case report

Giant Facial Lipoma - A Case Report

Thalles Moreira Suassuna1*, Flora Laís Malafaia da Silva2, Camila Oliveira Sá Barreto2, José Romar Baião de Almeida1, Flávio Henrique Real3

1Department of Oral and Maxillofacial Surgery, Hospital Getúlio Vargas, Brazil

2Departament of Dentistry, University of Pernambuco, Brazil

3Department of Oral and Maxillofacial Surgery, Federal University of Pará, Brazil

*Corresponding author: Thalles Moreira Suassuna, Department of Oral and Maxillofacial Surgery Hospital Getúlio Vargas. Trauma C. Av. General San Martin, S/N, Cordeiro- Recife, Pernambuco, Brazil. Tel: +5583988545056; Email: thallesms_@hotmail.com

Received Date: 28 August, 2017; Accepted Date: 02 September, 2017; Published Date: 08 September, 2017 

Citation: Suassuna TM, da Silva FLM, Sá Barreto CO, de Almeida JR, Real FH (2017) Giant Facial Lipoma - A Case Report. Dent Adv Res 2: 132. DOI: 10.29011/2574-7347.100032

1.      Abstract

 

Background: Lipomais the most frequent benign mesenchymal neoplasm’s that affect the human body. They are composed of mature adipocytes and are enveloped by a fibrous capsule. The oral vestibule and jugal mucosa are the most commonly affected intraoral sites, and the tumors are characterized by painless increase in size, soft consistency, yellowish color, sessile or pedunculated base, and slow growth rate.

 Objective: To report a case of giant facial lipoma and to review the main diagnostic and therapeutic aspects of this pathology.

 Case report: NRS, a 64-year-old female patient, presented with increasing facial volume for 7 years. Tumescence was observed from the genial to the mental regions, with intraoral and extra oral protuberance. Surgical removal was chosen as treatment.

 Final remarks: The histopathological analysis confirmed the diagnosis of lipoma. In cases of large lesions, surgery remains as the mainstay of treatment.

2.    Abbreviations: 

CT          :               Computed Tomographic

NRS        :               Patient Name Abbreviation

           

3.      Keywords: Lipoma, Oral Neoplasms, Oral Surgery

1.      Introduction

 Lipomas are benign neoplasm’s of mesenchymal origin [1] composed of mature adipocytes divided into lobules separated by fibrous septum and surrounded by a thin fibrous capsule [2,3].

They are the most frequent mesenchymal neoplasm’s that affect the human body, being commonly observed in the thorax and in extremities [1]; around 20% in the head and neck region; and only 4 to 5% in the oral cavity [4].

The intraoral sites affected by this tumor include the tongue, floor of the mouth, palate, oral vestibule, and jugal mucosa. The latter two sites are the most common, accounting for 50% of all intraoral cases [5,6].

The etiology of this tumor is uncertain, but endocrine disorders, infections, traumas, alcoholism, and inherited traits are believed to be predisposing factors [6].

This type of tumor is uncommon among children, and individuals older than 40 years tend to be more frequently affected at varying rates. There is no predilection for race and its distribution between genders seems to be balanced, with a slight predominance of male individuals, as pointed out by some studies [6,7].

When lipomas affect the oral cavity, they exhibit a painless increase in size, mobility, soft consistency, and a yellowish color [8]. Most tumors measure 10 to 19 mm; however, their size may be a lot bigger due to their progressive growth [9].

As lipomas are asymptomatic, they are neglected by patients, and many of them only seek medical care when the tumor has reached a large size and is compromising functional activities, such as chewing and speaking, or interfering with the placement of dental prostheses [10].

Given that lipomas do not resolve spontaneously and have a progressive growth, surgical intervention is usually recommended. Treatment of oral lipomas, including all histological types, consists of complete surgical excision. After this procedure, recurrence is rare [4].

The aim of this study is to review the clinical and therapeutic aspects of lipomas, especially those in the oral cavity, and to describe an uncommon clinical case of a 64-year-old patient with a giant facial lipoma.

 2.      Case Report

 NRS, 64-year-old, diabetic and hypertensive female patient presented with increasing facial volume for about 7 years. She complained of sporadic pain and trauma to the region before the development of the tumor. On physical examination, there was a flaccid, mobile lesion measuring approximately 12 cm from the right genial region to the mention, circumscribed to the soft tissues, without hyperalgesia, with evident intraoral and extra oral involvement. Oral mucosal tissue looked normal (Figure 1 A-B). The ultrasound scan revealed a thicker hypoechoic region, not well circumscribed, with lipomatous appearance in subcutaneous planes and more superficial lesion in the anterior jugal mucosa (Figure 1C).

