Treating Chronic Pain: Injection of Joints and Soft Tissues

Extra Digital Glomus Tumor: A Rare Cause for Undiagnosed Chronic Pain in Unusual Sites

Plastic Surgery Case Studies ◽

10.1177/2513826x19828796 ◽

2019 ◽

Vol 5 ◽

pp. 2513826X1982879

Author(s):

Haneen Asaad ◽

Gaber M. A. Osman ◽

Abdulrahman Ibraheam

Keyword(s):

Chronic Pain ◽

Soft Tissues ◽

Glomus Tumor ◽

Normal Structure ◽

Cold Sensitivity ◽

Nerve Fibres ◽

Glomus Tumors ◽

Clinical Triad ◽

Extradigital Glomus ◽

Malignant Behavior

Glomus tumor, also known as Glomangioma, originates in the neuromyoarterial glomus, a normal arteriovenous shunt abundantly supplied with nerve fibres and fulfilling a temperature-regulating function. The classic location of the glomus tumor is the subungual region, but it can occur elsewhere in the skin, soft tissues, nerves, stomach, nasal cavity, and trachea. There is some question as to whether this is a true neoplasm or simply a normal structure. Glomus tumor constitutes 1% to 5% of all hand tumors. It usually occurs at the subungual region and more commonly in aged women. Its classical clinical triad consists of pain, tenderness, and temperature intolerance, especially cold sensitivity. Glomus tumors are usually benign, but on rare occasions may exhibit an uncertain or malignant behavior as with glomangiosarcoma. In this article, we present a case of a 60-year-old female patient diagnosed with extradigital glomus tumor of the palm of right hand.

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Rapid Critical Point Drying of Tissues in a Parr Bomb

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100095261 ◽

1972 ◽

Vol 30 ◽

pp. 400-401

Author(s):

C.A. Baechler ◽

W. C. Pitchford ◽

J. M. Riddle ◽

C.B. Boyd ◽

H. Kanagawa ◽

...

Keyword(s):

Critical Point ◽

Critical Pressure ◽

Soft Tissues ◽

Biological Tissues ◽

Critical Temperatures ◽

Air Drying ◽

The Past ◽

Critical Point Drying ◽

Great Stress ◽

Infiltration Techniques

Preservation of the topographic ultrastructure of soft biological tissues for examination by scanning electron microscopy has been accomplished in the past by using lengthy epoxy infiltration techniques, or dehydration in ethanol or acetone followed by air drying. Since the former technique requires several days of preparation and the latter technique subjects the tissues to great stress during the phase change encountered during air-drying, an alternate rapid, economical, and reliable method of surface structure preservation was developed. Turnbill and Philpott had used a fluorocarbon for the critical point drying of soft tissues and indicated the advantages of working with fluids having both moderately low critical pressures as well as low critical temperatures. Freon-116 (duPont) which has a critical temperature of 19. 7 C and a critical pressure of 432 psi was used in this study.

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SEM analysis of fish scale cross sections: A technique study

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100124124 ◽

1992 ◽

Vol 50 (1) ◽

pp. 744-745

Author(s):

M.E. Lee ◽

A. Moller ◽

P.S.O. Fouche ◽

I.G Gaigher

Keyword(s):

Electron Microscopy ◽

Scanning Electron Microscopy ◽

Cross Sections ◽

Soft Tissues ◽

Close Association ◽

Sem Analysis ◽

Fish Scale ◽

Fish Scales ◽

Micro Structures ◽

Scanning Electron

Scanning electron microscopy of fish scales has facilitated the application of micro-structures to systematics. Electron microscopy studies have added more information on the structure of the scale and the associated cells, many problems still remain unsolved, because of our incomplete knowledge of the process of calcification. One of the main purposes of these studies has been to study the histology, histochemistry, and ultrastructure of both calcified and decalcified scales, and associated cells, and to obtain more information on the mechanism of calcification in the scales. The study of a calcified scale with the electron microscope is complicated by the difficulty in sectioning this material because of the close association of very hard tissue with very soft tissues. Sections often shatter and blemishes are difficult to avoid. Therefore the aim of this study is firstly to develop techniques for the preparation of cross sections of fish scales for scanning electron microscopy and secondly the application of these techniques for the determination of the structures and calcification of fish scales.

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Biological and biomedical applications of collagenous biomaterials

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100161849 ◽

1990 ◽

Vol 48 (3) ◽

pp. 856-857

Author(s):

Yasushi P. Kato ◽

Michael G. Dunn ◽

Frederick H. Silver ◽

Arthur J. Wasserman

Keyword(s):

Biomedical Applications ◽

Soft Tissues ◽

Collagen Fibers ◽

Bone Collagen ◽

Cover Slip ◽

Fibroblast Migration ◽

Cellular Expression ◽

Defect Repair

Collagenous biomaterials have been used for growing cells in vitro as well as for augmentation and replacement of hard and soft tissues. The substratum used for culturing cells is implicated in the modulation of phenotypic cellular expression, cellular orientation and adhesion. Collagen may have a strong influence on these cellular parameters when used as a substrate in vitro. Clinically, collagen has many applications to wound healing including, skin and bone substitution, tendon, ligament, and nerve replacement. In this report we demonstrate two uses of collagen. First as a fiber to support fibroblast growth in vitro, and second as a demineralized bone/collagen sponge for radial bone defect repair in vivo.For the in vitro study, collagen fibers were prepared as described previously. Primary rat tendon fibroblasts (1° RTF) were isolated and cultured for 5 days on 1 X 15 mm sterile cover slips. Six to seven collagen fibers, were glued parallel to each other onto a circular cover slip (D=18mm) and the 1 X 15mm cover slip populated with 1° RTF was placed at the center perpendicular to the collagen fibers. Fibroblast migration from the 1 x 15mm cover slip onto and along the collagen fibers was measured daily using a phase contrast microscope (Olympus CK-2) with a calibrated eyepiece. Migratory rates for fibroblasts were determined from 36 fibers over 4 days.

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