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A rare case of sebaceous adenoma of the palate, with literature review

Published online by Cambridge University Press:  29 March 2011

K G Somashekara*
Affiliation:
Department of ENT, Kempegowda Institute of Medical Sciences, Bangalore, Karnataka, India
S Lakshmi
Affiliation:
Department of ENT, Kempegowda Institute of Medical Sciences, Bangalore, Karnataka, India
N S Priya
Affiliation:
Department of Oral Pathology, Vokkaligara Sangha Dental College, Bangalore, Karnataka, India
*
Address for correspondence: Dr K G Somashekara, 463/1, 7th Cross, 12th Main, Rajmahal Vilas Extension Sadashivanagar, Bangalore 560080, Karnataka, India E-mail: dr_lakshmi_kumar@yahoo.com
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Abstract

Objective:

We present the first reported case of sebaceous adenoma of the palate, to our knowledge.

Method:

Case report and review of the English language literature, with a focus on the pathological spectrum of sebaceous glands.

Case report:

A woman presented with a growth on the hard palate, which was excised and examined. Histopathological analysis showed features of sebaceous adenoma. Further evaluation with Sudan Black B special stains and Ki 67 immunohistochemistry was performed.

Conclusion:

Sebaceous adenomas in the oral cavity are very rare, with only 10 cases previously reported in the English language literature. Sebaceous adenoma of the palate has not previously been reported, to our knowledge. We discuss the role of special stains and immunohistochemistry in the diagnosis of this tumour.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 2011

Introduction

Sebaceous glands are prominent adnexal components of the skin which are predominantly seen on the face and scalp. Normal glands vary in size from 0.2 to 2 mm in diameter, with the largest appearing in the skin of the nose and the concha of the ear.Reference Batsakis and el-Naggar1 Sebaceous glands secrete sebum.Reference Marx and Stern2 Sebaceous differentiation in the oral mucosa and salivary glands is an expected normal finding; however, sebaceous neoplasms do occur in these regions, albeit rarely and with low recurrence potential.

We present a rare case of sebaceous adenoma of the palate, together with a review of the literature.

Case report

A 38-year-old woman presented with a growth in the hard palate of eight months' duration.

On examination, the lesion was situated in the right posterior part and did not cross the midline. It was a well circumscribed, ovoid, firm, non-tender swelling with a smooth, pink surface, and measured 2 × 1.5 cm (Figure 1).

Fig. 1 Photograph of the lesion.

Fine needle aspiration cytology was performed and showed features of a benign lesion; however, the exact nature of the lesion could not be conclusively determined.

Routine haematological and urine examinations were normal.

A computed tomography scan showed a well circumscribed, non-enhancing, 2.1 × 1.2 cm lesion confined to the hard palate. Scalloping of the bone was evident without any erosion, suggestive of benign pathology. There was no evidence of calcification or necrosis (Figure 2).

Fig. 2 Coronal computed tomography scan showing the tumour, with dimensions as marked.

The palatal mass was excised completely with a 2 mm margin of apparently normal mucosa.

The patient was fed nasogastrically for five days, followed by a soft diet for two weeks.

Macroscopic examination of the excised lesion showed a single, ovoid tissue mass measuring 3 × 2 × 0.3 cm. The cut surface consisted of grey-white tissue.

Microscopic examination of haematoxylin and eosin stained sections showed stratified squamous epithelium with stroma showing focal collections of sebaceous cells in lobules. These lobules contained undifferentiated cells in the periphery and mature sebocytes with clear cytoplasm in the centre. Sheets, islands and cystic spaces of squamous epithelial cells and sebaceous cells were seen, without any cellular atypia or mitosis. A focal area of dense lymphoplasmacytic infiltrate was seen. There was no mucoid element. A diagnosis of sebaceous adenoma of the palate was made (Figure 3).

