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"Histomorphological study of salivary gland neoplasms: a 2 year study".

INTRODUCTION: Salivary gland neoplasms are a relatively uncommon group of neoplasms that seem to present a disproportionate degree of diagnostic uncertainty relative to their actual numbers. They can show a striking range of morphological diversity between different tumor masses. In addition, hybrid tumors, differentiation and the propensity for some benign tumors to progress to malignancy can confound histopathological interpretation (1,2).

Salivary gland neoplasm are quite uncommon, but they do elicit considerable medical interest because of their multifaceted clinical presentation, varied histologic appearances & the associated difficulties in predicting the diagnosis (3).

However there are no reliable criteria to differentiate on clinical grounds the benign from the malignant lesions and morphologic evaluation is necessary (4).

The present study was undertaken to study the spectrum of histomorphological features of various salivary gland neoplasms

AIMS:

1. To study the age, sex and site incidence of salivary gland neoplasms

2. To study the histomorphological features of salivary gland neoplasms

MATERIAL AND METHODS: The present histomorphological study of salivary gland neoplasms is a two year prospective study done at J.J.M medical college, Davangere. The material for the study comprised of specimens received in the department of pathology J.J.M. medical college, from patients admitted to chigateri general hospital, Bapuji hospital and Women & children hospital attached to J.J.M medical college, Davangere.

The specimens consisted of incisional biopsies and resected salivary gland lesions with or without the draining lymph nodes of that region.

The details of the specimens noted include dimensions, appearance of the external surface and the cut surface and involvement of surgical margins. They were fixed in 10% neutral buffered formalin for 24 to 48 hours. Large specimens were cut serially at a distance of 1cm before fixing.

After fixation, representative areas were selected for paraffin embedding, including the tumor proper and the margin of the tumor with surrounding tissue. Sections of 3 - 5 micron thickness were cut and stained with hematoxylin and eosin. Microscopic examination of the stained sections was performed.

OBSERVATIONS AND RESULTS: There were 53 cases of salivary gland neoplasms. Out of these 38 were benign neoplasms and 15 were malignant neoplasms.

Benign neoplasms consisted of 24 pleomorphic adenomas, four cases of basal cell adenoma, two cases each of warthin tumor, myoepithelioma, schwannoma & inflammatory pseudotumor & one case each of hemangioma & lipoma were seen.

Malignant neoplasms consisted of six mucoepidermoid carcinomas, four adenoid cystic carcinomas, and one case each of acinic cell carcinoma, malignant myoepithelioma, carcinoma ex pleomorphic adenoma, salivary duct carcinoma and undifferentiated carcinoma.

GENDER AND AGE: Fifteen benign neoplasms were seen in males and 23 benign neoplasms were reported in females. Among malignant tumors, ten were seen in males and the remaining five were reported in females. In the present study, the salivary gland neoplasms presented over a wide range of age from five months to 79 years. The mean age was 42.74 years. Mean age for benign neoplasms was 41.64 years and mean age for malignant neoplasms was 45.53 years

Parotid gland was the commonest site for various tumors, notable exception being adenoid cystic carcinoma, which showed predilection for the minor salivary glands and submandibular glands.

In our study, 24 pleomorphic adenomas were reported. They accounted for 45.27% of all salivary gland tumors & 63.2% of the benign tumors. They presented as painless slowly growing swellings. Most of them occurred in the parotid gland with submandibular gland being the second most common site.

Grossly, these tumors ranged in size from 0.5 to 6cm in their greatest dimension. The shape of the tumors varied from irregular to globular & lobulated. Most of the tumors were firm in consistency & showed partial to complete capsulation. Cut section revealed solid, grey white homogenous areas. Cystic changes hemorrhage & mucoid areas were seen in a few cases. No intralesional lymph nodes were seen.

