The Impact of Hypo Allergic Diet to Control of Fever Attacks in Children with Periodic Fever, Aphthous Stomatitis, Pharyngitis, Cervical Adenitis (PFAPA) Download PDF

Journal Name : SunText Review of Pediatric Care

DOI : 10.51737/2766-5216.2024.044

Article Type : Research Article

Authors : Shiari R, Khave LJ, Mirzaee AZ, Shiari S , Babaei D

Keywords : Periodic fever, Aphthous stomatitis, Pharyngitis, PFAPA, Allergy

Abstract

Background: Periodic Fever, Aphthous stomatitis, Pharyngitis, and Cervical Adenitis (PFAPA) is the most common cause of periodic fever syndrome in childhood.

Objectives: Although steroids are effective in controlling fever episodes, no medication has proved to be helpful for the prophylaxis of febrile episodes.

Methods: Herein, we evaluated the allergic profile in 33 confirmed cases of PFAPA and its correlation to PFAPA occurrence, symptoms, and role in treatment.

Results: In the skin prick test studies, a few allergens demonstrated a larger proportion in the study population and probably stronger associations with PFAPA occurrence.

Conclusions: It is essential to educate patients and their families on the management of food allergies and to review their risk of developing fever attacks in PFAPA patients.


Introduction

The syndrome of periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis (PFAPA) is the most common auto inflammatory periodic fever disorder first described in 1987 for the first time [1-2]. The condition is characterized by regular episodes of high fever (?39°), often mentioned as clockwork mechanism [3], every 3 to 8 weeks with completely asymptomatic intervals in between generally starting before the age of five (2). The fever is accompanied by at least one of the three cardinal signs: aphthous stomatitis, pharyngitis, and cervical adenitis. Other heterogeneous clinical features such as headache, skin rashes, arthralgia, gastrointestinal symptoms and others may be present [4]. In fact, PFAPA seems to have a broader spectrum of manifestations than previously assumed [5]. The incidence has been reported 2.3 cases per 10000 in a Norwegian study, yet the worldwide epidemiologic patterns may differ [6]. The pathogenesis of the disease is yet to be discovered. Though numerous studies have explored the hereditary patterns of the disorder [8-9], genetic background [10-17], inflammatory and prop-inflammatory cytokines role in the diseases course, environmental factors associated with the syndrome [18] and potential involvement of microbiological agents [19], the precise cause of PFAPA remains unclear and with no specific diagnostic biomarker, the diagnosis is only based on clinical judgments and criteria [20,21]. Considering the unclear role of inflammation in the development of the syndrome, there may be a link with other disorders involving disregulated immune responses and inflammation namely allergies which has not yet been studied in the medical literature. Allergy is defined as an abnormal atypical immune response directed against non-infectious environmental substances (allergens), characterized by the role of allergen-specific IgEs, T helper 2 cells and other cytokines [22] and correlation to many disorders is coming to light every day. Despite the benign and self-limited nature of the disease, maintaining normal growth and development [23,24], adulthood relapses have been reported [25] and symptoms may persist for years. Also, notable negative impacts on life quality and psychosocial functioning are worrisome. [26] In this study, we aimed to assess the allergic profile (via prick test) in 33 confirmed cases of PFAPA and its correlation to PFAPA occurrence, symptoms and role in treatment.


Methods

Study population and Design

Thirty-three patients with confirmed PFAPPA diagnosis, treated in a Clinic of Pediatric Rheumatology were enrolled in the study retrospectively between 2020 and 2021. All patients were less than 10 years of age. Patients were selected if they met the Thomas, 1999 criteria as described in (Table 1).

 

Figure 1: Frequency of cardinal signs in patients with PFAPA.

All other diagnosis was excluded through the course of routine check-ups. Serum cytokine profiles, neutrophil activation during attacks and genetic profiles were taken into consideration in diagnostically difficult cases. The medical records gathered included demographic data, medical history, disease onset and course, signs and symptoms, family history, laboratory findings and treatment measures. All patients went through a prick test and had a complete genetic and allergy analysis profile under investigation. A large wheal was considered as a true allergy. If no wheal appears, it was unlikely that there was allergic to the test. The study was approved by the Shahid Beheshti University of Medical Sciences Ethics Committee


Results

The study reviewed medical records of 33 patients diagnosed with PFAPA based on the Thomas et al, 1999 criteria. The baseline characteristics of the patients are presented in (Table 1). A total of 18 patients were male (54.54%). The mean age of patients was 3.29 (SD 1.28) at the onset of fevers (87.8% under the age of 5) and 4.48 at the time of final diagnosis of PFAPA. The mean interval between each flare up is 31 days (ranging between 2 to 7 weeks) and the mean duration of fever was 4.07 days with mean body temperature measuring 39.9°. All patients had at least one of the three cardinal clinical manifestations. Aphthous stomatitis presented in 78.7%, pharyngitis in 84.8% and cervical adenitis in 60.6%. Other symptoms included exudative pharyngitis (69.6%), arthralgia (27.2%), myalgia (12.1%), skin rashes (12.1%), and headache (18.1%). Gastrointestinal symptoms included abdominal pain (81.8%), nausea and vomiting (12.1%) and diarrhea (6.06%) (Table 2). 

