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Biomedical subjects

M Voge

Publications and source records attributed to M Voge.

At least 19 recordsLinked to original sources

Enterobiasis: a histopathological study of 259 patients.

Enterobius worms or their eggs, or both, are present in preserved tissue sections or tissue specimens of 259 patients whose medical records are on file at the Armed Forces Institute of Pathology, Washington D.C., U.S.A. The most common site of infection (86.5%) was found to be the lumen of the appendix, where the worms provoke no reaction. Of the 259 patients 11 (4.2%) had worms and/or eggs in granulomas of the abdominal and pelvic peritoneum, and an equal number had granulomas on the peritoneum of the salphinx or on the surface of the ovary. There were also ectopic worms and/or eggs in granulomas on the peritoneum of the small and large intestines (2.7%). These Enterobius granulomas form around degenerating adult worms, around discrete eggs, around clusters of eggs, and, we believe, also around the tracks of migrating worms. Three patients (1.2%) had worms in perianal abscesses. A necrotic granuloma, removed from the lung of one patient, surrounded a degenerating adult worm. This suggests that the worm, carried to the lung as an embolus, impacted in a pulmonary arteriole. A stool specimen of one patient contains eggs of Enterobius, and that of another patient contains an adult Enterobius. This is the largest recorded histopathological study of enterobiasis in man.

Adolescent↗

Cysticercosis. A modern day plague.

The authors describe the magnitude of the cysticercosis problem and describe the organism, the clinical features of the disease, the propensity of the organism for development in the central nervous system, pathologic considerations, clinical diagnosis, and treatment.

Adolescent↗

Scanning electron microscopy of tegument-free sensory receptor of Schistosoma mansoni.

Immersion of adult Schistosoma mansoni in buffered trypsin for a short time removed the sponge-like tegument to the level of the basal lamina, effectively uncovering the basal lamina and intact sensory receptors. Stripping the tegument from the cilium and sensory bulb exposed the crown of the bulb and its axon-like process. A cilium protrudes from the bulbs through a collar-like supporting structure that resembles the rim and spokes of a wheel. The exposed axon-like process of some bulbs penetrated the basal lamina without ramifying and disappeared into the musculature; the ramifying process of others remained on the upper surface of the lamina for some distance. Identical micromorphology of the sensory receptor by Transmission Electron Microscopy (TEM) (Silk and Spence, 1969; Hockley, 1973), and the similar appearance of the surface of the bulb and cilia and the ciliary supporting structure by Scanning Electron Microscopy (SEM) suggests that all of the receptors probably perform the same sensory function.

Animals↗

Secretory/excretory antigens produced by tetrathyridia of Mesocestoides corti defined by SDS--PAGE and HPLC.

Antigens derived from culture medium in which metacestodes of Mesocestoides corti Hoeppli, 1925, had been maintained were studied by sodium-dodecyl-sulfate--polyacrylamide gel electrophoresis (SDS--PAGE) and high performance liquid chromatography (HPLC). By SDS--PAGE a minimum of 18 Coomassie-staining bands were discerned, of which 4 major bands and 4 major peaks by HPLC of similar molecular weights were observed. The HPLC eluate peaks were analyzed for antigenic activity in vitro by double diffusion in two dimensions, and in vivo in a rabbit. The rabbit had been artificially sensitized with a dialyzable leukocyte extract, showing transfer-factor-like activity, from peritoneal exudate cells removed from mice infected with tetrathyridia. All of the HPLC fractions reacted with rabbit antibody prepared against secretory/excretory antigens, but the sensitized rabbit responded only to two fractions. It is now possible by HPLC to fractionate complex antigens without denaturing them and to elucidate further the role they play during infection.

Animals↗

Circulating antigens in infections of mice by tetrathyridia of Mesocestoides corti Hoeppli, 1925.

