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South African Journal of Surgery

On-line version ISSN 2078-5151
Print version ISSN 0038-2361

S. Afr. j. surg. vol.55 n.2 Cape Town Jun. 2017

 

CASE REPORTS

 

Lingual Fibrolipoma - A rare clinicopathological entity

 

 

S MungulI; S MaharajII; S D MasegeIII

IDepartment of Otorhinolaryngology, Helen Joseph Hospital, University of the Witwatersrand
IISenior Specialist, Department of Otorhinolaryngology/Head and Neck Surgery, Charlotte Maxeke Johannesburg Academic Hospital, University of the Witwatersrand, Parktown
IIIHead of Division, Department of Otorhinolaryngology/Head and Neck Surgery, Chris Hani Baragwanath Academic Hospital, University of the Witwatersrand, Soweto

Correspondence

 

 


ABSTRACT

Lipoma is a relatively common benign tumour occurring at sites of the body which are rich in adipose tissue. Due to sparsity of adipose tissue within the oral cavity, lipoma rarely presents in this region. Fibrolipoma of the tongue is a rare lesion. There are only 14 cases reported in the literature.
An 85-year-old patient presented with a painless mass on the tongue interfering with eating. There were no risk factors for malignancy and no family history of malignant diseases. Although intraoperatively the lesion was locally infiltrative, histopathology revealed a rare benign fibrolipoma.
Mainstay of treatment is surgical excision, but the lesion may pose a dilemma for Surgeons as difficulties associated with removal, due to the fibrous and adherent nature of the growth to surrounding tissue, may be mistaken for a cancerous growth.

Keywords: Fibrolipoma, Lipoma, Tongue, Malignant, Fibrous


 

 

Case presentation

An 85-year-old male presented to our hospital with a three-year history of a painless mass on the lateral aspect of the right side of the tongue. There was no history of repeated trauma to the tongue. There were no risk factors for malignancy on history and no other co-morbidities. Clinical examination revealed a healthy 85-year-old gentleman with no evidence of weight loss. Ear Nose and Throat examination was unremarkable. Oral cavity examination showed an approximately 3 x 3 cm sub-mucosal, regular, well-defined, non-tender, rubbery mass on the right side of the tongue, with no surface ulceration. No neck nodes were palpable. The sensation and mobility of the tongue was intact, with no apparent involvement of the floor of mouth.

A contrast Computed Tomography (CT scan) showed an oval-shaped, well-circumscribed and homogenous right tongue mass measuring 4.5 x 2.8 cm with no bony involvement and no enlarged lymph nodes. A fine needle aspirate (FNA) showed mainly blood and adipose tissue and was deemed inadequate for diagnostic evaluation.

Due to the frequency of malignancy in patients with tongue masses at our institution, excisional biopsy was planned under general anaesthesia via an intra-oral approach. Because investigations carried out on the lesion, including Fine Needle Aspirate Cytology (FNA) and CT scan suggested a diagnosis of a lipoma, we expected a straight forward excision of the lesion. Intraoperatively the lesion was encapsulated, firmly adherent to the surrounding tissues but not infiltrative.

Macroscopic examination of the excised lesion revealed a well circumscribed, encapsulated portion of tissue, measuring 3.5 x 3.2 x 3.0 cm. On sectioning, the mass was soft and homogenous with a yellow cut surface.

Histologic evaluation of the mass confirmed representation of encapsulated, lobulated fibro-adipose tissue comprising of mature adipocytes which showed no variation in size. There were no hypercellular areas and no areas of fat necrosis present within the specimen. The histological features were therefore consistent with a benign fibro-lipoma. Outpatient follow-up was uneventful, with no recurrence.

 

Discussion

Lipomas are the most common benign tumours occurring in anatomical sites with adipose tissue throughout the body. Approximately 13-20% of head and neck tumours comprise lipoma,4 with 1-5% of lipomas presenting in the oral cavity.4-6

The buccal mucosa is the most common site for lipoma, with the tongue being the second commonest site.

