Monosomy 21, a Sole Abnormality in an Elderly Man with Non-CLL-Type Monoclonal B-cell Lymphocytosis.

OBJECTIVES: Monoclonal B-cell lymphocytosis (MBL) is a light-chain restricted proliferation of mature B cells fewer than 5000 cells/µL without additional clinical or hematologic abnormalities. Sibling studies of individuals genetically susceptible to chronic lymphocytic leukemia (CLL) first identified monoclonal B cells in otherwise healthy persons, and studies show a 3% to 14% prevalence for MBL in persons over 40 years of age. Non-CLL-type MBL accounts for less than 20% of all MBL cases, and its progression is incompletely characterized. Here we present the case of an 85-year-old man with CD5-, CD19+, CD20 bright, and lambda-restricted lymphoid cells whose immunophenotypic findings are suggestive for a precursor lesion to marginal zone lymphoma (MZL). Karyotyping showed monosomy 21 without additional cytogenetic changes in three of the 35 cells examined. Monosomy 21 as a sole abnormality in CLL has been detected in just 11 cases between 1984 and 2003. As a sole abnormality in splenic and nodal marginal zone lymphoma, only three instances of monosomy 21 have been recorded on the Mitelman Database of Chromosome Aberrations and Gene Fusions in Cancer. The significance of monosomy 21 as a marker for oncogenesis remains unclear.

Effects of Bio-Impedance Sensor Placement Relative to the Arterial Sites for Capturing Hemodynamic Parameters.

Accurate measurement of the heart pulse waveform based on blood volume changes inside the arteries is crucial for reliable estimation of hemodynamic parameters such as blood pressure and cardiac output. Placement of blood volume sensors such as bio-impedance sensors close to the arterial sites is essential for the accurate measurement of the pulse waveform. The effect of sensor location relative to the wrist arteries on the pulse waveform had not been studied previously on human subjects. In this paper, we explore the effect of arterial and off-arterial placement of the bio-impedance sensor on important pulse waveform features such as pulse transit time (PTT), which is the travel time of the arterial pressure pulse between two sensors, and diastolic peak error (DPE), a measure of pulse signal sharpness. Placing the current injection and voltage sensing electrodes of a bio-impedance sensor on the radial artery provide greater accuracy for such features. We find that arterial PTT has a significantly lower standard deviation compared to off-arterial PTT indicating better signal quality. Similarly, we observe that DPE is much smaller for arterial bio-impedance which confirms our expectations. Based on these features, the location of the artery can be determined using an array of sensors placed around the artery.