Microscopically, majority of the tumors consisted of myxoid and chondromyxoid areas with epithelial & myoepithelial cells arranged in various patterns. The tumors had a capsule of varying thickness & completeness. In some tumors the epithelial components were predominant & the tumor cells were arranged in the form of ducts, solid sheets, tubules & strands. In few tumors either myxoid or chondroid areas were predominant. Hyaline areas were seen in a few cases along with areas of pseuodocartilage and mucin. One case of pleomorphic adenoma showed large areas of infarction, with adjacent myxoid areas.

Two cases of warthin's tumor were reported. Cut surface was grey white with variable sized cysts. Microscopically the tumors revealed the classical histopathological features of warthin tumor.

Two cases of myoepithelioma were encountered in our study. One case was seen in hard palate. Grossly both the tumors were well delineated & grey white, measuring 2-4cm in greatest dimensions. Cut surface was grey white. Microscopy of both the tumors showed tumor cells composed of elongated spindle to oval cells having scanty to moderate clear to eosinophilic cytoplasm. The cells were arranged in bundles with focal microcystic areas in one case. One case showed plasmacytoid cells having eccentric nuclei & eosinophilic cytoplasm. Stroma was scanty with focal areas of hyalinization, myxoid change & fibrosis.

Four cases of basal cell adenoma were encountered in our study. They were of size ranging between 2-6cm in the greatest dimension. Microscopically tumors were well encapsulated, bordered by normal salivary tissue. The tumor cells were small, round to oval in shape having scanty basophilic cytoplasm & hyperchromatic nuclei. The tumor cells were arranged in solid groups, nests, cords, trabeculae & sheets with peripheral palisading in some of the cell nests. Stroma was scanty with areas of fibrosis & hyalinization.

Two cases of schwannoma were reported in the present study. The tumors were globular to irregular in shape & varied in size from 2-6cm in the greatest dimension.

Microscopy showed tumor tissue composed of bundles of elongated spindle shaped cells, having plump nuclei & verocay bodies with nuclear palisading. One case of hemangioma was noted in this study. Cut surface showed spongy, lobular mass infiltrating the glandular tissue.

Microscopy showed lobules of salivary gland tissue with intervening fibrofatty stroma having multiple thin walled vascular spaces containing red blood cells.

A case of lipoma ms 6 x 4 x 3 cm was encountered in our study which showed classical microscopic features of a lipoma. We encountered two cases of inflammatory pseudotumor which were also included in our study. The two tumors were firm, nodular swellings measuring 2cm to 5cm in their greatest dimensions. Cut surface was grey white, well delineated & whorled in one case. Microscopy showed spindle cells intimately mixed with collagen fibres & variable amounts of plasma cells, lymphocytes, polymorphs & foamy histiocytes. One case showed spindle cells forming vague fascicles.

Malignant tumors: Fifteen cases of malignant neoplasms were encountered is our study. The most common malignant tumor was mucoepidermoid carcinoma, accounting for six cases. Grossly, these tumors varied in size from 2-6cm in greatest dimension. Cut surface of the tumors was grey white to grey brown with cystic spaces containing mucinous fluid. Definitive capsule was not appreciated in majority of the tumors.

Microscopy: All tumors were poorly delineated & consisted of mucous secreting cells lining the cystic spaces. Epidermoid cells were in the form of clumps or strands or as multilayered masses beneath the mucous secreting epithelium along with a group of intermediate type of cells were seen between these two layers. The three cellular components varied in population. Stroma showed lymphocytic infiltration. Few cases showed clear cells & epithelial pearl formations. These tumors were graded into high grade mucoepidermoid carcinoma, intermediate grade mucoepidermoid carcinoma & low grade mucoepidermoid carcinoma. Low grade tumors show predominance of mucous secreting cells with formation of cystic spaces lined by mucus cells. Nuclear atypia & mitoses were not observed. Cystic spaces in low-grade tumors were filled with mucin & also showed mucin pools in which the tumor cells were floating. Intermediate grade tumors showed a greater tendency to form solid nests of squamous pearls & intermediate cells with less prominent cystic spaces. Same degree of nuclei atypia and mitotic activity were seen.

