alexa Epithelial-Myoepithelial Carcinoma of Parotid Gland: A Cytological Challenge with Histological Correlation | OMICS International
ISSN: 2157-7099
Journal of Cytology & Histology
Like us on:
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Epithelial-Myoepithelial Carcinoma of Parotid Gland: A Cytological Challenge with Histological Correlation

Iván Fernández-Vega*, Nelson Fuentes-Martínez, Guillermo E Mendoza, Jorge Santos-Juanes and Florentino Fresno-Forcelledo

Pathology Department of Central University Hospital of Asturias, Oviedo, Spain

*Corresponding Author:
Iván Fernández-Vega
Pathology Department
Central University Hospital of Asturias
33006, Oviedo, Spain
E-mail: [email protected]

Received Date: December 19, 2012; Accepted Date: December 28, 2012; Published Date: December 31, 2012

Citation: Fernández-Vega I, Fuentes-Martínez N, Mendoza GE, Santos-Juanes J, Fresno-Forcelledo F (2012) Epithelial-Myoepithelial Carcinoma of Parotid Gland: A Cytological Challenge with Histological Correlation. J Cytol Histol 3:156. doi:10.4172/2157-7099.1000156

Copyright: © 2012 Fernández-Vega I, 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.

Visit for more related articles at Journal of Cytology & Histology

Abstract

Background: Epithelial-Myoepithelial Carcinoma (EMC) is a rare type of malignant tumor of salivary gland accounting for less than 1.5% of all salivary neoplasms. Differential diagnosis of this tumor is complicated, especially by cytological examinations. Case: We present the case of an 86-year-old female who presented clinically with a bulky lesion behind her right ear. Fine needle aspiration cytology with immunocytochemistry has been performed and the patient was diagnosed with a biphasic neoplasm, epithelial-myoepithelial, highly suggestive of EMC. She underwent a wide surgical excision and diagnostic was confirmed by histological examinations, which showed a tumor composed of ducts with double cell lining surrounded by a basement membrane in a sclerotic stroma. Immunohistochemistry was carried on to highlight the biphasic cell pattern. The patient is free of disease after 20 months of surgical procedure. Conclusion: Although there isn’t any antibody that confirms the diagnosis of EMC, due to the difficulty to make a correct diagnostic of this lesion by cytology, we have highly recommended the use of immunocytochemistry assay as an important tool to confirm the double-cell pattern, which in together with a clinical course may help in the diagnostic of EMC. Cytology and histology correlation are rarely reported.

Keywords

Fine needle aspiration; Carcinoma; Salivary glands; Immunohistochemistry

Highlighted Boxes

Established facts

Biphasic pattern of EMC is a relevant cytological feature to orientate the diagnosis of this exceedingly rare malignant salivary gland tumor.

Novel insights

Nonspecific antibodies such as CD117 and P-63, can help us to make a good diagnostic approach in cytological smears.

Introduction

Case Report

An 86 year old female with a history of painless longstanding bulky lesion over her right parotid gland. Since, last 5 months to date she noted a fast growing. Cervical adenopathy and her right facial nerve function were unaffected. Ultrasonography and computed tomography of the head and neck revealed a non-homogeneously solid mass measuring 6.5 × 4.5 cm in her right parotid gland with a skin protuberance, an external jugular vein displacement and possibility of a sternocleidomastoid muscle infiltration. There wasn´t evidence of jaw affectation. The tumor’s interface with the parotid gland was clearly defined. Clinically and radiologically the tumor suggested a malignant neoplasm. The patient underwent Fine Needle Aspiration Cytology (FNAC) from mass with 23G needle. Cytology revealed both epithelial and stromal components. Cells were frequently arranged in pseudopapillary formations, with slightly eosinophilic stromal cores on May-Grünwald-Giemsa (MGG) stain (Figure 1a). Epithelial cells were in clusters or singles, with spindle cells in a scanty myxoid stromal background (Figure 1b). There wasn´t evidence of cellular atypia so, immunocytochemistry was performed in order to rule out the possibility of malignant tumor. Eventually, immunocytochemistry highlighted the biphasic nature of this tumor with epithelial cells positive for CD 117 (Figure 1c) and myoephitelial cells positive for P-63 (Figure 1d). Clinical course together with cytological findings were consistent with a biphasic malignant parotid gland neoplasm called EMC. A right parotidectomy was performed including adjacent soft tissue and skin (Figure 2a).

