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An Official Publication of the Indian Association of Oral and Maxillofacial Pathologists


 
  Table of Contents    
CASE REPORT  
Year : 2014  |  Volume : 18  |  Issue : 1  |  Page : 102-106
 

Primary diffuse large B-cell lymphoma in the anterior hard palate: A rare case report with review of literature


1 Department of Oral Pathology, Institute of Dental Sciences, Bhubaneswar, Odisha, India
2 Department of Oral Medicine and Radiology, Institute of Dental Sciences, Bhubaneswar, Odisha, India
3 Department of Conservative Dentistry and Endodontics, Institute of Dental Sciences, Bhubaneswar, Odisha, India
4 Department of Oral and Maxillofacial Surgery, Institute of Dental Sciences, Bhubaneswar, Odisha, India

Date of Web Publication6-May-2014

Correspondence Address:
Satya Ranjan Misra
Prasanti, Kathogola Road, Mangalabag, Cuttack 753 001, Odisha
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0973-029X.131927

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   Abstract 

Diffuse large B-cell lymphomas (DLBCLs) are defined as neoplasms of large transformed B cells, i.e. with nuclear diameter more than twice that of a normal lymphocyte. These account for 30-40% of all adult non-Hodgkin's lymphomas (NHL). Intraoral lymphomas are relatively rare and often difficult to diagnose in clinical settings. In this case report, we describe a case of primary DLBCL affecting the anterior part of the hard palate of an elderly male patient. DLBCL of anterior part of hard palate is yet to be reported in the English literature, even though DLBCL cases involving the posterior palate have been recorded, thus making the present case to be first of its kind. Emphasis has also been given on the subclassification, differential diagnosis and prognostic antibody factors determining the outcome of DLBCL.


Keywords: Anterior hard palate, diffuse large B-cell lymphoma, non-Hodgkin′s lymphoma


How to cite this article:
Sahoo SR, Misra SR, Mishra L, Mishra S. Primary diffuse large B-cell lymphoma in the anterior hard palate: A rare case report with review of literature. J Oral Maxillofac Pathol 2014;18:102-6

How to cite this URL:
Sahoo SR, Misra SR, Mishra L, Mishra S. Primary diffuse large B-cell lymphoma in the anterior hard palate: A rare case report with review of literature. J Oral Maxillofac Pathol [serial online] 2014 [cited 2019 Dec 13];18:102-6. Available from: http://www.jomfp.in/text.asp?2014/18/1/102/131927



   Introduction Top


Diffuse large B-cell lymphoma (DLBCL) is a subtype of non-Hodgkin's lymphoma (NHL) characterized by diffuse proliferation of large neoplastic B-lymphoid cells with nuclear size equal to or exceeding normal macrophage nuclei or more than twice the size of a normal lymphocyte (>20 μm). [1] Affected patients are usually in their seventh decade of life and clinically a rapidly enlarging and often symptomatic mass is typically seen. [2] It is frequently reported in the mediastinum, gastrointestinal tract, bone marrow, central nervous system, breast and testes. [3] NHLs of the oral cavity are rare and account for only 2-3% of all the lymphomas reported. [4] In the maxillofacial region, the most commonly affected site of NHL is the Waldeyer's ring, nasopharynx and base of the tongue. [5] However, the incidence of primary DLBCL in the oral cavity has not been previously specified in the literature. Apart from Waldeyer's ring, in the oral cavity, DLBCL can involve maxillary alveolus, maxillary vestibule and posterior palate. [4] Currently, the treatment of DLBCL consists of radiotherapy, chemotherapy or both. Importantly, DLBCL may be cured in a significant percentage of patients, depending on the initial characteristics of the tumor and the host. [6]

This article reports a case of primary DLBCL affecting anterior part of hard palate in a 76-year-old male patient, which is first case of its kind considering the unusual location.


