |
Notes |
---|---|---|---|---|---|
Bond et al., 2020[6] |
13 months old (female) |
Subdural empyema |
Meropenem and surgical evacuation |
Recovery |
First case of sterile empyema |
Milligan et al., 2013[9] |
3 weeks old (female) |
Meningitis |
Cefotaxime and gentamicin |
Recovery |
|
Park et al., 2004[13] |
7 months old (male) |
Meningitis and subdural empyema |
Ceftriaxone, metronidazole and surgical evacuation |
Recovery |
History of meningitis |
Paul et al., 2020[15] |
32 + 5 gestational weeks (male) |
Meningitis and sepsis |
Meropenem and gentamicin |
Recovery |
Preterm infant due to fetal distress |
Sinha et al., 2006[11] |
6 days old (female) |
Meningitis |
Cefotaxime, gentamicin, and meropenem |
Recovery |
Mother had chorioamnionitis before the delivery |
Staudt et al., 2016[20] |
1 day old (male) |
Cephalohematoma and osteomyelitis |
Vancomycin, meropenem and surgical evacuation |
Recovery |
Delivered via vacuum extraction |
Thomas et al., 2007[17] |
2 months old (male) |
Brain abscess |
Unspecified antibiotics and surgical evacuation |
Discharged |
Patient discharged on oral chloramphenicol with no follow-up |
Verboon-Maciolek et al., 1995[18] |
8 days old (male) |
Brain abscess |
Cefotaxime, gentamicin, and surgical evacuation |
Recovery |
Cultures of pus aspirated from the abscess were sterile |
Name |
Age (gender) |
Description of the infection |
Treatment |
Outcome |
Notes |
---|---|---|---|---|---|
Abdalla et al., 2006[5] |
38 years old (female) |
Brain abscess |
Cefepime and surgical evacuation |
Death |
History of craniotomy due to a motor vehicle accident |
Águeda et al., 2013[19] |
9 years old (male) |
Brain abscess and subdural empyema |
Ceftriaxone, vancomycin, ceftriaxone, and surgical evacuation |
Recovery |
History of chronic suppurative otitis media |
Isaacs et al., 1987[7] |
78 years old (female) |
Meningitis |
Pefloxacin mesylate |
Death |
The reason of death was coronary heart disease |
Lu et al.,1999[12] |
55 years old (female) |
Brain abscess and meningitis |
Imipenem/ cilastatin and surgical evacuation |
Recovery |
The patient underwent caniotomy, then developed the infection |
Mastroianni et al., 1994[8] |
45 years old (male) |
Meningitis |
Netilmicin and ceftriaxone |
Death |
History of AIDS |
Ndiaye et al., 2010[14] |
12 years old (male) |
Meningoencephalitis |
Cefotaxime and gentamicin |
Recovery |
History of chronic otitis media |
Patil et al., 2010[3] |
12 years old (male) |
Brain abscess and meningitis |
Amikacin, ceftriaxone, and metronidazole |
Recovery |
History of chronic suppurative otitis media |
Rau et al., 2002[16] |
Not reported (not reported) |
Brain abscess |
Third-generation cephalosporins and surgical evacuation |
Recovery |
|
Samonis et al., 2001[10] |
25 years old (female) |
Meningitis |
Cefotaxime and amikacin |
Death |
|
Present study |
53 Years old (male) |
Skin, skull, encephalitis, epidural abscess, and subdural empyema |
Gentamicin, ceftriaxone, and surgical evacuation |
Death |
History of hypertension, diabetes, epilepsy, and brain tumor treated with craniotomy |
In the cohort of patients > 2 years old ([Table 2]), the mortality rate was high, reaching 50%. Three patients had a history of chronic suppurative otitis media. Brain abscess and meningitis have been previously reported as possible intracranial complications of chronic suppurative otitis media.[21]
Only three cases described osteomyelitis caused by M. morganii.[20] [22] [23] Staudt et al. reported a case of skull osteomyelitis and infected cephalohematoma with M. morganii in a 1-day old infant.[20] Our case is the second case of skull osteomyelitis and the fourth case of osteomyelitis in general. Subdural empyema can be caused by a superimposed infection of a previous SDH.[6] The identification of M. morganii is based on culturing the biopsy on MacConkey agar or blood agar.[3] In our case, both were negative for the aspirated pus but positive for the superficial scalp lesions. The rate of negative pus culture from subdural empyema is reported to range from 7 to 53%.[24] In our case, possible sources of such a rare pathogen might be iatrogenic from the previous burr-hole drainage to clear the SDH, but the infection was in the contralateral side from the intracranial potential space created from his previous tumor excision,[25] which was performed 20 years before.
