Abstract |
A study of 14 personal patients and 16 others in the literature shows that (1) IgD myelomatosis often presents at a significantly younger age than other forms of myelomatosis, and (2) during life extraosseous tumour can be detected in about two-thirds of these patients.The IgD form represents 1.5% of myelomatosis and shows an increased incidence of osteolytic lesions, hypercalcaemia, and renal failure, together with heavy Bence Jones proteinuria (90% type L).Like only Bence Jones myelomatosis, the IgD form seems to behave clinically in a more vicious manner.
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Authors | J R Hobbs, A A Corbett |
Journal | British medical journal
(Br Med J)
Vol. 1
Issue 5641
Pg. 412-4
(Feb 15 1969)
ISSN: 0007-1447 [Print] England |
PMID | 4179168
(Publication Type: Journal Article)
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Chemical References |
- gamma-Globulins
- Bence Jones Protein
|
Topics |
- Adult
- Age Factors
- Aged
- Bence Jones Protein
(urine)
- Blood Protein Disorders
(complications)
- Bone Resorption
(etiology)
- Female
- Humans
- Hypercalcemia
(etiology)
- Kidney Failure, Chronic
(etiology)
- Male
- Middle Aged
- Multiple Myeloma
(complications)
- Neoplasm Metastasis
- Proteinuria
(complications)
- gamma-Globulins
(analysis)
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