   Case report Top


A 76 year old eastern-Indian male patient reported to the dental hospital with a complaint of swelling in the palate since 2 months. History revealed that the swelling started as a small lesion and gradually grew in size. There was no toothache or pain associated with it, but as the size increased there was trauma from the mandibular anterior teeth causing ulceration and pain in the swelling. There was no history of any discharge from the swelling. The patient had nasal stuffiness and seromucous discharge from the nose on the left side since 15 days, which did not respond to medications.

On examination, a single well-circumscribed swelling was seen on the anterior hard palate, ovoid in shape, measuring about 3 cm in greatest diameter, with the surface color resembling that of normal mucosa, margins were well defined and the swelling crossed the midline on the left side with surface ulceration [Figure 1]. On palpation there was slight tenderness, the swelling was firm in consistency, sessile, attached to the underlying bone, not yielding to pressure, non-fluctuant and non-reducible. Fine-needle aspiration cytology was done, but no aspirate was obtained. Correlating the history and clinical features, a provisional diagnosis of a malignant soft tissue neoplasm was made.
Figure 1: Swelling in the anterior hard palate with surface ulceration

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Antral carcinoma, malignant neoplasm of the salivary glands, lymphoma, sarcoma and malignant melanoma were considered in the differential diagnosis. Because the site was anterior part of the hard palate where salivary glands are absent and due to the mucosal color of the swelling, salivary gland neoplasm and malignant melanoma were ruled out. Radiologic and histopathologic investigations were done to confirm the diagnosis.

Periapical, occlusal and panoramic radiographs revealed generalized destruction of alveolar bone in the anterior maxilla with perforation of the antrum bilaterally. A contrast-enhanced computed tomography scan was performed and it revealed a large contrast-enhancing lobulated soft tissue attenuated mass measuring 57 × 45 mm in size, involving the maxillary alveolus extending up to the maxillary antrum bilaterally [Figure 2]. Extensive contiguous bone destruction was seen along with extension into the premaxillary soft tissue subcutaneous fat [Figure 2]. The submandibular salivary glands were enlarged bilaterally.
Figure 2: CT scan of the maxilla, sagittal, (a) coronal (b) and axial (c) sections showing a space occupying hypodense lesion in the anterior maxilla (red arrow) with perforation and extension into the maxillary antrum. CT: Computed tomography

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An incisional biopsy was done and histological examination of biopsy specimen revealed diffuse proliferation of large atypical lymphoid cells with high nuclear cytoplasmic ratio, coarse chromatin and prominent nucleoli with few abnormal mitotic figures [Figure 3]. The features were suggestive of large cell lymphoma. Immunohistochemistry showed weak cluster of differentiation (CD) 3 positivity, strong CD20 and CD45 positivity confirming the B-cell origin of lymphocytes [Figure 4]. Correlating the clinical, histopathological and immunohistological features, a final diagnosis of primary diffuse large B-cell lymphoma of anterior palate was given.
Figure 3: Photomicrograph showing centroblasts (red arrows),i.e. large atypical pleomorphic lymphocytic nucleus with multiple nucleoli (H & E stain, x400)

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Figure 4: CD20 immunostaining showing strong positivity indicating B-cell origin of lymphocytes (IHC stain, x200)

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The patient was sent to a medical oncologist for chemotherapy. He was given cyclophosphamide 1200 mg, adriamycin 75 mg and vincristine 2 gm thrice weekly for a total of six cycles. Following chemotherapy, the palatal swelling resolved completely but areas of hypermelanosis were observed [Figure 5]. Patient was asymptomic without any evidence of recurrences during the 18 months follow-up period.
Figure 5: Post-chemotherapy photo showing complete resolution of the lesion followed by hypermelanosis after resolution of the swelling (red arrow)

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   Discussion Top


Malignant lymphomas constitute a group of neoplastic proliferation process of the lymphocytes and their precursor cells. Hodgkin's disease is characterized histologically by the presence of multinucleated  Reed-Sternberg cells More Details. All other neoplasms of lymphoid system are referred to as NHL and are derived predominantly from the cells of B-lymphocyte series. [6] Till date seven case series containing a total of 202 cases on extranodal NHL have been published in English literature. Of these 202 cases only five (2.4%) are reported in palate (all in posterior hard palate), which makes it a rare site for occurrence. However, primary DLBCL occurring in anterior part of hard palate is yet to be published in literature. DLBCL, being a heterogenous neoplasm shows variable clinical, morphologic, immunophenotypic, cytogenetic and genetic features. [7] This is often reflected in their marked biological heterogeneity and highly variable clinical course. [3]

