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Table of Contents   
CASE REPORT  
Year : 2017  |  Volume : 28  |  Issue : 4  |  Page : 457-460
Gingival fibromatosis with hypertrichosis syndrome: Case series of rare syndrome


Department of Oral and Maxillofacial Surgery, Balaji Dental and Craniofacial Hospital, Chennai, Tamil Nadu, India

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Date of Web Publication16-Aug-2017
 

   Abstract 

Gingival fibromatosis with hypertrichosis syndrome is an extremely rare genetic condition characterized by profound overgrowth of hair and gums, as well as other variable features. Gingival fibromatosis is characterized by a large increase in the gingival dimension which extends above the dental crowns, covering them partially or completely. They were found to have a genetic origin, may also occur in isolation or be part of a syndrome, or acquired origin, due to specific drugs administered systemically. Congenital generalized hypertrichosis is a heterogeneous group of diseases with continuing excessive growth of terminal hair without androgenic stimulation. It has informally been called werewolf syndrome because the appearance is similar to that of a werewolf. Various syndromes have been associated with these features such as epilepsy, mental retardation, cardiomegaly, or osteochondrodysplasia. As so far very few cases have been reported in literature, we are reporting a series of three cases with management of the same. The excess gingival tissues, in these cases, were removed by conventional gingivectomy under general anesthesia. The postoperative result was uneventful and the patient's appearance improved significantly. Good esthetic result was achieved to allow patient to practice oral hygiene measures. Though this is not a serious condition clinically, psychosocial trauma cannot be neglected owing to the cosmetic disfigurement it produces.

Keywords: Gingival fibromatosis, hypertrichosis, werewolf syndrome

How to cite this article:
Balaji P, Balaji S M. Gingival fibromatosis with hypertrichosis syndrome: Case series of rare syndrome. Indian J Dent Res 2017;28:457-60

How to cite this URL:
Balaji P, Balaji S M. Gingival fibromatosis with hypertrichosis syndrome: Case series of rare syndrome. Indian J Dent Res [serial online] 2017 [cited 2019 Oct 21];28:457-60. Available from: http://www.ijdr.in/text.asp?2017/28/4/457/213040

   Introduction Top


Gingival fibromatosis with hypertrichosis (GFH) syndrome is an extremely rare condition of genetic origin characterized by the excessive growth of gingival tissue with abnormal facial and body hairs. Gingival diseases of genetic origin are uncommon conditions and their most common clinically evident form is known as hereditary gingival fibromatosis (HGF). It may occur singly or in association with other inherited syndromes.[1] This condition is also known as elephantiasis gingivae, diffuse fibroma, familial elephantiasis, idiopathic fibromatosis, HGF, and congenital familial fibromatosis. It is inherited as an autosomal dominant trait and has an incidence of 1:350,000.[2],[3] Hypertrichosis may be congenital or acquired. People with congenital hypertrichosis were often referred to as “wolf men,” “werewolves,” and “ape-men” in the 19 century, and perhaps even today, they are crowd-drawers at sideshow acts.[4] Various syndromes have been associated with gingival fibromatosis and hypertrichosis condition which have other features such as epilepsy, mental retardation, cardiomegaly, or osteochondrodysplasia.


   Case Reports Top


Case 1

A 10-year-old girl reported with the complaint of everted lips and swollen gums with coarse hair present over the entire body since birth. She also complained of delayed eruption of permanent teeth. There was no medical history and no systemic abnormalities. The girl was born out of nonconsanguineous marriage and she had average growth and achieved normal developmental milestones. Hypertrichosis, with extremely bushy hairs over the chin, cheeks, and also in the mid forehead with retruded nasal bridge, is seen. Profuse growth of dark brown hair was present on both the upper and lower limbs and in the mid back. On intraoral examination, gingival enlargement involving the upper dentition was found. Teeth were completely covered with gingival overgrowth and lips were incompetent due to abnormality in thickness. In both the jaws, dentition appeared to be normal, as it led to functional disturbances while eating and chewing and esthetic concern. The treatment plan was to do debulking of the lips and gingivectomy procedures [Figure 1]a,[Figure 1]b,[Figure 1]c,[Figure 1]d.
Figure 1: (a–d) Preoperative frontal, lateral, worm's eye and intraoral views

