scholarly journals Atypical Streptococcal Meningitis with Fatal Cerebrovascular Complications: A Case Report

2020 ◽  
Vol 12 (3) ◽  
pp. 87-96
Author(s):  
Gabriel D. Pinilla-Monsalve ◽  
Daniel F. Torres-Cutiva ◽  
Juan P. Fernández-Cubillos

Bacterial meningitis is an infectious pathology that remains a public health challenge. The most frequent etiological agent is Streptococcus pneumoniae, which is also associated with higher rates of mortality and sequels. However, less is known about the clinical presentation of atypical non-pneumoniae streptococcal meningitis. Here, we studied a 23-year-old man with no medical background who presented with projectile vomiting, states of consciousness alteration, unilateral cranial nerve palsy, and meningeal signs. Neuroimaging showed tonsillar herniation, regions of empyema, right transverse and sigmoid sinuses thrombosis, and multiple arterial subcortical infarcts. Cerebrospinal fluid suggested bacterial infection; blood and abscess cultures were positive for Streptococcus constellatus. The patient received antibiotics with no clinical improvement. He deteriorated over the following days, the abolishment of brainstem reflexes was observed, and brain death was declared. Streptococcal meningitis produced by atypical species is a potential cause of lethal cerebrovascular complications, even in immunocompetent patients.

Author(s):  
JA Mailo ◽  
J Pugh ◽  
FD Jacob

Background: Focal neurological deficits occur in approximately 15% of children with bacterial meningitis. However, cranial nerve involvement such as facial-nerve palsy is uncommon in non-tuberculous bacterial meningitis. Methods: Case Report. Review of the literature was conducted on Pubmed for the search terms: facial nerve palsy and meningitis. Results: We present the case of a 4-year old right-handed girl who presented with a new onset unilateral facial nerve palsy preceded by 5-day history of fever and headaches. The patient had meningeal signs and was identified to have Streptococcal Meningitis. MRI of the brain showed a large previously undiagnosed intranasal encephalocele. The facial palsy resolved within 7 days of antibiotic treatment. Conclusions: Our case represents an unusual combination of facial nerve palsy in context of Streptococcal Meningitis secondary to intranasal encephalocele.


2015 ◽  
Vol 166 (5) ◽  
pp. 1187-1192.e1 ◽  
Author(s):  
Daniel Tibussek ◽  
Adriane Sinclair ◽  
Ivanna Yau ◽  
Sarah Teatero ◽  
Nahuel Fittipaldi ◽  
...  

2016 ◽  
Vol 9 (3) ◽  
pp. 792-795 ◽  
Author(s):  
Shadi Hamouri ◽  
Duha Al Shorafat

Leptomeningeal carcinomatosis is rare, and its precise incidence is unknown. It is associated with a wide spectrum of solid and hematological malignancies. To complicate its diagnosis, the clinical presentation of leptomeningeal carcinomatosis can be variable. We report a case of a 38-year-old male with bilateral facial nerve paralysis as first presentation of lung adenocarcinoma. To our knowledge, this is the only case describing bilateral facial nerve palsy as the first and only manifestation of lung adenocarcinoma.


2017 ◽  
Author(s):  
Daniel Caroff ◽  
Chanu Rhee

Viral, fungal, and “atypical” bacterial pathogens are important causes of infections in critically ill patients. Many of these pathogens predominantly cause disease in immunosuppressed patients, but immunocompetent patients can also face serious illness or death. Understanding the risk factors and clinical syndromes caused by these pathogens is necessary to quickly identify patients who may need specialized diagnostics and treatment and is an essential component of training for any provider who practices in the intensive care unit. In this review, we discuss the most relevant aspects of clinical presentation, epidemiology, diagnosis, and management of these infectious agents, with a particular focus on respiratory tract infections. New advances in the diagnosis and treatment of influenza, invasive Candida infections, aspergillosis, and Legionella are highlighted. This review contains 3 figures, 5 tables, and 94 references. Key words: Candida, influenza, invasive pulmonary aspergillosis, Legionella pneumophilia, viral pneumonia


Author(s):  
Tiffanie-Marie Borg ◽  
Amy Sarah Warwick ◽  
Mas Ahmed

In this article we summarise the educational aspects regarding the clinical presentation, diagnosis and management of children presenting with facial nerve paralysis, highlighting the importance of family history. We report two cases of hereditary facial nerve paralysis managed by the authors: one a child with familial facial nerve palsy, and the other a child with Melkersson–Rosenthal syndrome. The history in both cases revealed multiple family members with the same disorder.


