An unusual case of multiple myeloma with extramedullary dissemination and co-existing systemic non-necrotic granulomas is described. Immunoperoxidase staining revealed that both lymph node and bone marrow infiltrating plasma cells contained the same IgG-lambda type paraprotein, and that the granuloma epithelioid histiocytes contained intracytoplasmic lysozyme. As there was no evidence of either systemic infection or sarcoidosis, the non-necrotic granulomas may represent the host's response to the myeloma, not unlike the reaction observed in Hodgkin's disease or solid tumours. A causal association cannot, however, be entirely excluded
Cutaneous manifestations associated with myelodysplastic syndromes (MDS) are uncommon and can occur ...
Bone marrow sarcoidosis is extremely rare. The association between sarcoidosis and lymphoproliferati...
Sarcoidosis is a systemic granulomatous disease in which medullary involvement is a rare extrapulmon...
The association of sarcoidosis with multiple myeloma is not well known. Including this case report, ...
The existence of a sarcoidosis-lymphoma syndrome has been previously proposed since the relation bet...
Some reports correlate the administration of all forms of interferon with the development or exacerb...
ULTIPLE myeloma is a disorder in which malignant plasma cells accumulate in the bone marrow and prod...
Abstract: We report a case of a woman, who initially presented with an non-secreting multiple myelom...
Context The sarcoidosis is an idiopathic multisystem inflammatory disease characterized by the prese...
We report on a rare case of multiple myeloma with atypically large cells containing a great amount o...
The development of noncaseating granulomas in a patient with underlying malignancy and no symptoms o...
multiple myeloma to respond to antigen challenge is well recognized. Response to antigen involves an...
A rare variant of multiple mieloma, non-secretory multiple myeloma (NSM), is reported. Diagnosis of ...
Systemic mastocytosis (SM) is a disease characterized by a clonal infiltration of mast cells affecti...
Multiple myeloma is the third most common form of haematological malignancy after non-Hodgkin’s lym-...
Cutaneous manifestations associated with myelodysplastic syndromes (MDS) are uncommon and can occur ...
Bone marrow sarcoidosis is extremely rare. The association between sarcoidosis and lymphoproliferati...
Sarcoidosis is a systemic granulomatous disease in which medullary involvement is a rare extrapulmon...
The association of sarcoidosis with multiple myeloma is not well known. Including this case report, ...
The existence of a sarcoidosis-lymphoma syndrome has been previously proposed since the relation bet...
Some reports correlate the administration of all forms of interferon with the development or exacerb...
ULTIPLE myeloma is a disorder in which malignant plasma cells accumulate in the bone marrow and prod...
Abstract: We report a case of a woman, who initially presented with an non-secreting multiple myelom...
Context The sarcoidosis is an idiopathic multisystem inflammatory disease characterized by the prese...
We report on a rare case of multiple myeloma with atypically large cells containing a great amount o...
The development of noncaseating granulomas in a patient with underlying malignancy and no symptoms o...
multiple myeloma to respond to antigen challenge is well recognized. Response to antigen involves an...
A rare variant of multiple mieloma, non-secretory multiple myeloma (NSM), is reported. Diagnosis of ...
Systemic mastocytosis (SM) is a disease characterized by a clonal infiltration of mast cells affecti...
Multiple myeloma is the third most common form of haematological malignancy after non-Hodgkin’s lym-...
Cutaneous manifestations associated with myelodysplastic syndromes (MDS) are uncommon and can occur ...
Bone marrow sarcoidosis is extremely rare. The association between sarcoidosis and lymphoproliferati...
Sarcoidosis is a systemic granulomatous disease in which medullary involvement is a rare extrapulmon...