Case Reports in Dentistry

Case Reports in Dentistry / 2019 / Article

Case Report | Open Access

Volume 2019 |Article ID 4210347 |

Jean-Claude Abou Chedid, Michel Salameh, Abbass El-Outa, Ziad E. F. Noujeim, "Papillon-Lefèvre Syndrome: Diagnosis, Dental Management, and a Case Report", Case Reports in Dentistry, vol. 2019, Article ID 4210347, 7 pages, 2019.

Papillon-Lefèvre Syndrome: Diagnosis, Dental Management, and a Case Report

Academic Editor: Sukumaran Anil
Received27 Jan 2019
Accepted03 Mar 2019
Published21 Apr 2019


Aim. This paper revisits Papillon-Lefèvre syndrome (PLS), addresses its diagnostic update and dental management, and reports a case of a 5-year-old Lebanese patient with consanguineously married parents. Background. PLS, also known as “keratoris palmoplantaris with periodontopathia” and “hyperkeratosis palmoplantaris with periodontosis,” is an extremely rare autosomal-recessive trait that combines a diffuse palmoplantar hyperkeratosis and a severe generalized, progressive prepubertal form of a precocious form of juvenile, aggressive periodontitis. Case Description. We are reporting a 5-year-old boy that sustained a spontaneous loss of all his primary teeth. At consultation, he was under treatment for hyperkeratosis of his palms and soles. Detailed family history of the child revealed that the patient’s parents, grandparents, and relatives were consanguineously married and two of his cousins displayed similar clinical signs (palmoplantar hyperkeratosis and premature loss of deciduous and most of the permanent teeth). Conclusion. PLS is an extremely rare disorder that usually becomes apparent from approximately 1-5 years of age. Genetic counseling should always be suggested to parents of affected children, informing them of chances of their offspring having the inherited disease.

1. Introduction

Papillon-Lefèvre syndrome (PLS) is a very rare genodermatosis of autosomal-recessive inheritance. It is an ectodermal dysplasia, and a type IV palmoplantar keratosis [1]. It was named, in 1924, by French physicians M.M. Papillon and Paul Lefèvre [1] and is characterized by a hyperkeratosis of soles of feet and palms of the hands (palmar-plantar) and extensive, severe, aggressive, and prepubertal periodontitis, leading to premature loss in both deciduous and permanent dentitions.

PLS prevalence is estimated between 1/250,000 and 1/1,000,000 in the general population [2, 3].

PLS disorder can be hereditary, acquired, or associated with other syndromes, but in most described cases, PLS is genetic, resulting from mutations on both alleles of the cathepsin C gene (CTSC) on chromosome 11q14.2. Most PLS patients are homozygous for CTSC mutations [47].

2. Case Report

A 5-year-old boy presented to the Department of Pediatric Dentistry of the Faculty of Dental Medicine at Saint-Joseph University of Beirut, Lebanon, with a chief complaint of loosening of all primary teeth, followed by their spontaneous loss. The patient’s medical history showed that he was undergoing a dermatological treatment for the “hyperkeratosis of his palms and soles”; the treating dermatologist referred the patient to the dentist after having suspected PLS. A detailed family history revealed that the patient’s parents, grandparents, and relatives were consanguineously married and two of his cousins exhibited similar clinical signs (palmoplantar hyperkeratosis and premature loss of deciduous and permanent teeth).

Intraoral examination revealed that many primary teeth (teeth 54, 52, 51, 61, 62, 64, 74, 72, 71, 81, and 82) were missing while remaining teeth (teeth 85, 84, 83, 73, 75, 65, 63, 53, and 55) exhibited plaque accumulation, multiple caries, and generalized grade III mobility with the formation of periodontal pockets (Figure 1); gingival tissues surrounding these teeth were inflamed, edematous, and tender to palpation, while those of edentulous regions appeared normal and nontender to palpation. Dental and periodontal abscesses were noticed on teeth 85 and 75. Panoramic radiograph displayed several floating teeth with generalized horizontal and vertical bone loss (Figure 1).

