A 57-year-old male, known case of chronic inflammatory demyelinating polyneuropathy with POEMS Syndrome (Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes) presented with generalized weakness. Peripheral blood smear findings were within normal limits. Bone marrow smears showed mild increase in lymphoid cells including many lymphoplasmacytoid cells and increased in plasma cells. Bone marrow biopsy revealed hypercellular marrow spaces with small and large lymphoid aggregates interstitially and in paratrabecular location along with few plasma cell clusters. On immunohistochemistry, these lymphoid aggregates were CD20 positive with lambda restriction, and CD 56, CD5 and CD10 negative [ ABSTRACT Waldenström macroglobulinemia (WM) is a rare indolent variant of non-Hodgkin's lymphoma characterised by lymphoplasmacytic infiltration of bone marrow (BM) associated with a serum IgM paraprotein. The WHO classification states that the neoplastic cells of WM usually are positive for monotypic surface immunoglobulin light chain, IgM, CD19, and CD20 and are negative for CD5, CD10, and CD23. Serum monoclonal protein detection by serum protein electrophoresis and bone marrow aspirate and biopsy are required for WM diagnosis, monitoring and response assessment. Pathologist must dissuade themselves from making a hasty decision on calling a complete response in WM when neoplastic B cell component is absent. Evaluation of clonality of any residual plasma cells must be done in all cases of WM to evaluate the presence and extent of residual or persistent disease. Role of additional therapy targeted at these residual plasma cells in WM can be evaluated as tools for achieving complete remission. Herein, we present a case of WM with residual monotypic plasmacytosis in BM, without B lymphocytes after therapy.