High grade tumors were predominantly solid consisting of epidermoid cells with occasional pearls & these tumors showed increased degree of nuclear atypia & mitotic activity.

Four cases of adenoid cystic carcinoma were reported in our study. Two cases were seen in intraoral minor salivary glands and two cases were reported in the submandibular gland. Grossly the tumors presented as ill defined infiltrative growths, measuring 0.5to 4cm in their greatest dimension. Cut surface was grey white to grey brown with cystic areas. Microscopy showed tumor tissue composed of basaloid cells. These tumor cells were small, round to oval having scanty cytoplasm with hyperchromatic nuclei. They were arranged in solid groups, cords, trabeculae & in cribriform patterns separated by hyaline stroma. One tumor showed atypical mitotic activity. Hyaline cylinders & mucoid areas were seen in one tumor. A case of acinic cell carcinoma was reported which was 4 x 3 x 2 cm in greatest dimensions macroscopically. Microscopy showed tumor tissue arranged in the form of small nests, sheets & papillary fronds. It was composed of small round to polygonal cells having pale blue or clear cytoplasm. A few cells showed vacuolated cytoplasm. Nuclei were uniform, small & situated either centrally or eccentrically. These tumor cells were arranged in papillary cystic pattern & separated by fibrovascular septa. A single case of malignant myoepithelioma was reported in the present study. The tumor was grey white, nodular & measured 3 x 3 x 2 cm. Microscopy showed lobules of tumor cells. The tumor cells were short, spindle shaped having clear to pale eosinophilic cytoplasm with pleomorphic nuclei. Mitoses were frequent. Stroma was scanty & showed areas of hemorrhage & necrosis. One case of carcinoma ex pleomorphic adenoma was seen in our study. Macroscopically, the tumor was irregular & grey brown with infiltrating areas, but the surgical margins were free. Microscopically the malignant component was characterized by widespread cellular pleomorphism & a high mitotic count. Large areas of necrosis were present. The malignant component was poorly differentiated carcinoma. Markedly hyalinized areas were seen adjacent to the carcinoma. Small area of pleomorphic adenoma was also present.

A case of salivary duct carcinoma was reported showing cribriform & solid pattern with prominent comedo necrosis. Histologically it resembled intraductal carcinoma of breast. Also seen were cords, nests and single cells. The tumor cells had abundant eosinophilic cytoplasm, large pleomorphic vesicular nuclei & prominent nucleoli. The stroma was densely fibrous. A case of undifferentiated carcinoma was reported which showed polygonal to spindle cells having abundant cytoplasm with mitosis along with areas of hemorrhage & necrosis

DISCUSSION: The various benign & malignant neoplasms of the salivary glands encountered in our study have been compared with similar neoplasm in other studies

Our study showed an overall mean incidence of 26.5 cases per year for all neoplasms. Jones et al (5) & Bhargava et al (6) have reported a slightly higher incidence than our study where as Sousa et al (7) & Gupta et al (8) showed a lower incidence. The frequency of benign & malignant neoplasms was almost similar to other studies. In our study the mean age for benign tumors was lower than the mean age for the occurrence of malignant tumors.

Our study showed a female preponderance similar to that recorded by Vargas et a (19), Jones et al (5), Sengupta et al (10), Sharkey et al (11) & Budhraja et al (12). However Renehan et al (13) observed a male preponderance and Sousa et al (7) found an overall equal sex distribution. The site distribution of the salivary gland tumors in the present study is in agreement with the results obtained in other series, with a predilection for the parotid gland.

The commonest benign tumor in our study is pleomorphic adenoma, which showed a peak incidence in the 5th decade & predilection for parotid gland. Our finding was in accordance with the results of other studies. However Vargas et al (9), Gupta et al (8) & Sharkey et al (11) noted a lower age incidence.

