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An Official Publication of the Indian Association of Oral and Maxillofacial Pathologists


 
  Table of Contents    
CASE REPORT  
Year : 2014  |  Volume : 18  |  Issue : 1  |  Page : 114-117
 

Plexiform neurofibromatosis involving face and oral cavity


1 Department of Periodontics, Missions Sankarachariyar Dental College, Salem, Tamil Nadu, India
2 Depatment of Prosthodontia, Vinayaka Missions Sankarachariyar Dental College, Salem, Tamil Nadu, India
3 Department of Oral Medicine and Radiology, Sree Mookambika Institute of Dental Sciences, Kanyakumari, Tamil Nadu, India
4 Department of Oral Medicine and Radiology, Vishnu Dental College, Bhimavaram, Andhra Pradesh, India

Date of Web Publication6-May-2014

Correspondence Address:
Gajendra Veeraraghavan
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0973-029X.131932

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   Abstract 

Plexiform neurofibromas (PNFs) are one of the most common and debilitating complications of neurofibromatosis type I (NF-I). They account for substantial morbidity, disfigurement, functional impairment and are life threatening. PNFs can also be subjected to transformation into malignant peripheral nerve sheath tumor (MPNST). This complication is refractory to treat due to paucity of effective therapies for malignant soft tissue sarcomas in general and also the delay in diagnosis from a preexisting tumor. We report a case of PNF of face involving oral cavity with literature review.


Keywords: Café- au- lait macules, facial plexiform neurofibromatosis, peripheral nerve sheath tumor, von Recklinghausen′s


How to cite this article:
Jayachandran D, Sunantha S, Gopalaiah H, Veeraraghavan G. Plexiform neurofibromatosis involving face and oral cavity . J Oral Maxillofac Pathol 2014;18:114-7

How to cite this URL:
Jayachandran D, Sunantha S, Gopalaiah H, Veeraraghavan G. Plexiform neurofibromatosis involving face and oral cavity . J Oral Maxillofac Pathol [serial online] 2014 [cited 2019 Dec 7];18:114-7. Available from: http://www.jomfp.in/text.asp?2014/18/1/114/131932



   Introduction Top


A neurofibroma is a benign nerve sheath tumor in the peripheral nervous system. At least eight forms of neurofibromatosis are recognized, the most common form being neurofibromatosis type I (NF-I) or von Recklinghausen's disease. NF-I is an autosomal dominant genetically inherited disease, which can result in a range of symptoms from physical disfiguration, pain to cognitive disability. Neurofibromas arise from nonmyelinating-type schwann cells that exhibit biallelic inactivation of the NF-I gene that codes for the protein neurofibromin. [1] This protein is responsible for regulating the retrovirus associated DNA sequences (RAS) mediated cell growth signaling pathway. In contrast to schwannomas, another type of tumor arising from schwann cells, neurofibromas incorporate many additional types of cells and structural elements in addition to schwann cells, making it difficult to identify and understand all the mechanisms through which they originate and develop. [2] NF-I is estimated to occur in one in every 3000 births with no sex predilection. [3],[4],[5],[6],[7] Although, in principle, diagnosis of NF-I should be possible through genetic testing, only two-thirds of cases can be diagnosed and moreover, genetic testing cannot predict severity of the disease. The diagnosis of NF-I is still dependent on identification of the cardinal signs of the disease, two or more of which must be present to establish the diagnosis. Some researchers say that neurofibromas alone are pathognomonic of the disease. The condition can cause disfigurement by entwining important supportive structures. [8],[9] Plexiform neurofibromas (PNFs) are uncommon and occur almost exclusively in about 5-15% patients with NF-I. [10] PNFs are benign tumors that originate from nerve sheath cells, subcutaneous or visceral peripheral nerves that can involve multiple fascicles. [1] PNF presents at birth and often progresses during early childhood at a growth rate and pattern that vary significantly and unpredictably. [3],[4],[5],[6],[7] Because of the involvement of multiple fascicles of nerves and tissues and the spread of PNF, there is high risk of neurological and functional destruction when surgical resection is carried out. Therefore surgical interventions are frequently postponed as long as possible from the early childhood. Most cases require repeated surgeries, as they are limited to debulking and PNFs often regrow later. [9]


