Infectious mononucleosis lymphoadenitis showing histologic findings indistinguishable from toxoplasma lymphadenitis. A report of three cases

• Published in: Pathology, research and practice research and practice, 2010-06, Vol.206 (6), p.361-364
• Main Authors: Kojima, Masaru, Kashimura, Makoto, Itoh, Hideaki, Noro, Masahiro, Matsuda, Hazuki, Tsukamoto, Norihumi, Akikusa, Bunshiro, Masawa, Nobuhide, Morita, Yukio
• Format: Article
• Language: English
• Subjects: Adult; Antibodies, Viral - blood; Antigens, Viral - immunology; Clinical findings; Diagnosis, Differential; DNA, Protozoan - analysis; DNA, Protozoan - isolation & purification; Female; Humans; Immunohistochemistry; In Situ Hybridization; Infectious mononucleosis; Infectious Mononucleosis - blood; Infectious Mononucleosis - pathology; Lymph node/toxoplasmic lymphadenitis; Lymphadenitis - blood; Lymphadenitis - microbiology; Lymphadenitis - pathology; Male; Polymerase Chain Reaction; RNA, Viral - analysis; RNA, Viral - isolation & purification; Toxoplasmosis - pathology; Young Adult
• ISSN: 0344-0338; 1618-0631
• DOI: 10.1016/j.prp.2009.12.010

Lymph node lesions in infectious mononucleosis (IM) show a marked histologic diversity. We report here three cases of IM lymphadenitis with histologic findings indistinguishable from those of toxoplasmic lymphadenitis. The histologic findings of the three cases presented here showed a histologic triad of toxoplasmic lymphadenitis, including (i) numerous lymphoid follicles with hyperplastic germinal centers; (ii) small clusters or single epithelioid histiocytes; and (iii) multiple foci of monocytoid B-cells. Moreover, all three lesions contained isolated or small clusters of epithelioid histiocytes within the hyperplastic germinal centers and the periphery of lymphoid follicles, which are the most specific histologic findings of toxoplasmic lymphadenitis. However, serologic findings confirmed EBV infection in all three cases. On in situ hybridization, numerous Epstein-Barr virus (EBV)-encoded small RNA (EBER)-positive cells were demonstrated in the germinal center, as well as in interfolicular areas in all three cases. Toxoplasmosis gondii infection was excluded in at least one case, based on serologic findings. Polymerase chain reaction analysis also demonstrated that there was no T. gondii DNA in the remaining two cases. Two of our three cases showed atypical clinical presentations, including an absence of atypical lymphocytosis in peripheral blood in two cases, age more than 30 years, and an absence of systemic symptoms in one case. It appears that previous descriptions emphasize the differential diagnostic problems between IM lymphadenitis and malignant lymphomas. However, from a therapeutic perspective, it is important to discriminate IM lymphadenitis from toxoplasmic lymphadenitis particularly in patients showing atypical clinical features.