cytology-histology-cytosmear-showing

Figure 1: a-b: Cytosmear showing a pseudopapillary structures with a myoepithelial background. Biphasic pattern, central low-cuboidal ductal cells surrounded by clear myoepithelial cells; May-Gr├╝nwald- Giemsa, x400. c) CD117 antibody highlighting the ductal component; Immunoperoxidase stain, x400. d) P-63 antibody, nuclear positivity in myoepithelial cells; Immunoperoxidase stain, x1000.

cytology-histology-parotidectomy-including

Figure 2: a) A total right parotidectomy including adjacent soft tissue and skin. b) Tumor features showing a bad-bordered lobulated mass with a gray/ yellowish surface and some hemorrhagic areas. Non-tumoral parotid gland is illustrated in the right upper part.

Cutting sections from formalin fixed tumour did show a poorly circumscribed greyish mass, arranged in a globular pattern with a haemorrhagic core, measuring 6 cm in higher diameter (Figure 2b). Histopathology sections displayed a normal parotid structure and a uniform nesting arrangement of tumor cells being separated by a thin fibrous connective tissue capsule (Figure 3a). There were two cell types, an outer layer of clear myoepithelial cells and an inner layer of cuboidal eosinophilic duct-like cells. These cells were further enveloped on outside by a well defined basement membrane material (Figure 3b). There wasn´t evidence of nuclear atypia but some mitotic figures were seen.

cytology-histology-normal-parotid

Figure 3: Histology. a) Normal parotid gland separated from tumor by a connective tissue capsule; H&E, x100. b) Biphasic pattern, an inner ductal cells and outer clear myoepithelial cells; H&E, x200. c) Cytokeratin 8 positivity in the epithelial component; Immunoperoxidase stain, x400. d) Smooth muscle actin positivity in the myoepithelial component; Immunoperoxidase stain, x400. e) CD117 present in the epithelial groups; Immunoperoxidase stain, x400. f) P-63 positivity in the myoepithelial cells nuclei; Immunoperoxidase stain, x600.

Immunohistochemistry assay was also made. Epithelial cells were strongly positive for cytokeratin 8 (Figure 3c) and CD 117 (Figure 3f). Myoephitelial cells did stain with smooth muscle actin (Figure 3d) and P-63(Figure 3e). S100 was also positive in myoephitelial cells showing nuclear and cytoplasmatic staining. Both groups of cells were negative for GFAP and PSA. Ki-67 was up to 20% mainly in the myoepithelial component. Thus, the final diagnosis of EMC of the right parotid gland was made. Since the surgery the patient has done well, without evidence of either local recurrence or metastases.

Discussion

Firstly described by Donath et al. in 1972 [2], EMC wasn’t included in the World Health Organization classification of salivary gland tumors until 1991 [8]. Higher incidence is in older persons with a female predominance, and affect principally the parotid gland, more than the others salivary glands [7]. Furthermore, most patients tend to present an asymptomatic enlarging mass from weeks to months, whereas others exhibited signs of malignancy such as pain or facial paralysis.

Although radiological signs can approach to the malignancy, EMC is a pathological challenge particularly when the diagnostic is not suspected. In cytology smears differential diagnosis must be done with myoepithelioma, pleomorphic adenoma, monomorphic adenoma, adenoid cystic carcinoma and polymorphous low grade adenocarcinoma. Klijanienko et al. have published a quantitative differential diagnosis of EMC on cytology smears taking into account both , stroma and cells features, such as papillary formations, clear cells, cuboidal/basal cells, plasma-shape myoepithelial cells, squamous cells, cellular atypia, chondromixoid stroma, mucoid stroma, hyaline deposits and crystalloids. Sometimes these characteristics are overlapping between one tumor and another, however up to 84,6% of EMC are diagnosed as suspicious/malignant as this authors demonstrated. In the other hand, only 7.7% of cases were diagnosed as a benign tumor such as pleomorphic adenoma. Finally, they conclude that failure to distinguish between these entities is not dramatic, because all of them lead to surgical excision [9].