Extraoral examination of the patient revealed hyperkeratosis on the dorsum surface of his hands (Figure 2) and feet (Figure 3).

Routine hematological examination (CBC and blood chemistry profile) and liver function tests were normal. In addition, a genetic test was performed at the Saint Joseph University Faculty of Medicine/Laboratory of Molecular Biology, Beirut; PCRs (polymerase chain reaction) followed by fluorescent Sanger sequencing of exons 3 to 7 of CTSC gene, for the affected child, revealed no mutation. However, PCR amplification of exons 1 and 2 did not result in any product, suggesting that affected child harbored a homozygous deletion of the 5UTR region and exons 1 and 2.

Level of patient’s cooperation was assessed during the first clinical examination, and it was decided to implement the treatment under general anesthesia, at hospital. A written informed consent form was signed by the child’s parents after having discussed with them all the steps of the treatment planning, from extraction of all remaining teeth to the fabrication of an immediate removable complete denture (RCD). The importance of oral hygiene was emphasized, and enforcement of oral hygiene habits was advocated.

At hospital, the first dose of amoxicillin (50 mg/kg) and clavulanic acid was administered through IV route before beginning the surgery and it was continued for the following postoperative seven days. In order to maintain a stable occlusion, two impressions of maxilla and mandible were taken with the remaining teeth in place using an addition silicon material. All remaining teeth were extracted, and all extraction sockets were irrigated with a 0.12% chlorhexidine digluconate solution. No sutures were needed, and impressions were directly transferred to the dental laboratory in order to be casted.

Two weeks after extractions, maxillary and mandibular RCDs were fabricated (Figure 4(a)) and inserted in the mouth (Figure 4(b)). No pressure spots were noticed, and occlusion showed no interferences. Patient and parents were taught the proper oral hygiene measures for RCDs; they were also informed of the need for regular dental visits (one week after the insertion and every three months afterwards) in order to reexamine the appliances and, when necessary, replace or reline them according to arch growth and eruption of the permanent teeth. Eight-month follow-up revealed the erupting mandibular central incisors (Figure 5).

3. Discussion

3.1. Consanguinity in PLS

Consanguineous marriage [8] is matrimony between persons who are closely related. It is defined as a union between two individuals who are related as second cousins or closer, with an inbreeding coefficient () equal or higher than 0.0156; representing a measure of the proportion of loci at which the offspring of a consanguineous union is expected to inherit identical gene copies from the father and mother. This includes unions termed first cousins and second cousins. In some Arab communities where unions occur between double first cousins, the highest inbreeding coefficients are reached, and in some regions of South India where uncle-niece marriages occur, reaches 0.125 [8].

Increased genetic risks to the offspring represent the main negative impact of consanguineous marriages. Indeed, consanguineous unions may lead to an increased expression of autosomal-recessive disorders, and the closer the biological relationship between parents, the greater is the probability that their offspring will inherit similar copies of one or more detrimental recessive genes [9]. Consanguinity does not increase the risk for autosomal-dominant diseases when only one of the parents is affected nor for X-linked recessive conditions if neither parent is affected [8].

Premarital screening and preconception counseling programs are important in raising public’s awareness of possible genetic diseases and their prevention by knowing more on consanguinity as a risk factor for the expression of recessive disorders. In Shiraz, Southern Iran, among 2,686 couples presenting for genetic counseling during a period of 4 years, 85% had consanguineous relationships and 74% were first cousins [10].

In preconception counseling for consanguinity, it is important to make the difference between families with no known genetic disorder and those with a known inherited or genetic one. Taking a detailed family history and constructing a four-generation pedigree (offspring, siblings, parents, aunts, uncles, grandparents, nieces, nephews, and first cousins) are obligatory [9]. Collection of information is implemented by addressing very specific questions that could lead to the detection of a genetic or hereditary disorder in the extended family; these questions should include any relevant information about any of the following pathologies in blood relatives: (1)Congenital anomalies or birth defects(2)Learning disability or mental retardation (or disability)(3)Inherited blood disorder(4)Undiagnosed severe condition or anomaly(5)Early vision and/or hearing impairment(6)Failure to thrive or developmental delay(7)Epilepsy(8)Unexplained infant (or neonatal) death in the offspring

Consanguinity is a deeply rooted social trend among one-fifth of the world population mostly residing in the Middle East, North Africa, and West Asia, as well among some emigrants from these regions now residing in Europe, North America, and Australia. In these highly consanguineous populations and communities, premarital counseling on consanguinity is almost absent. Around one billion of the current global population live in regions and communities with an obvious preference for consanguineous (blood relatives) marriages. In such communities and regions, though cousin marriages are customary, there are inconsistencies among healthcare providers in counseling for consanguinity possible consequences and sequelea [9].

