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Dive into the research topics where Thomas H. Morton is active.

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Featured researches published by Thomas H. Morton.


Oral Surgery, Oral Medicine, Oral Pathology | 1989

Oral mucosal lesions: Association with the presence of antibodies to the human immunodeficiency virus

Sandra L. Melnick; David Engel; Edmond L. Truelove; Timothy A. DeRouen; Thomas H. Morton; Mark M. Schubert; Carol Dunphy; Robert W. Wood

To assess the relationship between oral lesions and antibodies to the human immunodeficiency virus, oral examinations of 803 homosexual males were conducted at the time of serologic testing. Nineteen percent were HIV seropositive. Thirty percent of antibody-positive subjects had one or more oral lesion(s), as compared with 7% of antibody-negative subjects (p less than 0.001). The presence of oral lesions was significantly associated with HIV seropositivity: a subject was 5.7 times as likely to have serum antibodies if he had one or more oral lesions (95% confidence interval, 3.5 to 9.1; p less than 0.001). This significant association with HIV seropositivity was only partially explained by cigarette smoking (adjusted odds ratio 3.1; 1.4-6.8; less than 0.006). Specific conditions that were significantly associated with seropositivity included candidiasis, hairy leukoplakia, periodontal disease, and Kaposis sarcoma. Other diseases identified included acute necrotizing ulcerative gingivitis, mucocutaneous ulcerations, and oral warts. Oral findings may occur earlier in the natural history of infection than previously reported.


Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology | 2003

Intraoral melanoma: Long-term follow-up and implication for dental clinicians. A case report and literature review

Gao Man Gu; Joel B. Epstein; Thomas H. Morton

Primary intraoral melanoma is a rare neoplasm with a poor prognosis, accounting for 1% to 8% of all melanoma in Europe and the United States. The incidence (12%) and 5-year survival rate (17.4%) are higher in Japan. We report a case of oral lentiginous melanoma in a Japanese-American man who survived disease-free for more than 5 years after surgery, radiation therapy, and chemotherapy but developed chronic mucositis of the palate under the denture in the primary radiated field. This lesion responded to antifungal therapy. Subsequent multiple biopsies ruled out the recurrence of melanoma but demonstrated prolonged melanocytic hyperplasia and focal epithelial atypia. We reviewed clinical differences in oral melanoma reported in the United States and Japanese literature, and describe the wide variety of oral clinical features of postoperative radiation and chemotherapy, as well as the oral tissue changes caused by denture-induced mucositis and candidiasis in such patients. Dental clinicians should conduct a thorough head, neck, and oral follow-up with increased vigilance in patients with a history of prior cancer.


Oral Surgery, Oral Medicine, Oral Pathology | 1994

Histopathologic evaluation of proliferating cell nuclear antigen (PC10) in oral epithelial hyperplasias and premalignant lesions

Winston Y F Huang; Marc D. Coltrera; Mark M. Schubert; Thomas H. Morton; Edmond L. Truelove

As the therapeutic options for malignant lesions expand, early accurate diagnosis of premalignancy is becoming increasingly important in the concept of cancer prevention. Because it has been hypothesized that abnormal cell proliferation is related to subsequent malignant transformation, many proliferation markers such as proliferating cell nuclear antigen have been studied in a variety of malignant tumors. In oral surface epithelium, proliferating cell nuclear antigen activity is restricted to basal layers of normal squamous mucosa. In this preliminary study, 169 formalin-fixed, paraffin-embedded oral epithelial lesions, including 28 carcinomas in situ, 82 epithelial dysplasias, 21 epithelial atypia, and 38 typical epithelial hyperplasias, were studied with a monoclonal antibody, PC10, to determine whether proliferating cell nuclear antigen suprabasal expression correlated with premalignancy. The findings revealed that with progression of lesions toward malignancy, there was a significant predilection for basal/suprabasal staining pattern for proliferating cell nuclear antigen as compared with the strictly basal staining pattern seen in normal and benign epithelial conditions. One unexpected staining pattern, suprabasal positive stain only, was also noted mostly in reactive hyperplasia and dysplasia. The data suggested that a positive basal/suprabasal staining pattern for proliferating cell nuclear antigen is indicative of premalignancy in oral epithelial lesions.


Journal of Interprofessional Care | 2008

Piloting team simulations to assess interprofessional skills

Lynne Robins; Douglas M. Brock; Thomas H. Gallagher; Deborah Kartin; Taryn Lindhorst; Peggy Soule Odegard; Thomas H. Morton; Basia Belza

Medical Education and Biomedical Informatics, Department of Medical Education and Biomedical Informatics, University of Washington School of Medicine, Department of Rehabilitation Medicine, University of Washington, University of Washington School of Social Work, Department of Pharmacy, University of Washington School of Pharmacy, University of Washington School of Dentistry, and Biobehavioral Nursing and Health Systems, University of Washington School of Nursing, Seattle, Washington, USA


International Journal of Oral Surgery | 1983

Melanoma metastatic to the mandible: Report of a case

Robert W.T. Myall; Thomas H. Morton; Philip Worthington

Metastasis of a tumor to the jaws can simulate an infection, but the presence of paraesthesia and loose teeth or inadequate response to treatment should alert the clinician to a more serious cause. A malignant melanoma metastatic to the jaws illustrates these points.


