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Showing 1 to 12 of 60 entries
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Polyclonal Bence Jones Proteinuria Associated with Reactive Plasmacytosis.

Leukemia & lymphoma

Tarlton SW, Ariad S, Lewis D, Rowe P, Mendelow BV.
PMID: 27457302
Leuk Lymphoma. 1990;3(2):151-6. doi: 10.3109/10428199009050990.

A 43 year old black male patient presented with progressive respiratory symptoms, fever and malaise of short duration accompanied by mild epistaxis. Physical examination revealed generalised lymphadenopathy and hepatosplenomegaly. Peripheral blood examination showed a striking plasmacytosis. Further investigation revealed...

Prognostic factors associated with solitary plasmacytoma.

OncoTargets and therapy

Guo SQ, Zhang L, Wang YF, Sun BC, Zhang LY, Zhang J, Wang G, Zhang YZ.
PMID: 24259986
Onco Targets Ther. 2013 Nov 14;6:1659-66. doi: 10.2147/OTT.S53248. eCollection 2013.

Solitary plasmacytoma (SP) is a rare tumor with low incidence. The aim of this study was to investigate the clinical features, treatment strategies, and relative prognostic factors of 66 patients with SP. These patients made up 10.25% of the...

Disseminated plasma cell myeloma presenting as massive pleural effusion.

European clinical respiratory journal

Babu KA, Sundararajan L, Prabu P, Parameswaran A.
PMID: 26664659
Eur Clin Respir J. 2015 Nov 24;2. doi: 10.3402/ecrj.v2.27028. eCollection 2015.

Plasma cell myeloma (PCM) is a hematologic malignancy of plasma cell origin and usually associated with the presence of lytic bone lesions. Pleural effusions are rarely associated with PCM and most often signify a concurrent disease process. Malignant myelomatous...

The Nitrogen-Distribution in Bence-Jones' Protein, with a Note upon a New Colorimetric Method for Tryptophan-Estimation in Protein.

The Biochemical journal

Lüscher E.
PMID: 16743116
Biochem J. 1922;16(5):556-63. doi: 10.1042/bj0160556.

No abstract available.

Immunological differences of crystalline Bence-Jones proteins.

The Biochemical journal

Hektoen L, Welker WH.
PMID: 16747184
Biochem J. 1940 Apr;34(4):487-9. doi: 10.1042/bj0340487.

No abstract available.

An analysis of Bence-Jones protein.

The Biochemical journal

Devine J.
PMID: 16747340
Biochem J. 1941 Mar;35(3):433-45. doi: 10.1042/bj0350433.

No abstract available.

Markers of tumor burden : an overview.

Methods in molecular medicine

Roulston JE.
PMID: 21340761
Methods Mol Med. 2001;39:109-20. doi: 10.1385/1-59259-071-3:109.

Since ancient times, cancer has been known to humankind. The ancient Greeks and Romans have left us with writings in which various treatment options are discussed (1). Disease processes and causes were not well understood, however; the humoral pathology...

CLASSIFICATION OF MYELOMA PROTEINS, BENCE JONES PROTEINS, AND MACROGLOBULINS INTO TWO GROUPS ON THE BASIS OF COMMON ANTIGENIC CHARACTERS.

The Journal of experimental medicine

Mannik M, Kunkel HG.
PMID: 19867218
J Exp Med. 1962 Nov 30;116(6):859-77. doi: 10.1084/jem.116.6.859.

Antisera to normal 7S gamma-globulin and to Bence Jones proteins permit the grouping of myeloma proteins (gamma and beta 2A types), Bence Jones proteins, and the Waldenström type macroglobulins into two fundamental antigenic groups. The antigenic determinants responsible for...

Multiple myeloma presenting as an intracranial plasmacytoma: a case report.

Cases journal

Terada T.
PMID: 20062687
Cases J. 2009 Nov 30;2:9110. doi: 10.1186/1757-1626-2-9110.

Multiple myeloma presenting as an intracranial tumor (plasmacytoma) is very rare. An 81-year-old woman was admitted to our hospital because of gait disturbance. A blood laboratory test revealed a mildly increased lactate dehydrogenase (236 IU/L) and glucose (121 mg/dl)....

A Case of Light Chain Deposition Disease (LCDD) in a Young Patient.

Indian journal of clinical biochemistry : IJCB

Mahto M, Mohapatra S, Sumitra G, Kaushik S, Mishra TK, Saxena A.
PMID: 23024482
Indian J Clin Biochem. 2011 Oct;26(4):420-2. doi: 10.1007/s12291-010-0105-z. Epub 2011 Jan 11.

Light chain disease is a variant of multiple myeloma in which the malignant population of marrow cells produces free monoclonal light chains but no heavy chain or complete immunoglobulin. The monoclonal light chains are small enough to be freely...

Late-onset Familial Amyloidotic Polyneuropathy with Bence Jones Proteinuria and Cardiomyopathy.

Journal of neurosciences in rural practice

García de León SC, González AH, Alonso CO, Lobo LB.
PMID: 28694632
J Neurosci Rural Pract. 2017 Jul-Sep;8(3):448-450. doi: 10.4103/jnrp.jnrp_498_16.

Familial amyloidotic polyneuropathy is a genetically determined disease characterized by deposition of an anomalous transthyretin. A high index of suspicion is needed for this multisymptomatic and lethal disease to be diagnosed. The patient was a 70-year-old male examined due...

Light Chain Deposition Disease Diagnosed Using Computed Tomography-Guided Kidney Biopsy.

Cureus

Shimamura Y, Ogawa Y, Takizawa H, Hayashi T, Sakurai Y.
PMID: 34159010
Cureus. 2021 May 18;13(5):e15102. doi: 10.7759/cureus.15102.

Light chain deposition disease (LCDD) is characterized by the deposition of monoclonal immunoglobulin light chains in the kidney, which can cause end-stage kidney disease if not treated. While kidney biopsy is required for definitive diagnosis, choosing an appropriate biopsy...

Showing 1 to 12 of 60 entries