Morganella morganii also contains an inducible ampC β -lactamase gene, making it resistant to penicillin and to first- and second-generation cephalosporins.[26] In addition, overproduction of ampC β -lactamase by the loss of ampD gene expression can cause treatment failure with third-generation cephalosporins.[26] In our case, the antibiotic susceptibility test showed resistance to cefixime, a third-generation cephalosporin. This was also noted by Sinha et al., who described a case of cefotaxime-resistant M. morganii during treatment due to overexpression of ampC β -lactamase.[11] Thus, the use of third-generation cephalosporins should be monitored continuously even if the bacterium showed an initial susceptibility and response. Third-generation cephalosporins, meropenem, and gentamicin were the most used antibiotics in the literature ([Tables 1] and [2]). In most cases, surgical evacuation by burr-hole drainage or craniotomy was performed. In our case, the patient underwent craniectomy due to the presence of osteomyelitis. The mortality rate when the surgical evacuation was performed was 20%, compared with 37.5% when the surgical evacuation was not performed. Therefore, surgical management with the administration of the appropriate antibiotics is needed to increase the chances of survival.
#
Conclusion
In the present case report, we reported a very rare case of M. morganii infection in an adult patient that involved the scalp, the skull, and the epidural and subdural spaces with unusual presentation and unknown risk factors. Clinical presentation and mortality rate may differ according to age. The use of surgical evacuation resulted in a decreased mortality rate.
#
#
Conflict of Interests
The authors have no conflict of interests to declare.
Contribution of the Authors
Daoud S. S.: Supervision and critical review of the manuscript.
Jarrar S.: Supervision and literature review.
Ababneh O. E.: Writing of the manuscript, data collection, and review.
Jbarah O. F.: Writing and editing of the manuscript, data collection, and review.
Ethics Approval and Consent to Participate
Written informed consent was obtained from the patient for publication of the case report and any related images.
-
References
- 1 Liu H, Zhu J, Hu Q, Rao X. Morganella morganii, a non-negligent opportunistic pathogen. Int J Infect Dis 2016; 50: 10-17 DOI: 10.1016/j.ijid.2016.07.006.
- 2 Bandy A. Ringing bells: Morganella morganii fights for recognition. Public Health 2020; 182: 45-50 DOI: 10.1016/j.puhe.2020.01.016.
- 3 Patil AB, Nadagir SD, Lakshminarayana S, Syeda FM. Morganella morganii, subspecies morganii, biogroup A: An unusual causative pathogen of brain abscess. J Neurosci Rural Pract 2012; 3 (03) 370-372 DOI: 10.4103/0976-3147.102631.
- 4 CARE Checklist— CARE Case Report Guidelines. Accessed April 13, 2021. https://www.care-statement.org/checklist
- 5 Abdalla J, Saad M, Samnani I, Lee P, Moorman J. Central nervous system infection caused by Morganella morganii. Am J Med Sci 2006; 331 (01) 44-47 DOI: 10.1097/00000441-200601000-00013.
- 6 Bond E, Stadler JA. Subdural empyema caused by Morganella morganii . Surg Neurol Int 2020; 11 (216) 216 DOI: 10.25259/SNI_136_2020.
- 7 Isaacs RD, Ellis-Pegler RB. Successful treatment of Morganella morganii meningitis with pefloxacin mesylate. J Antimicrob Chemother 1987; 20 (05) 769-770 DOI: 10.1093/jac/20.5.769.
- 8 Mastroianni A, Coronado O, Chiodo F. Morganella morganii meningitis in a patient with AIDS. J Infect 1994; 29 (03) 356-357 DOI: 10.1016/S0163-4453(94)91450-8.
- 9 Milligan KL, Barenkamp SJ. Neonatal meningitis due to Morganella morganii. Clin Pediatr (Phila) 2013; 52 (05) 462-464 DOI: 10.1177/0009922811435166.
