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Year 2019

Volume: 4 , Issue: 4

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IP Journal of Diagnostic Pathology and Oncology


Multiple primary tumour of parotid gland and duodenum in an elderly male: An unusual rare case report


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Author Details : E S Keerthika Sri, S Sowmya*, K Shanmugasamy, K Anandrajvaithy

Volume : 4, Issue : 3, Year : 2019

Article Page : 241-244


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Abstract

Introduction: Patients with multiple primary malignancies (MPMs) are progressively increasing and
MPM includes metachronous and synchronous tumours. Synchronous tumour is defined as two or more
neoplasms identified simultaneously in the same patient or a second tumour identified up to six months
after the initial diagnosis. In India, the incidence of synchronous colorectal adenocarcinoma varies and
according to the literature, ranges from 2 to 5%.
Case presentation: In the present case scenario a 68 year old male presented with left pre auricular
swelling for 2 months duration along with right axillary swelling f or the past one month with history
of loss of appetite and significant weight loss. Cytology of parotid swelling showed features of
mucoepidermoid ca rcinoma (MEC) of salivary gland and right axillary swelling revealed metastatic
deposits from adenocarcinoma. In addition, the axillary node excision biopsy revealed metastatic deposits
from mucoepidermoid carcinoma. Pan endoscopy guided biopsy showed features of adenocarcinoma of
duodenum.
Conclusion: Strong clinical acumen and suspicion are required to identify cases of MPM and to
differentiate them from metastatic disease. While synchronous tumour is known to occur among colorectal
region and below diaphragm, MPM involving head and neck region [parotid] and sub diaphragmatic region
(duodenum) makes this case report unique.

Keywords: Duodenal carcinoma, Mucoepidermoid carcinoma, Synchronous tumour.

Doi : 10.18231/j.jdpo.2019.050

How to cite : Sri E S K, Sowmya S, Shanmugasamy K, Anandrajvaithy K, Multiple primary tumour of parotid gland and duodenum in an elderly male: An unusual rare case report. IP J Diagn Pathol Oncol 2019;4(3):241-244

Copyright © 2019 by author(s) and IP J Diagn Pathol Oncol. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) (creativecommons.org)