Frequently, the initial symptoms of a large B-cell lymphoma of the oral cavity are a painless swelling, a nonhealing ulcer, fever, sweats and weight loss. A painless lymph node enlargement or a submucosal lesion in the junction between hard and soft palate are highly suspicious. Oral lymphoma often is a component of a disseminated disease process that may involve regional nodes as well. Other times, it may represent a primary extranodal disease confined to oral cavity or jaws, which is very rare. [8]

The etiology of DLBCL remains unknown. They may originate de novo or represent progression from a less aggressive lymphoma, such as follicular lymphoma or small lymphocytic lymphoma. Underlying immunodeficiency is a significant risk factor and DLBCL in the setting of immunodeficiency is more often Epstein-Barr virus-positive than sporadic DLBCL. [9]

Lymphomas can be diagnosed using hematoxylin and eosin-stained sections, but immunophenotyping is currently the most common technique. Modern hematology relies on immunophenotyping to distinguish between benign and malignant diseases, as well as for a more detailed subtyping. [10] The DLBCL can be subclassified depending on cytomorphology, gene expression profile and reactiveness toward specific antibodies [Table 1] [11] . The histologic and immunohistochemical differential diagnosis for DLBCL includes Burkitt's lymphoma, lymphoblastic lymphoma, diffuse mixed lymphoma, true histiocytic lymphoma and the classical Hodgkin's lymphoma [Table 2].
Table 1: Subclassifi cation of diffuse large B-cell lymphoma affecting oral cavity

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Table 2: clinical, histological and immunological differential diagnosis of DLBCL

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DLBCLs express CD45 (leukocyte common antigen) and pan-B-cell antigens (CD19, CD20 and CD79). In some cases, expression of one or more of these antigens may be lacking. [14] CD20 is expressed on B cells from the mature precursor B cell until the pre-plasma cell stage of differentiation. It is a highly specific marker for B-cell lineage and most DLBCL show homogenously bright staining for CD20. [15] [Table 3] [13],[16] shows the normal B-cell differentiation process, respective expression of specific antibody and prognosis in each stage. The post-germinal center (GC) B-cells are multiple myeloma oncogene 1 (MUM1) positive, which when expressed more can be prognostically unfavorable. MUM1 expression denotes the final step of intra-GC B-cell differentiation and subsequent steps of B-cell maturation toward plasma cells. [17] CD138 expression is usually restricted to cells exhibiting plasmablastic differentiation and to plasma cells. CD3 is a T-cell marker that is associated with the T-cell receptor and transmits the activation signal to the cytoplasm. It is highly restricted in its expression to T-lymphoid cells and is an excellent marker, as it is retained following neoplastic transformation. [18]
Table 3: DLBCL affecting different stages of B-cell differentiation, subsequent antibody positivity and prognosis

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Variability in the immunophenotypes of DLBCL, indicates that this comprises a heterogeneous group of tumors. More than 25% of DLBCL have a translocation t(14;18) and most of them express bcl-2 with or without a translocation. Chromosomal rearrangements affecting the bcl-6 gene (regulator of germinal centre formation) at 3q27 are seen in 30% of DLBCL extranodal tumors. The bcl-6 is required for GC formation, antibody-affinity maturation and T-helper-2-mediated responses. [19] The bcl-6 also inhibits lymphocyte activation by inhibiting the expression of CD69 and CD44 and inhibits differentiation of GC B-cells towards plasma cells. [20] Mutations and deletion of p53 are common in DLBCL. The bcl-6 and bcl-2 are the strongest predictors of survival. [21]

DLBCLs may exhibit more than one chromosomal rearrangement and are then referred to as 'double-hit' or 'triple-hit' lymphomas. 'Double-hit' lymphomas are associated with older age, usually present with an advanced stage of disease and show an aggressive clinical behavior. They normally have a poor prognosis, even when treated with intensive chemotherapy regimens. [22] Nevertheless, in the case presented, the patient was free of symptoms 18 months after initial diagnosis.

