Vet Pathol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Smrkovski, O. A.
Right arrow Articles by Tobias, K. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Smrkovski, O. A.
Right arrow Articles by Tobias, K. M.
Vet Pathol 43:374-377 (2006)
© 2006 American College of Veterinary Pathologists


BRIEF COMMUNICATIONS AND CASE REPORTS

Carcinoma ex Pleomorphic Adenoma with Sebaceous Differentiation in the Mandibular Salivary Gland of a Dog

O. A. Smrkovski, A. K. LeBlanc, S. H. Smith, C. J. LeBlanc, W. H. Adams and K. M. Tobias

Abstract

A carcinoma ex pleomorphic adenoma was diagnosed in the left mandibular salivary gland of an 8-year-old female spayed dog. The animal presented with a large nonpainful swelling in the left submandibular region. A computed tomography scan detected an irregularly enhancing soft tissue mass that was closely associated with the left external ear canal and extended to the left wing of the atlas. On surgical exploration, the mass was intimately associated with the left mandibular salivary gland. Both the mass and the adjacent gland were removed, and the diagnosis was determined by histopathology. The tumor was comprised of basaloid and low columnar epithelial cells, many glandular units formed by well-differentiated sebocytes, and multifocal regions of necrosis, mineralization, and hemorrhage. Salivary gland tumors with sebaceous differentiation are very rare in animals, with one previously reported case in a cat.


Key words: Carcinoma; dogs; salivary gland; tumor.

An 8-year-old female spayed Basset Hound was presented to the University of Tennessee Veterinary Teaching Hospital because of a mass located in the left submandibular area. The mass was first noticed by the owners 2–3 months prior to presentation and was gradually increasing in size. The dog was otherwise healthy and exhibited no clinical signs associated with the mass. At presentation, the mass was subcutaneous, fixed, and firm on palpation. Fine needle aspirate of the mass revealed many streaming erythrocytes and nucleated cells, suggesting a mucinous background. The heterogeneous cell population consisted of a few large aggregates of well-differentiated salivary secretory epithelial cells and several large clusters of uniform, basophilic cells exhibiting a high nuclear-to-cytoplasmic ratio. The aspirate was considered to be of salivary gland origin; differentials for the mass included basal cell tumor or a well-differentiated ductular tumor.

A computed tomography (CT) scan showed a focal, well-circumscribed, heterogenous-density mass measuring approximately 44 (dorsoventral dimension) x 35 (mediolateral dimension) x 48 (rostrocaudal dimension) mm arising within the left mandibular salivary gland (Fig. 1). The mass was expansive within the gland, effacing the adjacent gland parenchyma. Postcontrast images revealed nonuniform enhancement of the mass with normal strong uniform enhancement of the adjacent compressed glandular tissue. There was mild enlargement of one of the adjacent submandibular lymph nodes. Imaging diagnosis was of a discrete mass arising within the left mandibular salivary gland with mild associated lymphadenomegaly. Primary consideration was given to a neoplastic process.


Figure 01
View larger version (138K):
[in this window]
[in a new window]
 
Fig. 1. Postcontrast axial CT image at the level of the larynx. The dog is imaged in dorsal recumbency. A heterogeneously enhancing mass (spanned by vertical white line) is present within the left mandibular salivary gland (large arrowhead). The dorsal portion of the salivary gland (small arrowheads) is effaced by the expansion of the mass within the gland parenchyma. The right mandibular salivary gland (arrow) is normal. Bar = 1-cm increments.
Fig. 2. Carcinoma ex pleomorphic adenoma; dog. Border between the neoplasm and preexisting salivary tissue with intervening fibrous capsule. Within the neoplasm (right) there are foci of ductal and squamous differentiation. Hematoxylin and eosin. Bar = 200 µm.
Fig. 3. Carcinoma ex pleomorphic adenoma; dog. Within the neoplasm there is a cluster of well-differentiated sebocytes, consistent with sebaceous differentiation. Elsewhere, the pattern is more ductular. Hematoxylin and eosin. Bar = 100 µm.
Fig. 4. Carcinoma ex pleomorphic adenoma; dog. Cluster of myoepithelial cells within a mucinous stroma. These areas were infrequent, but this one is accompanied by islands of squamous cells. Necrosis is evident in the top left corner. Hematoxylin and eosin. Bar = 100 µm.

 
Surgical excision of the mass and an enlarged left submandibular lymph node was performed. Grossly, the mass was intimately associated with the left mandibular salivary gland. The salivary gland itself, however, was compressed by the mass to the periphery and did not appear to be involved.