   Case report Top


A 56-year-old female patient presented to the dental clinic, with a history of growth on the lip and tongue. Lesions are also noted on face, both sides of the chin and jaws [Figure 1]. The patient reported that the face-disfiguring growth started at birth and continuously increased in size since then. Patient complained of difficulty in speech, occasional pain and itching on the face. The patient came to hospital with these lesions for the first time and had not taken any prior treatment for the same. There was no known evidence of hereditary disease in the family and none of the other relatives had a known history of this disease. On physical examination, she was pale and face was disfigured with growth of completely overhanging skin folds typically termed as elephantiasis skin. The patient presented with macrocheilia and macroglossia. The café-au-lait macules (with some measuring over 5.5 mm) as well as several freckles were observed in the axilla, back and chest. Imaging modalities did not reveal any bone abnormality.

An incisional biopsy was taken from the lip lesion. Five-micrometer sections were made and stained with hematoxylin and eosin (H and E) and 3-μm sections were taken for S-100 immunohistochemical staining.
Figure 1: Clinical image showing diffuse swelling involving the tongue and lower lip

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Histopathological features

The H and E stained section shows [Figure 2] cellular neoplasm composed of combined proliferation of schwann's cells, fibroblast, perineural cells and axon cells. Schwann cells are spindle cells with wavy nuclei arranged in bundles. The endoneurium showed myxoid changes. The interstitium showed thickened fibroblast bundles interspersed with scattered spindle cells and also shows plexiform features. Immunohistochemistry [Figure 3] showed S-100 positivity in the cytoplasm of tumor cells, which confirms their schwannian origin. On the basis of clinical and histopathological features, a clinical diagnosis of NF-I and PNF was made [Table1].
Table 1: Histological feature of our case in comparison
with the literature


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Figure 2: The photomicrograph of the sections shows bundles of Schwann cells in myxomatous stroma (H&E stain, 100)

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Figure 3: The photomicrograph showing tumor cells positive for S-100 protein (IHC stain, 100)

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   Discussion Top


PNFs can grow from nerves in the skin or from more deeper nerve bundles. They can be very large. Internal PNFs are very difficult to remove completely because they are extended through multiple layers of tissue and the attempt would damage healthy tissue or organs. PNFs occur earlier in life and are thought to be congenital defects.

PNF is a rare type of generalized neurofibromatosis, which occurs due to overgrowth of neural tissue in the subcutaneous fat or deeper tissues in the body. It is usually considered to be a hamartoma rather than a typical tumor. [10] They originate from nerve sheath cells, subcutaneous or visceral peripheral nerves and can involve multiple fascicles. Malignant changes in 2.4-29% of patients with neurofibromatosis have been reported. [11] The condition is autosomally dominant, with variable penetration and presents as multiple nodules of various sizes, which are firm and non-tender, often associated with café-au-lait spots and spindle deformities. Two types of PNF that have been recognized are (i) diffuse type/elephantiasis neurofibromatosis and (ii) nodular neurofibromatosis. [8] PNF can occur anywhere along a nerve and may appear on the abdomen, [11],[12] face, [10],[13],[14] orbit and globe, [15] legs, [10] scalp, neck, chest, pelvis or spinal cord and frequently involve the cranial and upper cervical nerves. [13] The fifth, ninth and tenth cranial nerves are most commonly involved. [16] The condition can be quite disfiguring, as in this case, presenting as hemifacial hypertrophy, occurring secondary to a plexiform tumor involvement. [17] Symptoms ranging from minor discomfort to extreme pain may occur. [8],[16],[18] Complications include bleeding from trauma, neurological deficits, limited limb and psychological disturbance because of abnormal anatomy. [10] There is evidence that only 50% of PNF patients have a positive family history of the disease and the remaining represent spontaneous mutation. Although most individuals who develop neurofibromatosis are not born with café-au-lait macules, these skin lesions develop during the first 3 years of life and were observed in our patient. Lisch nodules that are hamartomas of the iris, which appear dome-shaped and are found superficially around the eyes on slit lamp examination, helped us to confirm the disease. Axillary freckling (observed in our patient) and inguinal freckling often develop during puberty. [8] Various neurologic abnormalities, acoustic nerve involvement and deafness as well as gliomas of the optic nerve may occur. [10],[16],[17],[18]

The patient in our case fulfilled many of the criteria; she had more than six café-au-lait macules, PNF and fleckles in the axilla, but there was no evidence of central nervous system (CNS) tumors, macrocephaly, mental deficiency, seizures, short stature or sclerosis.