Tongue lipomas, which may be single, multiple or part of a syndrome, most commonly occur on the lateral border of the tongue, and have a male predilection.2 They may present as single or multiple lesions and may either be solitary or manifest as part of a syndrome such as Gardner Syndrome.

Fibrolipoma, a histologic variant of lipoma, is characterised by mature adipose tissue which is separated into lobules by fibrous strands. These tumours are surrounded by a fibrous connective tissue capsule, which gives rises to multiple fibrous bands which often adhere to surrounding tissue3 making a clear distinction between benign and malignant lesions doubtful, as it was with our patient.

Macroscopically, these lesions may be oval and of variable size, appear yellow in colour due to a thin translucent membrane, and with a soft to semi-firm consistency, depending on the degree of the fibrous connective tissue component.4,6

The clinical course of lingual fibrolipoma is usually asymptomatic, with an average duration of 3.2 years prior to excision. Patients classically present with a painless, slow growing lesion and generally only seek medical attention for aesthetic or functional issues such as chewing, swallowing or phonation dysfunction.4 The appearance and pseudo-infiltrative nature of fibrolipoma may induce doubt clinically as to whether the lesion is truly benign.3 In addition, since one cannot with certainty clinically distinguish between fibrolipoma and malignant infiltrating lesions such as liposarcoma, histologic evaluation is essential.

Computed Tomography scan features of fibrolipoma include that of an oval homogenous mass with well-defined borders. Although cytological evaluation may be attempted, it rarely provides diagnostic value in such cases of fibrolipoma of the tongue.3

Surgical excision is the mainstay of treatment and recurrence of fibrolipoma is rare following total excision.4 The main objective of presenting this case is to create awareness of this rare clinical entity which may at times mimic a malignant growth.

 

Conclusion

Lipoma of the tongue is a rare clinicopathological entity and fibrolipoma specifically, is exceptionally rare, with as few as 14 reported cases worldwide.3 The histological features of this subtype of lipoma render it significant as it may masquerade as a malignancy on clinical examination, and it is therefore important to be aware of such an entity.3 Surgical excision is thus essential to histologically distinguish fibrolipoma from infiltrating malignant lesions, and is the mainstay of treatment.

 

 

 

 

 

Figure 4

 

Acknowledgement

We would like to acknowledge Dr Farzana Mahomed, Oral Histopathology Department, University of the Witwatersrand, for preparing and providing us with the slides.

Funding

None

Conflict of Interest

None declared

Consent

Dr Mungul takes full responsibility for the integrity of the content of the manuscript. Assisted by Dr Masege.

 

REFERENCES

1. Srinivasan K, Hariharan N, Parthiban P, Shyamala R. Lipoma of the tongue - A rare site for a common tumour. Indian J Otolaryngol Head Neck Surg. Mar 2007;59(1):83-4.         [ Links ]

2. Baonerkar HA, Vora M, Sorathia, R, Shinde S. The lipoma of tongue - a rare site for a tumour: case report and review of the literature. Indian J Dent. Oct-Dec 2015;6(4):207-10.         [ Links ]

3. Iaconetta G, Friscia M, Cecere A, Romano A, Orabona GDA, Califano L. Rare fibrolipoma of the tongue: A Case Report. J Med Case Rep. 2015;9:177.         [ Links ]

4. Manjunatha BS, Pateel GS, Shah V. Oral fibrolipoma-a rare histological entity: report of 3 cases and review of literature. J Dent (Tehran) 2010;7:226-31.         [ Links ]

5. de Visscher JG. Lipomas and fibrolipomas of the oral cavity. J Maxillofac Surg. 1982;10:177-81. doi: 10.1016/S0301-0503(82)80036-2        [ Links ]

6. Colella G, Biondi P, Caltabiano R, Vecchio GM, Amico P, Magro G. Giant intramuscular lipoma of the tongue: a case report and literature review. Cases J. 2009;22:7906.         [ Links ]

 

 

Correspondence:
Dr SD Masege
dipuo.masege@wits.ac.za

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