COVID 19 vaccination as a trigger of acute genital ulcers in an immunocompromised adolescentcase study and … – BioMed Central

When diagnosing external genital ulcers in women, both endo- and exogenous causes should be considered. The specialists should pay attention to both infectious and non-infectious reasons [9].Numerous factors such as infectious, inflammatory, immunological, neoplastic, traumatic, or medication-induced causes need to be taken into account [10].In adolescents the most common causes of AGU are: herpes simplex virus (HSV), Epstein-Barr virus, cytomegalovirus, human immunodeficiency virus (HIV), Behcets disease, Crohns disease (CD), ulcerative colitis, celiac disease, cyclic neutropenia, periodic fever syndromes and leukemia [9].

A thorough physical examination should be performed following detailed history-taking, because a patients childhood diseases can have a significant impact on their current health problems. Our patient was diagnosed with PFAPA syndrome in the past. This disease is a complex auto-inflammatory disorder diagnosed on the basis of clinical symptoms such as periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis. The course of the disease is characterized by alternating periods of relapses and remissions, and the main symptoms are often accompanied by gastrointestinal disorders [11]. Beside the chief complaint, our patient presented abdominal pain, nausea and vomiting.

PFAPA syndrome is associated with a polygenic predisposition to impaired functioning of the innate immune system. The interaction of genetic susceptibility and environmental factors, including infections, predisposes individuals to the occurrence of the disease and its recurrence in the autoimmune mechanism [11, 12]. People suffering from PFAPA display increased activation of CD4Th1 and Th17 lymphocytes [13]. This molecular susceptibility results in the dysfunction of antigen-presenting cells, e.g. monocytes, and in dysregulation of T cells. Monocytes produce higher levels of pro-inflammatory cytokine IL-12, which stimulates CD4 and CD8 lymphocytes to produce excessive amounts of IFN- and lipopolysaccharides (LPS) [14].Moreover, the expression of the IL-10 gene decreases, resulting in a reduction of anti-inflammatory IL-10 cytokine [13]. In addition, down regulation of CCR1 (CC motif chemokine receptor 1) predisposes to a reduced migration of monocytes [15]. Depletion of these cells in inflammatory diseases may lead to increased migration of microorganisms through the permeable mucous membrane, which results in ulceration [14]. In PFAPA, the classical complement pathway is activated, while the alternative pathway remains unchanged. During PFAPA flare-ups, the levels of T-cell chemokines (IP-10/CXCL10, MIG/CXCL9), G-CSF (granulocyte colony-stimulating factor), and pro-inflammatory cytokines IL-1, IL-6, IL-12, IL-18 are all increased, and the complement system is activated [11, 12]. PFAPA is a consequence of excessive intracellular protein complexes response with the participation of pro-inflammatory factors such as caspase-1, IL-6, IP-10 (interferon gamma-induced protein 10) and interleukin 1 receptor antagonist (IL1Ra), but the levels of other pro-inflammatory factors, such as TNF (tumor necrosis factor) and MCP-1 (monocyte chemoattractant protein-1), remain relatively steady.

During PFAPA attacks, the complete blood count shows increased levels of neutrophils and monocytes, with low levels of lymphocytes and eosinophils [12, 16]. The disease usually responds to treatment with corticosteroids [11]. The administration of antibiotics is not justified due to the autoimmune basis of the disease. Tonsillectomy provides a 7097% long-term remission of the PFAPA syndrome [17].

PFAPA syndrome may predispose to the occurrence of AGU [13, 18]. However, AGUs are a very rare and atypical manifestation of PFAPA. The presence of vulvar ulcers in PFAPA patients is influenced by reduced IL-10 (anti-inflammatory cytokine) and CCR1 levels [13, 14]. According to Scattoni et al. this atypical symptom should be regarded as a potential and useful indicator of PFAPA [18].

In the present study, we took into consideration the influence of the PFAPA syndrome on the development of labial ulceration in our patient. The immune and genetic determinants that caused the PFAPA syndrome could also lead to the appearance of ulcers after the occurrence of provoking factors. The patient's leukocyte, neutrophil, and eosinophil levels resembled those typically found in PFAPA syndrome. The vulvar lesions were accompanied by fever episodes, abdominal pain, nausea, and vomiting. Additionally, our patient did not undergo a tonsillectomy, a procedure reducing the risk of the PFAPA syndrome recurrence.

