Abstract
Necrotizing fasciitis (NF) is a severe infection involving the superficial fascial layers, subcutaneous cellular tissue, and possibly skin. It usually has a fulminant evolution, rapidly leading to death in the absence of early diagnosis and aggressive surgical treatment. We herein report a rare case of NF secondary to a traumatized occipital psoriatic plaque in an alcoholic 47-year-old woman and compare this case with the published literature. The NF extended to the entire scalp, right face, and posterior and lateral cervical region. Despite the initially guarded prognosis, the patient’s survival emphasizes the importance of aggressive surgical treatment with wide excision of all necrotic structures without any aesthetic compromise.
Keywords
Introduction
The term “necrotizing fasciitis” (NF) was coined by Wilson in 1952. 1 This condition was earlier described by Hippocrates and subsequently compared with “hospital gangrene” by the Confederate Army surgeon Joseph Jones because of its severity, pattern of infection, fulminant progression, and extension along the superficial fascial layers with involvement of the subcutaneous cellular tissue, skin, and underlying muscles.2,3 NF involving the scalp and cervical and facial region has rarely been described.4–7 Septic venous thrombosis and thromboangiitis obliterans in the papillary dermis can lead to marked tissue necrosis.8,9 In patients with improper surgical management of NF, death is induced by progressive organ failure. 10 The etiology of NF varies in the literature; reported causes include dento-periodontal foci 11 associated or unassociated with diabetes mellitus, intravenous drug use and abuse, 12 trauma compromising the skin barrier,13,14 and postoperative complications or even idiopathic causes.4,15 Regardless of the causal factor, any type of infection is likely to be worsened by alcoholism, diabetes mellitus, renal failure, malignancy, immunological deficiencies, nutritional disorders such as obesity, increased age, and even metabolic syndrome in young adults. 16 The development of NF on the background of psoriasis vulgaris with or without alcoholism has rarely been reported.17,18 A multimicrobial pattern of NF with predominance of streptococcal bacteria is more frequent than a monomicrobial pattern, and the prognosis is guarded if the diagnosis is delayed.10,19–21 Successful surgical treatment must be initiated within the first 24 hours after onset22,23 to prevent complications such as mediastinitis, aspiration pneumonia, septic shock, or internal jugular vein thrombosis.9,10
We herein present a rare case of NF of the scalp with an emphasis on its unusual onset and severe evolution. This case is being reported to make clinicians aware of the extreme importance of rapid diagnosis and treatment to prevent death in patients with NF. Presentation of this case was approved by the Ethics Committee of the Clinical Emergency County Hospital. The patient consented to the reporting of her case, and the authors respected her confidentiality by using anonymous information and pictures that do not expose the patient’s facial features.
Case report
A 47-year-old Caucasian woman with a 26-pack-year history of cigarette smoking, 10-year history of consumption of more than 1 glass of alcohol per day, and untreated chronic psoriasis vulgaris was found unconscious on the floor of her house in May 2017. She had been previously treated at a regional hospital with meropenem (intravenous infusion of 1 g powder for solution every 12 hours for 2 days). Interhospital transfer to the Oral and Maxillofacial Surgery (OMFS) Clinic of Cluj Napoca, Romania was performed for evaluation and treatment of an extensive infection of an occipital excoriated psoriatic plaque. Upon admission to the OMFS department, the patient had a normal temperature, tachypnea, tachycardia, hypotension, tumefaction in the right area of her face and neck, bilateral palpebral microabscesses, a large occipital psoriatic plaque of 10 × 7 cm, and massive crepitations in the occipital and posterior cervical regions (Figure 1). Within 1 hour, emergency surgery was performed and involved a wide posterior cervical incision from the contralateral margin of the trapezius muscle to the right lateral cervical region, extending along the anterior margin of the right sternocleidomastoid muscle. This was complemented by a right submandibular incision from the right mastoid process to the mental region. Extensive necrosis affected the occipital epicranial galea, posterior cervical fascia, and right superficial cervical fascia from the right temporozygomatic arch to the superior border of the right clavicle (Figure 2(a)). We performed wide excision, applied a sterile dressing, and carried out extensive washing with oxygenated water and povidone-iodine solution. A postoperative contrast-enhanced computed tomography scan revealed no additional fluid or gas collections in the superficial fascial layer or deep cranial, facial, and cervical layers. After 3 days of empirical antibiotic therapy (vancomycin 1000 mg, imipenem 500 mg, and metronidazole 500 mg powder for solution, infused intravenously every 12 hours), we performed a limited right lateral cervical and supraclavicular necrectomy with complete excision of the platysma muscle, partial excision of the lateral cervical skin flap, total necrectomy of the splenius capitis muscles, and partial necrectomy of the semispinalis capitis muscles (Figure 2(b)). The postoperative outcome was favorable in the right face and lateral and cervical regions despite leukocytosis (11.000 ×103/dL) and fever (38.8°C). Three days later, bacteriological wound drainage and drug sensitivity testing showed

First postoperative day – Clinical appearance of the occipital psoriatic plaque after the initial posterior cervical incision.

Intraoperative view. (a) Superficial necrotic area of the right sternocleidomastoid muscle and right supraclavicular fossa. (b) The two semispinalis muscles after excision of the superficial splenius capitis muscles as well as the interstitium between these muscles after excision of the posterior cervical line. (c) Necrectomy of the epicranial galea. (d) Necrectomy of the right temporal fascia.

(a, b) Final outcome of the scalp and posterior cervical and laterocervical regions with secondary granulation prior to plastic reconstruction. (c) Final outcome of reconstruction of the occipital scalp and posterior cervical region with a trapezius muscle flap. (d) Final outcome of reconstruction of the laterocervical region with a free skin graft.
Discussion
NF most frequently affects the abdomen and limbs.
24
NF of the head and neck is rare;5–7,9,11,12,25,26 it is a hidden
27
but not forgotten disease,
28
such as tuberculosis of the oral cavity.
29
In such cases, the impact of immunosuppression caused by psoriasis,
17
herpes zoster,
27
alcoholism,
18
uncontrolled diabetes mellitus, and chronic renal failure must be considered. Correct diagnosis of NF is frequently difficult because it can mimic soft tissue cellulitis, erysipelas, or lymphedema.
27
This confusion often leads to inadequate, less aggressive treatment and delayed intervention (>48 hours), increasing the mortality rate to 50%,2,10 especially in cases involving interhospital transfer.
30
From a microbiological viewpoint, NF is classified into four main types.
31
Type I is generally plurimicrobial, characterized by the combination of aerobic with at least one anaerobic or facultative anaerobic species with synergistic virulence between them.
32
Type II is a monomicrobial infection most frequently caused by group A
In conclusion, rapid diagnosis and surgical therapy of NF are crucial for patient survival. Despite the occurrence of a rare type of NF secondary to a neglected multimicrobial infected occipital psoriatic plaque after minor trauma, aggressive surgery with no compromise in favor of the patient’s aesthetic appearance followed by plastic reconstruction were successfully performed in a 47-year-old alcoholic woman.
Footnotes
Declaration of conflicting interest
The authors declare that there is no conflict of interest.
Funding
This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.
