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Lymphomas of different histological types can occur at the same anatomical site (composite lymphoma) or at different sites, and can arise simultaneously or sequentially [1, 2]. Reports of patients in whom histologically distinct lymphomas occur simultaneously at different sites are rare [3, 4]. Among these rare cases, the simultaneous occurrence of T- and B-cell lymphomas is extremely rare [5]. To the best of our knowledge, composite involvement of T- and B-cell lymphomas in the bone marrow (BM) have not been reported so far. We report a case of composite BM involvement by T- and B-cell lymphomas.  A 52-yr-old woman presented with abdominal discomfort. She had a history of hepatitis B-related liver cirrhosis and was taking lamivudine. She had lost 4 kg of weight in the previous 4 months. Laboratory investigation revealed pancytopenia (white blood cells, 1.7×109/L [reference range: 4-10×109/L]; hemoglobin, 11.0 g/dL [12-16 g/dL]; and platelets, 75×109/L [150-350×109/L]), elevated levels of liver enzymes (aspartate transaminase, 75 IU/L [0-40 IU/L]; alkaline phosphatase, 129 IU/L [40-120 IU/L]; γ-glutamyltransferase, 99 IU/L [8-35 IU/L]), and an increased level of lactate dehydrogenase (315 IU/L [120-250 IU/L]). Dynamic computed tomography revealed an ill-defined, 3-cm lesion in the left lateral segment of the liver and multiple abdominal and mediastinal lymphadenopathies. Esophagogastroduodenoscopy revealed a 3-cm ulcerofungating mass between the antrum and the lower body of the stomach. A liver core needle biopsy identified a peripheral T-cell lymphoma, not otherwise specified, and an endoscopic biopsy of the stomach identified a diffuse large B-cell lymphoma (DLBL). A BM biopsy revealed BM involvement by DLBL with a nodular infiltration pattern, which was corroborated by positive immunohistochemical staining for CD3 and CD20. CD20-positive lymphocytes were present in nodular aggregates. CD3-positive lymphocytes were present in small lymphocytes surrounding CD20-positive lymphocytes suggesting reactive T lymphocytes. A cytogenetic study of BM revealed an apparently normal karyotype. The patient was started on the combination chemotherapy regimen including rituximab, cyclophosphamide, doxorubicin, vincristine and prednisolone (R-CHOP).  After 6 cycles of R-CHOP, the liver mass and lymphadenopathies had disappeared. However, a follow-up BM biopsy revealed BM involvement by T-cell lymphoma and DLBL. Immunohistochemical staining showed medium to large sized PAX5-positive lymphocytes with a marked interstitial infiltration pattern (Fig. 1A, B), and the cells were also CD79a-positive. Peritrabecular and interstitial infiltration of small to medium sized CD3-positive lymphocytes was also prominent (Fig. 1C, D). Rearrangements of the T-cell receptor gamma locus (TRG) and immunoglobulin heavy locus (IGH) were studied in BM (after the 6th cycle of R-CHOP), liver, and stomach (at diagnosis) specimens using the BIOMED-2 multiplex PCR protocol [6]. A 170-bp monoclonal TRG rearrangement was detected in the liver sample (Fig. 2A), while TRG in the BM had a larger 160-bp peak with a smaller 170-bp peak (Fig. 2B). IGH gene rearrangements were not detected in the stomach sample or in the BM aspirate, and the BM aspirate had a normal karyotype. After the 8th R-CHOP cycle, computed tomography and positron emission tomography findings suggested involvement of multiple lymph nodes (celiac, splenic hilar, and abdominal paraaortic lymph nodes). The patient died of pneumonia 1 yr after diagnosis.    Fig. 1  Bone marrow biopsy after 6 cycles of rituximab, cyclophosphamide, doxorubicin, vincristine and prednisolone (R-CHOP) combination chemotherapy. (A, B) Neoplastic B lymphocytes infiltrating in an interstitial pattern was immunohistochemically analyzed by ...      Fig. 2  T cell receptor gamma locus (TRG) rearrangement analyzed by using BIOMED-2 multiplex PCR. Horizontal axis represents amplicon size (base pairs) and vertical axis represents fluorescence intensity. (A) A monoclonal TRG rearrangement was detected at 170 ...    In our TRG rearrangement study, monoclonal TRG rearrangements were detected in both liver and BM samples, but the sizes of amplicons were slightly different, that is a finding that may be explained by clonal evolution [7]. We speculate that there is BM involvement on the basis of a subclone from the hepatic T-cell lymphoma. Moreover, a small peak corresponding to a 170-bp PCR product was observed in a BM sample, which suggests that the same clone present in the liver sample was also present in the BM sample. Monoclonal IGH rearrangements were not detected in the stomach or BM sample. As monoclonal IGH rearrangements are detected in approximately 80% of DLBL cases using BIOMED-2 multiplex PCR [8], the fact that rearrangement of IGH was not detected in the stomach sample is not unusual.  T- and B-cell lymphomas simultaneously developed in this patient. Moreover, a follow-up examination suggested BM involvement by both these lymphomas. To our knowledge, this is the first report of a patient with BM involvement by both T- and B-cell lymphomas. Factors contributing to the development of synchronous primary lymphomas have not been investigated, and a case with involvement of the same site by two different lymphomas has not been reported; however, primary composite lymphomas have been reported [9]. The clinical significance of BM involvement by both T- and B-cell lymphomas is unknown, although the simultaneous development of more than one histological type of lymphoma is associated with a poor prognosis [1]. The present patient died 1 yr after her diagnosis, suggesting that composite BM involvement may also be associated with a poor prognosis.

annals of laboratory medicine

The First Case Report of Composite Bone Marrow Involvement by Simultaneously Developed Peripheral T-Cell Lymphoma, Not Otherwise Specified, and Diffuse Large B-Cell Lymphoma