scholarly journals A Methodological Evaluation of Volumetric Measurement Techniques including Three-Dimensional Imaging in Breast Surgery

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
H. Hoeffelin ◽  
D. Jacquemin ◽  
V. Defaweux ◽  
J L. Nizet

Breast surgery currently remains very subjective and each intervention depends on the ability and experience of the operator. To date, no objective measurement of this anatomical region can codify surgery. In this light, we wanted to compare and validate a new technique for 3D scanning (LifeViz 3D) and its clinical application. We tested the use of the 3D LifeViz system (Quantificare) to perform volumetric calculations in various settings (in situ in cadaveric dissection, of control prostheses, and in clinical patients) and we compared this system to other techniques (CT scanning and Archimedes’ principle) under the same conditions. We were able to identify the benefits (feasibility, safety, portability, and low patient stress) and limitations (underestimation of the in situ volume, subjectivity of contouring, and patient selection) of the LifeViz 3D system, concluding that the results are comparable with other measurement techniques. The prospects of this technology seem promising in numerous applications in clinical practice to limit the subjectivity of breast surgery.

2009 ◽  
Vol 67 (2) ◽  
pp. 215-230 ◽  
Author(s):  
Masahiko Furusawa ◽  
Kazuo Amakasu

Abstract Furusawa, M., and Amakusu, K. 2010. The analysis of echotrace obtained by a split-beam echosounder to observe the tilt-angle dependence of fish target strength in situ. – ICES Journal of Marine Science, 67: 215–230. A method of echotrace analysis (ETA), proposed by Furusawa and Miyanohana in 1988 utilizes successive echodata from an individual fish to obtain the target-strength (TS) pattern as a function of fish tilt angle and behaviour. The method can be applied to data from an echosounder with any beam configuration, single-, dual-, and split-beam. However, the method has not been applied rigorously to split-beam sounder data, which provide most comprehensive and accurate information. The aim of this work is to establish an accurate and practical ETA method for split-beam echosounder data. Although the basic theory had already been developed, some theoretical and practical enhancement was needed; smoothing of an echotrack by linear and quadratic regressions, correction for transducer motion, and comparison of an observed TS pattern with a prolate-spheroid theoretical model. The analysis starts from careful selection of a single echotrace on an echogram and ends with a composite display of results including a three-dimensional fish track and a TS pattern as a function of the tilt angle of the fish. The method was applied to typical echotrace examples, and utility and practicality were confirmed. A means of increasing the number of applicable echotraces is discussed.


Author(s):  
W. G. Johnston ◽  
J. H. Rosolowski ◽  
J. H. Rosolowski ◽  
T. Lauritzen

The development of rapid and reliable techniques for measuring void swelling produced in metals by heavy ion bombardment is an important part of our investigation of possible alloys suitable for fast reactor structural materials. Conventional transmission electron microscopy (TEM) measurements of void numbers and sizes with sterescopy has permitted us to observe up to about 50% swelling without evidence of saturation for certain alloys bombarded with 5 MeV nickelions. Measurement of swelling beyond this was not feasible with standard TEM techniques since void size had become comparable to the foil thickness (Fig. 1). In the case of high voltage electron microscopy where greater foil thicknesses can be used, the overlapping of many voids limited measurement. There are additional disadvantages and limitations of TEM measurement techniques. Throughout the range of swelling, inhomogenity of void distributions hampers the selection of representative areas (Fig. 2).


Author(s):  
J. P. Revel

Movement of individual cells or of cell sheets and complex patterns of folding play a prominent role in the early developmental stages of the embryo. Our understanding of these processes is based on three- dimensional reconstructions laboriously prepared from serial sections, and from autoradiographic and other studies. Many concepts have also evolved from extrapolation of investigations of cell movement carried out in vitro. The scanning electron microscope now allows us to examine some of these events in situ. It is possible to prepare dissections of embryos and even of tissues of adult animals which reveal existing relationships between various structures more readily than used to be possible vithout an SEM.