- 10 Samonis G, Anatoliotaki M, Apostolakou H, Souglakos J, Georgoulias V. Fatal septicemia and meningitis due to Morganella morganii in a patient with Hodgkin's disease. Scand J Infect Dis 2001; 33 (07) 553-555 DOI: 10.1080/00365540110026665.
- 11 Sinha AK, Kempley ST, Price E, Sharma BK, Livermore DM. Early onset Morganella morganii sepsis in a newborn infant with emergence of cephalosporin resistance caused by depression of AMPC β-lactamase production. Pediatr Infect Dis J 2006; 25 (04) 376-377 DOI: 10.1097/01.inf.0000207474.25593.2d.
- 12 Lu CH, Chang WN, Chuang YC. Resistance to third-generation cephalosporins in adult gram-negative bacillary meningitis. Infection 1999; 27 (03) 208-211 DOI: 10.1007/BF02561530.
- 13 Park E, Lee S, Oh P. et al. KK-KJ of, 2004 undefined. A case of subdural abscess caused by Morganella morganii. KoreaMed. Accessed June 29, 2021. http://www.koreamed.org/SearchBasic.php?RID=1314300
- 14 Ndiaye M, Sène MS, Sow AD, Seck LB, Coulibaly T, Diagne NS, Touré K, Diop AG, Ndiaye MM. Meningoencephalitis due to Morganella Morganii: A case report. Bull Soc Pathol Exot 2010; 103 (04) 230-232 DOI: 10.1007/s13149-010-0055-y.
- 15 Paul SP, Newman LM, Mubashar Y, Turner PC. Morganella morganii: a rare cause of early onset neonatal sepsis and meningitis. Br J Hosp Med (Lond) 2020; 81 (10) 1-3 DOI: 10.12968/hmed.2020.0037.
- 16 Rau CS, Chang WN, Lin YC. et al. Brain abscess caused by aerobic Gram-negative bacilli: clinical features and therapeutic outcomes. Clin Neurol Neurosurg 2002; 105 (01) 60-65 DOI: 10.1016/S0303-8467(02)00103-8.
- 17 Thomas VA, Sathish KumarT, Agarwal I, Chacko AG. Unusual cause of brain abscess in an infant. J Pediatr Neurosci [serial online] 2007 [cited 2022 Nov 4];2:94-5. Available from: https://www.pediatricneurosciences.com/text.asp?2007/2/2/94/36776
- 18 Verboon-Maciolek M, Vandertop WP, Peters ACB, Roord JJ, Geelen SPM. Neonatal brain abscess caused by Morganella morgagni. Clin Infect Dis 1995; 20 (02) 471 DOI: 10.1093/clinids/20.2.471.
- 19 Águeda S, Leitão A, Rocha G, Guimarães H. Cerebral Abscess and Empyema due to Morganella morganii. [Internet]. [cited 2022Nov4]. Available from: https://www.longdom.org/open-access/cerebral-abscess-and-empyema-due-to-morganella-morganii-2161-0665.1000147.pdf Pediatr Ther 2013; 3: 147 DOI: 10.4172/2161-0665.10001.
- 20 Staudt MD, Etarsky D, Ranger A. Infected cephalohematomas and underlying osteomyelitis: a case-based review. Childs Nerv Syst 2016; 32 (08) 1363-1369 DOI: 10.1007/s00381-016-3084-4.
- 21 Sharma N, Jaiswal AA, Banerjee PK, Garg AK. Complications of Chronic Suppurative Otitis Media and Their Management: A Single Institution 12 Years Experience. Indian J Otolaryngol Head Neck Surg 2015; 67 (04) 353-360 DOI: 10.1007/s12070-015-0836-5.
- 22 Zhu J, Li H, Feng L. et al. Severe chronic osteomyelitis caused by Morganella morganii with high population diversity. Int J Infect Dis 2016; 50: 44-47 DOI: 10.1016/j.ijid.2016.07.016.
- 23 Harris MC, DeRosa DC, West PA. Subacute osteomyelitis of the Pediatric Talus: A first report of Brodie's abscess from Morganella Morganii. Case Reports in Orthopedics 2019; 2019: 1-4
- 24 Osborn MK, Steinberg JP. Subdural empyema and other suppurative complications of paranasal sinusitis. Lancet Infect Dis 2007; 7 (01) 62-67 DOI: 10.1016/S1473-3099(06)70688-0.
