Malignant lymphoma with a high content of epithelioid histiocytes: Report of a T-cell variant of so-called lennert lymphoma and review of the literature

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Abstract
The present report describes the first case of well‐differentiated nodular lyraph‐ocytic lymphoma evolving into Lennert lymphoma of T‐cell origin. A 58‐year‐old white female developed malignant lymphoma, well‐differentiated, lympho‐cytic type, nodular, with focal bone marrow involvement (stage IV) in May 1975. She received 16 cycles of cyclophosphamide and prednisone combination chemotherapy which was completed in October 1976. A complete remission was achieved. In December 1976, she relapsed and was treated with cyclophosphamide, vincristine, bleomycin, and prednisone until May 1977. Lympha‐denopathy decreased until August 1978, but then increased again. Biopsy of an axillary lymph node was interpreted as Lennert lymphoma. She received methotrexate, cyclophosphanide, vincristine, adriamycin, and prednisone beginning in September 1978. When last seen in November 1979, she was in partial remission. Lymphoid cells obtained from lymph node which was involved with Lennert lymphoma consisted of 93% standard E‐rosettes and 83% gravity E‐rosettes. Cytoplasmic immunoglobulin on frozen sections was negative, but acid phosphatase (ACP) and alpha‐naphthyl acetate esterase reactions were strongly positive. These findings support a T‐cell proliferation in Lennert lymphoma. A review of the literature reveals only four cases of Lennert lymphoma of T‐cell origin.