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1.
W V Med J ; 96(1): 364-6, 2000.
Article in English | MEDLINE | ID: mdl-10734801

ABSTRACT

An extremely rare case of pulmonary epitheloid hemangioendothelioma (PEH), previously known as intravascular bronchoalveolar tumor (IVBAT), in a 38-year-old female is presented. This patient had a history of rheumatoid arthritis and bilateral multiple small pulmonary nodules which progressed over the years. The histopathological diagnosis of PEH was confirmed by immunohistochemical stains. Prognosis of this tumor is very unpredictable. There is no effective treatment for pulmonary epitheloid hemangioendothelioma.


Subject(s)
Hemangioendothelioma, Epithelioid/pathology , Lung Neoplasms/pathology , Lung/pathology , Adult , Biopsy , Female , Humans , Prognosis
2.
W V Med J ; 94(5): 276-8, 1998.
Article in English | MEDLINE | ID: mdl-9803886

ABSTRACT

This article presents a rare case of metastatic glioblastoma multiforme (GM) to the cervical lymph node. In spite of very aggressive tumor behavior, extracranial metastasis from intra-cerebral GM is rare. Only a few cases are reported in the world literature. This infrequent extracranial metastasis may be due to the fact that patients do not live long enough to manifest metastases or result from the fact that brain tissue has some structural differences from other tissues in the body. This tumor can be easily mistaken for other anaplastic tumors like malignant melanoma, malignant lymphoma, or anaplastic carcinoma. Positive glial fibrillary acidic (GFA) protein stain (an immunoperoxidase stain) of this metastatic tumor can eliminate all other time consuming, expensive, and exhausting procedures for the patient.


Subject(s)
Brain Neoplasms/pathology , Glioblastoma/secondary , Parietal Lobe , Adult , Fatal Outcome , Female , Glioblastoma/pathology , Humans , Lymphatic Metastasis , Neck
3.
J Orthop Sports Phys Ther ; 19(5): 232-41, 1994 May.
Article in English | MEDLINE | ID: mdl-8199615

ABSTRACT

Before discussing adjustments in the fees for the clinical services of industrial rehabilitation, the Medical Free Guide Committee of the Maryland Industrial Commission requested a copy of the clinical standards for these services. However, there were no multidisciplinary standards for industrial services that had state-wide approval. Therefore, a committee was formed to write the standards. Following a review of the literature and unpublished work from other associations and state organizations, standards were developed. Constructive criticism was solicited from national and local professionals and organizations with demonstrated interest and experience in providing or using these services or with experience writing standards. Further comment was solicited from individuals in the state of Maryland before final editing. Because of the dearth of outcome studies supporting the efficacy of clinical services in industrial rehabilitation, the standards describing a level of expectation from clinical services have become important for state organizations responsible for making decisions on reimbursement for clinical services. This paper summarizes the process used for the development of clinical standards of industrial rehabilitation services.


Subject(s)
Occupational Medicine/standards , Rehabilitation, Vocational/standards , Contraindications , Goals , Humans , Job Description , Work Capacity Evaluation
5.
Hum Genet ; 59(4): 297-307, 1981.
Article in English | MEDLINE | ID: mdl-6949855

ABSTRACT

Clinical and cytogenetic studies are reported on 13 patients with Wolf-Hirschhorn syndrome. The oldest of the living twelve probands is 24 years of age. Three of these patients had a translocation involving the short arm of chromosome 4, and in one of these the anomalous chromosome was inherited from the father. Another three patients were believed, on the basis of GTG-staining, to have a translocation although the origin of the translocated chromatin could not be identified. In the remaining seven patients the anomalous chromosome appeared to be a simple deletion, although in two cases a translocation could not be ruled out. Cytogenetic studies in these patients suggest that the critical deletion involved in Wolf-Hirschhorn syndrome is within 4p16.


Subject(s)
Abnormalities, Multiple/genetics , Chromosome Deletion , Chromosomes, Human, 4-5 , Adolescent , Adult , Child , Child, Preschool , Chromosome Banding , Dermatoglyphics , Female , Genetic Markers , Growth Disorders/genetics , Humans , Infant , Infant, Newborn , Intellectual Disability/genetics , Male , Pedigree , Syndrome , Translocation, Genetic
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