Table 1: Thomas criteria for PFAPA diagnosis.

1

Regular recurrent fevers with <5 years of age of onset

2

Constitutional symptoms in the absence of upper respiratory infection, malignancies, autoimmune diseases, or hereditary autoinflammatory

Diseases with at least 1 of the following cardinal signs:

Aphthae

Cervical lymphadenitis

Pharyngitis

3

Exclusion of cyclic neutropenia

4

Completely asymptomatic interval between episodes

5

Normal growth and development


Table 2: Frequency of cardinal signs in patients with PFAPA.   

Clinical findings

Pharyngitis

Aphthous stomatitis

Cervical adenitis

Percentages

84.40%

78.80%

60.60%

Table 3: Prick test Results.

Allergen

Proportion

Std. Err.

[95% Conf.

Interval]

Trees

0.193548

0.072131

0.046237

0.34086

Birch

0.032258

0.032258

-0.03362

0.098138

Grass mixture

0.225807

0.076337

0.069907

0.381706

Weeds mixture

0.129032

0.061205

0.004034

0.25403

Rye grass

0.032258

0.032258

-0.03362

0.098138

Bermuda grass

0.032258

0.032258

-0.03362

0.098138

Timothy

0.032258

0.032258

-0.03362

0.098138

Ragweed

0.032258

0.032258

-0.03362

0.098138

Russian thistle

0.032258

0.032258

-0.03362

0.098138

Sycamore

0.032258

0.032258

-0.03362

0.098138

Cladosporiom

0.032258

0.032258

-0.03362

0.098138

Aspergillus

0.064516

0.044853

-0.02709

0.156118

Alternaria

0.032258

0.032258

-0.03362

0.098138

Penicillium

0.032258

0.032258

-0.03362

0.098138

Pteronyssinus

0.258065

0.079889

0.09491

0.42122

Farina

0.258065

0.079889

0.09491

0.42122

Cat

0.096774

0.053978

-0.01346

0.207012

Dog hair

0.129032

0.061205

0.004034

0.25403

Cockroach

0.096774

0.053978

-0.01346

0.207012

Mosquito

0.032258

0.032258

-0.03362

0.098138

Corn moth

0.032258

0.032258

-0.03362

0.098138

Feather mix

0.032258

0.032258

-0.03362

0.098138

Egg-Y

0.225807

0.076337

0.069907

0.381706

Egg-W

0.193548

0.072131

0.046237

0.34086

Beef

0.193548

0.072131

0.046237

0.34086

Walnut

0.193548

0.072131

0.046237

0.34086

Peanut

0.290323

0.082873

0.121074

0.459571

Almond

0.129032

0.061205

0.004034

0.25403

Garlic

0.096774

0.053978

-0.01346

0.207012

Pepper green

0.032258

0.032258

-0.03362

0.098138

Pepper black

0.096774

0.053978

-0.01346

0.207012

Shrimp

0.096774

0.053978

-0.01346

0.207012

Tuna

0.096774

0.053978

-0.01346

0.207012

Banana

0.096774

0.053978

-0.01346

0.207012

Strawberry

0.032258

0.032258

-0.03362

0.098138

Cereals

0.16129

0.067151

0.024151

0.29843

Potato

0.16129

0.067151

0.024151

0.29843

Tomato

0.322581

0.085347

0.148279

0.496882

Cocoa

0.064516

0.044853

-0.02709

0.156118

Wheat

0.129032

0.061205

0.004034

0.25403

Rice

0.290323

0.082873

0.121074

0.459571

Soya

0.193548

0.072131

0.046237

0.34086

Chicken

0.096774

0.053978

-0.01346

0.207012

Sesame

0.258065

0.079889

0.09491

0.42122

Cow milk

0.129032

0.061205

0.004034

0.25403

Barley

0.129032

0.061205

0.004034

0.25403

Hazelnut

0.032258

0.032258

-0.03362

0.098138

Pistachio

0.032258

0.032258

-0.03362

0.098138


The past medical history of patients with a higher focus on disorders with an allergic pathophysiologic basis was gathered and showed a considerable co-occurrence with PFAPA: 81.8% had previous allergies; 24.2% reported Dermatitis and 66.6% reported GERD; 9% had Asthma. History of similar signs and symptoms in first and second degree family members was 12.1% and only one case of autoimmune disorders (3%) in the family was reported. In the skin prick test studies, a few allergens demonstrated a larger proportion in the study population and probably stronger associations with PFAPA occurrence. These allergens are as followed: Overall allergy to trees was 0.19 (SD 0.072), to grass mixture was 0.22 (SD 0.076) and to weed mixture was 0.12 (SD 0.061). Birch, Rye grass, Bermuda grass, timothy, ragweed and Russian thistle and sycamore among botanical allergens all had a proportion of almost 3% each in our study population. In the animal, dust and danders allergies, allergy to mites (d pteronyssinus and d farina was reported in one-quarter of patients followed by dog hair with 12% in the second place and other allergens showed in (Table 3). In the food allergen category, tomato was the most common (32.2%), followed by rice and peanut (29.03%), sesame (25.8%), egg yolk (22.58%) – vs egg white (19.35%) - and other allergens seen in (Table 2). Positive allergy test for cow milk was seen in 12.9% of the population and green paper, strawberry, hazelnut and pistachio had the lowest distribution: approximately 3%.


Discussion

In this study we analyzed the frequencies of various allergens in children with PFAPA. In the food allergen category, tomato was the most common (32.2%), followed by rice and peanut (29.03%), sesame (25.8%), egg yolk (22.58%) – vs egg white (19.35%)- and other allergens seen in Table 2. Positive allergy test for cow milk was seen in 12.9% of the population and green paper, strawberry, hazelnut and pistachio had the lowest distribution: approximately 3%. These results suggest that there is considerable association between allergies and attacks of fever in PFAPA which need for further investigation. In 27 patients, treatment (Singular and cimetidine) along with allergen contact cessation resulted in complete regression of fever episodes, suggesting the effective role of allergy control of fever in PFAPA patients. The baseline characteristics of the patients are presented in Table 1. A total of 18 patients were male (54.54%), compatible to the slight male sex preference of the disorder in the previous studies [27-29].

Conclusions

Although food allergy is rarely the etiology of PFAPA, it is important to monitor allergic diet because they have a higher risk of developing PFAPA. It is essential to educate patients and their families on the management of food allergy and to review their risk of developing fever attacks in PFAPA.