PNF can cause pain, disfigurement, neurological and other clinical deficits. PNFs have the potential to cause severe clinical complications if they occur in certain areas. [19] About 10% of PNFs undergo transformation into a malignant peripheral nerve sheath tumor (MPNST). [20] The formation of malignant tumor from neurofibroma is associated with the loss of expression of the cyclin-dependent kinase inhibitor 2A (CDKN2A) or TP53 gene in nonmyelinating schwann cells that also exhibit biallelic inactivation of the NF-I gene. [21]

The primary treatment option for PNF was surgery. [21] Removal of PNF is difficult because they can be large and cross tissue boundaries. However, besides pain, PNFs are sometimes removed due to the possibility of malignant transformation. Once a PNF has undergone malignant transformation, radiation and chemotherapy can be used as treatment. However, radiation is generally not used as a treatment for PNFs because of concerns that this could actually promote malignant transformation. [22]

Angiotensin-converting enzyme (ACE) inhibitors have been proposed as a novel treatment of neurofibromas. ACE inhibitors are currently used to treat hypertension and congestive heart failure; to help remodeling and avert reinfarction after myocardial infarction; to ameliorate diabetic nephropathy and other renal diseases. ACE inhibitors work by indirectly downregulating transforming growth factor-beta (TGF-β), which is a growth factor that has been shown to influence the development of tumors. [23]

Gene therapy for the neurofibromin 1 gene represents the ultimate solution to prevent the cluster of maladies that are enabled by the mutation. [24],[25]

The strategy adopted for our patient with neurofibromatous lesion presenting on lip and tongue was surgical excision because of the dimension of the lesion, interference with the function and esthetics of the patient. The patient underwent surgery and 6 months postoperative follow up without registering any complaints or apparent signs of recurrence of the lesion. It was decided to keep the patient under observation and review her once every 6 months for as long as possible.


   Conclusion Top


The disfiguring nature of facial PNF can be psychologically traumatic for most patients and requires good counseling. PNF is conclusive evidence for arriving at a diagnosis of NF-I. A few but not all cardinal signs may be seen in patients with NF-I. Patients with PNF should be periodically recalled to rule out recurrence or malignant conversion.


   Acknowledgment Top


Authors thank Dr. Sekar, MDS, Professor, Oral Pathology, Vinayaka Missions Dental College, Salem and Dr. Shylaja, MBBS, DCH, Department of Pathology, Government medical college, Dharmapuri, Tamil nadu for their assistance in the preparation of this manuscript.

 
   References Top

1.Kleihues P and Cavenee WK. Pathology and genetics of tumours of the nervous system. World Health Classification of Tumours. 1 st edition. Lyon; IARC Press; 2000.  Back to cited text no. 1
    
2.Huson SM. Neurofibromatosis 1: A clinical and genetic overview. In: Huson SM, Hughes RAC, editors. The Neurofibromatoses. London: Chapman and Hall Medical; 1994. p. 160-203.    Back to cited text no. 2
    
3.Cawthon RM, Weiss R, Xu GF, Viskochil D, Culver M, Stevens J, et al. A major segment of the neurofibromatosis type I gene: cDNA sequence, genomic structure, and point mutations. Cell 1990;62:193-201.  Back to cited text no. 3
    
4.Viskochil D, Buchberg AM, Xu G, Cawthon RM, Stevens J, Wolff RK, et al. Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type I locus. Cell 1990;62:187-92.  Back to cited text no. 4
    
5.Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, et al. Type I neurofibromatosis gene: Identification of a large transcript disrupted in three NF1 patients. Science 1990;249:181-6.  Back to cited text no. 5
    
6.Gutmann DH, Aylsworth A, Carey JC, Korf B, Marks J, Pyeritz RE, et al. The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. JAMA 1997;278:51-7.  Back to cited text no. 6
    
7.Kam JR, Helm TN. Neurofibromatosis. Available from: http://www.emedicine.medscape.com/article/1112001-Overview [Last accessed on 2009 Nov 14].  Back to cited text no. 7
    