Two circulating antigens were detected in the serum of ICR/Timco female mice infected intraperitonealy with tetrathyridia of the cestode Mesocestoides corti Hoeppli, 1925. One circulating antigen appeared by day 2 postinfection (p.i.) and remained in all mice until at least 90 days p.i. A second antigen appeared in the serum on day 14 p.i. and disappeared from all mice by day 28 p.i. Infected mouse serum also contained antibodies against one secretory/excretory antigen and two antigens in crude homogenate, as judged by double diffusion in two dimensions (Ouchterlony). Immune deposits were observed in the kidney tissue of Rockland mice by transmission electron microscopy, and their identity as products of tetrathyridia was confirmed by immunofluorescence. Further studies showed that the main antibody subclass associated with the mesangial immune deposits was 7S gamma l, and that other subclasses of IgG and IgM were not involved. Antigen was found in the proximal renal tubules of infected mice, as demonstrated by fluorescein-labeled IgG fraction of rabbit antitetrathyridia secretory/excretory antigen antisera. The presence of tetrathyridia antigen in the urine of infected mice was confirmed using the Ouchterlony technique.

Animals↗

Diagnostic clinical parasitology: IV. Identification of the blood parasites?

This is the fourth article in a series of articles entitled "Diagnostic Clinical Parasitology" and contains information on the recovery and identification of human blood parasites. The organisms covered include those that cause the diseases malaria, babesiosis, leishmaniasis, and trypanosomiasis. Some of the filarial worms, which can be considered "blood parasites," have been discussed in the third article in the series, "Identification of the Helminths." Although some of these organisms may rarely be encountered in the laboratory in clinical specimens, they will probably have to be identified in proficiency testing specimens, some of which may not always be representative of patient clinical material. The differences between potential organism recovery from patients coming from endemic areas and from those individuals who become infected with no prior exposure to the organism will also be emphasized. Often, for a number of different reasons, organism recovery and subsequent identification may be more difficult than the textbook imply. It is very important for the technologist to recognize this fact, particularly when dealing with a possibly fatal infection, ie, Plasmodium falciparum.

Animals↗

Diagnostic clinical parasitology: I. Proper specimen collection and processing.

This article (first of a series of four papers on diagnostic clinical parasitology) presents various collection methods and diagnostic procedures which are available for laboratory diagnosis of human parasitic infections. The information presented includes the pros and cons of each method discussed. When a laboratory selects various procedures, this decision should be based on a thorough understanding of the value and limitations of each technique selected. The topics to be included in the next three presentations include: protozoa, helminths, and blood parasites.

Ether↗

Diagnostic clinical parasitology: II. Identification of the intestinal protozoa.

This article (the second in a series of four papers on clinical diagnostic parasitology) presents information on the diagnostic morphology of the protozoa which infect humans. The description of morphological characteristics includes information on atypical morphology as well as the classic descriptions. Because these organisms are the most difficult to identify, extensive detail is included to illustrate the morphological variability.

Amoeba↗

Fine structure of a racemose cysticercus from human brain.

The surface of a racemose cysticercus from the human brain was studied by scanning electron microscopy and the tegument of the cyst by transmission electron microscopy. The surface of the larva is covered by microvilli of uniform shape and size. The glycocalyx of the microvilli bears knotlike areas positive for acid mucopolysaccharides. Microvilli are interconnected by a fine, electron-dense network. The tegumental and subtegumental tissues vary in thickness from one region to the next, and the tissues below the vesicular layer are scattered irregularly, in a seemingly disordered manner.

Animals↗

Fine structure of the tegument of Mesocestoides tetrathyridia by scanning and transmission electron microscopy.

The tegumental surface of tetrathyridial stages of the tapeworm, Mesocestoides corti, was studied by scanning and transmission electron microscopy. Two structural types of microvilli were observed--blade-shaped or conical ones, and elongated, slender microvilli. The distribution and relative frequency of the two types of microvilli differs in different areas of the body surface. Host peritoneal cells were observed attached to the blade-shaped microvilli by slender cytoplasmic projections.

Animals↗