Blastoid Mantle Cell Lymphoma of the Palate: Report of a Rare Aggressive Entity and Review of the Literature

• Published in: Head & neck pathology (Totowa, N.J.) N.J.), 2022-06, Vol.16 (2), p.631-642
• Main Authors: Georgaki, Maria, Theofilou, Vasileios Ionas, Pettas, Efstathios, Piperi, Evangelia, Stoufi, Eleana, Panayiotidis, Panayiotis, Nikitakis, Nikolaos G.
• Format: Article
• Language: English
• Subjects: Case Reports; Dentistry; Medicine; Medicine & Public Health; Oral and Maxillofacial Surgery; Otorhinolaryngology; Pathology
• ISSN: 1936-0568; 1936-055X; 1936-0568
• DOI: 10.1007/s12105-021-01391-9

Mantle cell lymphoma (MCL) is a well-defined, non-Hodgkin lymphoma of B-cell origin displaying diverse morphological phenotypes and variable disease course. The World Health Organization recognizes two aggressive histopathologic variants of this type of lymphoma: pleomorphic and blastoid MCL. To date, only few cases of MCL affecting the oral cavity have been reported. Additionally, the involvement of the oral and maxillofacial area by aggressive MCL subsets is considered extremely rare with only two patients reported in the English language literature to the best of our knowledge. Herein, we describe a 69 year-old male with a prior history of MCL of the right lateral pharyngeal wall developing a recurrent lesion extending to the palatal mucosa as diffuse ulceration and exhibiting histomorphological features of blastoid MCL. We also review the pertinent literature with emphasis on the diagnostic challenges and distinction between the different MCL variants.