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Surgical procedure

Under general anesthesia and nasotracheal intubation, lidocaine gel was applied 30–45 min before the procedure. The lip was held taut between the thumb and forefinger. Using a number 15 blade, incisions were first made along the newly outlined margin, excess tissue was removed and suturing was done. Generally, gingivectomy is done when there is moderate gingival enlargement or when aberrations are present or when there is asymmetrical or unesthetic gingival topography. Pocket depth was measured by inducing bleeding points. Initial incision was placed apical to the bleeding point and 45° bevel was given to the root. The gingival tissues covering the teeth were removed placing an incision leaving a 2 mm gingival margin around the teeth and were excised. Excess gingival tissue was excised and zinc oxide eugenol pack was placed. After 5–14 days, surface epithelialization was completed. Immediate result of the treatment was a dramatic cosmetic improvement in her outlook and socialization also greatly improved [Figure 2], [Figure 3].
Figure 2: Intraoperative views. (a) Incision placed leaving 2 mm attached gingiva. (b and c) Removal of excess gingival tissue. (d) Excised gingival and lip tissue

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Figure 3: (a) Lip debulking. (b and c) Immediate postoperative view after removal of excess lip and gingival tissues. (d) Postoperative frontal view

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Case 2

A 6-year-old girl presented with the chief complaint of gum enlargement over the upper and lower teeth regions. The girl was born out of nonconsanguineous marriage and presented with excessive hair on the whole body. She had average growth and achieved normal developmental milestones. Clinical examination showed a mentally alert, well-built girl with hypertrichosis, presenting with extremely bushy eyebrows with downy growth of hair on the cheeks, chin, upper lip, and chin. On intraoral examination, generalized gingival hyperplasia was present covering the anatomical crowns of the deciduous teeth as well as the permanent teeth. Lips were incompetent due to gingival hyperplasia [Figure 4], [Figure 5], [Figure 6] (for surgical procedure, refer Case 1).
Figure 4: (a and b) Preoperative image. (c) Intraoperative view

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Figure 5: (a-c) Removal of excess gingival tissue

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Figure 6: (a and b) Postoperative view

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Case 3

An 8-year-old girl was brought to our hospital for the treatment of overgrown gums in the upper and lower teeth. She was born out of a nonconsanguineous marriage with an uneventful antenatal and postnatal history, as described by the mother. There were no associated systemic complications in the child. On examination, terminal hair had a generalized distribution over the entire body sparing the palms, soles, and the mucosal surfaces. Intraoral examination revealed pink, hyperplastic, and stippled gingiva with an altered dental architecture covering almost all teeth except for occlusal surface of all the four molars, and she was planned for gingivectomy procedure (for surgical procedure, refer Case 1).


   Discussion Top


Congenital generalized hypertrichosis (CGH) represents a heterogeneous group of conditions that are phenotypically and genetically distinct; it is characterized by excessive universal hair growth as the hallmark feature that is disproportionate when compared to normal individuals of that age, sex, and race and it is not dependent on androgenic hormones.[5] Various genetic syndromes have been associated with hypertrichosis condition such as Ambras syndrome, Barber Say syndrome, and Cantu syndrome.

Gingival fibromatosis may be familial or idiopathic.[2] The familial variation may occur with a number of other inherited syndromes when it could be associated with some of the following, for example, Zimmermann–Laband syndrome,[6],[7] Murray–Puretic–Drescher (juvenile hyaline fibromatosis),[8] Rutherfurd, Cross, Cowden syndrome, multiple hamartomas, and tuberous sclerosis.[9],[10]

The gingival overgrowth usually begins at the time of eruption of permanent dentition or less frequently with the eruption of primary dentition.[9] In our cases, case 1 reported that the gingival enlargement started since birth but it almost covered the entire teeth at the time of teeth eruption of permanent dentition, and hence there was delayed eruption of permanent dentition. The extent and severity of fibromatosis in this case has covered almost all teeth, thereby causing difficulty in mastication and speech.

