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Review
. 2002 Nov;55(11):868-71.
doi: 10.1136/jcp.55.11.868.

Anaplastic lymphoma kinase (ALK) protein expressing lymphoma after liver transplantation: case report and literature review

Affiliations
Review

Anaplastic lymphoma kinase (ALK) protein expressing lymphoma after liver transplantation: case report and literature review

V Costes-Martineau et al. J Clin Pathol. 2002 Nov.

Abstract

Most post transplantation lymphoproliferative disorders (PTLDs) are Epstein-Barr virus (EBV) associated B cell proliferations. We report a case of aggressive anaplastic large cell lymphoma expressing the anaplastic lymphoma kinase (ALK) protein in a 58 year old man who had previously undergone liver transplantation. A definite diagnosis was not possible on histopathological examination. Immunostaining clearly showed a predominant population of small irregular lymphocytes, admixed with large cells strongly positive for CD30, epithelial membrane antigen, and the ALK protein. Neoplastic cells were of the T/cytotoxic phenotype. In situ hybridisation with EBV encoded early RNA probes showed only a few scattered positive non-neoplastic small lymphocytes. Polymerase chain reaction analysis of immunoglobulin and T cell receptor rearrangements was negative. The NPM-ALK fusion transcript associated with the t(2;5) translocation was detected by reverse transcription polymerase chain reaction. A review of the literature revealed 76 cases of T cell PTLD, showing a broad spectrum of morphological features and clinical behaviour. Most of these cases were EBV negative (61 of 76) and occurred after renal transplantation (48 of 76). To our knowledge, this is the first case of ALK positive lymphoma occurring in the setting of organ transplantation. This observation stresses the need for accurate immunostaining for diagnosing this rare, apparently aggressive, lymphoma in immunosuppressed patients.

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Figures

Figure 1
Figure 1
(A) The lymph node had a hypocellular appearance with residual small lymphoid follicles. The capsule is shown on the left side. (B,C) Lymphoid cells were loosely dispersed in an oedematous stroma, rich in venules. (D,E) Higher magnifications showed small to medium sized lymphoid cells dispersed in a oedematous stroma, with accentuation of the cellularity around the venules. (F) Rare large cells with the features of hallmark cells (eccentrically located reniform or embryo-like nucleus and abundant amphophilic cytoplasm) were present.
Figure 2
Figure 2
(A) Immunostaining for CD30 revealed a greater number of neoplastic cells than could be appreciated on routine histological sections. (B) ALK staining was observed in both the nuclei and cytoplasm of the tumour cells.

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