Fever and arthralgia as the initial symptoms of primary bone marrow diffuse large B-cell lymphoma: A case report

Introduction

Primary bone marrow diffuse large B-cell lymphoma (DLBCL) is an uncommon type of non-Hodgkin's lymphoma (NHL). DLBCL may involve nodal or extranodal sites (1); however, initial presentation in the bone marrow occurs infrequently (2–6). Extranodal involvement of the bone marrow as an isolated and unique localization of aggressive NHLs has been reported (7), including cases of anaplastic large cell lymphoma or DLBCL.

The rapid diagnosis of primary bone marrow DLBCL is challenging, as the clinical symptoms and signs are nonspecific. In addition, the clinical features, optimal management, diagnostic procedures and prognostic factors associated with this disease remain to be elucidated (8). Recently, the diagnostic criteria for primary bone marrow lymphoma (PBML) have been proposed, and the clinicopathological features of this extremely rare tumor have also been documented (7). The current study presents the case of a patient with primary bone marrow DLBCL who was admitted to the hospital with symptoms of fever and arthralgia. A correct initial diagnosis of primary bone marrow DLBCL was determined by multiple bone marrow biopsies at different locations.

Case report

A 41-year-old male patient was admitted to the Affiliated Hospital of Jining Medical University (Jining, China) on August 4th, 2014, with initial complaints of a high fever and arthralgia. The patient also presented with recent onset of pharyngalgia, coughing, weight loss and malaise. Following admission, a physical examination revealed that the patient's body temperature was 39.4°C; however, lymphadenopathy and hepatosplenomegaly were not observed. Blood tests indicated leukopenia and anemia [white blood cell (WBC) count, 2.75×109/l (normal, 3.5–9.5×109/l); red blood cell (RBC) count, 2.62×1012/l (normal, 4.3–5.3×1012/l); hemoglobin (HGB) level, 100 g/l (normal, 130–175 g/l)], elevated lactate dehydrogenase (LDH) levels (1,191 U/l; normal, 90–240 U/l) and elevated C-reactive protein (CRP) levels (39.83 mg/l; normal, 0–10 mg/l). All other results, including comprehensive serology and screening for autoimmune antibodies, were unremarkable. A bone marrow puncture of the right posterior iliac crest was a dry tap. No abnormalities were detected (data not shown). Contrast-enhanced computed tomography (CT; SOMATOM Definition Flash CT; Siemens Healthcare, Erlangen, Germany) confirmed no hepatosplenomegaly, and malignancy could not be confirmed.

In the following week, pancytopenia, LDH elevation, direct bilirubin elevation, CRP elevation and B symptoms were not resolved. These results indicated no lymph node and extranodal involvement, but suggested bone marrow involvement. Bone marrow aspiration was repeated in the left posterior iliac crest and sternum, and a bone marrow biopsy of the left posterior iliac crest was performed. Resected tissues were formalin-fixed, paraffin-embedded and cut into sections (2–4 µm) using a RM2235 rotary microtome (Leica, Wetzlar, Germany). Peripheral blood samples and bone marrow aspirate smears were stained with Wright-Giemsa (Beijing Leagene Biotech Co., Ltd., Beijing, China) for morphological evaluation (Olympus L100 S600; Olympus, Tokyo, Japan). Formalin-fixed specimens were stained with hematoxylin and eosin (Beyotime Institute of Biotechnology, Shanghai, China) for histological evaluation. Large lymphoma cells were present in the marrow aspirates on Wright-Giemsa-stained (Fig. 1A) and leukocyte peroxidase (myeloperoxidase)-stained (Fig. 1B) slides.

Figure 1. Bone marrow biopsy smears. Large lymphoma cells were present in the marrow aspirates: (A) Wright-Giemsa staining and (B) leukocyte peroxidase (myeloperoxidase) staining (magnification, ×1,000).

