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Sialolipoma of Minor Salivary Gland in Uvula Basak K*, Kayipmaz S and Karadayi N

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Research Article Open Access

Basak et al., Oral Hyg Health 2014, 2:5

http://dx.doi.org/10.4172/2332-0702.1000159

Case Report Open Access

Oral Hygiene & Health

Volume 2 • Issue 5 • 1000159 Oral Hyg Health

ISSN: 2332-0672 JOHH, an open access journal

Keywords: Sialolipoma; Minor salivary gland; Uvula

Introduction

Lipomatous lesions of the salivary glands are rare accounting for less than 0.5% of all parotid gland tumours [1]. Although distinct microscopic variants of lipoma of the salivary glands, e.g. angiolipoma, fibrolipoma, pleomorphic lipoma and spindle-cell lipoma have been reported [2-5]. Term of sialolipoma was first used by Nagao et al. [6].

The patients were from birth to 84 years old, and average of age was 55.7 years [6-11]. Male cases were slightly more common than female ones

6

. Sialolipoma was reported to occur in both major and minor salivary glands [1-5].

Case Report

A forty five-year-old male patient was presented with a mass on uvula. The specimen was a capsulated, yellow coloured, soft tissue, 1.3 cm in greatest diameter. Cut surface was solid and yellow. Whole- mount section showed that tumor composed by mature adipocytes, salivary gland parenchymal tissue and lymphoid follicles surrounded by a fibrous capsule. Salivary gland component consists acinar and ductal elements (Figure 1). In some areas, glandular components were atrophic. Lymphoid follicles and focal fibrosis were seen (Figure 2).

Oncocytic, sebaceous, and squamous metaplasia was not observed.

Discussıon

Sialolipomas were predominantly composed of adipose tissue and showed expansive growth with fibrous capsule. Sialolipomas were previously reported at parotid and submandibular glands [11,12]

and can occur almost any site other than the salivary glands [6,10].

Qayyum et al. reviewed 35 cases and documented that sialolipoma of minor salivary gland were reported only in adults [10]. The glandular components closely resembled the normal salivary gland parenchyma without any atypia, albeit with the presence of minor metaplastic changes [6]. In our case, metaplastic changes were not observed but contain

*Corresponding author: Kayhan Basak, Dr.Lütfi Kırdar Kartal Education and Research Hospital, Department of Pathology, Semsi Denizer Cad. E-5 Karayolu, Cevizli Mevkii, 34890 Kartal, Istanbul, Turkey, Tel: 90 216 4413900; Fax: 90 216 3520083; E-mail: kayhan.basak@sbkeah.gov.tr

Received August 06, 2014; Accepted August 21, 2014; Published August 26, 2014

Citation: Basak K, Kayipmaz S, Karadayi N (2014) Sialolipoma of Minor Salivary Gland in Uvula. Oral Hyg Health 2: 159. doi: 10.4172/2332-0702.1000159 Copyright: © 2014 Basak K, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Lipomatous lesions of the salivary glands are rare, accounting for less than 0.5% of all parotid gland tumours.

Distinct microscopic variants of lipoma of the salivary glands, e.g. angiolipoma, fibrolipoma, pleomorphic lipoma and spindle-cell lipoma have been reported. A 45 year-old male patient with mass on uvula was presented. The specimen was capsulated, yellow coloured, soft tissue with 1.3 cm in greatest diameter. Whole-mount section showed tumor composed by mature adipocytes, salivary gland parenchymal tissue and lymphoid follicles surrounded by a fibrous capsule. Salivary gland component consist acinar and ductal elements. In some areas, glandular components were atrophic. Lymphoid follicles and focal fibrosis were seen. Oncocytic, sebaceous, and squamous metaplasia were not observed. Sialolipomas were composed predominantly of adipose tissue and showed expansive growth with fibrous capsule. Sialolipomas were reported at parotid gland, submandibular gland, hard and soft palate. To our knowledge, such a case in uvula localization was not previously presented.

Sialolipoma of Minor Salivary Gland in Uvula

Basak K*, Kayipmaz S and Karadayi N

Department of Pathology, Semsi Denizer Cad. E-5 Karayolu, Cevizli Mevkii, Istanbul, Turkey

Figure 1: Capsulated nodular lesion have lots of mucinous acinus between mature lipocytes(H&E, whole section, original magnification x40).

Figure 2: Mucinous glands and mononuclear inflamatory infiltrate (H&E, original magnification x200).

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Citation: Basak K, Kayipmaz S, Karadayi N (2014) Sialolipoma of Minor Salivary Gland in Uvula. Oral Hyg Health 2: 159. doi: 10.4172/2332-

0702.1000159

Page 2 of 2

Volume 2 • Issue 5 • 1000159 Oral Hyg Health

ISSN: 2332-0672 JOHH, an open access journal

inflammatory infiltration with lymphoid follicles. Immunohistological and ultrastructural studies confirmed that the glandular components become entrapped during lipomatous proliferation, rather than representing true neoplastic elements [6]. These findings suggested sialolipoma as a distinct variant of salivary gland lipoma.

References

1. Ellis GL, Auclair PL (1996) Tumors of the Salivary Glands. Atlas of Tumor Pathology. Washington DC: Armed Forces Institute of Pathology.

2. Reilly JS, Kelly DR, Royal SA (1988) Angiolipoma of the parotid: case report and review. Laryngoscope 98: 818-821.

3. Hatziotis JC (1971) Lipoma of the oral cavity. Oral Surg Oral Med Oral Pathol 31: 511-524.

4. Graham CT, Roberts AH, Padel AF (1998) Pleomorphic lipoma of the parotid gland. J Laryngol Otol 112: 202-203.

5. de Moraes M, de Matos FR, de Carvalho CP, de Medeiros AM, de Souza LB (2010) Sialolipoma in minor salivary gland: case report and review of the literature. Head Neck Pathol 4: 249-252.

6. Nagao T, Sugano I, Ishida Y, Asoh A, Munakata S, et al. (2001) Sialolipoma: a

report of seven cases of a new variant of salivary gland lipoma. Histopathology 38: 30-36.

7. Hornigold R, Morgan PR, Pearce A, Gleeson MJ (2005) Congenital sialolipoma of the parotid gland first reported case and review of the literature. Int J Pediatr Otorhinolaryngol 69: 429-434.

8. Ramer N, Lumerman HS, Ramer Y (2007) Sialolipoma: report of two cases and review of the literature. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 104: 809-813.

9. Bansal B, Ramavat AS, Gupta S, Singh S, Sharma A, et al. (2007) Congenital sialolipoma of parotid gland: a report of rare and recently described entity with review of literature. Pediatr Dev Pathol 10: 244-246.

10. Qayyum S, Meacham R, Sebelik M, Zafar N (2013) Sialolipoma of the parotid gland: Case report with literature review comparing major and minor salivary gland sialolipomas. J Oral Maxillofac Pathol 17: 95-97.

11. Herrera ÓM, Rodríguez RR, Noriega JCL (2013) Surgical excision of sialolipoma.

Report of clinical case. Revista Odontológica Mexicana 17:121-124.

12. Agaimy A, Ihrler S, Markl B, Lell M, Zenk J, et al (2013) Lipomatous Salivary Gland Tumors: A Series of 31 Cases Spanning Their Morphologic Spectrum With Emphasis on Sialolipoma and Oncocytic Lipoadenoma. Am J Surg Pathol 37:128-137.

Citation: Basak K, Kayipmaz S, Karadayi N (2014) Sialolipoma of Minor Salivary Gland in Uvula. Oral Hyg Health 2: 159. doi: 10.4172/2332-0702.1000159

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