References

  1. Marshall GS, Edwards KM, Butler J, Lawton AR. Syndrome of periodic fever, pharyngitis, and aphthous stomatitis. J Pediatr. 1987; 110: 43-46.
  2. Thomas KT, Feder HM, Lawton AR, Edwards KM. Periodic fever syndrome in children. J Pediatric. 1999; 135: 15-21.
  3. Cattalini M, Soliani M, Rigante D, Lopalco G ,Lannone F, Galeazzi L, et al. Basic characteristics of adults with periodic fever, aphthous stomatitis, pharyngitis, and adenopathy syndrome in comparison with the typical pediatric expression of disease. Mediators Inflamm. 2015.
  4. Feder HM, Salazar JC. A clinical review of 105 patients with PFAPA (a periodic fever syndrome). Acta Paediatr. 2010; 99: 178?184
  5. Manthiram K, Li SC, Hausmann JS, Amarilyo G, Barron K, Kim H, et al. Physicians’ perspectives on the diagnosis and management of periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome. Rhematol Int. 2017; 37: 883-889
  6. Forsvoll J, Kristoffersen EK, Oymar K. Incidence, clinical characteristics and outcome in Norwegian children with periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis syndrome; a population-based study. Acta Paediatr. 2013; 102: 187-192.
  7. Kraszewska-GBomba B, Matkowska-Kocjan A, Szenborn L. The Pathogenesis of Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Cervical Adenitis Syndrome: A Review of Current Research. Mediators of Inflamm. 2015.
  8. Perko D, Debeljak M, Toplak N, Avcin T. Clinical features and genetic background of the periodic fever syndrome with aphthous stomatitis, pharyngitis, and adenitis: a single center longitudinal study of 81 patients. Mediators Inflamm. 2015.
  9. Manthiram K, Nesbitt E, Morgan T, Edwards K. Family history in periodic fever, aphthous stomatitis, pharyngitis, adenitis (PFAPA) syndrome. Pediatrics. 2016; 138.
  10. Gioia SAD, Bedoni N, von Scheven-Gete A, Vanoni F, Superti-Furga A, Hofer M, et al. Analysis of the genetic basis of periodic fever with aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome. Sci Rep. 2015; 5: 10200.
  11. Kolly L, Busso N, von Scheven-Gete A, Bagnoud N, Moix I, Holzinger D, et al. Periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis syndrome is linked to dysregulated monocyte IL-1b production. J Allergy Clin Immunol. 2013; 131: 1635-1643.
  12. Stojanov S, Lapidus S, Chitkara P, Feder H, Salazar JC, Fleisher TA, et al. Periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) is a disorder of innate immunity and Th1 activation responsive to IL-1 blockade. Proc Natl Acad Sci USA. 2011; 108: 7148-7153.
  13. Berkun Y, Levy R, Hurwitz A, Meir-Harel M, Lidar M, Livneh A, et al. The familial Mediterranean fever gene as a modifier of periodic fever, aphthous stomatitis, pharyngitis, and adenopathy syndrome. Semin Arthritis Rheum. 2011; 40: 467-472.
  14. Celiksoy MH, Ogur G, Yaman E, Abur U, Fazla S, Yildiran A, et al. Could familial Mediterranean fever gene mutations be related to PFAPA syndrome? Pediatr Allergy Immunol. 2016; 27: 78-82.
  15. Dagan E, Gershoni-Baruch R, Khatib I, Mori A, Brik R. MEFV, TNF1rA, CARD15 and NLRP3 mutation analysis in PFAPA. Rheumatol Int. 2010; 30: 633-636.