Neurosurgery ◽  
2006 ◽  
Vol 58 (4) ◽  
pp. E791-E791 ◽  
Author(s):  
Shigeo Ohba ◽  
Tomoru Miwa ◽  
Takeshi Kawase

Abstract OBJECTIVE AND IMPORTANCE: Schwannomas originating from the trochlear nerve without neurofibromatosis are extremely rare. Thirty-four cases have previously been reported in the literature, and only 25 cases were pathologically diagnosed. In addition, intratumoral hemorrhage in intracranial schwannomas is also rare. Approximately 30 cases of intracranial schwannomas with intratumoral hemorrhage have been reported. CLINICAL PRESENTATION: A 42-year-old man presented with left hemiparesis and right trochlear nerve palsy. Magnetic resonance imaging revealed an abnormal cystic lesion beside the brainstem. His symptoms rapidly worsened after enlargement of the mass because of intratumoral hemorrhage. INTERVENTION: Gross total removal of the tumor was performed via the anterior transpetrosal approach. The tip of the trochlear nerve was fanned out and unified with the tumor. The tumor was diagnosed as a schwannoma. CONCLUSION: The patient's hemiparesis improved postoperatively, and he was discharged 1 week after the operation. Magnetic resonance imaging performed 4 months later revealed no regrowth of the tumor. Only right trochlear nerve palsy has persisted. This report is the second case of intratumoral hemorrhage from a trochlear nerve schwannoma.


2010 ◽  
Vol 16 (1) ◽  
pp. 17-21 ◽  
Author(s):  
A. Santillan ◽  
W.E. Zink ◽  
J. Knopman ◽  
H.A. Riina ◽  
Y.P. Gobin

Palsy of the third cranial nerve (oculomotor nerve, CNIII) is a well-known clinical presentation of posterior communicating artery (P-com) aneurysm. We report a series of 11 patients with partial or complete third nerve palsy secondary to P-com aneurysm. All were treated with endovascular embolization within seven days of symptom onset. Third nerve palsy symptoms resolved in 7/11 (64%), improved in 2/11 (18%) and did not change in 2/11 (18%) patients


Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 5048-5048
Author(s):  
Mohamed Jumayli ◽  
Emily Chen ◽  
Hossein Sadrzadeh

Abstract Background: Primary cardiac lymphoma (PCL) is rare extranodal subtype of non-Hodgkin's lymphoma (NHL) .It is extremely rare in immunocompetent patients. PCL usually occurs in adults mean age of 62.1 years with male predominance. Primary cardiac Burkitts lymphoma (PCBL) is small subgroup of the PCL. Characteristics, presentation and the optimal management guideline of BL have not been clearly defined. Method: We performed PubMed searches using the particular terms including but not limited to primary, cardiac, burrkit's , lymphoma to identify reported adult cases of PCBL.Different Variables including demographic, immune status, clinical presentation, radiographic and other clinical variables were analyzed. Result: This is the largest study of PCBL up to now.We analyzed 10 cases of adult PCBL including 9 reported cases in literature and one case who presented to our facility.Majority of patients were older than 65 (7/10), which is consistent with other studies of Burrkit's lymphoma in immunocompetent patients particularly in sporadic type. This can be secondary to similarity of pathogenesis and oncogenesis of PCBL to sporadic type. Although age at presentation ranged from 30 to 85 years old, only (2/10) were younger than 40. .All reported PCBL in our analysis including the one who presented to our facility were HIV negative and immunocompetent state. Thus we propose that PCBL can be categorized as a subtype of sporadic BL (SBL) but interestingly PCBL was more common in older patients in contrast with SBL as is more common in younger individuals, with a peak incidence at age 30 in adults. Most of patients (7/10) were male, which is also consistent with other studies of majority of NHL subgroups including cardiac lymphoma. As expected all patients except one presented with cardiac symptoms. Dyspnea was the most prominent presenting symptom comparing to palpitation, syncope or chest pain. It is most likely secondary to large pericardial effusion, which was present in all patients, rather than the mass effect. Interestingly one case had no cardiac mass identified and PCBL was diagnosed with pericardial analysis. These demonstrate the importance of evaluation for and analysis of possible pericardial effusion in patients, who present with dyspnea As noted, our analysis showed that all patient except the one who presented to our facility, presented with cardiac mass (9/10). Similar to other studies of cardiac lymphoma, right heart particularly right atrium was the most common location of the cardiac mass. Cardiac lymphoma should be highly considered in patient with right atrial mass. Interestingly, Outcomes and chemotherapy response were variable; 3/10 cases reported favorable response to chemotherapy , however two cases with variable burrkit type and other chromosomal abnormalities had poorer prognosis. Due to rarity and low number of the cases ,outcome analysis adjusted with treatment regimen was not performed in our study. Conclusion: There is no comprehensive treatment analysis study for burrkit lymphoma . Due to complexity of pathogenesis and different behavior of this type of lymphoma, an efficient and optimal diagnostic, treatment and management guidelines for Burrkit lymphoma and its subtypes need to be developed. Table 1. Age Gender(Male : M, Female : F) Presenting Symptom Mass Location pericardial effusion Diagnosed by Chromosomal abnormalities HIV status Reference 79 F Dyspnea Left Ventricle (LV) Positive (pos) Pericardial analysis variant type-(8,22)(q24,q11), no c-myc negative (neg) J. Kuroda et al. elderly M Not available (NA) positive mass location NA NA NA NA neg S. Fatimi et al 61 F Dyspnea Right atrium (RA) +Right ventricle (RV) pos Excisional biopsy variant type- 49, XX, +X, t(8;14)(q24;q32), −14, +der(14)(3;8;14) (q27;q24;q32), +18, +20 neg Piero Maria Stefani et al. 33 M Dyspnea RA pos Excisional biopsy NA neg Chang-Fu Peng et al. 44 F Abdominal Discomfort RA pos Pericardial analysis t(8;14) neg Dimitrios et al. 77 M Dyspnea large mass , location NA pos Autopsy of mass t(8;14) neg Takai K. et al. 70 M Dyspnea RA pos Excisional biopsy t(8;14) neg M.De Filippo et al. 74 M Dyspnea RA pos Pericardial analysis NA neg Sylvie et al. 67 M syncope bi-atrial + LV pos Excisional biopsy t(8;14) neg Francesco Santini et al. 84 M Dyspnea No mass pos Pericardial analysis t(8;14) neg Presented to our facility Disclosures No relevant conflicts of interest to declare.