Surgical treatment was indicated and after preoperative tests, the lesion was rejected. After direct incision of the mucosa, a soft yellowish mass was observed. Because of evident surgical distinction between the lesion and the tissues, a blunt dissection was performed until complete excision of the lesion (Figure 2). No vital structures were directly affected, but the dissection eventually showed close contact between the lesion and the skin.

Even though the gross aspect of the lesion was highly suggestive of lipoma, the specimen was sent for histopathological analysis, which did not detect malignancies and confirmed the diagnosis (Figure 3). The patient had an uneventful recovery and did not have any recurrence, as evidenced in her follow-up visit 2 years after the surgery (Figure 4).

3.      Discussion

 The etiology of lipomas is quite controversial, including endocrine disorders, inflammation, and local trauma[7]. Literature reviews suggest that Caucasian men aged 49 to 60 years without a family history of lipoma are the most frequently affected group, with no predilection for the affected side[11,12]. Gender predominance does not appear to be remarkable. In the present report, lipoma affected a female patient.

 These gelatin-like smooth-surfaced tumors are often asymptomatic, mobile, and free of ulcerations. Superficial blood vessels are more evident on the tumor as it develops, owing to distension of the mucosa over the lesion. Despite the discrete yellowish color detected clinically, deep lesions may not interfere in the color of epithelial tissue6. Moreover, curiously enough, these tumors tend to float when placed in a 10% formaldehyde solution as they are less dense than the solution [13].

 Due to clinical similarities in some cases, other diagnostic possibilities should be included in the differential diagnosis, such as epidermis and oral lymphoepithelial cysts [14]. While the latter have a smaller size and develop mainly in the first decades of life, they are sub mucosal, mobile, and painless nodules with a light yellow color, thus bearing resemblance to lipomas [6,14]. Therefore, histopathological analysis is still the most accurate method for confirming the diagnosis [14], as observed in the present report.

 Lipomas microscopically differentiate too little from the surrounding healthy adipose tissue. Classically, they are fatty masses, but other mesenchymal elements could be present, producing histological variants, which eventually have a negligible impact on treatment and prognosis. These variants are widely acknowledged and include angiolipoma, pleomorphic lipoma, intramuscular lipoma, and fibrolipoma [5,15].

 These tumors are often found in obese individuals. If calorie intake and body fat are reduced, lipomas do not decrease in size, due to the independent metabolism of these lesions [6].

 Imaging exams have an important diagnostic value. Computed Tomographic (CT) scans are useful in determining the accurate location of the lesion, and they usually reveal a hypodense mass circumscribed by a thin capsule that is not enhanced by contrasting agents [11,12]. CT and ultrasound scans were used as complementary exams in the present study.

 Magnetic resonance is also useful, as the margin of lipomas tends to be clearly visible in this kind of exam. The visualization of the capsule based on the black margin substantially aids in the final diagnosis. Such distinction cannot be made by CT scans [11,12,16].

 Ultrasonography can also be used. It is easy and quick to use, inexpensive, and provides good identification of superficial tissues, which are usually hypoechoic. However, this diagnostic modality has poor image resolution [16].

 This type of lesion is treated preferably by surgical excision [17,18], but some authors have described satisfactory results with the use of electrocautery and laser for removal of intraoral lipomas [19]. Cases of recurrence are uncommon, but in case of intramuscular variants, there could be recurrence, and it is widely known that liposarcomas may develop after recurrent lipomas. Despite the low rates of recurrence after surgical excision, postoperative follow-up is important and the prognosis is good in most cases [18,19]. In the case reported herein, the lesion was totally removed, with no evidence of recurrence after 2 years.

 4.      Final Remarks

 Lipoma is a relatively common pathology in the maxillofacial region, and histopathological analysis plays an essential role in ruling out malignancies. Whenever possible, diagnostic resources help choose the treatment plan and surgical approach which is the most effective method of treatment.


Figure 1(A-C): A) Extra oral tumescence extending from the genial region to the mention. B) Intraoral image showing vestibular bulging. C) Ultrasound scans showing thicker hypoechoic layer, not well circumscribed, and lipomatous aspect in subcutaneous planes.





Figure 2: A) Incision in right oral mucosa for lesion exposure. B) Dissection and determination of lesion borders. C) Total excision of the tumor. D) Gross image of the surgically removed tissue.






Figure 3:A) Low-power photomicrograph showing fatty cells and connective tissues with capillary blood vessels. B) Histological examination showing mature adipocytes.