- 25 Agrawal A, Timothy J, Pandit L, Shetty L, Shetty JP. A Review of Subdural Empyema and Its Management. Infect Dis Clin Pract [Internet] [cited 2022Nov4]. 2007; 15 (03) 149-153 Available from: https://journals.lww.com/infectdis/fulltext/2007/05000/A_Review_of_Subdural_Empyema_and_Its_Management.6.aspx
- 26 Jacoby GA. AmpC beta-lactamases. Clin Microbiol Rev 2009; 22 (01) 161-182 DOI: 10.1128/CMR.00036-08.
Address for correspondence
Publication History
Received: 15 March 2022
Accepted: 01 August 2022
Article published online:
29 September 2023
© 2022. Sociedade Brasileira de Neurocirurgia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Thieme Revinter Publicações Ltda.
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil
-
References
- 1 Liu H, Zhu J, Hu Q, Rao X. Morganella morganii, a non-negligent opportunistic pathogen. Int J Infect Dis 2016; 50: 10-17 DOI: 10.1016/j.ijid.2016.07.006.
- 2 Bandy A. Ringing bells: Morganella morganii fights for recognition. Public Health 2020; 182: 45-50 DOI: 10.1016/j.puhe.2020.01.016.
- 3 Patil AB, Nadagir SD, Lakshminarayana S, Syeda FM. Morganella morganii, subspecies morganii, biogroup A: An unusual causative pathogen of brain abscess. J Neurosci Rural Pract 2012; 3 (03) 370-372 DOI: 10.4103/0976-3147.102631.
- 4 CARE Checklist— CARE Case Report Guidelines. Accessed April 13, 2021. https://www.care-statement.org/checklist
- 5 Abdalla J, Saad M, Samnani I, Lee P, Moorman J. Central nervous system infection caused by Morganella morganii. Am J Med Sci 2006; 331 (01) 44-47 DOI: 10.1097/00000441-200601000-00013.
- 6 Bond E, Stadler JA. Subdural empyema caused by Morganella morganii . Surg Neurol Int 2020; 11 (216) 216 DOI: 10.25259/SNI_136_2020.
- 7 Isaacs RD, Ellis-Pegler RB. Successful treatment of Morganella morganii meningitis with pefloxacin mesylate. J Antimicrob Chemother 1987; 20 (05) 769-770 DOI: 10.1093/jac/20.5.769.
- 8 Mastroianni A, Coronado O, Chiodo F. Morganella morganii meningitis in a patient with AIDS. J Infect 1994; 29 (03) 356-357 DOI: 10.1016/S0163-4453(94)91450-8.
- 9 Milligan KL, Barenkamp SJ. Neonatal meningitis due to Morganella morganii. Clin Pediatr (Phila) 2013; 52 (05) 462-464 DOI: 10.1177/0009922811435166.
- 10 Samonis G, Anatoliotaki M, Apostolakou H, Souglakos J, Georgoulias V. Fatal septicemia and meningitis due to Morganella morganii in a patient with Hodgkin's disease. Scand J Infect Dis 2001; 33 (07) 553-555 DOI: 10.1080/00365540110026665.
- 11 Sinha AK, Kempley ST, Price E, Sharma BK, Livermore DM. Early onset Morganella morganii sepsis in a newborn infant with emergence of cephalosporin resistance caused by depression of AMPC β-lactamase production. Pediatr Infect Dis J 2006; 25 (04) 376-377 DOI: 10.1097/01.inf.0000207474.25593.2d.
- 12 Lu CH, Chang WN, Chuang YC. Resistance to third-generation cephalosporins in adult gram-negative bacillary meningitis. Infection 1999; 27 (03) 208-211 DOI: 10.1007/BF02561530.
- 13 Park E, Lee S, Oh P. et al. KK-KJ of, 2004 undefined. A case of subdural abscess caused by Morganella morganii. KoreaMed. Accessed June 29, 2021. http://www.koreamed.org/SearchBasic.php?RID=1314300
- 14 Ndiaye M, Sène MS, Sow AD, Seck LB, Coulibaly T, Diagne NS, Touré K, Diop AG, Ndiaye MM. Meningoencephalitis due to Morganella Morganii: A case report. Bull Soc Pathol Exot 2010; 103 (04) 230-232 DOI: 10.1007/s13149-010-0055-y.