When PLS is genetic, it is transmitted as an autosomal-recessive trait, and 20-40% of patients are children of consanguineously married parents [11].

In their original paper, back in 1924, Papillon and Lefèvre reported [1] the case of two siblings who were the products of a first-cousin mating, and the condition described in their paper featured two hallmarks which were a premature loss of deciduous and permanent dentitions and diffuse transgradient palmoplantar keratosis. Consanguinity is now recognized as a risk factor [12] for PLS, and many articles reported PLS cases in the same family [1315]. Considering that consanguineous marriage is customary in Lebanese society, potential parents are to be warned that this leads to an increased birth prevalence of infant with severe recessive disorders; consequently, this kind of marriage should be discouraged, and genetic counseling should be advocated. Families at increased risk should be identified, and carrier testing should be implemented when feasible [16].

3.2. Clinical Manifestations

PLS becomes clinically apparent from the ages of 1 to 5; dry scaly patches of palms and soles (palmar-plantar hyperkeratosis) and severe, aggressive, and early-onset periodontitis are its main clinical features, but additional symptoms may be associated to it, such as pyogenic skin infections, nail dystrophies, and hyperhidrosis. Patches of the skin usually develop around the age of 1 to 5; they are mostly confined to the undersides of feet and hands, but they may appear on elbows and knees. In rare cases, upper portions of hands and feet, eyelids, and other parts of the body may be affected as well. Affected skin is often thick and red, but texture and color may vary; skin lesions may worsen during cold weather, and walking is often uncomfortable and painful.

Patients affected with PLS may also exhibit generalized hyperhidrosis (excessive perspiration), leading to unpleasant, malodorous odors. Most patients with PLS have hypotrichosis (sparse hair on the scalp and body), dirty colored skin, and very fragile nails that easily break off, but some of them may release excessive amounts of keratine in hair follicles, causing rough papules on the skin.

Only some individuals affected by PLS may experience other kinds of infections such as furunculosis, respiratory tract infections, and hidradenitis suppurativa (painful and swollen lesions in the breast, groin, and armpit).

3.3. Craniofacial, Oral, Dental, and Periodontal Aspects

Dental and periodontal manifestations [3] of PSL become apparent by the age of 2-3 years; they start with severe gingivitis and rapid periodontal destruction, followed by premature exfoliation of all deciduous teeth by the age of 4 to 5. The same sequence of events recurs as the permanent dentition erupts, leading to its early shedding, and without treatment, most of the permanent teeth may fall by the same mechanism by the age of 16 years. Consequences of this premature tooth loss will affect the patient’s daily functions, such as mastication and speech.

Gingival and periodontal tissues are involved (gingivitis, gingival ulcers, periodontal pockets, and severe, aggressive periodontitis) in PLS. Aggregatibacter actinomycetemcomitans plays an important role in the progression of periodontal infections and inflammations. Treponema denticola, Porphyromonas gingivalis, and Fusobacterium nucleatum are also suggested as causative agents [17].

At eruption of deciduous teeth, gums appear red, inflamed, and sometimes bleedy and enlarged. In some cases, all oral mucosae may appear erythematous (stomatitis), with possible perioral lymphadenopathies. Halitosis may also develop in some individuals. Apart from that, discrepancies in the arch length and psychological problems may follow [18].

In rare people affected with PLS, dry scaly patches of the skin (hyperkeratosis) may appear on lips, cheeks, and eyelids, and in some rare adult patients, cysts may develop on eyelids and calcium may accumulate in the skull, causing intracranial calcifications [19, 20].

