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Case Reports
. 2017 Apr;30(2):186-189.
doi: 10.1080/08998280.2017.11929579.

Asian-variant intravascular large B-cell lymphoma

Affiliations
Case Reports

Asian-variant intravascular large B-cell lymphoma

Derrick W Su et al. Proc (Bayl Univ Med Cent). 2017 Apr.

Abstract

Intravascular large B-cell lymphoma (IVLBCL) is a rare and deadly malignancy involving the growth of lymphoma cells within vessel lumina of all organ types. IVLBCL is further divided into the hemophagocytic Asian variant and a classical Western variant. Both variants are difficult to diagnose by imaging, and although diagnostic criteria have been developed to guide workup, histopathological examination remains imperative. Treatment of IVLBCL remains difficult given the high mortality of the disease, but rituximab has emerged as a promising therapeutic option when combined with various cytotoxic regimens. The two main variants of IVLBCL generally manifest in their respective Asian or Western populations, and crossover between ethnicities is rare. We present the second described case of Asian-variant IVLBCL in an African American individual.

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Figures

Figure 1.
Figure 1.
Representative hematoxylin and eosin sections of atypical intravascular lymphocytes infiltrating capillaries of (a) lung, (b) thalamus, (c) esophagus, (d) bladder, (e) pancreas, and (f) psoas muscle. CD20 stain of (g) spleen and (h) bladder.
Figure 2.
Figure 2.
(a) Bone marrow, hematoxylin and eosin stain, and (b) CD68 immunohistochemical stain highlighting numerous hemophagocytic histiocytes.

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