For flow cytometry, 50 µl aliquots of cell suspensions were incubated at room temperature (22–25°C) with the following fluorescent monoclonal mouse anti-human antibodies (BD Biosciences, San Jose, CA, USA) for 30 min: Cluster of differentiation (CD)45-peridinin-chlorophyll protein complex (cat. no. 564106), CD10-phycoerythrin (PE; cat. no. 561002), CD20-fluorescein isothiocyanate (FITC; cat. no. 556632), CD34-allophycocyanin (APC; cat. no. 560940), CD11c-APC (cat. no. 559877), CD5-FITC (cat. no. 561896), CD19-PE (cat. no. 561741) and immunoglobulin κ (cat. no. 555861) and λ (cat. no. 562893) light chains. Next, 2.5 ml ammonium chloride (BD Biosciences) was added for 10 min to lyse the RBCs. The cells were centrifuged at 190 × g for 5 min using the Cence H1650R centrifuge (Cence, Changsha, China) and washed with phosphate-buffered saline. The second cell pellet was resuspended in 0.5 ml PBS containing 1% formaldehyde (Polysciences Inc., Warrington, PA, USA). Cells were analyzed using a FACSCalibur flow cytometer (BD Biosciences). Data were quantified using CellQuest software (BD Biosciences). Flow cytometry confirmed the presence of lymphoma in the aspirates, which revealed positivity for cluster of differentiation (CD)20, CD19, CD10 and λ light chain, and negativity for CD5, CD11c and κ light chain (Fig. 2).

Figure 2. Immunophenotype of the bone marrow cells as detected by flow cytometric analysis. (A) CD45 was used to gate B lymphocytes. (B-G) Cells were positive for (B, C and G) CD20 (positive rate >20%), (B) CD10, (E) CD19 and (F) λ light chain, and negative for (D) CD11c, (D and E) CD5 and (G) κ light chain. CD, cluster of differentiation; FITC, fluorescein isothiocyanate; PE, phycoerythrin; APC, allophycocyanin; SSC, side scatter.

Biopsy specimens revealed focal hyperplasia of large abnormal lymphoid cells and bone marrow necrosis (Fig. 3A–B). Bone marrow biopsy specimens were formalin-fixed, paraffin-embedded and cut into 2–4-µm sections using the RM2235 rotary microtome. Each section was stained with hematoxylin and eosin and used for immunostaining. Immunohistochemical analyses were performed using an autostainer (Benchmark XT system; Ventana Medical Systems, Inc., Tucson, AZ, USA) according to the manufacturer's protocol. The following ready-to-use mouse monoclonal primary antibodies were used: CD43 (cat. no. 14690602), CD10 (cat. no. 14368806), CD20 (cat. no. 140316020), CD38 (cat. no. 141124341), terminal deoxynucleotidyl transferase (cat. no. 140508197), Ki67 (cat. no. 14690209) and CD79a (cat. no. 14620803) (ZSGB-BIO, Beijing, China); and CD34 (cat. no. END-R-7-CE; Leica). Following incubation with the primary antibodies at 4°C overnight, sections were incubated with a monoclonal biotin-conjugated goat anti-mouse IgG secondary antibody (cat. no. Kit-9710; ready-to-use; Fuzhou Maixin Biotech. Co., Ltd., Fuzhou, China) at 37°C for 30 min, followed by peroxidase-labeled streptavidin and diaminobenzidine chromogen (Ventana UltraView Universal DAB Detection Kit; Ventana Medical Systems, Inc.). Evaluation was then performed using an Olympus BX51 microscope (Olympus Corporation, Tokyo, Japan). All immunostaining was performed using a BenchMark XT automated immunostaining device (Ventana Medical Systems, Inc.). Immunohistochemical staining indicated that the abnormal cells were positive for CD20, melanoma associated antigen (mutated) 1, CD79a, Ki-67 and silver staining; and negative for CD10, CD34, CD38, CD43 and terminal deoxynucleotidyl transferase (Fig. 3C–L). This immunophenotype matches that previously ascribed to DLBCL (9). A diagnosis of primary bone marrow DLBCL was made based on these results.