Among the malignant tumors, mucoepidermoid carcinoma was the commonest with a male preponderance and a peak age of incidence being 30-69 years. Similar observations were reported by Gupta et al (8) & Sharkey et al (11).

Parotid gland is the most common site for mucoepidermoid carcinoma in over study. Present study did not encounter any case in minor salivary glands as reported by other studies. The age, sex, & site distribution of our cases were similar to the findings of other studies for all other types of tumors.

HISTOMORPHOLOGY: In our study majority of pleomorphic adenomas consisted of myxoid & chondromyxoid areas with the epithelial & myoepithelial cells arranged in various patterns. Similar findings have been reported by Mendenhall w.m et al (14). One case showed necrosis in a hyalinized area. Alves FA et al (15) also reported similar findings. In our study all pleomorphic adenomas had focally thin capsules. A similar observation made by Stennert et al (16). The microscopic observations made in all other benign neoplasms in our study were similar to the findings reported by other authors.

Malignant tumors: Among the six mucoepidermoid carcinomas, predominant type was of intermediate grade. Similar results were reported by Healey et al (17) & Acceta et al (18). However Eneroth et al 19 have found a preponderance of high grade tumors & Renehan et al (13) have found a preponderance of low grade tumors. This discrepancy may be due to the subjective differences in the grading of the tumors. The microscopic findings observed were similar to the findings reported by other authors. In the present study adenoid cystic carcinoma constituted 7.55% of all tumors and 26.7% of all malignant tumors. Our findings are similar to the findings of other authors except the findings of Nascimento et al (20) where there was a slightly higher incidence. In our study, tumors measured between 0.5cm to 4cm in greatest dimension, which is similar to that observed by Evans and Cruikshank (21), Batsakis JG (22) and Ellis, Auclair and Gnepp. The microscopic findings we observed were similar to the observations made by Evans and Cruikshank (21), Lucas RB (23) and Ellis, Auclair and Gnepp. One case of acinic cell carcinoma which was encountered in the present study was papillary cystic type microscopically with typical histology. Similar findings were reported by Calmenero C et al. (24)

In our case of Carcinoma ex pleomorphic adenoma the tumor showed irregular grey brown infiltrating areas, with areas of necrosis & hemorrhage. The malignant areas consisted of epithelial cells with an increased nuclear to cytoplasmic ratio, prominent nucleoli & frequent mitoses. Small area of pleomorphic adenoma was seen. The histologic pattern in our case was that of a poorly differentiated carcinoma. Similar observations were made by Wenig & Gnepp (25). One case of undifferentiated carcinoma was reported in our study which showed polygonal to spindle cells. They were arranged in sheets & thin cords separated by fibrovascular stroma.

A case of malignant myoepithelioma is reported in our study which showed spindle shaped cells having clear to pale eosinophilic cytoplasm with pleomorphic nuclei. Frequent mitoses were present. Stroma showed areas of necrosis. Similar observations were made by Ellis, Auclair, & Gnepp (26) & Savera et al (27). We also encountered a case of salivary duct carcinoma. Histologically it resembled ductal carcinoma of breast. It showed cribriform & solid pattern with central comedo type necrosis. A case of undifferentiated carcinoma was also reported in our study which showed polygonal to spindle cells arranged in thin cords separated by fibrovascular stroma. Cellular pleomorphism & mitosis were present. There were areas of necrosis & hemorrhage. Similar cases were reported by Eversole & Gnepp (28).

CONCLUSION: It is concluded that some of our results are in harmony with those of other authors.. On the other hand, some of our results are different from published literature. Further more population based surveys are needed to define the epidemiology of salivary gland neoplasms.

REFERENCES:

(1.) Barnes L, Eveson JW, Reuichart P, Sidrawsky D. WHO classification of tumours. Pathology and Genetics of Head and Neck Tumours : Lyon : IARC Press; 2005. p. 209281.