3.4. Differential Diagnosis

To distinguish between PLS and palmoplantar hyperkeratosis syndromes, occurrence of severe, aggressive, and early-onset destructive periodontitis has to be taken into consideration [21].

Many disorders share similar clinical and genetic features with PLS [22]: (1)The association with severe, aggressive, and early-onset periodontitis is unique to PLS and Haim-Munk syndrome (HMS). HMS (known also as “palmoplantar keratoderma with periodontitis and arachnodactyly and acroosteolysis” or “Cochin Jewish disorder”) is a skin condition caused by a cathepsin C gene mutation; it is an extremely rare disorder of keratinization of recessive inheritance that manifests with scaly, red, and thickened patches of the skin of soles of the feet and palms of the hands (palmoplantar hyperkeratosis), pes planus (flat foot), arachnodactyly (a peculiar deformity of terminal phalanges of hands and feet), acroosteolysis, atrophic changes of nails (onychogryphosis), a radiographic deformity of fingers, recurrent abscess formations, and a severe early-onset periodontitis. PLS cases were reported worldwide while HMS ones were only described among descendants of a religious isolate originally from Cochin, India. Consanguinity is a major feature of both conditions.(2)Palmoplantar ectodermal dysplasia (PPED) is a skin condition that includes 8 types: PPED type 1 or pachyonychia congenita which is autosomal dominant, PPED type 2, PPED type 3 or acrokeratoelastoidosis, PPED type 4 which resembles the PLS, PPED type 5 or oculocutaneous tyrosinemia type II or Richner-Hanhart syndrome which is autosomal recessive, PPED type 6 or Olmsted syndrome, PPED type 7, and PPED type 8 or Meleda disease or “mal de Meleda” or “acral keratoderma” which is autosomal recessive.(3)von Feer’s disease (acrodynia, pink disease, mercurialism, erythredema, and Swift-Feer disease) affects children which is characterized by dusky pink discoloration in hands and feet, loss of teeth, hair, and nails, red lips, cheeks, and nose, transient rashes, hypotonia, photophobia, kidney dysfunction, peripheral neuropathy (paresthesia, itching, burning sensation, and pain), and neuropsychiatric symptoms (insomnia, emotional lability, and memory impairment). Mercury intoxication/poisoning is incriminated as a causative factor of this disease.

Other pathologies and syndromes sharing clinical features with PLS [22] include palmoplantar hyperkeratosis (Unna-Thost syndrome), palmoplantar hyperkeratosis-punctate, Vohwinkel’s syndrome, Vörner’s localized epidermolytic palmoplantar keratoderma, Howel-Evans syndrome, Gamborg-Nielsen syndrome, and Greither’s transgrediens and progrediens palmoplantar keratoderma.

Some PLS patients were reported to have palmoplantar keratosis and periodontal destruction in their permanent dentition, with no periodontal destruction observed in their deciduous one [21, 23, 24].

A cohort study including 47 patients [25] supported the concept that the two major components of PLS (periodontal destruction and palmoplantar keratosis) appeared to be unrelated to each other; in this study, skin and oral changes developed early in life, with no exception. Dermatological involvement showed no correlation with age, while periodontal infection was significantly worse in young age with primary teeth. Finally, a strong correlation was found between feet and hand condition, although the scores for the feet were significantly higher, and no significant correlation could be demonstrated between the severity of skin affections and the level of periodontal destruction [25].

4. Conclusion

PLS periodontosis ultimately leads to premature loss of deciduous and permanent dentitions at a very young age. This devastating periodontitis is attributed to a point mutation of the cathepsin C gene. Prognosis of dentition in these patients is poor, and most of them ultimately become edentulous, except for third molars, and end up with a small maxilla and mandible. In almost half of the patients, PLS displays an enhanced susceptibility to systemic and cutaneous infections, such as skin abscesses, furunculosis, hidradenitis suppurativa, and respiratory tract infections. Patients may also sustain nail dystrophies, follicular hyperkeratosis, dural calcifications, and malodorous hyperhidrosis; on very rare occasions, PLS may be associated with squamous cell carcinoma and malignant melanoma.