Figure 3. Histopathological and immunohistochemical features of the bone marrow biopsy. Images of the bone marrow biopsy showed involvement of large abnormal lymphoid cells with focal clusters. (A) Hyperactivity of the bone marrow (hyperplasia) and (B) necrotic zone (hematoxylin and eosin staining; magnification, ×400). The tumor cells were (C) positive for CD20 (magnification, ×400), (D) positive for melanoma associated antigen (mutated) 1 (magnification, ×400), (E) negative for CD10 (magnification, ×100), (F) negative for CD34 (magnification, ×200), (G) negative for CD38 (magnification, ×200), (H) negative for CD43 (magnification, ×400), (I) positive for CD79a (magnification, ×400), (J) positive for Ki-67 (magnification, ×100), (K) negative for terminal deoxynucleotidyl transferase (magnification, ×100), and (L) positive for silver staining (magnification, ×400). CD, cluster of differentiation.

In August 2014, the patient was administered with four cycles of chemotherapy with cyclophosphamide, vincristine, epirubicin and prednisone (CHOP regimen) plus etoposide as part of a 3-week standard cycle, as follows: Etoposide [50 mg/(m2x day)], vincristine [0.4 mg/(m2 × day)] and epirubicin [15 mg/(m2 × day)] administered via continuous intravenous (i.v.) drip for 96 h; cyclophosphamide (750 mg/m2, i.v., day 5); and prednisone [60 mg/(m2 × day), orally, days 1–5]. Cerebrospinal fluid examination showed no obvious lymphomatous infiltration (data not shown). Following one course of chemotherapy, remission of symptoms was observed. The patient's temperature returned normal, and the arthralgia reduced. Blood tests indicated a WBC count of 6.10×109/l, RBC count of 2.37×1012/l and HGB level of 67 g/l, and the bone marrow tests indicated partial remission. If the patient achieved complete remission, another two cycles of CHOP chemotherapy would be administered as consolidation therapy. If not, other chemotherapy regimens would be explored. The last follow-up was conducted on May 7, 2015, however, the patient has since been lost to follow-up.

Discussion

Extranodal DLBCLs have specific clinicopathological features that are dependent on the organ of origin (3). Previous reports have shown that invasion of lymphoma cells may be detected in the brain, adrenal glands, kidney and skin in autopsy cases (10–17). However, DLBCL primarily arising from the bone marrow is an extremely rare entity, with only a few retrospective studies and sporadic cases reported in the literature (4,18–22). Previously, Wong et al (23) reported 14 cases of large cell lymphoma with initial manifestation in the bone marrow, of which 4 exhibited a B-cell phenotype, 3 a T-cell phenotype, and 1 a non-T non-B phenotype. The majority of patients had ‘swinging’ fever and peripheral blood cytopenia. However, in the present case, the patient complained only of fever and arthralgia as the initial symptoms. This presentation is extremely rarely reported.

The diagnosis of primary bone marrow DLBCL is difficult due to the absence of guidelines regarding clinical features, optimal management, diagnostic procedures and prognostic factors (8). As no lesions were observed in the present case, and only fever and joint pain were reported, multiple bone marrow biopsies in different locations were performed. DLBCL is most commonly diagnosed using positron emission tomography (PET)-CT (24,25). By contrast, the current study relied on multiple bone marrow biopsies combined with the clinical findings, physical examination, morphology and flow cytometry results. The findings of the present case corresponded to the diagnostic criteria of PBML previously proposed (7). Notably, the patient in the present case complained primarily of joint pain. This may have resulted from bone marrow necrosis. However, this should be studied further.

The optimal therapy for PBML has still not been proposed. Autologous hematopoietic stem cell transplantation or multi-agent chemotherapy with rituximab plus CHOP regimen followed by involved field radiotherapy are typically the chosen treatment options (17,26–29). However, the exact roles and effects of these treatments are unclear due to the extremely low incidence of the disease. In the present study, the patient received CHOP regimen plus etoposide, and achieved a reduction in the fever and arthralgia, in addition to partial remission as indicated by bone marrow tests.

In conclusion, DLBCL primarily arising from the bone marrow is an extremely rare entity. The present case demonstrates that awareness should be raised of bone marrow DLBCL, particularly in patients presenting with fever and arthralgia. In addition, when lymphoma is suspected, it is imperative to perform multiple bone marrow biopsies in various locations. The long-term outcome and the prognosis of DLBCL require further investigation with more cases.

Acknowledgements

This study was supported by the Science and Technology Program of Shandong Province, China (grant no. 2012YD18066) and the Health and Family Planning Commission of Shandong Province (grant no. 9,2012).

References