(2.) Chan JK, Cheuk W. Salivary gland tumors. Chapter 7, In : Fletcher CDM, editor. Diagnostic histopathology of tumors. 3rd ed. china: Churchill Livingstone Elsevier; 2007. p. 239-325

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(4.) Lingel MW, Kumar V. Head and Neck. Chapter 16, In : Kumar V, Abbas AK, Fausto N, editors. Robbins and Cotran Pathologic basis of disease. 7th ed, Philadelphia : Saunders; 2004. P. 790-91

(5.) Jones AV, Craig GT, Speight PM, Franklin CD. The range and demographics of salivary gland tumours diagnosed in a UK population. Oral Oncology 2007

(6.) Bhargava S, Sant MS, Arora MM. Histomorphologic spectrum of tumours of minor salivary glands. Ind J Cancer 1982; 19:134-140

(7.) Sousa J, Desa O. Salivary gland tumours : An analysis of 62 cases. Indian Journal of Cancer 2001; 38:38-45

(8.) Gupta SK, Sengupta P, Sarkar SK. Primary tumours of salivary glands. J Ind Med Assoc 1975; 65(10):277-280.

(9.) Vargas PA, Gerhard R, Filho JFA, Castro IV. Salivary gland tumours in a Brazilian population : A retrospective study of 124 cases. Rev Hosp Clin Fac Med S. Paulo 2002; 57(6):271-276

(10.) Sengupta SK, Banerjee AK, Datta BN. Primary tumours of salivary glands : An analysis of 111 tumours. Ind J Pathol Bacteriol 1973; 16:32

(11.) Sharkey FE. Clinicopathologic study of 366 salivary gland tumours. Am J Clin Pathol 1977; 67:272-278

(12.) Budhraja SN, Pasupathy, Perianayagam. Salivary gland tumours in Pondicherry. Ind J Surg 1974; 36:235-239

(13.) Renehan A, Gleave EN, Mancock BD, Smith P, McGurk M. Long term follow up of over 1000 patients with salivary gland tumours treated in a single centre. Br J Surg 1996; 83:1750-1754

(14.) Mendenhall WM, Mendenhall CM, Wrning JW, Malyapa RS, Mendenhall NP. Salivary gland pleomorphic adenoma. Am J Clin Oncol 208 February; 31(1):95-99.

(15.) Alves FA, Perez DEC, Almeida OP, Lopes MA, Kowalski LP. Pleomorphic adenoma of the submandibular gland. Clinicopathological and Immunohistochemical features of 60 cases in Brazil. Arch Otolaryngol Head Neck Surg 2002 Dec; 128:1400-1403

(16.) Stennert E, Lichius GD, Klussmann JP, Arnold G. Histopathology of pleomorphic adenoma in the parotid gland : A prospective unselected series of 100 cases. Laryngoscope 2001; 111:2195-2200.

(17.) Healey WA, Perzin KH, Smith L. Mucoepidermoid carcinoma of salivary gland origin : Classification, clinicopathologic correlations and results of treatment. Cancer 1970; 26:368-388

(18.) Acceta PA, Gray GF, Hunter RM, Rosenfeld L. Mucoepidermoid carcinoma of salivary glands. Arch Pathol Lab Med 1984; 108:321-325.

(19.) Eneroth EM, Hjertman L, Muberger G, Soderberg G. Mucoepidermoid carcinomas of the salivary glands, with special reference to the possible existence of a benign variety. Acta Otolaryngol 1972; 73:68-74.

(20.) Nascimento AG, Amarel ALP, Prado LAF, Kligerman J, Silveira TRP. Adenoid cystic carcinoma of salivary glands : A study of 61 cases with clinicopathologic correlation. Cancer 1986; 57:312-319.