Conventional treatment of PLS is mainly based on the use of oral retinoids which often attenuate signs of palmoplantar keratoderma and, somehow, slow the resorption of the alveolar bone on the remaining teeth. Etretinate, a synthetic retinoid, lately showed very promising results in the medical treatment of PLS. Antibiotics are also prescribed in treating recurrent infections.

A very good oral hygiene with concomitant use of chlorhexidine mouth rinses should also be recommended to patients in order to slow the aggressive progression of periodontitis. Finally, deciduous and remaining teeth are often extracted and replaced, either by conventional removable dentures or dental osseointegratable implants.

Successful periodontal management of PLS patients is the key to improve the prognosis of the dentition, preventing or delaying primary and permanent tooth loss. It is mandatory that all dental professionals be familiar and aware of this disease as well as the importance of its early diagnosis and management.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this paper.


  1. M. M. Papillon and P. Lefèvre, “Deux cas de kératodermie palmaire et plantaire symétrique familiale (maladie de Meleda) chez le frère et la sœur. Coexistence dans les deux cas d'altérations dentaires graves,” Bulletin de la Société Française de Dermatologie et de Vénéréologie, vol. 31, pp. 82–87, 1924. View at: Google Scholar
  2. B. Dalgic, A. Bukulmez, and S. Sari, “Eponym: Papillon-Lefèvre syndrome,” European Journal of Pediatrics, vol. 170, no. 6, pp. 689–691, 2011. View at: Publisher Site | Google Scholar
  3. P. J. Dhanrajani, “Papillon-Lefèvre syndrome: clinical presentation and a brief review,” Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, vol. 108, no. 1, pp. e1–e7, 2009. View at: Publisher Site | Google Scholar
  4. T. C. Hart, P. S. Hart, D. W. Bowden et al., “Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome,” Journal of Medical Genetics, vol. 36, no. 12, pp. 881–887, 1999. View at: Google Scholar
  5. A. Wani, N. Devkar, M. Patole, and Y. Shouche, “Description of Two New Cathepsin C Gene Mutations in Patients With Papillon-Lefèvre Syndrome,” Journal of Periodontology, vol. 77, no. 2, pp. 233–237, 2006. View at: Publisher Site | Google Scholar
  6. N. A. Cagli, S. S. Hakki, R. Dursun et al., “Clinical, genetic, and biochemical findings in two siblings with Papillon-Lefèvre syndrome,” Journal of Periodontology, vol. 76, no. 12, pp. 2322–2329, 2005. View at: Publisher Site | Google Scholar
  7. T. C. Hart, P. S. Hart, M. D. Michalec et al., “Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C.,” Journal of medical genetics, vol. 37, no. 2, pp. 88–94, 2000. View at: Publisher Site | Google Scholar
  8. H. Hamamy, “Consanguineous marriages. Preconception consultation in primary health care settings,” Journal of Community Genetics, vol. 3, no. 3, pp. 185–192, 2012. View at: Publisher Site | Google Scholar
  9. R. L. Bennett, A. G. Motulsky, A. Bittles et al., “Genetic counseling and screening of consanguineous couples and their offspring: recommendations of the national society of genetic counselors,” Journal of Genetic Counseling, vol. 11, no. 2, pp. 97–119, 2002. View at: Publisher Site | Google Scholar
  10. M. Fathzadeh, M. A. Babaie Bigi, M. Bazrgar, M. Yavarian, H. R. Tabatabaee, and S. M. Akrami, “Genetic counseling in Southern Iran: consanguinity and reason for referral,” Journal of Genetic Counseling, vol. 17, no. 5, pp. 472–479, 2008. View at: Publisher Site | Google Scholar