- 15 Paul SP, Newman LM, Mubashar Y, Turner PC. Morganella morganii: a rare cause of early onset neonatal sepsis and meningitis. Br J Hosp Med (Lond) 2020; 81 (10) 1-3 DOI: 10.12968/hmed.2020.0037.
- 16 Rau CS, Chang WN, Lin YC. et al. Brain abscess caused by aerobic Gram-negative bacilli: clinical features and therapeutic outcomes. Clin Neurol Neurosurg 2002; 105 (01) 60-65 DOI: 10.1016/S0303-8467(02)00103-8.
- 17 Thomas VA, Sathish KumarT, Agarwal I, Chacko AG. Unusual cause of brain abscess in an infant. J Pediatr Neurosci [serial online] 2007 [cited 2022 Nov 4];2:94-5. Available from: https://www.pediatricneurosciences.com/text.asp?2007/2/2/94/36776
- 18 Verboon-Maciolek M, Vandertop WP, Peters ACB, Roord JJ, Geelen SPM. Neonatal brain abscess caused by Morganella morgagni. Clin Infect Dis 1995; 20 (02) 471 DOI: 10.1093/clinids/20.2.471.
- 19 Águeda S, Leitão A, Rocha G, Guimarães H. Cerebral Abscess and Empyema due to Morganella morganii. [Internet]. [cited 2022Nov4]. Available from: https://www.longdom.org/open-access/cerebral-abscess-and-empyema-due-to-morganella-morganii-2161-0665.1000147.pdf Pediatr Ther 2013; 3: 147 DOI: 10.4172/2161-0665.10001.
- 20 Staudt MD, Etarsky D, Ranger A. Infected cephalohematomas and underlying osteomyelitis: a case-based review. Childs Nerv Syst 2016; 32 (08) 1363-1369 DOI: 10.1007/s00381-016-3084-4.
- 21 Sharma N, Jaiswal AA, Banerjee PK, Garg AK. Complications of Chronic Suppurative Otitis Media and Their Management: A Single Institution 12 Years Experience. Indian J Otolaryngol Head Neck Surg 2015; 67 (04) 353-360 DOI: 10.1007/s12070-015-0836-5.
- 22 Zhu J, Li H, Feng L. et al. Severe chronic osteomyelitis caused by Morganella morganii with high population diversity. Int J Infect Dis 2016; 50: 44-47 DOI: 10.1016/j.ijid.2016.07.016.
- 23 Harris MC, DeRosa DC, West PA. Subacute osteomyelitis of the Pediatric Talus: A first report of Brodie's abscess from Morganella Morganii. Case Reports in Orthopedics 2019; 2019: 1-4
- 24 Osborn MK, Steinberg JP. Subdural empyema and other suppurative complications of paranasal sinusitis. Lancet Infect Dis 2007; 7 (01) 62-67 DOI: 10.1016/S1473-3099(06)70688-0.
- 25 Agrawal A, Timothy J, Pandit L, Shetty L, Shetty JP. A Review of Subdural Empyema and Its Management. Infect Dis Clin Pract [Internet] [cited 2022Nov4]. 2007; 15 (03) 149-153 Available from: https://journals.lww.com/infectdis/fulltext/2007/05000/A_Review_of_Subdural_Empyema_and_Its_Management.6.aspx
- 26 Jacoby GA. AmpC beta-lactamases. Clin Microbiol Rev 2009; 22 (01) 161-182 DOI: 10.1128/CMR.00036-08.
![](https://www.thieme-connect.de/media/10.1055-s-00028832/202303/thumbnails/10-1055-s-0042-1758211-i2200018-1.jpg)
![Zoom Image](/products/assets/desktop/css/img/icon-figure-zoom.png)
![](https://www.thieme-connect.de/media/10.1055-s-00028832/202303/thumbnails/10-1055-s-0042-1758211-i2200018-2.jpg)
![Zoom Image](/products/assets/desktop/css/img/icon-figure-zoom.png)