With the help of complementary deoxyribonucleic acid (cDNA) microarray techniques, the gene expression profiles of DLBCL have been evaluated and the two distinct molecular forms, the GC-like (GCB) and the activated B-cell-like (non-GCB) DLBCL were identified. GCB lesions express genes normally expressed by GC B cells and the non-GCB DLBCL express genes normally induced during in vitro activation of peripheral blood B cells. [8]

Bhattacharyya and colleagues in their study of 13 primary DLBCLs proposed that non-GCB lesions predominate and may exhibit a poorer prognosis with half of the patients succumbing to their disease, whereas majority of the GCB group continues to be disease free. [11] Pathologists and clinicians should be aware of this trend and should consider adding GCB classification to their reports when referring patients with oral DLBCL for further treatment and evaluation. However, stratification of DLBCL by immunohistochemitry is possible and is a relatively inexpensive, readily available and effective method of delineating the subtypes of DLBCL.

Current treatment of DLBCL usually begins with multi agent chemotherapy, typically CHOP (cyclophosphamide, hydroxydoxorubicin, oncovin and prednisone). Despite the initial response to therapy, more than half the patients succumb to the disease. [23] Early stage disease care involves either chemotherapy alone or a combination of chemotherapy and radiotherapy. The chemotherapy usually involves three cycles of CHOP. Patients are considered for bone marrow transplantation if remission is not maintained. The role of surgery is severely limited in the treatment of DLBCL. Other drugs used in multi agent chemotherapy for advanced stage disease usually involve various combinations of methotrexate, bleomycin, doxorubicin, vincristin, dexamethasone, leukcovorin, etoposide, mechlorethamine, procarbazine and cytarabine. [16]

Considering the rare occurrence of primary DLBCL in oral cavity, it has become essential for an oral physician to be aware of this aggressive lesion to aid in the early diagnosis thereby contributing to an increased life expectancy of these patients. The diagnosis of these tumors is complicated considering the nonspecific nature of the presenting symptoms. Therefore, a proper clinical evaluation, histology as well as immunohistochemical evaluation of biopsy specimen may aid in early diagnosis and effective management.

 
   References Top

1.Pileri SA, Dirnhofer S, Went P, Ascani S, Sabattini E, Marafioti T, et al. Diffuse large B-cell lymphoma: One or more entities? Present controversies and possible tools for its subclassification. Histopathology 2002;41:482-509.  Back to cited text no. 1
    
2.Campo E, Swerdlow SH, Harris NL, Pileri S, Stein H, Jaffe ES. World Health Organization classification of tumors. Pathology and genetics of tumors of haematopoietic and lymphoid tissues. Lyon: IARC Press; 2001.  Back to cited text no. 2
    
3.Coiffier B. Diffuse large cell lymphoma. Curr Opin Oncol 2001;13:325-34.  Back to cited text no. 3
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4.Kolokotronis A, Konstantinou N, Christakis I, Papadimitriou P, Matiakis A, Zaraboukas T, et al. Localized B-cell non-Hodgkin's lymphoma of oral cavity and maxillofacial region: A clinical study. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2005;99:303-10.  Back to cited text no. 4
    
5.Coiffier B. State-of-the-art therapeutics: Diffuse large B-cell lymphoma. J Clin Oncol 2005;23:6387-93.  Back to cited text no. 5
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6.Eisenbud L, Sciubba J, Mir R, Sachs SA. Oral presentations in non-Hodgkin's lymphoma: a review of thirty-one cases. Part II. Fourteen cases arising in bone. Oral Surg Oral Med Oral Pathol 1984;57:272-80.  Back to cited text no. 6
    