Furthermore, as emphasized by researchers, the incidence of PFAPA syndrome rose during the COVID-19 pandemic [14].

An effective vaccination against SARS-CoV-2 was a vital tool to halt the spread of the pandemic; however, some predisposed people may have presented adverse reactions to the vaccination. Several cutaneous side effects were observed, e.g. delayed large local reactions and eruptions.

Recently, cases of AGU associated with COVID-19 vaccinations have been reported [2, 5, 19]. Of the 94 cases of vulvovaginal ulceration reported in the female adolescent age group, there was evidence that at least 37 were AGUs. In addition, up to December 2022, there were approximately 12 case reports published in scientific literature on genital ulceration after COVID-19 vaccine administration in non-sexually active adolescent patients. In majority, the events occurred after the second dose, usually within 1week. Common symptoms included pain-related difficulty in urination, defecation, sitting and walking. Fever, vulvar swelling and fatigue were also noted. Despite a different approach, the ulcers were usually self-limiting and healed between 2 to 6weeks [20].

The most frequently reported altered effects of vaccines are pain and swelling. Mucosal changes (bleeding gums, oral sores and ulcers) may occur after administration of diphtheria, tetanus, acellular pertussis and polio vaccines [19]. Incidences of lichen planus, a chronic inflammatory disease which affects the stratified squamous epithelium and frequently involves the oral and genital mucosa, have been reported after hepatitis B vaccination. In all likelihood, the immune system recognizes epitopes similar/identical to proteins of the virus on keratinocytes and induces immunological response and apoptosis of these cells [21].

Once an mRNA vaccine is administered,the spike protein, a viral receptor-binding protein, is produced by ribosomes in muscle cells. Subsequently, it binds to the host receptor angiotensin-converting enzyme 2 and triggers a robust CD8+and CD4+cell mediated response, inducing the production of neutralizing antibodies and memory of B and T-cells. COVID-19 vaccinations induce an autoimmune response by several pathways, including the development of specific autoantibodies, the effects of certain vaccine adjuvants, and molecular mimicry [22].

The SARS-CoV-2 spike protein and lung surfactant proteins share 13 out of 24 pentapeptides and the respiratory system is the most frequently attacked system in the case of COVID-19 infection. A similar mechanism of cross-reactions between the virus proteins and a variety of human antigens could possibly lead to autoimmunity against other organs, including the formation of mucosal and skin lesions induced by the coronavirus invasion as well as COVID-19 vaccines [22].The side effects of a vaccination might as well be due to transient bursts of IFN-I expression, effective antibody production, oxidative stress and DNA-damage, which may stimulate hyperinflammatory conditions. Another explanation indicates that in the case of mRNA vaccines, mRNA presents as both antigen and adjuvant, and might be so identified by Toll-like receptors, which trigger inflammation and immunity [22]. Nevertheless, the pathophysiology of AGUs after vaccination remains poorly understood.

A rare problem following COVID-19 vaccination described in the literature is Behcet's disease, and it is also possible that AGUs after vaccination are the first manifestation of this condition [23].

Behcets disease (BD) should also be evaluated in our patients history of aphthous lesions in the mouth and genital ulceration. Behcets disease is a rare inflammatory disorder diagnosed based on clinical symptoms and specific characteristics. According to the new criteria, a patient who scores4 points is classified as having BD. Characteristic signs and symptoms include ocular lesions (2), genital aphthosis (2), oral aphthosis (2), skin lesions (1), neurological manifestations (1), vascular manifestations (1) and, optionally, a positive pathergy test (1) [24]. In addition, BD is often associated with the neutrophil to lymphocyte ratio (NLR) being increased while the hemoglobin (HB) level is decreased. Additionally, there is an increase in the erythrocyte sedimentation rate (ESR) and CRP, and the human leukocyte antigens (HLA-B51) test shows positive results [25].

