Literature DB >> 18327777

Lymphadenomatous carcinoma of the sublingual gland: report of a first case in an unusual localization.

Yong-Dae Kwon1, Stefan Biesterfeld, Torsten Hansen, Andreas Schwerdtfeger, Martin Kunkel.   

Abstract

BACKGROUND: Lymphadenomatous carcinoma of the salivary gland is a very rare tumor, which hitherto occurred exclusively in the parotid gland. This report describes a case of lymphadenomatous carcinoma of the sublingual gland, which is thought to be the first report of this special entity. METHODS AND
RESULTS: A 36-year-old man was seen with slowly growing mass on his right floor of mouth. Upon surgical removal, the mass was well encapsulated. Microscopic examination revealed a biphasic appearance with islands of neoplastic epithelial cells presenting against a dense lymphoid stroma, while the epithelial compartment showed features of malignancy. During 30-months of close follow-up, there has not been any sign of local recurrence or metastasis.
CONCLUSION: The clinical behavior, the age of the patient, and the sublingual localization differentiate this lesion from the sebaceous type, favoring lymphadenomatous carcinoma as a distinct clinical entity. Copyright (c) 2008 Wiley Periodicals, Inc. Head Neck 2008.

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Year:  2008        PMID: 18327777     DOI: 10.1002/hed.20814

Source DB:  PubMed          Journal:  Head Neck        ISSN: 1043-3074            Impact factor:   3.147


  1 in total

Review 1.  NUT Midline Carcinoma of the Sublingual Gland: Clinical Presentation and Review.

Authors:  Nolan B Seim; Ramez H W Philips; Lynn Schoenfield; Theodoros N Teknos; James W Rocco; Amit Agrawal; Enver Ozer; Ricardo L Carrau; Stephen Y Kang; Matthew O Old
Journal:  Head Neck Pathol       Date:  2017-03-27
  1 in total

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