(21.) Evans RW, Cruickshank AH. Epithelial tumours of the salivary glands. Vol.1, Philadelphia : WB Saunders C; 1970

(22.) Batsakis JG. Tumours of the head and neck. 23rd ed. Baltimore: Williams and Wilkins Co; 1979

(23.) Lucas RB. Pathology of tumours of the oral tissues. 4th ed. London: Williams Clower; 1984

(24.) Calmenero C, Patron M, Sterra I. Acinic cell carcinoma of the salivary glands. A review of 20 new cases. Journal of Cranio-Maxillofacial Surgery 1991; 19(6):260-266.

(25.) Wenig BM, Gnepp DR. Malignant mixed tumors. Chapter 20, In : Ellis GL, Auclair PL, Gnepp Dr, editors. Surgical pathology of the salivary glands. Vol. 25, Philadelphia : WB Saunders Company; 1991. p. 350-368.

(26.) Goode RK, Ellis GL, Auclair PL, Gnepp DR. Other malignant epithelial neoplasms. Chapter 27, In : Elli GL, Auclair PL, Gepp DR, editors. Surgical pathology of the salivary glands. Vol. 25, Philadelphia : WB Saunders Company; 1991. p. 455-488.

(27.) Savera AT, Sloman A, Huvos AG, Klimstra DS. Myoepithelial carcinoma of the salivary glands. A clinicopathologic study of 25 patients. Am J Surg Pathol 2000; 24:761-774.

(28.) Eversole M, Eversole LR, Gnepp DR. Undifferentiated carcinoma. Chapter 25, In : Ellis GL, Auclair PL, Gnepp DR, editors. Surgical pathology of the salivary glands. Vol. 25, Philadelphia: WB Saunders Company; 1991. p. 422-440.

Mohammad Shahid Iqbal, Aisha Tabassum, Chatura. K. R, Sateesh K. Malkappa, P. K. Basavaraja

[1.] Assistant Professor, Department of Pathology, Kamineni Institute of Medical Sciences. Narketpally, Nalgonda

[2.] Assistant Professor, Department of Pathology, Kamineni Institute of Medical Sciences. Narketpally, Nalgonda

[3.] Professor, Department of Pathology, J. J. M. Medical College, Davangere, Karnataka.

[4.] Assistant Professor, Department of Microbiology, Kamineni Institute of Medical Sciences. Narketpally, Nalgonda

[5.] Professor, Department of Pathology, J. J. M. Medical College, Davangere, Karnataka.

CORRESPONDING AUTHOR

Dr. Mohammad Shahid Iqbal, Assistant Professor, Department of Pathology, Kamineni Institute of Medical Sciences, Sreepuram, Narketpally 508254 Nalgonda (dist). A.P

E-mail: drshahidkbn@yahoo.com

Ph: 0091 8143108536
TABLE 01: TYPE OF BENIGN AND MALIGNANT NEOPLASMS AND THEIR GENDER
DISTRIBUTION

Neoplasms                    No.         Male (%)     Female (%)

Benign
Pleomorphic adenoma          24          09 (37.3)    15 (62.5)
Warthin tumor                02          02 (100)     00
Basal cell adenoma           04          01 (25)      03 (75)
Myoepithelioma               02          00           02 (100)
Schwannoma                   02          00           02 (100)
Hemangioma                   01          01 (100)     00
Lipoma                       01          01 (100)     00
Inflammatory pseudotumor     02          01 (50)      01 (50)
Malignant
Mucoepidermoid carcinoma     06          04 (66.6)    02 (33.3)
Adenoid cystic carcinoma     04          02 (50)      02 (50)
Acinic cell carcinoma        01          01 (100)     00
Malignant myoepithelioma     01          01 (100)     00
Carcinoma ex pleomorphic     01          00           01 (100)
Adenoma
Salivary duct carcinoma      01          00           00

Undifferentiated carcinoma   01          01 (100)     00
Total                        53 (100%)   25 (47.16)   28 (52.83)