Fig. 3 Photomicrograph of the tumour showing a lobule with undifferentiated cells at the periphery and mature sebocytes in the centre. (H&E; ×40)

Staining with Sudan Black B stain demonstrated the presence of sebum (Figure 4).

Fig. 4 Photomicrograph of tumour preparation stained with Sudan Black B, demonstrating the presence of sebum. (×10)

Immunohistochemical analysis using the Ki 67 marker showed focal positive expression.

The results of special staining and immunohistochemical analysis confirmed the final diagnosis of sebaceous adenoma.

The patient was followed up for six months, over which time her palatal mucosa healed well.

After obtaining informed consent, a diagnostic colonoscopy was performed to exclude Muir–Torre syndrome. The colonoscopy was normal.

Discussion

Sebaceous glands are holocrine glands in which the cell dies and secretions are discharged. These glands are normal skin appendages present throughout the skin, with the exception of the palms and soles.Reference Marx and Stern2 Ectopic sebaceous glands are principally found in the major salivary glands, and are rarely seen in minor salivary glands.Reference Batsakis and el-Naggar1, Reference Gnepp3

In the oral cavity, sebaceous glands normally appear as yellow-white spots, termed Fordyce spots, and are commonly seen on the vermillion border of the lip, the labial and buccal mucosa, and the retro-molar region.Reference Daley4

Sebaceous gland lobules are less common in children because the pilosebaceous system does not reach full development until after puberty.Reference Dent, Hunter and Svirsky5

Sebaceous adenomas are rare, benign tumours arising from sebaceous glands in the oral cavity.Reference Batsakis and el-Naggar1 They account for 0.1 per cent of all sebaceous gland neoplasms.Reference Gnepp3 The mean age of initial clinical presentation is 58 years, and the male to female ratio is 1.6:1.

Approximately 149 primary sebaceous tumours of salivary gland origin have been reported in the English literature (see Table I).Reference Marx and Stern2Reference Daley4, Reference Pilch6 However, only 10 cases of intraoral sebaceous adenoma have been reported in the English language literature, with common sites being the buccal mucosa and retromolar area.Reference Lezzi, Rubini, Fioroni and Piattelli7 No cases of sebaceous adenoma of the palate have previously been reported.

Table I Distribution of sebaceous glands in oral cavity

Ca = carcinoma

The presence of sebaceous glands, or evidence of sebaceous differentiation, has been noted in submandibular and parotid salivary glands. Their presence in the oral cavity is thought to originate in the intralobular ducts of the salivary glands.Reference Batsakis and el-Naggar1 However, an opposing school of thought states that the presence of sebaceous lobules derives from the inclusion of ectoderm in the oral cavity at the time of fusion of the maxillary and mandibular processes, during embryonic development.Reference Dent, Hunter and Svirsky5

Histological examination of sebaceous adenoma shows an encapsulated tumour consisting of nests of sebaceous cells in a fibrous stroma. These are well demarcated lesions with a multilobular pattern. The tumour comprises three types of cells: undifferentiated germinal cells (at the periphery), mature sebocytes and intermediate cells.Reference Marx and Stern2

The secretory product of sebaceous glands is called sebum. Sebum comprises a mixture of lipids, including triglycerides, waxes, squalene, and cholesterol and its esters. Sebum may have weak antibacterial and antifungal properties.Reference Junqueira8

Sudan Black B stain demonstrates the presence of sebum within sebaceous adenomas.