2020 ◽  
Vol 12 (1) ◽  
pp. 58-62
Author(s):  
Johanna Cecilia Enríquez Cruz ◽  
Adriana Elizabeth Araujo Yánez ◽  
Sayonara del Rocío Zaputt Cabrera

BACKGROUND: Disseminated cutaneous Herpes Zoster is defined as the presence of more than 20 vesicles outside the area and adjacencies of the primarily affected dermatome, the involvement of more than 2 contiguous dermatomes or the presence of systemic disease. Its prevalence among immunodepressed patients is 10- 40%, but between immunocompetent patients only isolated cases are reported. We present a case of an elderly immunocompetent patient, with no pathological history, that developed HZCD. CASE REPORT: An 89 year old woman, with no medical background, presented with 10 day evolution itchy, painful blistering lesions on the inner right thigh and the proximal third of the ipsilateral leg. Days after the lesions disseminated and the patient received topical treatment, she couldn’t specify the treatment; after 3 days her general condition worsened, and she was brought to the Emergency Room. EVOlUTION: Patient was diagnosed with Disseminated Herpes Zoster. She had a good outcome, after completing the intravenous antiviral treatment and she was discharged with no complications, after 10 days of being hospitalized. CONClUSION: Diagnosis of disseminated herpes zoster should be considered in both immunocompetent and immunocompromised patients. The outcome strongly depends on the promptness of the specific therapy instauration. KEYWORDS: HERPES ZOSTER, SKIN DISEASES, VESICULOBULLOUS, ANTIVIRAL AGENTS


Author(s):  
Dheeraj Lambor ◽  
Kanhai R. Naik ◽  
Carnegie DeSa ◽  
Swati Lambor ◽  
Ruby Samuel

<p><strong>Background: </strong>Necrotizing otitis externa is an infection affecting immune-compromised and elderly diabetic patients resulting in complications with significant morbidity and mortality. We present our experience with this disease, along with the investigative tools and treatment modalities that benefitted most. The objective being to analyze the course of the disease and the benefit of having an institutional protocol for its management.</p><p><strong>Methods: </strong>This is a retrospective observational study on patients diagnosed with necrotizing otitis externa between 2013-2019.</p><p><strong>Results: </strong>Out of 38 patients 36 were diabetics, the commonest clinical presentation included otalgia in 37 patients, granulations in 35, facial nerve palsy in 14 and <em>Pseudomonas aeruginosa</em> was isolated in 19 patients. They were managed with multidrug combination antibiotic therapy, topical dressing and drops with 27 showing improvement.</p><p><strong>Conclusions: </strong>We recommend a diagnostic triad for NOE comprising of otalgia in an elderly diabetic patient with granulations in the external auditory canal. It is best managed by controlling diabetes, appropriate antibiotic combination, topical dressing, and sometimes surgical debridement.</p>


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