| Literature DB >> 34178349 |
Erina Fujiwara1, Takeshi Tsuda1,2, Kento Wada1, Sadanori Waki1, Yukiko Hanada1, Hiroshi Nishimura1.
Abstract
Cervical abscesses develop in the tissue spaces between the cervical fascia. The rapid expansion of these abscesses can lead to fatal outcomes. We describe a case of a deep cervical abscess caused by Parvimonas micra. He was referred to our department with complaints of sore throat and neck pain. Ultrasonography revealed a hypoechoic area in the cervical interfascicular space. An ultrasound-guided puncture was performed to collect pus for bacteriological examination. Subsequently, a contrast-enhanced computed tomography scan revealed a multi-focal abscess extending from the left mandible to the left side of the neck, without any mediastinal abscess. An emergency drainage and antibacterial therapies were performed, and the patient progressed well. Parvimonas micra, a gram-positive anaerobic bacterium, was detected in the pus collected before incision, and appropriate antibiotics were immediately administered. The collection of pus prior to incision and drainage aids accurate identification of the causative organism and appropriate treatment.Entities:
Keywords: Cervical abscess; Parvimonas micra; ultrasound guided puncture
Year: 2021 PMID: 34178349 PMCID: PMC8202303 DOI: 10.1177/2050313X211024505
Source DB: PubMed Journal: SAGE Open Med Case Rep ISSN: 2050-313X
Figure 1.(a) Pre-operative cervical ultrasound image. Extensive hypoechoic areas with indistinct borders noted in the left mandible and just below the sternocleidomastoid muscle in the left neck. (b) Pre-operative contrast-enhanced computed tomography. A low-density area is seen from the left mandible to the left deep neck. The same area has a contrast effect on the margins and an internal septum.
Figure 2.(a) Susceptibility of various antimicrobial agents to Parvimonas micra. No resistance to any antimicrobial agent observed. (b) Post-hospitalization progress. On the day of admission, the abscess was punctured and incision and drainage were performed under general anesthesia. Antimicrobial agents were administered as shown in this figure. The patient’s symptoms improved quickly with a decrease in inflammation.
MIC: minimal inhibitory concentration; PCG: penicillin G; ABPC: ampicillin; ABPC/SBT: ampicillin/sulbactam; AMPC/CVA: amoxicillin/clavulanate; TAS/PIPC: tazobactam/piperacillin; CMZ: cefmetazole; CZX: ceftizoxime; IPM/CS: imipenem/cilastatin; MEPM: meropenem; CLDM: clindamycin; MINO: minocycline; CP: chloramphenicol; WBC: white blood cell; CRP: C-reactive protein.