TABLE 02: AGE DISTRIBUTION OF SALIVARY GLAND NEOPLASM

NEOPLASMS          AGE GROUP (YEARS)
                   0-9   10-19   20-29   30-39   40-49   50-59

BENIGN
PLEOMORPHIC        0     1       4       5       9       4
ADENOMA
BASAL CELL         0     0       0       0       2       1
ADENOMA
WARTHIN TUMOR      0     0       0       0       0       0
MYOEPITHELIOMA     0     0       0       1       0       1
SCHWANNOMA         0     1       0       0       0       0
HEMANGIOMA         1     0       0       0       0       0
LIPOMA             0     0       0       0       0       1
INFLAMMATORY       0     0       0       1       0       0
PSEUDOTUMOR
MALIGNANT
MUCOEPIDERMOID     0     1       1       0       2       0
CARCINOMA
ADENOID CYSTIC     0     0       1       0       2       1
CARCINOMA
ACINIC CELL        0     0       0       0       0       0
CARCINOMA
MALIGNANT          0     0       0       0       1       0
MYOEPITHELIOMA
CARCINOMA EX       0     0       0       0       0       0
PLEOMORPHIC
ADENOMA
SALIVARY DUCT      0     0       1       0       0       0
CARCINOMA
UNDIFFERENTIATED   0     0       0       0       0       1
CARCINOMA
TOTAL              1     3       7       7       16      9

NEOPLASMS          AGE GROUP (YEARS)
                   60-69   70-   TOTAL
                           79

BENIGN
PLEOMORPHIC        0       1     24
ADENOMA
BASAL CELL         1       0     04
ADENOMA
WARTHIN TUMOR      1       1     2
MYOEPITHELIOMA     0       0     2
SCHWANNOMA         1       0     2
HEMANGIOMA         0       0     1
LIPOMA             0       0     1
INFLAMMATORY       1       0     2
PSEUDOTUMOR
MALIGNANT
MUCOEPIDERMOID     2       0     6
CARCINOMA
ADENOID CYSTIC     0       0     4
CARCINOMA
ACINIC CELL        1       0     1
CARCINOMA
MALIGNANT          0       0     1
MYOEPITHELIOMA
CARCINOMA EX       0       1     1
PLEOMORPHIC
ADENOMA
SALIVARY DUCT      0       0     1
CARCINOMA
UNDIFFERENTIATED   0       0
CARCINOMA
TOTAL              7       3     53

TABLE 03: SITE DISTRIBUTION OF SALIVARY GLAND NEOPLASMS

NEOPLASMS            NO.     PAROTID      SUBMANDIBULAR   MINOR
                     OF      GLAND        GLANDS          SALIVARY
                     CASES                                 GLANDS

BENIGN
PLEOMORPHIC          24      20           04              00
ADENOMA
BASAL CELL ADENOMA   04      03           00              01
ARTHIN TUMOR         02      02           00              00
MYOEPITHELIOMA       02      01           00              01
SCHWANNOMA           02      01           01              00
HEMANGIOMA           01      01           00              00
LIPOMA               01      01           00              00
INFLAMMATORY         02      02           00              00
PSEUDOTUMOR
MALIGNANT
MUCOEPIDERMOID       06      06           00              00
CARCINOMA
ADENOID CYSTIC       04      00           02              02
CARCINOMA
ACINIC CELL          01      01           00              00
CARCINOMA
MALIGNANT            01      01           00              00
MYOEPITHELIOMA
CARCINOMA EX         01      01           00              00
PLEOMORPHIC
ADENOMA
SALIVARY DUCT        01      01           00              00
CARCINOMA
UNDIFFERENTIATED     01      01           00              00
CARCINOMA
TOTAL                53      42(79.25%)   07(13.21%)      04(7.54%)
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Title Annotation:ORIGINAL ARTICLE
Author:Iqbal, Mohammad Shahid; Tabassum, Aisha; Chatura, K.R.; Malkappa, Sateesh K.; Basavaraja, P.K.
Publication:Journal of Evolution of Medical and Dental Sciences
Article Type:Report
Date:Jan 28, 2013
Words:3947
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