In the way to improve our knowledge about salivary gland tumors, we could find in the English literature that Seethala et al. recently published a frequent positivity (69,2%) of c-kit (CD117) in EMC [10]. However, Andreadis et al. [11] have lately demonstrated that CD117 was also expressed in a wide group of malignant salivary gland tumors, such as adenoid cystic carcinoma, acinar cell carcinoma and basal cell adenocarcinoma. By the way, they have also seen a CD117 expression in benign salivary gland pathology, for example inflammatory disease.

In order to differentiate EMC from others malignancies, is important to take into account that biphasic nature (epithelial and myoepithelial) is the most relevant finding. This pattern can be present in smears, but it´s better seen in histology and is characterized by a tubular or ductal structures composed of basal myoepithelial and luminal epithelial cells, these latest look like normal intercalated salivary gland ducts. We confirmed the double-cell pattern on smear and on histology sections. In the former, immunocytochemistry displayed a strong positivity for CD117 (Figure 1c) and strong nuclear positivity for P-63 (Figure 1d) in myoepithelial cells. In formalin fix tissue, immunohistochemistry revealed a positivity for cytokeratin 8 (Figure 3c) and CD117 (Figure 3f), and intense dye with smooth muscle actin (Figure 3d) and P-63 (Figure 3e) in the myoephitelial cells. Although PSA is considered highly specific marker for prostate carcinoma, several authors have demonstrated focal immunostaining for PSA in pleomorphic adenoma, mucoepidermoid carcinoma, and ductal carcinoma of salivary gland [12]. Aberrant expression of PSA was recently described by Venetia et al. in one case of dedifferentiated EMC [13]. In the present case PSA was negative.

In conclusion, we remark the biphasic pattern of EMC as a cytological strategy to orientate the diagnosis of this exceedingly rare malignant salivary gland tumor; however, non-specific antibodies can help us to make a good diagnostic approach, although they may be useful. Our patient is free of disease since surgery.

References

Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Recommended Conferences

Article Usage

  • Total views: 11868
  • [From(publication date):
    September-2012 - Dec 14, 2017]
  • Breakdown by view type
  • HTML page views : 8099
  • PDF downloads : 3769
 

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

Agri & Aquaculture Journals

Dr. Krish

[email protected]

1-702-714-7001Extn: 9040

Biochemistry Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Business & Management Journals

Ronald

[email protected]

1-702-714-7001Extn: 9042

Chemistry Journals

Gabriel Shaw

[email protected]

1-702-714-7001Extn: 9040

Clinical Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Engineering Journals

James Franklin

en[email protected]

1-702-714-7001Extn: 9042

Food & Nutrition Journals

Katie Wilson

[email protected]

1-702-714-7001Extn: 9042

General Science

Andrea Jason

[email protected]

1-702-714-7001Extn: 9043

Genetics & Molecular Biology Journals

Anna Melissa

[email protected]

1-702-714-7001Extn: 9006

Immunology & Microbiology Journals

David Gorantl

[email protected]

1-702-714-7001Extn: 9014

Materials Science Journals

Rachle Green

[email protected]

1-702-714-7001Extn: 9039

Nursing & Health Care Journals

Stephanie Skinner

[email protected]

1-702-714-7001Extn: 9039

Medical Journals

Nimmi Anna

[email protected]

1-702-714-7001Extn: 9038

Neuroscience & Psychology Journals

Nathan T

[email protected]

1-702-714-7001Extn: 9041

Pharmaceutical Sciences Journals

Ann Jose

[email protected]

1-702-714-7001Extn: 9007

Social & Political Science Journals

Steve Harry

[email protected]

1-702-714-7001Extn: 9042

 
© 2008- 2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version