Abstract
A 68-year-old man presented with facial cellulitis and found to have Neisseria meningitidis bacteraemia with no evidence of infection outside of the facial soft tissue. He was treated with a course of intravenous ceftriaxone and transitioned to oral amoxicillin on discharge with significant improvement of his symptoms. N meningitidis is best recognised as a causal agent of bacterial meningitis. To our knowledge N meningitidis cellulitis has only been described in 12 other cases. In this case series we describe and summarise our case, along with the 12 cases already reported in the literature. We report this case series to highlight the importance of recognising N meningitidis in the differential in patients presenting with acute skin and soft tissue infections especially involving the periorbital, head and neck regions.
Background
The case illustrates the importance of recognising Neisseria meningitidis as an uncommon but notable cause of cellulitis in immunocompetent hosts even in the absence of bacterial meningitis. It should thus be considered in the differential in patients presenting with acute cellulitis especially when the cellulitis affects the periorbital, head and neck regions.
Case presentation
A 68-year-old Chilean man presented with 2 days of facial swelling, which began in the lateral upper lip. The patient was presumptively diagnosed with food-related angioedema and treated with diphenhydramine and methylprednisolone then discharged home on a prednisone taper. The facial swelling worsened despite this treatment. On return to the emergency room (ER) the patient was febrile to 38.2°C, with marked erythema and oedema involving the right cheek, jaw and proximal neck. After additional questioning, he reported sustaining a small laceration during a recent shave at a barber. Labs were significant for a leukocytosis of 16 000 with a left shift. A maxillofacial CT scan demonstrated soft tissue stranding of the right cheek and submandibular gland with no fluid collection. Treatment was begun with intravenous clindamycin but the erythema and oedema worsened, thus antibiotic coverage was broadened to vancomycin and piperacillin-tazobactam. The patient was then admitted to the medicine floor.
Investigations
On hospital day 2 blood cultures returned with Gram-negative diplococci, subsequently speciated as N meningitidis.
Differential diagnosis
The differential diagnosis for acute cellulitis of the facial region includes Staphylococcus aureus, Streptococcus pneumoniae and Streptococcus pyogenes. Haemophilus influenza type B was once a common cause of facial cellulitis especially in children, but has now become rare due to widespread vaccination.1 As this case demonstrates, N meningitidis should also be considered in the differential of acute cellulitis.
Treatment
Antibiotics were narrowed to intravenous ceftriaxone 2 g four once daily blood cultures returned with N meningitidis and the erythema and oedema improved, after which the patient was discharged home on oral amoxicillin with the input of the infectious disease team.
Outcome and follow-up
During the patient's hospital stay, it was noted that the patient had a diffuse headache without meningeal signs and, due to the atypical bacteria, a lumbar puncture was performed to rule out meningitis. Cerebrospinal fluid (CSF) analysis revealed no evidence of infection. With improvement of his cellulitis, and improvement in his white cell count (WCC) count to 6000, the patient was discharged on oral amoxicillin 500 mg three times a day for 14 days, and told to follow-up with his primary care physician in Chili. It was advised that he be evaluated for endocarditis as well as complement deficiency as these conditions have been previously documented in association with N meningitidis cellulitis.2
Discussion
Facial cellulitis is a diagnosis commonly seen by internists, but rarely caused by Gram-negative organisms. N meningitidis is best recognised as a causal agent of bacterial meningitis. This infection can result in a variety of cutaneous sequelae including petechiae, ecchymosis and a maculopapular rash.3 Cellulitis is an uncommon manifestation of neisserial infection, with few reported cases in the literature. In children, six cases of N meningitidis have been reported.4–9 Of these children, one case was associated with meningitis.4 In adults, there have been six reported cases, only one of which was immunocompromised.8 10–13 Nearly all patients were reported to have concurrent bacteraemia. With the exception of one patient who died of concurrent complications and sepsis, all patients achieved complete resolution of their symptoms with antibiotic treatment. Table 1 provides a brief summary of cases of cellulitis caused by N meningitidis listed chronologically. Taken together these presentations suggest that N meningitidis has a predilection for the periorbital area, especially in children. In adults, it may also favour other structures in the face and neck with rare presentations in the upper and lower extremities.
Table 1.
| Age/sex | Site of cellulitis | Source of culture specimen | Serogroup | Other manifestations | Underlying conditions | Reference |
|---|---|---|---|---|---|---|
| 64 years/F | Right ankle calf | Cellulitic area | NA | None | CHF, DM, obesity, plasma cell dyscrasia | 10 |
| 9 years/F | Right periorbital area | Conjunctival exudate | C | Conjunctivitis, bacteremia, pericarditis | None | 6 |
| 8 months/M | Periorbital area | Blood | C | Bacteremia | None | 9 |
| 9 months/M | Right periorbital area | Blood | B | Bacteremia | None | 5 |
| 19 months/F | Right periorbital area | Blood, periorbital aspirate | C | Bacteraemia, conjunctivitis | None | 7 |
| 45 years/F | Left calf | Blood | Y | Bacteraemia, endocarditis | Hypocomplentemia, mixed connective tissue disease, poor LE circulation | 2 |
| 76 years/F | Face, neck | Blood | N/A | Bacteremia | DM, steroid dependent asthma | 11 |
| 44 years/F | Neck | Blood | Y | Bacteraemia, supraglottitis | None | 13 |
| 83 years/F | Left arm, hand | Blood | C | Bacteraemia | Pulmonary HTN, systemic HTN | 8 |
| 9 months/F | Left periorbital area | Conjunctival exudate | B | Conjunctivitis | None | 8 |
| 85 years/F | Left neck, Left shoulder, Left anterior chest | Blood | Y | Bacteraemia, sialadenitis | Stroke, polymyalgia rheumatica, sepsis | 12 |
| 4 months/F | Left periorbital area | CSF | B | Meningitis | None | |
| 85 years/M | Right periorbital area, right neck | Blood | ? | Bacteraemia | None | Present report |
CHF, congestive heart failure; CSF, cerebrospinal fluid; DM, diabetes mellitus; HTN, hypertension.
Our patient had no notable infectious risk factors, with exception of his age as well as a potential site of exposure secondary to a superficial wound the patient sustained in weeks prior to hospitalisation. Therefore, this case highlights the importance of recognising N meningitidis as a possible cause of cellulitis in immunocompetent hosts. This is particularly important as typical empiric agents for facial cellulitis do not treat this organism thus missing this diagnosis would leave patients at risk for progressive infection. Additionally, the case provides contributory evidence that neisserial infection, in the setting of acute cellulitis, has a predilection for the periorbital/facial region.
Learning points.
Best recognised as a causal agent of bacterial meningitis, Neisseria meningitidis is also a rare cause of cellulitis in immunocompetent hosts.
One potential treatment of N meningitidis cellulitis is a course of oral amoxicillin.
N meningitidis should be included in the differential in patients presenting with acute skin and soft tissue infections especially involving the periorbital, head and neck regions.
Footnotes
Contributors: All authors were involved in the creation of this article and approve the final manuscript submitted.
Competing interests: None.
Patient consent: Obtained.
Provenance and peer review: Not commissioned; externally peer reviewed.
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