MLT 106 exam 2 | Questions with 100% Correct
Answers | Verified | Latest Update 2026
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Terms in this set (83)
CASUED BY THE DEPOSITION OF TYPE III HYPERSENSITIVITY - IMMUNE COMPLEX
IMMUNE COMPLEXES IN BLOOD REACTIONS
VESSEL WALLS AND TISSUES
ALLERGIC VACULITIS AND EXAMPLES OF TYPE III HYPERSENSITIVITY
ERYTHEMA NODOSUM
PULMONARY REACTIONS SUCH AS
HYPERSESITIVITY PNEUMONITIS
(FARMERS LUNG)
SERUM SICKNESS
AUTOMIMMUNE SUCH AS
SYSTEMIC LUPUS AND
ERYTHEMATOUS
CONSISTS OF ONE OR MORE POLYCLONAL GAMMOPATHIES
HEAVY-CHAIN CLASSES AND BOTH
LIGHT-CHAIN TYPES
OFTEN SEEN IN CHRONIC POLYCLONAL GAMMOPATHIES
INFECTIONS SUCH AS:
CHRONIC LIVER DISEASE
RHEUMATOID CONNECTIVE TISSUE
AUTOIMMUNE DISEASE
, AN INCREASE IN MORE THAN ONE POLYCLONAL GAMMOPATHIES
IMMUNOGLOBULIN, AND
INVOLVES SEVERAL CLONES OF
PLASMA CELLS
REPRESENTS THE PRESENCE OF A MONOCLONAL GAMMOPATHY OF
MONOCLONAL PROTEIN IN UNDETERMINES SIGNIFICANCE (MGUS)
PATIENTS WITH NO FEATURES OF
MM OR RELATED MALIGNANT
DISORDERS
B CELL DISORDER WALDENSTROM'S PRIMARY
CHARACTERIZED BY THE MACCROGLOBULINEMIA (WM)
INFILTRATION OF
LYMPHOPLASMYTIC CELLS TO THE
BONE MARROW AND THE
PRESENCE OF AN IGM
MONOCLONAL GAMMOPATHY
MOST CONSISTENT THE INCESSANT SYNTHESIS OF A
IMMUNOLOGIC FEATURE OF MM DYSFUNCTIONAL SINGLE MONOCLONAL
PROTEIN OR IMMUNOGLOBULIN CHAINS OF
FRAGMENTS, W/ CONCURRENT SUPPRESSION
OF THE SYNTHESIS OF NORMAL FUNCTIONAL
ANTIBODIES
COMMON FINDING ON ROULEAUX
PERIPHERAL BLOOD SMEARS OF
MM
DIAGNOSITC MARKER OF PROTEINURIA
MULTIPLE MYELOMA >50% EXCRETING ABNORMAL AMOUNTS OF
BENCE JONES PROTEINS (BJP)
Answers | Verified | Latest Update 2026
Save
Terms in this set (83)
CASUED BY THE DEPOSITION OF TYPE III HYPERSENSITIVITY - IMMUNE COMPLEX
IMMUNE COMPLEXES IN BLOOD REACTIONS
VESSEL WALLS AND TISSUES
ALLERGIC VACULITIS AND EXAMPLES OF TYPE III HYPERSENSITIVITY
ERYTHEMA NODOSUM
PULMONARY REACTIONS SUCH AS
HYPERSESITIVITY PNEUMONITIS
(FARMERS LUNG)
SERUM SICKNESS
AUTOMIMMUNE SUCH AS
SYSTEMIC LUPUS AND
ERYTHEMATOUS
CONSISTS OF ONE OR MORE POLYCLONAL GAMMOPATHIES
HEAVY-CHAIN CLASSES AND BOTH
LIGHT-CHAIN TYPES
OFTEN SEEN IN CHRONIC POLYCLONAL GAMMOPATHIES
INFECTIONS SUCH AS:
CHRONIC LIVER DISEASE
RHEUMATOID CONNECTIVE TISSUE
AUTOIMMUNE DISEASE
, AN INCREASE IN MORE THAN ONE POLYCLONAL GAMMOPATHIES
IMMUNOGLOBULIN, AND
INVOLVES SEVERAL CLONES OF
PLASMA CELLS
REPRESENTS THE PRESENCE OF A MONOCLONAL GAMMOPATHY OF
MONOCLONAL PROTEIN IN UNDETERMINES SIGNIFICANCE (MGUS)
PATIENTS WITH NO FEATURES OF
MM OR RELATED MALIGNANT
DISORDERS
B CELL DISORDER WALDENSTROM'S PRIMARY
CHARACTERIZED BY THE MACCROGLOBULINEMIA (WM)
INFILTRATION OF
LYMPHOPLASMYTIC CELLS TO THE
BONE MARROW AND THE
PRESENCE OF AN IGM
MONOCLONAL GAMMOPATHY
MOST CONSISTENT THE INCESSANT SYNTHESIS OF A
IMMUNOLOGIC FEATURE OF MM DYSFUNCTIONAL SINGLE MONOCLONAL
PROTEIN OR IMMUNOGLOBULIN CHAINS OF
FRAGMENTS, W/ CONCURRENT SUPPRESSION
OF THE SYNTHESIS OF NORMAL FUNCTIONAL
ANTIBODIES
COMMON FINDING ON ROULEAUX
PERIPHERAL BLOOD SMEARS OF
MM
DIAGNOSITC MARKER OF PROTEINURIA
MULTIPLE MYELOMA >50% EXCRETING ABNORMAL AMOUNTS OF
BENCE JONES PROTEINS (BJP)