The pathomechanism of BD may depend on neutrophil-mediated mechanisms, that is, neutrophil hyperactivation via both a massive reactive oxygen species (ROS) production and neutrophil extracellular traps (NETs) release. BD patients have higher serum concentrations of sTNFR, leptin, sCD40L, and IL-6. Tumor necrosis factor alpha (TNF-alpha), leading neutrophils to disrupt the oral mucosa, is elevated in patients with recurrent aphthae, and affects endothelial cell adhesion and neutrophil chemotaxis. This is believed to be one of the molecular factors that are responsible for aphthous ulcers. As mentioned above in the present article, aphthous ulcers may occur both as a rare side effect of COVID-19 vaccination and as a consequence of high serum concentrations of sTNFR in BD [26].

,PFAPA syndrome and Behcets disease are characterized by similar pathomechanism. For this reason, they are often considered in the differential diagnosis [10, 13]. It is postulated that the same HLA type, specifically, HLA-B5 and HLA-B51, is involved in the development of both diseases [13, 14].Thus, ulceration in the vaginal area can be a symptom of PFAPA syndrome and Behcets disease.

The vulva can be affected by a variety of microorganisms including bacteria, viruses, fungi and parasites. Commonly, those infections are transmitted by sexual contact. However, in non-sexually active adolescents, genital infections might develop as well. AGU is commonly described as associated with a variety of infections including cytomegalovirus, herpes zoster virus (HZV), influenza type A and B, mumps virus, salmonella, mycoplasma and, most commonly, Epstein-Barr virus [4].

EBV causing infectious mononucleosis syndrome has been reported as a most common cause of AGU. Serologic testing for EBV in patients with vulvar ulcers demonstrated evidence of acute as well as prior infections [3]. Most patients develop systemic symptoms of IMS, and lymphadenopathy distant from the site of ulceration is also common; however, in the presented case the enlargement of lymph nodes has not been noted. Acute CMV infection has also been detected in patients with AGU and CMV inclusions found in cells of the vulva and cervix [3, 27]. As for the vulvar HZV infection, it is uncommon and often causes pain or a burning sensation. Lesions usually appear in a specific dermatomal distribution.

Herpes simplex virus, causing genital herpes, remains the most common factor of genital ulcers among sexually active females. However, it might also be responsible for ulcers in non-sexually active adolescents [4, 28]. There are two types of HSV. HSV-2 is considered to be the main cause of AGU, whilst HSV-1 is mostly linked to oral cavity lesions.

American pediatric and adolescent gynecology care providers suspect an 80% of HSV etiology at the onset of AGU diagnosis, therefore aggressive diagnosis of lesions should be delayed [29].

Since there is no single infectious agent identified as a cause of AGU, clinical examination and detection of viral genetic material or serologic tests play a pivotal role in the diagnostic process.

We also considered the possibility of vulvar cancer, although the incidence of genital cancers are rare in young females [30]. However, the macroscopic appearance of the vulvar lesion as an ulcer raised suspicions of oncological concern. There are two types of vulvar intraepithelial neoplasia (VIN). One of them, defined as differentiated (dVIN), is often associated with lichen sclerosus. The other refers to vulvar high-grade squamous intraepithelial lesions (vH-SIL) [31]. It is an HPV-related oncology condition that is specific to younger women and refers to intraepithelial neoplasia and squamous cell vulvar carcinoma (SVC) [32]. Moreover, given the increase in HPV infections and an early age of sexual initiation, there is a significant risk of vulvar cancer in younger age groups [33]. However, biopsy from vulvar lesions in children is debatable among many researchers unless there is a recurrence or a non-infectious etiology is suspected [29]. Most cases of vulvar ulceration in young women are self-limiting and respond to topical and systemic corticosteroid therapy. For these reasons, some authors recommend reducing extensive diagnostics [34].In our study, due to the extensive area of necrosis as well as the specificity of a hospital also providing oncological treatment, it was decided to collect material for histopathological examination. Biopsy excluded neoplastic invasion, therefore we ruled out vulvar cancer.

Link:

COVID 19 vaccination as a trigger of acute genital ulcers in an immunocompromised adolescentcase study and ... - BioMed Central