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Spontaneous Remission Of Leukemic Lymphoproliferative Disease

Han & Sokal, 1971Lymphoma

Cancer 27(3): March 1971; 586-595

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Abstract

Spontaneous remission was observed in 4 of approximately 400 patients with chronic lymphocytic leukemia or malignant lymphoma with leukemic manifestations. Findings prior to spontaneous remission in these patients included generalized lymphadenopathy and splenomegaly. In one patient, the remission followed an acute (presumably viral) infection. Relapse of disease after spontaneous remission, characterized by lymphadenopathy and tissue infiltration only, without lymphocytosis or bone marrow involvement, was seen in one patient with chronic lymphocytic leukemia and one with leukemic lymphosarcoma. Seven well-documented cases of spontaneous remission in leukemic lymphoproliferative disease were found in a survey of the literature. The patterns of normalization of the peripheral blood count seen in the pooled cases included both rapid declines of lymphocyte counts, consistent with active destruction of leukemic cells, and very slow decreases which suggested that the mechanism of remission was cessation of production of leukemic cells, with their subsequent disappearance at a rate consistent with their known long life span. Only one death from lymphoproliferative disease is recorded among these pooled cases.

Case Details

Personal Characteristics

H. B., a 69-year-old woman

Clinical Characteristics

Developed weakness and easy fatigability, experienced fullness in the left upper quadrant of her abdomen, moderate generalized lymphadenopathy, spleen was palpable 2 centimeters below the left costal margin, liver was palpable 3 centimeters below the right costal margin, hemoglobin was 11.2 gm/100 ml, platelet count 126,000/mm3, white blood cell count 40,000/mm3, with 87% lymphocytes, bone marrow aspirate showed infiltration with “a great number of lymphocytes,” with relative depression of other elements; megakaryocytes were normal

Remission Characteristics

Excellent partial remission, characterized by disappearance of lymphadenopathy and hepatosplenomegaly, rise in hemoglobin and significant fall in lymphocyte count, total white blood cell count fell to normal levels, lymphadenopathy and hepatosplenomegaly had regressed markedly, hemoglobin was 12.8 gm/100 ml, platelet count 280,000/mm3, white blood cell count 9,943/mm3 with 67% lymphocytes, normal lymphocyte count was reached in september 1966

Treatment & Mechanisms

Proposed Remission Mechanisms

Not discussed

Clinical Treatment

Treated with 2 courses of chlorambucil (first course, november 1956 to january 1957; second course, december 1959 to january 1960), given 2 units of blood and treated symptomatically

Additional Notes

Despite complete peripheral remission, the last bone marrow aspiration showed evidence of residual disease