Correspondence

Infiltrating Oral Lipoma a Rare Variant Dear Editor, Intramuscular infiltrating lipoma is a rare variant of lipoma first defined by Regan and his colleagues in 1946.[1] There are only few cases reported in literature. We report an unusual case of intramuscular lipoma of the tongue, present on the posterior lateral aspect, emphasizing the clinico-pathologic features. A 50-year-old female patient reported to the outpatient department of the Seema Dental College and Hospital, Rishikesh, India, with a chief complaint of swelling on the posterior lateral border of the tongue, present for 2 years [Figure 1]. Clinical examination revealed a well-defined oval swelling measuring 2 � 1 cm present on the lateral border of the tongue. On palpation, the swelling was soft, fluctuant, non-tender and mobile. A provisional diagnosis of intraoral lipoma was made. After routine blood examination, an excisional biopsy was performed under local anaesthesia and was further subjected to histopathological examination. The haematoxylin and eosin-stained slides showed a lipomatous tumour composed of mature adipocytes, uniform in size and shape, diffusely infiltrating the striated muscle fibres of the tongue, further confirmed by Masson’s trichome stain [Figure 2]. There was no recurrence at a follow-up period of 1 year. The first description of an oral lipoma was provided by Roux in 1848, who referred to it as a “yellow epulis.”[2] There is lack of consensus regarding its pathogenesis. Hormonal factor, trauma and chronic irritation are thought to play a role in the development of lipoma. However, trauma is widely accepted as a causative factor in the discovery of the lesion rather than the aetiology.[3] It is usually found in adults and there is no gender predilection.[2] The clinical course of oral intramuscular

Figure 1: Clinical picture showing the growth over the lateral aspect of the posterior tongue

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lipomas is usually asymptomatic, but, on rare occasions, it can cause muscle dysfunction or sensory changes due to pressure on the nerve trunks.[4] In the present case, the tumour interfered with speech, mastication and movement of tongue. Intramuscular lipomas are of primary importance because of their differential diagnosis with liposarcoma due to their large size, deep location and their ability to infiltrate the adjacent muscles and recur locally. Therefore, a detailed histological examination is essential for all intramuscular lipomas. Our case had no areas of lipoblastic proliferation, nuclear atypia and mitosis. Conservative surgical removal is the treatment of choice and the prognosis is good as recurrence is rare. In our case, although adipocytes infiltrated the striated muscle fibres, they were all mature and uniform in shape and size. In addition, no morphological features of liposarcoma were identified. To conclude, although rare, intramuscular lipomas can occur in the oral cavity. Complete resection should be emphasized during the first surgical operation, which is the key factor to avoid recurrence. This case reported here was unique because, firstly, it occurred on the posterior third of the tongue and not on the anterior two-third, as usually reported and, secondly, intramuscular or infiltrating lipomas are very rare.

Sujata Saxena, Pramod Bhimsein Jahagirdar, Dayananda Bagur Chidananda Department of Oral and Maxillo-Facial Pathology, Seema Dental College and Hospital, Rishikesh, Uttarakhand, India E-mail: [email protected]

Figure 2: Photomicrograph showing adipose tissue infiltrating muscle (Masson trichome, 10×)

Journal of Cutaneous and Aesthetic Surgery - Oct-Dec 2014, Volume 7, Issue 4

Correspondence

REFERENCES 1. 2. 3. 4.

Regan JM, Bickel WH, Broders AC. Infiltrating benign lipomas of the extremities. West J Surg Obstet Gynecol 1946;54:87-93. Rajendran R, Sivapathasundharam B. Shafer’s Textbook of Oral Pathology. 6th ed. India: Elsevier; 2009.194-95. Lin JJ, Lin F. Two entities in angiolipoma. A study of 459 cases of lipoma with review of literature on infiltrating angiolipoma. Cancer 1974;34:720-7. Piattelli A, Fioroni M, Rubini C. Intramuscular lipoma of the cheek: A case report. J Oral Maxillofac Surg 2000;58:817-9.

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DOI: 10.4103/0974-2077.150789

An Unusual Case of Lipoma Attached to the Frontalis Muscle Dear Editor, Lipomas are the most common benign mesenchymal tumours composed of adipose tissue, which account for almost 50% of all the soft-tissue tumours. Lipomas can occur at any age and can arise in any location, but are more frequently located on the trunk, chest, arm, shoulder and thigh. Lipomas are most frequently encountered in the subcutaneous tissues but very rarely they may be intermuscular or intramuscular, i.e., found within the muscle. We report an unusual case of frontalis-associated lipoma in a 25-year-old male patient because of its rarity.

We operated under local anaesthesia and made an incision through the skin and subcutaneous fat. However, the plane of swelling was noted to be intramuscular after incision and we reached out to the nodule through the frontalis muscle to reveal a well-circumscribed yellowish mass which was excised and sent for histopathological examination.

A 25-year male presented with a single asymptomatic swelling on the right side of the forehead since three years. Clinical examination showed a 2 × 3 cm firm, nontender, slightly mobile subcutaneous nodule on the right side of the forehead [Figure 1]. Clinically, these features suggested a differential diagnosis of liposarcoma, lipoma, epidermoid cyst, sebaceous cyst or osteoma. All the routine investigations were normal.

Lipomas are often seen in the subcutaneous plane whereas the intramuscular lipomas arise in a deeper plane. Intramuscular lipomas were first described in 1946 and they account for a very small number amongst the fatty tumours.[1]

Figure 1: A 25-year-old male with a swelling on the right side of the forehead

Figure 2: H&E 40× showing benign adipocytes with fibrovascular septae

Histopathology showed a circumscribed lesion covered by a thin fibrous capsule, composed of mature adipocytes in lobules which confirmed it to be a lipoma. No evidence of malignancy was noted [Figure 2]. The patient was followed up for 6 months and there has been no recurrence [Figure 3].

Fletcher et al. reported that intramuscular lipomas account for about 1.8% of fatty tumours and predominantly occur

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Infiltrating oral lipoma a rare variant.

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