  11. F. Acun Kaya, Z. Seyfioglu Polat, E. Akuzum Baran, and G. G. Tekin, “Papillon-Lefèvre syndrome. 3 years follow up: a case report,” International Dental and Medical Disorders, vol. 1, no. 1, pp. 24–28, 2008. View at: Google Scholar
  12. A. F. Shah, P. Tangade, and S. Agarwal, “Papillon–Lefevre syndrome: Reporting consanguinity as a risk factor,” The Saudi Dental Journal, vol. 26, no. 3, pp. 126–131, 2014. View at: Publisher Site | Google Scholar
  13. S. S. Pareek and A. K. Al-Aska, “Papillon-Lefevre syndrome. A report of six cases in one family,” International Journal of Dermatology, vol. 25, no. 10, pp. 638–641, 1986. View at: Publisher Site | Google Scholar
  14. A. K. Valeshabad, A. Mazidi, R. K. Valeshabad et al., “Papillon-Lefèvre Syndrome: A Series of Six Cases in the Same Family,” ISRN Dermatology, vol. 2012, Article ID 139104, 4 pages, 2012. View at: Publisher Site | Google Scholar
  15. Z. M. AlBarrak, A. S. Alqarni, E. P. Chalisserry, and S. Anil, “Papillon–Lefèvre syndrome: a series of five cases among siblings,” Journal of Medical Case Reports, vol. 10, no. 1, pp. 260–265, 2016. View at: Publisher Site | Google Scholar
  16. B. Modell and A. Darr, “Genetic counselling and customary consanguineous marriage,” Nature Reviews Genetics, vol. 3, no. 3, pp. 225–229, 2002. View at: Publisher Site | Google Scholar
  17. A. Stabholz, N. S. Taichman, and W. A. Soskolne, “Occurrence of Actinobacillus actinomycetemcomitans and anti-leukotoxin antibodies in some members of an extended family affected by Papillon-Lefèvre syndrome,” Journal of Periodontology, vol. 66, no. 7, pp. 653–657, 1995. View at: Publisher Site | Google Scholar
  18. B. Sreeramulu, N. D. V. N. Shyam, P. Ajay, and P. Suman, “Papillon–Lefèvre syndrome: clinical presentation and management options,” Clinical, Cosmetic and Investigational Dentistry, vol. 7, pp. 75–81, 2015. View at: Publisher Site | Google Scholar
  19. M. M. Brownstein and P. Skolnik, “Papillon-Lefèvre Syndrome,” Archives of Dermatology, vol. 106, no. 4, pp. 533-534, 1972. View at: Publisher Site | Google Scholar
  20. E. F. Corson, “Keratosis palmaris et plantaris with dental alternation,” Archives of Dermatology and Syphilology, vol. 40, p. 639, 1939. View at: Google Scholar
  21. E. Haneke, “The Papillon-Lefèvre syndrome: keratosis palmoplantaris with periodontopathy: report of a case and review of the cases in the literature,” Human Genetics, vol. 51, no. 1, pp. 1–35, 1979. View at: Publisher Site | Google Scholar
  22. T. C. Hart and L. Shapira, “Papillon-Lefèvre syndrome,” Periodontology 2000, vol. 6, no. 1, pp. 88–100, 1994. View at: Publisher Site | Google Scholar
  23. T. Q. Nguyen, K. E. Greer, G. B. Fisher Jr, and P. H. Cooper, “Papillon-Lefèvre syndrome: report of two patients treated successfully with isotretinoin,” Journal of the American Academy of Dermatology, vol. 15, no. 1, pp. 46–49, 1986. View at: Publisher Site | Google Scholar
  24. E. M. Rateitschak-Pluss and H. E. Schroeder, “History of periodontitis in a child with Papillon-Lefèvre syndrome. A case report,” Journal of Periodontology, vol. 55, no. 1, pp. 35–46, 1984. View at: Publisher Site | Google Scholar
  25. C. Ullbro, C. G. Crossner, T. Nederfors, A. Alfadley, and K. Thestrup-Pedersen, “Dermatologic and oral findings in a cohort of 47 patients with Papillon-Lefèvre syndrome,” Journal of the American Academy of Dermatology, vol. 48, no. 3, pp. 345–351, 2003. View at: Publisher Site | Google Scholar

Copyright © 2019 Jean-Claude Abou Chedid et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

Article of the Year Award: Outstanding research contributions of 2020, as selected by our Chief Editors. Read the winning articles.