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Herpetic esophagitis in a 7-year-old immunocompetent patient


Authors: Jabandžiev P. 1,2;  Jouza M. 1;  Pecl J. 1;  Urík M. 3;  Papež J. 1;  Pinkasová T. 1;  Slabá K. 1;  Trna J. 4,5;  Kyclová J. 6;  Vaculová J. 4;  Kunovsky L. 4,7
Authors‘ workplace: Department of Pediatrics, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic 1;  Central European Institute of Technology, Masaryk University, Brno, Czech Republic 2;  Department of Pediatric Otorhinolaryngology, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic 3;  Department of Gastroenterology and Internal Medicine, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic 4;  Department of Gastroenterology and Digestive Endoscopy, Masaryk Memorial Cancer Institute, Brno, Czech Republic 5;  Department of Pathology, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic 6;  Department of Surgery, University Hospital Brno, Faculty of Medicine, Masaryk University, Brno, Czech Republic 7
Published in: Gastroent Hepatol 2020; 74(3): 233-237
Category: Digestive Endoscopy: Case Report
doi: https://doi.org/10.14735/amgh2020233

Overview

Herpetic esophagitis is a disease dia­gnosed especially in immunocompromised patients. Although the disease is rare in immunocompetent individuals, the dia­gnosis should be considered in the presence of its acute triad of clinical symptoms – odynophagia, chest pain, and fever of unknown origin. Herpes simplex virus type 1 (HSV1) is the most common causative agent. In the majority of cases, the disease develops by re-activation of latent HSV1 infection or, rather rarely, by primo-infection. The basis of dia­gnosis is endoscopic examination of the esophagus with bio­psy and direct detection of the virus in the bio­ptic sample. In immunocompromised patients, treatment with acyclovir, which is the first-line virostatic in this indication, is always indicated. In immunocompetent patients, this is a self-limiting disease, where in most cases merely symptomatic treatment is sufficient. This case report describes an immunocompetent patient with a suddenly occurring typical triad of symptoms caused by herpetic esophagitis. The dia­gnosis was confirmed by the presence of viral DNA as determined by polymerase chain reaction from a sample taken during endoscopic examination. Due to the more severe course of the disease, the patient was treated with acyclovir and the general condition and local endoscopic findings then quickly improved.

Keywords:

endoscopy – children – herpetic esophagitis – acyclovir

Introduction

Along with cytomegalovirus and candida, herpes simplex virus (HSV) is one of the possible causative agents of ulcerative esophagitis in immunocompromised patients (e. g., HIV patients, immunosuppressed patients, patients with severe systemic disease or severe burns, patients with long-term corticosteroid therapy) [1,2]. Despite the high prevalence of primary and recurrent HSV infection in the population [3], clinically manifested herpetic esophagitis (HE) is rare in immunocompetent patients [4]. Isolated cases of HE in immunocompetent children are nevertheless described in the literature [5–11].

Case report

A 7-year-old patient who had previously been healthy was transferred to the Department of Pediatrics of the University Hospital Brno from the pediatric department of a district hospital. He was a normally thriving boy with adequate psychomotor development who had been properly vaccinated with no adverse manifestations. He had had no physiological morbidities up to that time and no allergic disease. He had not taken any medication for a long time. Before the occurrence of the clinical symptoms, the boy had spent a month of summer holidays in Montenegro. Otherwise, the epidemiological history obtained on admission was negative. Four days before the admission to the hospital, the boy had had a fever that reached a maximum of 38.5 °C. The fever had responded well to antipyretic therapy. The boy had no other problems. On the second day of the fever, dysphagia and odynophagia had occurred. After examination by a GP for children and adolescents, proton pump inhibitor therapy in the usual dosage had been recommended. Despite the established treatment, the swallowing problems worsened over subsequent days and the boy had to be hospitalized in the children’s ward of the district hospital. The possibility of having ingested a foreign body was excluded by the patient and parents. There had been no previous signs of primary immunodeficiency or other signs of gastrointestinal disease in the patient.

There was significant elevation of CRP (110 mg/l) in the baseline blood samples, mild leukocytosis in the blood count, and significant ketonuria without glycosuria in the urine. During hospitalization, a chest CT scan was performed but did not show any specific pathology. Parenteral nutrition was initiated and symptomatic therapy (proton pump inhibitor, nonsteroidal anti-inflammatory drugs) continued. For persisting difficulties without significant improvement, the boy was transferred for further examination to the university hospital.