  16. Maschio M, Oretti C, Ventura G, Pontillo A, Tommasini A. CARD15/NOD2 mutations are not related to abdominal PFAPA. J Pediatr. 2006; 149: 427.
  17. Cheung M, Theodoropoulou K, Lugrin J, Martinon F, Busso N, Hofer M, et al. Periodic fever with aphthous stomatitis, pharyngitis, and cervical adenitis syndrome is associated with CARD8 variant unable to bind the NLRP3 inflammasome. J Immunol. 2017; 198: 2063-2069.
  18. Kettunen S, Lantto U, Koivunen P, Tapiainen T, Uhari M, Renko M,et al. Risk factors for periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) syndrome: a case-control study. Eur J Pediatr. 2018; 177: 1201-1206.
  19. Freeman S, Bhatt A, Pedamallu C, King S, Duke F,Jung J, et al. A121: in search of infectious triggers of periodic Fever, aphthous stomatitis, pharyngitis and adenitis syndrome. Arthritis Rheumatol. 2014; 66: S158-S158.
  20. Krol P, Böhm M, Sula V, Dytrych P, Katra R, Nemcová D, et al. PFAPA syndrome: clinical characteristics and treatment outcomes in a large single-Centre cohort. Clin Exp Rheumatol. 2013; 31: 980-987.
  21. Hofer M, Pillet P, Cochard MM, Berg S, Krol P, Kone-Paut I, et al. International periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis syndrome cohort: description of distinct phenotypes in 301 patients. Rheumatol Oxf Engl. 2014; 53: 1125-1129.
  22. Galli SJ, Tsai M, Piliponsky AM. The development of allergic inflammation. Nature. 2008; 454: 445-454.
  23. Gentileschi S, Vitale A, Frediani B, Galeazzi M, Rigante D, Cantarini L, et al. Challenges and new horizons in the periodic fever, aphthous stomatitis, pharingitis and adenitis (PFAPA) syndrome. Expert Opin Orphan Drugs. 2017; 5: 165-171.
  24. Rigante D, Gentileschi S, Vitale A, Tarantino G, Cantarini L. Evolving frontiers in the treatment of periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis (PFAPA) syndrome. Isr Med Ass J. 2017; 19: 444-447.
  25. Vitale A, Orlando I, Lopalco G, Emmi G, Cattalini G, Frediani B, et al. Demographic, clinical and therapeutic findings in a monocentric cohort of adult patients with suspected PFAPA syndrome. Clin Exp Rheumatol. 2016; 34: 77?81.
  26. Grimwood C, Kone-Paut I, Piram M, Rossi-Semerano L, Hentgen V. Health-related quality of life in children with PFAPA syndrome. Orphanet J Rare Dis. 2018; 13: 132.
  27. Batu ED, Eroglu FK, Tsoukas P, Hausmann JS, Bilginer Y, Kenna MA, et al. Periodic fever, aphthosis, pharyngitis, and adenitis syndrome: analysis of patients from two geographic areas. Arthritis Care Res. 2016; 68: 1859-1865.
  28. Gunes M, Cekic S, Kilic SS. Is colchicine more effective to prevent periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis episodes in Mediterranean fever gene variants? Pediatr Int. 2017; 59: 655-660.
  29. Aviel YB, Harel L, Rumi MA, Brik R, Hezkelo N, Ohana O, et al. Familial Mediterranean fever is commonly diagnosed in children in israel with periodic fever aphthous stomatitis, pharyngitis, and adenitis syndrome. J Pediatr. 2018; 204: 270-274.