Author(s):  
D. Reis ◽  
B. Vian ◽  
J. C. Roland

Wall morphogenesis in higher plants is a problem still open to controversy. Until now the possibility of a transmembrane control and the involvement of microtubules were mostly envisaged. Self-assembly processes have been observed in the case of walls of Chlamydomonas and bacteria. Spontaneous gelling interactions between xanthan and galactomannan from Ceratonia have been analyzed very recently. The present work provides indications that some processes of spontaneous aggregation could occur in higher plants during the formation and expansion of cell wall.Observations were performed on hypocotyl of mung bean (Phaseolus aureus) for which growth characteristics and wall composition have been previously defined.In situ, the walls of actively growing cells (primary walls) show an ordered three-dimensional organization (fig. 1). The wall is typically polylamellate with multifibrillar layers alternately transverse and longitudinal. Between these layers intermediate strata exist in which the orientation of microfibrils progressively rotates. Thus a progressive change in the morphogenetic activity occurs.


Author(s):  
S. Naka ◽  
R. Penelle ◽  
R. Valle

The in situ experimentation technique in HVEM seems to be particularly suitable to clarify the processes involved in recrystallization. The material under investigation was unidirectionally cold-rolled titanium of commercial purity. The problem was approached in two different ways. The three-dimensional analysis of textures was used to describe the texture evolution during the primary recrystallization. Observations of bulk-annealed specimens or thin foils annealed in the microscope were also made in order to provide information concerning the mechanisms involved in the formation of new grains. In contrast to the already published work on titanium, this investigation takes into consideration different values of the cold-work ratio, the temperature and the annealing time.Two different models are commonly used to explain the recrystallization textures i.e. the selective grain growth model (Beck) or the oriented nucleation model (Burgers). The three-dimensional analysis of both the rolling and recrystallization textures was performed to identify the mechanismsl involved in the recrystallization of titanium.


Author(s):  
W.F. Marshall ◽  
A.F. Dernburg ◽  
B. Harmon ◽  
J.W. Sedat

Interactions between chromatin and nuclear envelope (NE) have been implicated in chromatin condensation, gene regulation, nuclear reassembly, and organization of chromosomes within the nucleus. To further investigate the physiological role played by such interactions, it will be necessary to determine which loci specifically interact with the nuclear envelope. This will not only facilitate identification of the molecular determinants of this interaction, but will also allow manipulation of the pattern of chromatin-NE interactions to probe possible functions. We have developed a microscopic approach to detect and map chromatin-NE interactions inside intact cells.Fluorescence in situ hybridization (FISH) is used to localize specific chromosomal regions within the nucleus of Drosophila embryos and anti-lamin immunofluorescence is used to detect the nuclear envelope. Widefield deconvolution microscopy is then used to obtain a three-dimensional image of the sample (Fig. 1). The nuclear surface is represented by a surface-harmonic expansion (Fig 2). A statistical test for association of the FISH spot with the surface is then performed.


Author(s):  
Greg V. Martin ◽  
Ann L. Hubbard

The microtubule (MT) cytoskeleton is necessary for many of the polarized functions of hepatocytes. Among the functions dependent on the MT-based cytoskeleton are polarized secretion of proteins, delivery of endocytosed material to lysosomes, and transcytosis of integral plasma membrane (PM) proteins. Although microtubules have been shown to be crucial to the establishment and maintenance of functional and structural polarization in the hepatocyte, little is known about the architecture of the hepatocyte MT cytoskeleton in vivo, particularly with regard to its relationship to PM domains and membranous organelles. Using an in situ extraction technique that preserves both microtubules and cellular membranes, we have developed a protocol for immunofluorescent co-localization of cytoskeletal elements and integral membrane proteins within 20 µm cryosections of fixed rat liver. Computer-aided 3D reconstruction of multi-spectral confocal microscope images was used to visualize the spatial relationships among the MT cytoskeleton, PM domains and intracellular organelles.


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