The initial clinical examination was without noteworthy changes. In a detailed supplement to the epidemiological history, it was found that 4 days prior to the onset of the patient’s complaints, his mother had had a significant eruption of herpes labialis. The patient himself had never had such symptoms. As a further step to the dia­gnosis, an esophagogastroduodenoscopic examination was performed. Significant inflammatory changes transitioning to longitudinal ulcerations in the distal third of the esophagus were revealed (Fig. 1A, B). In addition to the standard sampling of esophageal tissue, bio­psy material was also sent for bacteriological and mycological examination and also for the detection of HSV and cytomegalovirus by polymerase chain reaction (PCR).

1. A. Endoscopic imaging – view of distal esophagus. Ulceration covered by mucus, mucosa fragile to the touch, contact bleeding.
Obr. 1A. Endoskopický obraz – pohled na distální jícen. Ulcerace kryté hlenem, sliznice kâehká na dotek, kontaktně krvácející.
A. Endoscopic imaging – view of distal esophagus.
Ulceration covered by mucus, mucosa fragile to the touch,
contact bleeding.<br>
Obr. 1A. Endoskopický obraz – pohled na distální jícen.
Ulcerace kryté hlenem, sliznice kâehká na dotek, kontaktně
krvácející.

Fig. 1B. Endoscopic imaging – ulceration of the distal esophagus.
Obr. 1B. Endoskopický obraz – ulcerace distálního jícnu.
Fig. 1B. Endoscopic imaging – ulceration of the distal
esophagus.<br>
Obr. 1B. Endoskopický obraz – ulcerace distálního jícnu.

Given that this was a relatively unusual finding in a pediatric patient, empirical therapy with antibio­tics (cefuroxime), antifungal agent (fluconazole), and antiviral drug (acyclovir) were administered intravenously. Over the next two days, there was a significant subjective improvement in symptoms. The patient began to tolerate fluids and subsequently a semi-solid diet, and the fever disappeared.

The result of HSV DNA detection by PCR from the esophageal mucosa was positive. Histological examination of the tissue taken from the affected area of the esophagus confirmed the presence of nonspecific ulceration (necrosis and granulation tissue) (Fig. 2), but the pathognomonic features of herpesvirus infection (inclusion, multinucleated keratinocytes) were not found in the sample. Immunohistochemistry (anti-CMV antibody) and special staining (PAS, Grocott silvering) excluded the presence of cytomegalovirus and fungal infection.

2. Histological examination – base of ulceration consisting of granulation tissue with mixed inƪ ammatory infiltrate.
Obr. 2. Histologické vyšetření – spodina ulcerace tvořená smíšeně zánětlivě celulizovanou granulační tkání.
Histological examination – base of ulceration consisting of granulation
tissue with mixed inƪ ammatory infiltrate.<br>
Obr. 2. Histologické vyšetření – spodina ulcerace tvořená smíšeně zánětlivě
celulizovanou granulační tkání.
The presence of smooth muscle bundles verifies the depth of ulceration to the muscularis propria. Hematoxylin-eosin staining, magnification 30-times. Stars indicate smooth muscle bundles, vertical arrows indicate inflammatory infiltrate.
Přítomnost snopců hladké svaloviny dokumentuje hloubku ulcerace až ke svalovině muscularis propria. Barvení hematoxylin-eozinem, zvětšení 30krát. Hvězdičky – snopce hladké svaloviny, svislé šipky – zánětlivý infiltrát.

Due to the relatively unusual dia­gnosis, an immunological examination was performed. This did not indicate any impairment of immunity. After completing the results of the microbio­logical examination, the antimicrobial treatment was revised. Antiviral therapy was maintained until the result of the control esoph­agogastroduodenoscopy, which was performed 3 weeks after the dia­gnosis. Endoscopic and histopathological examination confirmed the complete disappearance of inflammatory changes in the esophagus.

Discussion

HE was first described in 1940 by Johnson [12] and confirmed histopathologically by the Pearce team 3 years later [13]. HE is regarded today as an opportunistic infection that usually affects patients with immune disorders [1]. The first larger set of endoscopic findings of immunocompromised patients in which the dia­gnosis was based on virus culture was described by McBan in 1991 [14]. In 2000, Ramathan et al published an overview of HE described in immunocompetent patients, including several children [4].