Figure 4: Extra oral aspect 2 years after the surgery.


  1. Misirlioglu M, Akyl YY, Adisen MZ, Okkesim A (2017) Differential Diagnosis of Parotid Lipoma in a Breast Ca Patient. Case Reports in Dentistry 1:1-4.
  2. VolpatoLER, Vasconcelos AC, Lambert NA, Castro PHS, Aburad A, et al. (2016) Lipoma of the Palate: An Uncommon Finding. Open Dent J 10: 643-646.
  3. Sanjuan A, Dean A, Garcia B, Alamillos F, Roldan E, et al. (2017) Condy­lar intramedullary intraosseouslipoma: Contribution of a new case and review of the literature. J Clin Exp Dent  9: 498-502.
  4. Vasconcelos BCE, Porto GG, Carneiro SCAS, Xavier RLF (2007) Lipomas ofthe oral Cavity. Rev Bras Otorrinolaringol 73: 848.
  5. Santos LAM, Barbalho JCM, Costa DFN, Silva CCG, Pereira VBS,Vasconcelos BEC (2014) RevCir Traumatol Buco-Maxilo-Fac 14: 29-44.
  6. Basheer S, Abraham J, Shameena P, Balan A (2013) Intraosseous lipoma ofmandiblepresenting as a swelling. J Oral MaxillofacPathol 17: 126-128.
  7. Egido-Moreno S, Lozano-Porras AB, Mishra S, Allegue-Allegue M, Marí-Roig A, et al. (2016) Intraorallipomas: Review of literature and report of two clinical cases. J ClinExp Dent 8: 597-603.
  8. Ohyama Y, Uzawa N, Yamashiro M, Yamaguchi S (2017) Congenitallipoma of the hard palate: case report. Brit J Oral Maxillofac Surg 55: 626-627.
  9. Taira Y, Yasukawa K, Yamamori I, Iino M (2011) Oral lipoma extending superiorly from mandibular gingivobuccal fold to gingiva: a case re­port and analysis of 207 patients with oral lipoma in Japan. Odontolo­gy 100: 104-108.
  10. Ponce JB, Ferreira GZ, Santos PSS, Lara VS (2016) Giant oral lipoma: a rareentity. An Bras Dermatol 91: 84-86.
  11. Fakhry N, Michel J, Varoquaux A, Antonini F, Santini L (2012) Is surgical excision of lipomas arising from the parotid gland systematically required?.Eur Arch Otorhinolaryngol 269:1839-1844.
  12. Starkman SJ, Olsen SM, Lewis JE, Olsen KD, Sabri A (2013) Lipomatous lesions of the parotid gland: analysis of 70 cases. Laryngoscope 123: 651-656.
  13. Bakshi SS, Priya M, Coumare VN, Vijayasundaram S, Karanam L (2015) A common tumor in an uncommon location: Lipoma of the palate. Ann Maxillofac Surg 5: 237-239.
  14. Jaeger F, Capistrano HM, de Castro WH, Caldeira PC, Vieira do Carmo MA, et al. (2015) Oral Spindle Cell Lipoma in a Rare Location: A Differential Diagnosis. Am J Case Rep 30: 844-848.
  15. Agarwal R, Kumar V, Kaushal A, Singh RK (2013) Intraorallipoma: a rare clinical entity. BMJ Case Rep 28.
  16. Pattipati S, Kumar MN, Ramadevi, Kumar BP (2013) Palatal lipoma: a case report. J Clin Diagn Res 7: 3105-3106.
  17. Tadataka T, Koichi S, Hiroshi N, Kumiko K,Mikihiko K (2014) Clinical characteristics of lipoma in the submandibular region: Report of a relatively uncommon case and review of the literature in Japan 2014. J OralMaxillofac Surg Med Pathol 27: 344-347.
  18. Raj AA, Shetty PM, Yadav SK (2014) Lipoma of the Floor of the Mouth: Report of an Unusually Large Lesion. J Maxillofac Oral Surg 13: 328-331.
  19. SathyakiDC, Swarup RJ, Mohan M, Varghese R (2014) Lipoma of the submandibular space. J Oral MaxillofacPathol 18: 149.

© by the Authors & Gavin Publishers. This is an Open Access Journal Article Published Under Attribution-Share Alike CC BY-SA: Creative Commons Attribution-Share Alike 4.0 International License. With this license, readers can share, distribute, download, even commercially, as long as the original source is properly cited. Read More About Open Access Policy.

Dentistry: Advanced Research

Update cookies preferences