Immunohistochemical analysis of sebaceous adenomas utilises Ki 67, a proliferative nuclear marker found to show higher expression in these tumours, compared with lower proliferation indices in normal glands and sebaceous hyperplasia.Reference Azevedo, Almeida, Netto, Miranda, Santos and Della Coletta9

Sebaceous adenoma should be differentiated from other, sebaceous-related lesions (see Table II).Reference Pilch6, Reference Daley10, Reference Lever11

Table II Oral cavity sebaceous lesions: differential diagnosis

Sebaceous adenomas do not recur after adequate excision, and the prognosis is excellent.Reference Marx and Stern2

  • Sebaceous adenomas rarely occur intraorally; only 10 cases have previously been reported in the English language literature

  • The first reported case of sebaceous adenoma of the palate is described

  • Complete excision is curative

Sebaceous adenomas are also found in Muir–Torre syndrome. This is an autosomal dominant condition characterised by a combination of sebaceous tumours of the skin and one or more internal malignancies, most commonly colon cancer.Reference Schwartz and Torre12 An association with intraoral sebaceous adenomas has not been reported. However, as only a tiny number of intraoral sebaceous adenomas have been reported, an association of such tumours with Muir–Torre syndrome cannot be excluded at this stage.

Conclusion

Sebaceous adenomas occur very rarely in the palate. Investigation using a combination of clinical and histopathological analysis is essential. Sudan Black B special staining and Ki 67 immunohistochemical evaluation add valuable information when differentiating this tumour from other sebaceous lesions of the oral cavity. A possible association with Muir–Torre syndrome should also be kept in mind. Following adequate excision, recurrence does not occur.

References

1Batsakis, JG, el-Naggar, AK. Sebaceous lesions of salivary glands and oral cavity. Ann Otol Rhinol Laryngol 1990;99:416–18Google Scholar
2Marx, RE, Stern, D. Oral Pathology, a Rationale for Diagnosis and Treatment, 1st edn.Chicago: Quintessence, 2003;282Google Scholar
3Gnepp, DR. Diagnostic Surgical Pathology of the Head & Neck, 2nd edn.Philadelphia: Saunders-Elsevier, 2009;508–9Google Scholar
4Daley, TD. The pathology of intraoral sebaceous glands. J Oral Pathol Med 1993;22:241–5Google Scholar
5Dent, CD, Hunter, WE, Svirsky, JA. Sebaceous gland hyperplasia: case report and literature review. J Oral Maxillofacial Surg 1995;53:936–8Google Scholar
6Pilch, BZ. Ch.8, Salivary Glands, Head and Neck Surgical Pathology, 1st edn.Philadelphia: Lippincott Williams & Wilkins, 2001;284349Google Scholar
7Lezzi, JG, Rubini, C, Fioroni, M, Piattelli, A. Sebaceous adenoma of cheek. Oral Oncol 2002;38:111–13Google Scholar
8Junqueira, LC. Basic Histology Text and Atlas, 10th edn.New York: McGraw Hill, 2003;379–80Google Scholar
9Azevedo, RS, Almeida, OP, Netto, JN, Miranda, AM, Santos, TC, Della Coletta, R et al. Comparative clinicopathological study of intraoral sebaceous hyperplasia and adenoma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2009;107:100–4Google Scholar
10Daley, TD. Intraoral sebaceous hyperplasia, diagnostic criteria. Oral Surg Oral Med Oral Pathol 1993;75:343–7Google Scholar
11Lever, WF. Histopathology of Skin, 7th edn.Philadelphia: JB Lippincott, 1990;538–9, 596–9, 634–5Google Scholar
12Schwartz, RA, Torre, DP. The Muir-Torre syndrome: a 25-year retrospect. J Am Acad Dermatol 1995;33:90104Google Scholar
Figure 0

Fig. 1 Photograph of the lesion.

Figure 1

Fig. 2 Coronal computed tomography scan showing the tumour, with dimensions as marked.

Figure 2

Fig. 3 Photomicrograph of the tumour showing a lobule with undifferentiated cells at the periphery and mature sebocytes in the centre. (H&E; ×40)

Figure 3

Fig. 4 Photomicrograph of tumour preparation stained with Sudan Black B, demonstrating the presence of sebum. (×10)

Figure 4

Table I Distribution of sebaceous glands in oral cavity

Figure 5

Table II Oral cavity sebaceous lesions: differential diagnosis