Four sections of the mass with adjacent salivary gland and two sections of the left submandibular lymph node were examined histologically (Figs. 2, 3, 4). Peripheral salivary gland tissue was compressed by an oval, well-demarcated, encapsulated, densely cellular multilobular mass, consisting of predominantly basaloid epithelial cells that occasionally invaded the capsule. They were arranged in narrow trabeculae, ducts, tubules, and solid sheets, supported by a moderate fibrous stroma. The basaloid cells had minimal eosinophilic cytoplasm and densely basophilic nuclei. Small areas were composed of cuboidal to low columnar cells occasionally forming acinar structures. These cells had small amounts of eosinophilic cytoplasm and basally located nuclei, with a stippled chromatin pattern and variably distinct nucleoli. There were infrequent clusters of spindle cells loosely spaced in a blue/gray, mucinous matrix, consistent with myoepithelial cells. Many glandular units formed by well-differentiated sebocytes were scattered throughout the mass, as is characteristic of sebaceous differentiation. These cells had abundant, clear, vacuolated cytoplasm and a small central hyperchromatic nucleolus. The overall mitotic index was 3–5 per 40x high-power field, with no mitotic activity or cellular atypia in the sebocytes. Occasional nests of squamous differentiation and keratinization were present but there was no cellular atypia within these areas. Small areas of the fibrous stroma had a glassy, hyalinized appearance.

Neoplastic cells did not extend to the surgical margins. There were multifocal regions of necrosis, with mineralization, hemorrhage, and cholesterol clefts within the mass. In the interstitium of the preexisting salivary gland, there was a mild to moderate lymphoplasmacytic and neutrophilic infiltrate, and acini adjacent to the mass were atrophied. Final diagnosis was a carcinoma ex pleomorphic adenoma (carcinoma arising in a mixed tumor) with sebaceous differentiation.

The left submandibular lymph node contained numerous hemosiderin-laden macrophages, histiocytes, red blood cells and prominent lymphoid follicles with large germinal centers. The changes in the lymph node were consistent with reactive lymphoid hyperplasia.

Discussion

Canine salivary gland tumors are broadly classified into benign and malignant subtypes, with the vast majority of epithelial origin and malignant in appearance.6 The mandibular gland is most commonly involved, with the parotid gland second in frequency.4,11 Salivary gland neoplasms are rare in dogs, with overall incidence of 1.6 benign tumors per 100,000 dogs at risk. For adenocarcinoma, the most common malignant salivary gland tumor, this figure was 3.1 per 100,000.5,6 Adenocarcinomas predominantly affect dogs between 10 and 12 years of age; there is no known breed or sex predilection for these tumors.11 Treatment for canine salivary gland neoplasia centers mainly on surgical removal of the affected gland. Special attention is given to regional lymph nodes and lung as possible sites of metastasis, because 17% and 8% of dogs in one study had lymph node and distant metastasis, respectively.4

The tumor described herein was most consistent with a carcinoma ex pleomorphic adenoma. The pleomorphic adenoma is the most common human salivary gland tumor, but it is rarely reported in dogs and cats.5,6,12 Although uncommon, pleomorphic adenomas account for most reports of primary benign epithelial tumors arising from canine salivary glands. Most examples in the dog have been identified in the parotid gland.5 The pleomorphic adenoma is described as containing a mixed population of epithelium, myoepithelium, and stroma, with no clear distinction between cell types.6 Features that led to this diagnosis were the fairly uniform population of ductal epithelial cells, clusters of myoepithelial cells, and areas of squamous differentiation. The diagnosis of carcinoma was based on large areas of necrosis, local capsular invasion, and high mitotic index.

One of the most unusual aspects of this neoplasm was the fairly frequent sebaceous differentiation. In humans, sebaceous differentiation of parotid and mandibular glands is a normal finding, because sebaceous glands are present in the epithelium of the mouth and lining of the major ducts of salivary glands.1 According to one study, approximately 10.5–42% of normal parotid and 6% of normal mandibular glands had such differentiation.8 Degree of differentiation ranges from a single sebaceous cell to a completely developed sebaceous gland, and differentiation is most commonly found in periductal areas of interlobular ducts. The reason for such aberrant location of sebaceous glands is still under investigation. The two hypotheses, neither of which has been sufficiently proved, are developmental derivation from dermis and sebaceous metaplasia. It is not known whether the aberrant sebaceous glands give rise to sebaceous tumors.8 However, sebaceous differentiation within salivary neoplasms seems to be considered less unusual in the human, where it is considered possible in any salivary neoplasm of ductal origin.1 No comparative studies of normal canine salivary glands are available to provide analogous data for sebaceous differentiation in this species.

