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LETTER TO EDITOR
Year : 2010  |  Volume : 47  |  Issue : 1  |  Page : 70-72
 

T-cell / histiocyte-rich B cell lymphoma mimicking Hodgkin's lymphoma


Department of Pathology, Cancer Institute (WIA), Chennai, India

Date of Web Publication12-Jan-2010

Correspondence Address:
U Majhi
Department of Pathology, Cancer Institute (WIA), Chennai
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0019-509X.58864

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How to cite this article:
Majhi U, Shirley S, Murhekar K M. T-cell / histiocyte-rich B cell lymphoma mimicking Hodgkin's lymphoma. Indian J Cancer 2010;47:70-2

How to cite this URL:
Majhi U, Shirley S, Murhekar K M. T-cell / histiocyte-rich B cell lymphoma mimicking Hodgkin's lymphoma. Indian J Cancer [serial online] 2010 [cited 2020 Nov 28];47:70-2. Available from: https://www.indianjcancer.com/text.asp?2010/47/1/70/58864


Sir,

T-cell / Histiocyte-rich large B-cell lymphoma (THRBCL) is characterized by a limited number of scattered, large, atypical B cells, embedded in a background of abundant T cells and frequently histiocytes. [1] THRBCL has a histological similarity between nodular lymphocyte predominant Hodgkin's lymphoma (NLPHL) and classical Hodgkin's lymphoma (cHL). [2] THRBCL usually presents in a more advanced stage, with involvement of liver, spleen, and bone marrow in greater frequency. [1],[2] We report nine cases of THRBCL diagnosed over a period of three years.

The cases were with age between 17 and 57 years, and eight were males. All presented with multiple cervical, axillary, and inguinal lymphadenopathy with hepatosplenomagaly. They had "B" symptoms and raised LDH levels. One case also had mediastinal lymphadenopathy. Six cases had advanced stage disease at presentation (three had bone marrow involvement, five had lung and / or pleural involvement). Five patients each had the international prognostic index (IPI) of 4 - 5 (high risk) and 3 (high intermediate) respectively, while one had IPI of 2 (low-intermediate), Median disease free survival after the start of treatment was 304 days (range: 30 - 870).

Immunohistochemical studies on lymph node biopsy specimens revealed a strong positive reaction for CD20 [Figure 1] and CD79a in all the cases, with 50 - 100% tumor cells showing a positive reaction. All patients were negative for CD15 [Table 1], while seven were positive for CD30 [Figure 2]. Three patients were positive for EBV and Bcl-2, while two were positive for Vimentin and EMA [Table 1]. The tumor cells showed CD 45 positivity. However, CD-45 positivity was difficult to evaluate, due to the positivity of the surrounding reactive lymphoid cells. The reactive cells were abundant and showed positivity for CD3 and CD45-RO. No rosette formation was seen around tumor cells with CD57. CD68 revealed a large number of histiocytes. A spherical meshwork of follicular dendritic cells was not seen with CD35.

Tumor cells of THRBCL always show positivity to CD45 and CD20 and usually to CD79α, and negative reaction to CD15, CD30, EBV, and Vimentin. [3],[4],[5] In our case-series, seven cases showed positivity for CD30 (CD30 positive giant cells had RS cell-like morphology), of which three were positive for EBV and two for Vimentin, suggesting a probable association with cHL-like phenotype. However, CD45 positivity and CD15 negativity in all cases argues against the diagnosis of cHL. Neoplastic cells in two cases co-expressed EMA and CD30, showing a closer association with NLPHL. [4],[5] CD57 positive rosettes around neoplastic cells in the background is characteristic of NLPHL. Absence of CD57 + rosettes in all the cases argues against the diagnosis of NLPHL. [2]

In conclusion, a small percentage of tumor cells of THRBCL showing features closely resembling classic Hodgkin's lymphoma as well as NLPHL probably suggest a biological overlap or "gray zone" between these entities. As the clinical behavior, management, and prognosis of THRBCL is different from other lymphoid malignancies, a detailed morphological and immunophenotypical analysis is essential, to distinguish it from NLPHL and c-HL.

 
  References Top

1.De Wolf-Peeters C, Delabie J, Campo E, Jaffe ES, Delsol G. T cell/histiocyte-rich B cell lymphoma. In: Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, et al, editors. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, Fourth edition, IARC WHO Classification of Tumours, No 2, WHO, Geneva: p. 238-9.  Back to cited text no. 1      
2.Boudová L, Torlakovic E, Delabie J, Reimer P, Pfistner B, Wiedenmann S, et al. Nodular lymphocyte-predominant Hodgkin's lymphoma with nodules resembling Tcell/histiocyte rich B-cell lymphoma:differential diagnosis between nodular lymphocyte predominant Hodgkin's lymphoma and T-cell/histiocyte-rich B-cell lymphoma. Blood 2003;102:3753-8.   Back to cited text no. 2      
3.Rüdiger T, Ott G, Ott MM, Müller-Deubert SM, Müller-Hermelink HK. Differential diagnosis between classic hodgkin's lymphoma, T-Cell-rich B-cell lymphoma, and paragranuloma by paraffin immunohistochemistry. Am J Surg Pathol 1998;22:1184-91.  Back to cited text no. 3      
4.Fraga M, Sánchez-Verde L, Forteza J, García-Rivero A, Piris MA. T-cell /histiocyte-rich large B-cell lymphoma is a disseminated aggressive neoplasm: differential diagnosis from Hodgkin's lymphoma. Histopathology 2002;41:216-29.  Back to cited text no. 4      
5.Abramson JS. T-cell/histiocyte-rich B-cell lymphoma: biology, diagnosis, and management. Oncologist 2006;11:384-92.  Back to cited text no. 5      


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