HE can be caused by human HSV types 1 and 2. Type 2 is, however, rarely the causative agent [6]. Nevertheless, 20% of adult HE patients have been reported to have concomitant oropharynx and genital involvement [4]. The HSV rarely attacks internal organs. In such cases as it does so, the esophagus is often affected but the lungs and kidneys very rarely. Cases with stomach involvement also have been described [15,16]. In a series of 1,307 autopsies performed in adults, a study from Japan found an incidence of HE in 1.8% patients [17]. HE can develop as a result of direct expansion in the primary infections of the orofacial region or as a result of reactivation of latent infection when invasion of the esophagus mucosa by anterograde neuronal migration had occurred via the vagus nerve [1].

One of the predisposing factors of HE in immunocompetent patients may be esophageal mucosal trauma. This predisposition may be gastroesophageal reflux disease, previous esophageal instrumental examination, long--term insertion of a nasogastric tube, or swallowing of a foreign body [5]. HE is typically manifested by a triad of symptoms: odynophagia, chest pain, and fever of unknown origin. These symptoms are usually accompanied by weight loss [4,14].

The dia­gnosis of HE consists of an endoscopic examination, exclusion of other causes (from infection, especially cytomegalovirus and candida), and confirmation of HSV’s presence. Bioptic examination almost always shows inflammatory changes of the mucosa, but only in some cases can the typical dia­gnostic signs of herpesvirus infection (i.e., intranuclear inclusion in the epithelium of the esophageal mucosa, either eosinophilic [Cowdry A type] or ground-glass [Cowdry B type]) be found [18]. Distinguishing of HSV and varicella-zoster virus is not possible with the use of light microscopy. In the past, the virus has been proven by a combination of immunohistochemical methods and cultivation [4,14]. Presently, due to its indisputable advantages, the detection of viral DNA by PCR is used [19].

The dia­gnosis is therefore usually based on clinical signs, upper gastrointestinal endoscopy, histology, microbio­logical examination, and then PCR, respectively. Serological examination may be another marker for dia­gnosis [20].

Other esophageal infections (cytomegalovirus, varicella-zoster virus, candida, or various bacterial agents), trauma, esophageal burns, and inflammatory diseases such as Crohn’s disease or Behcet’s disease may be considered in the differential dia­gnosis of ulcerative esophagitis [21].

Acyclovir, famciclovir, and valacyclovir are used to treat HE in immunocompromised patients [22].

HE in immunocompetent patients appears generally to be self-limiting [23]. The reasons for administering antiviral therapy may include expectation to reduce the length of the period of infection or to treat or prevent complications.

Primary HSV infection is a common disease in childhood. Positive antibodies to HSV 1 occur in as many as 90% of all adolescents. The highest incidence of the disease with clinical manifestation is around 2 years of age, and gingivostomatitis is the most common clinical form of the disease [5]. During primo-infection, HE can occur rather frequently and thus be underdia­gnosed. It is very likely that undia­gnosed esophagitis may also be suffered by patients with severe primo-infection (i.e., herpetic gingivostomatitis or pharyngitis), as well as patients with gastroesophageal reflux disease treated with proton pump inhibitors. HE in immunocompetent children is mostly represented by primo-infection, but it may also follow reactivation of latent infection. Although HSV infections of the visceral organs are the result of viremia, esophagitis as such is rather the result of a direct spread of oropharyngeal involvement. Boys are more affected than girls in a ratio of 3.4/1.

The described patient had been in contact with his mother who had symptoms of labial herpes 4 days before the onset of his symptoms. It can be assumed, therefore, that this was a primary HSV infection that then spread to the esophagus. This would correspond to the initial negative serological examination of HSV antibodies in the patient. Also, our patient showed no other clinical signs of immunodeficiency and the results of the immunological examination werenormal.

The clinical manifestations described in the literature (which means the triad of odynophagia, chest pain, and fever) were also present in this case.

Submitted/ Doručeno: 27. 3. 2020

Accepted/ Přijato: 29. 3. 2020

Lumír Kunovský, M.D., Ph.D.

Department of Gastroenterology and Internal Medicine, University Hospital Brno,

Faculty of Medicine, Masaryk University

Jihlavská 20

625 00 Brno, Czech Republic

e-mail: lumir.kunovsky@gmail.com


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