7.Harris NL, Jaffe ES, Stein H, Banks PM, Chan JK, Cleary ML, et al. A revised European-American classification of lymphoid neoplasms: A proposal from the International Lymphoma Study Group. Blood 1994;84:1361-92.  Back to cited text no. 7
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8.Lin AY, Tucker MA. Epidemiology of Hodgkin's disease and non-Hodgkin's lymphoma. In: Canellos GP, Lister TA, Sklar JL, editors. The Lymphomas. 1 st edition. Philadelphia: Saunders; 1998. p. 43-60.  Back to cited text no. 8
    
9.Duarte EC. Plasmablastic lymphoma of oral mucosal type: A case report. Oral Oncol Extra 2005;41:121-4.  Back to cited text no. 9
    
10.Hsi ED, Yegappan S. Lymphoma immunophenotyping: A new era in paraffin-section immunohistochemestry. Adv Anat Pathol 2001;8:218-39.  Back to cited text no. 10
    
11.Bhattacharyya I, Chehal HK, Cohen DM, Al-Quran SZ. Primary diffuse large B-Cell lymphoma of the oral cavity: Germinal center classification. Head Neck Pathol 2010;4:181-91.  Back to cited text no. 11
    
12.Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, et al. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. 4 th ed. Lyon: IARC Press;2008.  Back to cited text no. 12
    
13.de Leval L, Harris NL. Variability in immunophenotype in diffuse large B-cell lymphoma and its clinical relevance. Histopathology 2003;43:509-28.  Back to cited text no. 13
    
14.de Leval L, Braaten KM, Ancukiewicz M, Kiggundu E, Delaney T, Mankin HJ, et al. Diffuse large B-cell lymphoma of bone: An analysis of differentiation-associated antigens with clinical correlation. Am J Surg Pathol 2003;27:1269-77.  Back to cited text no. 14
    
15.Chang KL, Arber DA, Weiss LM. CD20: A review. Appl Immunohistochem 1996;4:1-15.  Back to cited text no. 15
    
16.Fisher RI, Gaynor ER, Dahlberg S, Oken MM, Grogan TM, Mize EM, et al. Comparison of a standard regimen (CHOP) with three intensive chemotherapy regimens for advanced non-Hodgkin's lymphoma. N Engl J Med 1993;328:1002-6.  Back to cited text no. 16
    
17.Sanchez-Beato M, Sanchez-Aguilera A, Piris MA. Cell cycle deregulation in B-cell lymphomas. Blood 2003;101:1220-35.  Back to cited text no. 17
    
18.Mason DY, Cordell J, Brown M, Pallesen G, Ralfkiaer E, Rothbard J, et al. Detection of T cells in paraffin wax embedded tissue using antibodies against a peptide sequence from the CD3 antigen. J Clin Pathol 1989;42:1194-200.  Back to cited text no. 18
    
19.Niu H. The proto-oncogene BCL-6 in normal and malignant B cell development. Hematol Oncol 2002;20:155-66.  Back to cited text no. 19
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20.Dent AL, Vasanwala FH, Toney LM. Regulation of gene expression by the proto-oncogene BCL-6. Crit Rev Oncol Hematol 2002;41:1-9.  Back to cited text no. 20
    
21.Lossos IS, Czerwinski DK, Alizadeh AA, Wechser MA, Tibshirani R, Botstein D, et al. Prediction of survival in diffuse large-B-cell lymphoma based on the expression of six genes. N Engl J Med 2004;350:1828-37.  Back to cited text no. 21
    
22.Frei M, Dubach P, Reichart PA, Schmitt AM, Mueller-Garamvölgyi E, Bornstein MM. Diffuse swelling of the buccal mucosa and palate as first and only manifestation of an extranodal non-Hodgkin 'double-hit' lymphoma: Report of a case. Oral Maxillofac Surg 2012;16:69-74.  Back to cited text no. 22
    
23.Vose JM. Current approaches to the management of non-Hodgkin's lymphoma. Semin Oncol 1998;25:483-91.  Back to cited text no. 23
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    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]
 
 
    Tables

  [Table 1], [Table 2], [Table 3]



 

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