melphalan and Polyradiculopathy

melphalan has been researched along with Polyradiculopathy* in 2 studies

Other Studies

2 other study(ies) available for melphalan and Polyradiculopathy

Article	Year
[A case of IgD plasmacytoma with unusual neurological symptoms]. Folia haematologica (Leipzig, Germany : 1928), 1977, Volume: 104, Issue:3 A disease in an IgD (lambda) plasmocytoma is described, where after therapy with Alkeran and prednisone a disappearance of all clinical and laboratory findings indicating an activity could be observed. However, there was a progressive development of a picture of encephalomyelitic and polyradicular neuritic syndrome in the female patient with all signs of a recidivous temporary intracranial hypertension which could not be cured. The aetiology of these processes could only be found by the autopsy which revealed an isolated massive infiltration of the meninges and the sheaths of the spinal cord nerves with atypical plasma cells. No signs of the tumour could be identified in other organs. Such localization of the disease, as it is described here, is the first observation of its king. Problems of clinical diagnosis and treatment are discussed. Topics: Encephalomyelitis; Female; Humans; Hypertension; Immunoglobulin D; Melphalan; Middle Aged; Neurologic Manifestations; Paralysis; Plasmacytoma; Polyradiculopathy; Prednisone	1977
[Patterns of plasmocytoma]. Schweizerische medizinische Wochenschrift, 1970, Apr-25, Volume: 100, Issue:17 Topics: Adult; Aged; Bone Marrow Examination; Bone Neoplasms; Cerebrospinal Fluid Proteins; Cyclophosphamide; Female; Fractures, Spontaneous; Humans; Male; Melphalan; Middle Aged; Multiple Myeloma; Neoplasm Metastasis; Plasma Cells; Polyradiculopathy; Radiography	1970

Article

Year

[A case of IgD plasmacytoma with unusual neurological symptoms].

Folia haematologica (Leipzig, Germany : 1928), 1977, Volume: 104, Issue:3

A disease in an IgD (lambda) plasmocytoma is described, where after therapy with Alkeran and prednisone a disappearance of all clinical and laboratory findings indicating an activity could be observed. However, there was a progressive development of a picture of encephalomyelitic and polyradicular neuritic syndrome in the female patient with all signs of a recidivous temporary intracranial hypertension which could not be cured. The aetiology of these processes could only be found by the autopsy which revealed an isolated massive infiltration of the meninges and the sheaths of the spinal cord nerves with atypical plasma cells. No signs of the tumour could be identified in other organs. Such localization of the disease, as it is described here, is the first observation of its king. Problems of clinical diagnosis and treatment are discussed.

Topics: Encephalomyelitis; Female; Humans; Hypertension; Immunoglobulin D; Melphalan; Middle Aged; Neurologic Manifestations; Paralysis; Plasmacytoma; Polyradiculopathy; Prednisone

1977

[Patterns of plasmocytoma].

Schweizerische medizinische Wochenschrift, 1970, Apr-25, Volume: 100, Issue:17

Topics: Adult; Aged; Bone Marrow Examination; Bone Neoplasms; Cerebrospinal Fluid Proteins; Cyclophosphamide; Female; Fractures, Spontaneous; Humans; Male; Melphalan; Middle Aged; Multiple Myeloma; Neoplasm Metastasis; Plasma Cells; Polyradiculopathy; Radiography

1970