8.Friedrich RE, Schmelzle R, Hartmann M, Fünsterer C, Mautner VF. Resection of small plexiform neurofibromas in neurofibromatosis type I children. World J Surg Oncol 2005;3:6.  Back to cited text no. 8
    
9.Sengupta SP. Manual of Long and Short Cases in Surgery. 1 st ed. Calcutta: New Centre Book Agency Publications; 1996.  Back to cited text no. 9
    
10.Patil K, Mahima VG, Shetty SK, Lahari K. Facial plexiform neurofibroma in a child with neurofibromatosis type I: A case report. J Indian Soc Pedod Prevent Dent 2007;25:30-5.  Back to cited text no. 10
    
11.Pui MH, Yang ZY, Li ZP. Computed tomography of abdominal neurogenic tumours. Australas Radiol 1998;42:183-7.  Back to cited text no. 11
    
12.Ferrozzi F, Zuccoli G, Bacchini E, Piazza P, Sigorini M, Virdis R. Extracerebral neoplastic manifestations in neurofibromatosis 1: Integrated diagnostic imaging. Radiol Med 1998;96:562-9.  Back to cited text no. 12
    
13.Wheeler JM. Plexiform neurofibromatosis (von Recklinghausen's disease) involving the choroid, ciliary body, and other structures. Trans Am Ophthalmol Soc 1936;34:151-62.  Back to cited text no. 13
[PUBMED]    
14.Sienkiewicz H, Wójtowicz PM. A case of plexiform neurofibroma of the face. Otolaryngol Pol 1985;39:253-6.  Back to cited text no. 14
    
15.Davis FA. Plexiform neurofibromatosis (Von Recklinghausen's disease) of the orbit and globe, with associated glioma of the optic nerve and brain: Report of a case. Trans Am Ophthalmol Soc 1939;37:250-71.  Back to cited text no. 15
    
16.Cunha KS, Barboza EP, Dias EP, Oliveria FM. Neurofibromatosis type I with periodontal manifestation. A case report and literature review. Br Dent J 2004;196:457-60.  Back to cited text no. 16
    
17.D'Ambrosio JA, Langlais RP, Young RS. Jaw and skull changes in neurofibromatosis. Oral Surg Oral Med Oral Pathol 1988;66:391-6.  Back to cited text no. 17
    
18.Neville BW, Damm DD, Allen CM, Bouquot JE. Oral and maxillofacial pathology. 2 nd ed. Philadelphia: Elsevier; 2002. p. 457 ?61.61.  Back to cited text no. 18
    
19.Kluwe L, Hagel C, Mautner V. Nervous system. Neurofibro. Altas Gent Cytogent Oncol Haematol. April 2007. URL: http://AtlasGeneticsOncology.org/Tumors/NeurofibromaID5098.html.  Back to cited text no. 19
    
20.Mautner VF, Friedrich RE, von Deimling A, Hagel C, Korf B, Knöfel MT, et al. Malignant peripheral nerve sheath tumours in neurofibromatosis type 1: MRI supports the diagnosis of malignant plexiform neurofibroma. Neuroradiology 2003;45:618-25.  Back to cited text no. 20
    
21.Packer RJ, Gutmann DH, Rubenstein A, Viskochil D, Zimmerman RA, Vezina G, et al. Plexiform neurofibromas in NF1: Toward biologic-based therapy. Neurology 2002;58:1461-70.  Back to cited text no. 21
    
22.Isler MH, Fogaça MF, Mankin HJ. Radiation induced malignant schwannoma arising in a neurofibroma. Clin Orthop Relat Res 1996;325:251-5.  Back to cited text no. 22
    
23.Namazi H. ACE inhibitors: A novel treatment for neurofibroma. Ann Surg Oncol 2008;15:1538-9.  Back to cited text no. 23
[PUBMED]    
24.Wetmore DZ, Garner CC. Emerging pharmacotherapies for neurodevelopmental disorders. J Dev Behav Pediatr 2010;31:564-81.  Back to cited text no. 24
    
25.Gottfried ON, Viskochil DH, Couldwell WT. Neurofibromatosis Type 1 and tumorigenesis: Molecular mechanisms and therapeutic implications. Neurosurg Focus 2010;28:E8.  Back to cited text no. 25
    


    Figures

  [Figure 1], [Figure 2], [Figure 3]
 
 
    Tables

  [Table1]



 

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   Case report
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