The microscopic features of the present cases were classic of gingival fibromatosis. The tissue showed excess amount of collagen in an avascular corium with the overlying parakeratinized epithelium.

The treatment need varies according to the degree of severity. The relative increase in the gingival mass necessitates the need for surgical intervention owing to the functional and esthetic compromise.

Whenever possible, the treatment should be performed after the complete eruption of permanent dentition. Recurrence is a common feature over varying periods. One report indicated that there is less chance of recurrence if the gingivectomy is delayed until permanent dentition is in place.[10]

As far as the management of hypertrichosis is concerned, long-term removal of hair in these patients poses to be a challenging concern. This in turn is dependent on the degree of hair growth, the patient's psychologic profile, and the issue of social acceptance.[11]

Since only very few cases have been reported in the literature, the duration of functional or cosmetic aspect of surgical treatment of GFH syndrome cannot be determined. There was no recurrence after 1 year of follow-up in all the three cases.


   Conclusion Top


GFH syndrome is a rare disorder characterized by varying degrees of attached gingival overgrowth with excessive facial and body terminal hairs. Esthetic and functional compromises of gingival enlargement often demand surgical intervention, albeit recurrence cannot be predicted. Good esthetic result was achieved without the recurrence of gingival overgrowth. After treatment, regular recalls are necessary to evaluate oral hygiene and stability of surgical treatment.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Newman MG, Takei HH, Klokkevold PR, Carranza FA. Carranza's Clinical Periodontology. 11th ed. St. Louis, Missouri: Saunders; 2010. p. 40.  Back to cited text no. 1
    
2.
Varma BR, Nayak RP. Clinical Periodontology. 2nd ed. New Delhi: Arya Medi Publishing House; 2009. p. 177.  Back to cited text no. 2
    
3.
Eley BM, Soory M, Manson JD. Periodontics. 6th ed. China: Churchill Livingstone, Elsevier; 2010. p. 113-4.  Back to cited text no. 3
    
4.
Winter GB, Simpkiss MJ. Hypertrichosis with hereditary gingival hyperplasia. Arch Dis Child 1974;49:394.  Back to cited text no. 4
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5.
Garcia-Cruz D, Figuera LE, Cantu JM. Inherited hypertrichoses. Clin Genet 2002;61:321-9.  Back to cited text no. 5
[PUBMED]    
6.
Laband P, Habib G, Humphrey G. Hereditary gingival fibromatosis: Report of an affected family with associated splenomegaly and skeletal and soft tissue abnormalities. Oral Surg Oral Med Oral Pathol 1964;17:339-51.  Back to cited text no. 6
    
7.
Oikawa K, Cavaglia AM, Lu D. Laband syndrome: Report of case. J Oral Surg 1979;37:120-2.  Back to cited text no. 7
[PUBMED]    
8.
Sciubba JJ, Niebloom T. Juvenile hyaline fibromatosis (Murray-Puretic-Drescher syndrome): Oral and systemic findings in siblings. Oral Surg Oral Med Oral Pathol 1986;62:397-409.  Back to cited text no. 8
[PUBMED]    
9.
Bansal A, Narang S, Sowmya K, Sehgal N. Treatment and two-year follow-up of a patient with hereditary gingival fibromatosis. J Indian Soc Periodontol 2011;15:406-9.  Back to cited text no. 9
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10.
James PL, Prasad SV. Gingival fibromatosis: Report of case. J Oral Surg 1971;29:55-9.  Back to cited text no. 10
[PUBMED]    
11.
Mysore SK, Trivedi A, Arora S, Gupta S. Werewolf syndrome associated with gingival fibromatosis: A rare case report. J Indian Acad Oral Med Radiol 2016;28:219-22.  Back to cited text no. 11
    

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Correspondence Address:
Preetha Balaji
Balaji Dental and Craniofacial Hospital, #30, Kavignar Bharathi Dasan Road, Teynampet, Chennai - 600 018, Tamil Nadu
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijdr.IJDR_367_17

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    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]



 

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