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1.
J Fr Ophtalmol ; 41(1): 62-77, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29246385

ABSTRACT

Sclerotic scatter involves the scattering of incident light by the limbal sclera followed by entry of part of the scattered light into the cornea, where some of the light travels through total internal reflection to the other side, where it scatters a second time in the limbal sclera. It is then visible in the form of a limbal scleral arc of light. Sclerotic scatter has been used for decades to spot and delineate corneal opacities, which disrupt and scatter the light travelling through total internal reflection. To implement the technique, the slit beam and the binoculars of the slit lamp should be dissociated so that the limbal sclera is illuminated, while the binoculars are centered on the cornea. The technique does not provide any information as to the depth of corneal opacities and therefore needs to be complemented by direct illumination. The second sclerotic scatter may also be used clinically, for instance for diode cycloablation, the posterior part of the arc of light projecting 0.5mm behind the scleral spur. This article aims to describe the phenomenon of sclerotic scatter, explaining how the slit-lamp should be set to use this technique, describing its clinical applications (in the opacified cornea and in the normal sclera), showing that the limbal scleral arc of light of sclerotic scatter may be seen under certain circumstances in daily life with the naked eye and, finally, explaining how the arc of light differs from peripheral light focusing ("Coroneo effect").


Subject(s)
Light , Scattering, Radiation , Sclera/physiology , Adaptation, Ocular/physiology , Cornea/physiology , Cornea/physiopathology , Corneal Opacity/diagnosis , Corneal Opacity/physiopathology , Humans , Sclera/physiopathology
2.
CDS Rev ; 91(5): 22-4, 1998.
Article in English | MEDLINE | ID: mdl-9760884

ABSTRACT

We dread mistakes because they are considered faults. The fear of making errors keeps us from extending ourselves professionally. We are more inclined to stay safe within the confines of current situations because there is comfort in its certainty. We tolerate less than ideal conditions because even if we are not prospering, we are, at least, not failing.


Subject(s)
Practice Management, Dental , Personnel Management , Personnel Selection
3.
Pharmacotherapy ; 6(6): 323-7, 1986.
Article in English | MEDLINE | ID: mdl-3822854

ABSTRACT

A 33-year-old obese, hypothyroid, white male with several medical problems was admitted to University Hospital in September 1984 for treatment of drug intoxication. Admitting medications included ethchlorvynol in addition to other central nervous system depressants. Initial serum concentrations were reported at 70 micrograms/ml in this somnolent yet totally conscious adult. Established therapeutic concentrations are 2-8 micrograms/ml, with toxic exceeding 20 micrograms/ml. A tolerance phenomenon seemed evident. Serum ethchlorvynol concentrations were monitored daily during early hospitalization and continued to be substantially greater than reported toxic concentrations. Kinetic values were as follows: total body clearance 9.92 ml/min, volume of distribution 68.0 liters, and half-life 78 hours. These values are unique in that they were calculated from a patient who had not suffered an acute overdose, thereby differing markedly from previously published values. The influence of hypothyroidism and hyperlipidemia on these markedly different values appears to be significant. Ethchlorvynol should probably be added to the list of drugs influenced by thyroid disease.


Subject(s)
Ethchlorvynol/blood , Hyperlipidemias/blood , Hypothyroidism/blood , Adult , Drug Administration Schedule , Drug Tolerance , Ethchlorvynol/adverse effects , Ethchlorvynol/therapeutic use , Humans , Hyperlipidemias/complications , Hypothyroidism/complications , Kinetics , Male , Time Factors
4.
Gynecol Oncol ; 24(3): 279-85, 1986 Jul.
Article in English | MEDLINE | ID: mdl-3013733

ABSTRACT

Condylomas of the genital tract can be found in 70% of patients who have cytologic evidence of human papilloma virus (HPV) infection or mild epithelial dysplasia (CIN I). Most male sexual partners of women with overt or subclinical HPV infections have no visible condylomas. Presently, there is no therapy for subclinically infected male partners. A screening test capable of detecting such HPV infections in males would be of value should effective therapy be discovered. Fifty-four men who were the current sexual partners of women with visible condylomata acuminata or with cytologic evidence of subclinical HPV infection or cervical neoplasia were asked to give a urine specimen for cytologic examination. The cytologist had no knowledge of the cytologic or histopathologic findings in the female partners. Of the 54 women, 39 (72%) had either visible genital condylomas or cytologic evidence of mild dysplasia or of HPV infection with or without mild dysplasia (CIN I). Twenty-five (63%) had histologic evidence of HPV infection with or without mild dysplasia. With one exception, urinary cytologic preparations from the study and from the control males were negative. No correlation could be found between cervical cytology and histology in the females and urinary cytologic findings in their current male partners. At the present time there is no screening test that can be utilized to detect male carriers with subclinical disease.


Subject(s)
Carrier State/urine , Condylomata Acuminata/etiology , Sex , Tumor Virus Infections/etiology , Uterine Cervical Neoplasms/etiology , Condylomata Acuminata/pathology , Female , Humans , Male , Papillomaviridae , Tumor Virus Infections/transmission , Tumor Virus Infections/urine , Uterine Cervical Neoplasms/pathology , Vaginal Smears
5.
Am J Surg Pathol ; 7(7): 691-7, 1983 Oct.
Article in English | MEDLINE | ID: mdl-6638259

ABSTRACT

We describe a rare variant of schwannoma characterized by a interconnecting multinodular growth mimicking a plexiform neurofibroma. The schwannoma recurred twice. The second recurrence was not excised and has not increased in size for 1 1/2 years. The patient is alive and well, 3 years and 4 months after the first excision with no clinical evidence of metastasis.


Subject(s)
Neurilemmoma/ultrastructure , Neurofibroma/ultrastructure , Vulvar Neoplasms/ultrastructure , Adult , Diagnosis, Differential , Female , Humans , Microscopy, Electron , Neoplasm Recurrence, Local
6.
Laryngoscope ; 86(4): 516-23, 1976 Apr.
Article in English | MEDLINE | ID: mdl-57560

ABSTRACT

Nasal cytograms, as an aid to diagnosis of pathological conditions of the nose and paranasal sinuses, have not been adopted by the majority of otolaryngologists. This situation exists because of technical problems with the preparation of a slide and the difficulty in finding someone competent and interested in its interpretation. The work of the Bryans has provided an analysis of the cytology of nasal secretions. Adopting their methods, we have been using the nasal cytogram in clinical practice and find it helpful in determining appropriate therapy for problems encountered in otolaryngological practice. In the authors' experience, profuse nasal mastocytosis is a consistent finding in cytograms from patients having varied symptoms that are associated with hypersensitivities that are not accompanied by positive objective findings. This is especially true in patients with constantly recurring headaches and those with a chronically obstructed nose. Once many mast cells are found by the cytogram, attempts are made to relieve these patients by selective dietary restrictions. These attempts are often successful. The nasal cytogram is also used to help explain periodic symptom flares in the long term allergy patient undergoing immunotherapy for inhalants, by identifying superimposed viral and bacterial infections.


Subject(s)
Nasal Mucosa/metabolism , Rhinitis, Allergic, Seasonal/diagnosis , Allergens , Cell Count , Cytodiagnosis/methods , Diagnosis, Differential , Environmental Exposure , Eosinophils , Food Hypersensitivity/immunology , Humans , Mast Cells/immunology , Mast Cells/ultrastructure , Nasal Mucosa/pathology , Rhinitis, Allergic, Seasonal/immunology , Staining and Labeling , Urticaria Pigmentosa
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