Biology of Blood and Marrow Transplantation | 2014

Proteomic Analysis of Saliva from Patients with Oral Chronic Graft-Versus-Host Disease

Ivana Devic; Min Shi; Mark M. Schubert; Michele E. Lloid; Kenneth T. Izutsu; Catherine Pan; Melody Missaghi; Thomas H. Morton; Lloyd Mancl; Jing Zhang; Richard B. Presland

Chronic graft-versus-host disease (cGVHD) is an immune-mediated disorder and is the major long-term complication of allogeneic hematopoietic stem cell transplantation (allo-HSCT). The oral mucosa, including the salivary glands, is affected in the majority of patients with cGVHD; however, at present there is only a limited understanding of disease pathobiology. In this study, we performed a quantitative proteomic analysis of saliva pooled from patients with and without oral cGVHD-cGVHD(+) and cGVHD(-), respectively-using isobaric tags for relative and absolute quantification labeling, followed by tandem mass spectrometry. Among 249 salivary proteins identified by tandem mass spectrometry, 82 exhibited altered expression in the oral cGVHD(+) group compared with the cGVHD(-) group. Many of the identified proteins function in innate or acquired immunity, or are associated with tissue maintenance functions, such as proteolysis or the cytoskeleton. Using ELISA immunoassays, we further confirmed that 2 of these proteins, IL-1 receptor antagonist and cystatin B, showed decreased expression in patients with active oral cGVHD (P < .003). Receiver operating curve characteristic analysis revealed that these 2 markers were able to distinguish oral cGVHD with a sensitivity of 85% and specificity of 60%, and showed slightly better discrimination in newly diagnosed patients evaluated within 12 months of allo-HSCT (sensitivity, 92%; specificity 73%). In addition to identifying novel potential salivary cGVHD biomarkers, our study demonstrates that there is coordinated regulation of protein families involved in inflammation, antimicrobial defense, and tissue protection in oral cGVHD that also may reflect changes in salivary gland function and damage to the oral mucosa.


Journal of Prosthetic Dentistry | 1990

Hyperostosis and fixed partial denture pontics: Report of 16 patients and review of literature

Thomas H. Morton; Eugene Natkin

A total of 19 hyperostoses underlying mandibular posterior fixed partial dentures were observed in 16 patients. In three patients the lesions were bilateral. Histologic examination of hyperostoses from eight patients showed that they were composed essentially of hyperplastic lamellar bone. Radiographic and clinical evidence suggested that subpontic hyperostoses are chronic, slow growing lesions with an exclusive predilection for the mandibular molar-premolar site. They appear to have variable growth rates and attain widely variable maximum size. The etiology of subpontic hyperostoses is unknown, but it is possible that inflammation, trauma, mandibular and occlusal function, and genetic factors, either individually or in combination, play a role in the initiation and development of these lesions. Subpontic hyperostoses have potential periodontal and restorative implications that may require their surgical removal.


Oral Surgery, Oral Medicine, Oral Pathology | 1987

Plexiform unicystic ameloblastoma of the maxilla

David G. Gardner; Thomas H. Morton; Jerry C. Worsham

Plexiform unicystic ameloblastomas have a marked predilection for occurring in the posterior part of the mandible. This article presents the first report of such a lesion in the maxilla.


Oral Surgery, Oral Medicine, Oral Pathology | 1984

Caries and periodontitis associated with an unerupted third molar

David A. Baab; Thomas H. Morton; Roy C. Page

Radiographic, gross, and histologic evidence is provided to demonstrate the development of caries and periodontal disease over a 5-year period in an unerupted tooth. The authors speculate on the pathogenesis of these disease processes.


Diabetes Spectrum | 2011

Non-periodontal oral manifestations of diabetes: a framework for medical care providers

Beatrice K. Gandara; Thomas H. Morton

In Brief In addition to periodontitis and dental caries, other oral conditions commonly occur commonly in patients with diabetes. These include fungal infections, salivary gland dysfunction, neuropathy, and mucosal disorders. Many of these lesions can be easily examined and documented by non-dental providers.

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Joel B. Epstein

University of Illinois at Chicago

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David E. Kleiner

National Institutes of Health

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Howard M. Shulman

Fred Hutchinson Cancer Research Center

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Mark M. Schubert

Seattle Cancer Care Alliance

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Mary E.D. Flowers

Fred Hutchinson Cancer Research Center

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Paul J. Martin

Fred Hutchinson Cancer Research Center

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Steven Z. Pavletic

National Institutes of Health

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