Primary sebaceous tumors of salivary gland origin are also rare.7 In humans, these tumors are broadly classified into 4 groups: sebaceous adenoma, sebaceous lymphadenoma, sebaceous lymphadenocarcinoma, and sebaceous carcinoma/adenocarcinoma.9 To date, the reports of salivary gland sebaceous adenoma come from the human literature, wherein sebaceous adenomas account for 0.1% of all salivary tumors. Sebaceous carcinomas are described as extremely rare.2 The mean age of human patients with these tumors is 61.4 years. The tumor is usually described as a slowly growing, firm, nonpainful swelling. Most patients do not exhibit any symptoms at the time of presentation. Treatment of choice is a complete surgical excision.3

The current case report describes a carcinoma ex pleomorphic adenoma in the salivary gland of a dog, a rare form of salivary neoplasia in this species. It also describes sebaceous differentiation within this tumor. This is a phenomenon that has not been previously reported in any canine salivary neoplasm, although a recent report describes a sebaceous carcinoma within the submandibular salivary gland of a cat.10 We believe this tumor most likely originated within the left mandibular salivary gland, for two reasons. First, there was no apparent involvement of the skin on histopathology, and second, the tumor was almost circumferentially surrounded by salivary tissue. This patient also had no prior history of cutaneous sebaceous neoplasia as a potential source of a metastatic lesion.

The prognosis for carcinoma ex pleomorphic adenoma in humans is guarded; the prognosis is more difficult to predict in animals, given its rarity. However, clinical follow-up found this patient to be alive and free of disease 12 months after surgery.

Acknowledgement

The authors thank Dr. Mike McCoy at the University of Tennessee Medical Center Department of Oral Surgery for his help in classifying this neoplasm.

References

  1. Cramer SF, Gnepp DR, Kiehn CL, Levitan J. Sebaceous differentiation in adenoid cystic carcinoma of the parotid gland. Cancer 46:1405–1410, 1980[Medline]
  2. Ellis GL, Auglair PL. Tumors of the Salivary Gland. Third Series. Armed Forces Institute of Pathology, Washington, DC. 1995
  3. Gnepp DR. Sebaceous neoplasms of salivary gland origin. Report of 21 cases. Cancer 53:2155–2170, 1984[Medline]
  4. Hammer A, Getzy D, Ogilvie G, Upton M, Klausner J, Kisseberth WC. Salivary gland neoplasia in the dog and cat: survival times and prognostic factors. J Am Anim Hosp Assoc 37:478–482, 2001[Abstract]
  5. Head KW, Cullen JM, Dubielzig RR, Else RW, Midsorp W, Patnaik AK, Tateyama S, van der Gaag I. Classification of Salivary gland tumors of Domestic Animals. Histological Classification of Tumors of the Alimentary System of Domestic Animals. Second Series. Armed Forces Institute of Pathology, Washington, DC. 2003
  6. Head KW, Else RW. Tumors of the skin and soft tissues. In: Tumors in domestic animals Meuten DJ, ed. 4th ed., 410–416.Iowa State Press. .
  7. Izutsu T, Kumamoto H, Kimizuka S, Ooya K. Sebaceous adenoma in the retromolar region: report of a case with a review of the English literature. Int J Oral Maxillofac Surg 32:423–426, 2003[Medline]
  8. Mariappan MR, Fadare O, Jain D. Sebaceous differentiation in salivary glands. Arch Path Lab Med 128:245–246, 2003
  9. Neville BW, Damm DD, Allen CM, Bouquot JE. Oral and Maxillofacial Pathology 2nd ed., 407,WB Saunders, Philadelphia, PA. 2002
  10. Sozmen M, Brown PJ, Eveson JW. Sebaceous carcinoma of the salivary gland in a cat. J Vet Med A 49:425–427, 2002[CrossRef]
  11. Spangler WL, Culbertson MR. Salivary gland disease in dogs and cats: 245 cases (1985–1988). J Am Vet Med Assoc 198:465–469, 1991[Medline]
  12. Wells GA, Robinson M. Mixed tumor of salivary gland showing histological evidence of malignancy in a cat. J Comp Pathol 85:77–85, 1975[Medline]
Request reprints from A. LeBlanc, The University of Tennessee, College of Veterinary Medicine, Small Animal Clinical Sciences, C247 Veterinary Teaching Hospital, 2407 River Dr., Knoxville, TN 37996 (USA). E-mail: aleblanc{at}mail.ag.utk.edu





This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Smrkovski, O. A.
Right arrow Articles by Tobias, K. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Smrkovski, O. A.
Right arrow Articles by Tobias, K. M.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS