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Dive into the research topics where Marilyn Dawlett is active.

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Featured researches published by Marilyn Dawlett.


Gynecologic Oncology | 2008

Gain of the 3q26 region in cervicovaginal liquid-based pap preparations is associated with squamous intraepithelial lesions and squamous cell carcinoma

Nancy P. Caraway; Abha Khanna; Marilyn Dawlett; Ming Guo; Nina Guo; E. Lin; Ruth L. Katz

BACKGROUND Chromosomal aberrations have been documented in cervical carcinomas, especially chromosome 3q. The human telomerase RNA gene (hTERC) is located in the chromosome 3q26 region, and its product, telomerase, is involved in the maintenance of chromosome length and stability. Upregulation of telomerase is in general associated with tumorigenesis. In this study, cervicovaginal specimens were analyzed by fluorescence in situ hybridization (FISH) for gain of chromosome 3q26 containing hTERC, and FISH findings were compared with the cytologic and histologic diagnoses. METHODS Slides prepared from 66 liquid-based preparations from cervical specimens with cytologic diagnoses of negative for squamous intraepithelial lesion or malignancy (NILM, n=4), atypical squamous cells of undetermined significance (ASC-US, n=15), low-grade squamous intraepithelial lesion (LSIL, n=20), high-grade squamous intraepithelial lesion (HSIL, n=24), or cervical squamous cell carcinoma (SCCA, n=3) were analyzed for aberrations of 3q26 using a commercially available two-color FISH probe. The results of the cytologic analysis and those of concurrent or subsequent biopsies, when available, were compared with the FISH-detected 3q26 abnormalities. The Wilcoxon rank-sum test was used to assess associations between 3q26 gains and diagnoses. RESULTS Gain of 3q26 was significantly associated with the cytologic diagnosis (p<0.0001). Patients with HSIL or SCCA cytology diagnoses had significantly higher percentages of cells with 3q26 gain than did patients with NILM or ASC-US cytologic diagnoses. CONCLUSIONS FISH can be performed on cervicovaginal liquid-based preparations to detect gain of 3q26. Gain of 3q26 is associated with HSIL and SCCA. This test may be an adjunct to cytology screening, especially high-risk patients.


Diagnostic Cytopathology | 2012

The triage efficacy of fine needle aspiration biopsy for follicular variant of papillary thyroid carcinoma using the Bethesda reporting guidelines

Elizabeth M. Kurian; Marilyn Dawlett; Jianping Wang; Yun Gong; Ming Guo

Diagnosis of follicular variant of papillary thyroid carcinoma (FVPTC) by ultrasound‐guided fine‐needle aspiration (FNA) is challenging. In this retrospective review, we evaluated triage efficacy (i.e., potential for triggering surgical intervention) in 44 archived FNA biopsies of surgically confirmed FVPTC obtained between December 2006 and December 2008. We compared the original FNA diagnoses with reclassified diagnoses based on 2007 National Cancer Institute (NCI)/Bethesda recommendations, and reviewed FNA cytologic features. Original FNA diagnoses included colloid nodule (7%, 3/44), atypical follicular cells (5%, 2/44), follicular lesion (11%, 5/44), follicular neoplasm (16%, 7/44), suspicious for malignancy/PTC (27%, 12/44), and papillary thyroid carcinoma (34%, 15/44). Reclassified diagnoses included indeterminate (5%, 2/44), colloid nodule (7%, 3/44), atypical cells of undetermined significance [ACUS] (7%, 3/44), Hurthle cell neoplasm (2%, 1/44), follicular neoplasm (7%, 3/44), suspicious for malignancy/PTC (25%, 11/44), and PTC (48%, 21/44). Triage efficacy was 77% (34/44) for original diagnoses versus 82% (36/44) for reclassified FNA diagnoses. We frequently observed cytologic features of PTC, such as nuclear grooves and fine chromatin; conversely, intranuclear inclusions, though present in 77% cases, were scant. Our review findings suggest that lack of characteristic cytologic features of PTC,coexistence with other thyroid lesions, and small tumor size arethe major obstacles to FNA diagnosis of FVPTC. Reclassification of thyroid FNA diagnoses does not significantly improve triage efficacy. Furthermore, FNA diagnoses of follicular neoplasm and suspicious for malignancy are valuable in patients with FVPTC because they trigger triage toward surgical intervention. Diagn. Cytopathol. 2012;40:E69–E73.


Cancer Cytopathology | 2013

Ultrasound‐guided fine‐needle aspiration biopsy of thyroid bed lesions from patients with thyroidectomy for thyroid carcinomas

Lichao Zhao; Yun Gong; Jianping Wang; Marilyn Dawlett; Lei Huo; Nancy P. Caraway; Ming Guo

To evaluate the efficacy and the limitation of fine‐needle aspiration (FNA) biopsy in thyroid bed lesions, a retrospective review was performed of the medical records of thyroid cancer patients who underwent ultrasound‐guided FNA biopsy of the thyroid bed at The University of Texas MD Anderson Cancer Center over a 5‐year period.


Cancer Cytopathology | 2013

The role of human papillomavirus type 16/18 genotyping in predicting high-grade cervical/vaginal intraepithelial neoplasm in women with mildly abnormal papanicolaou results

Ming Guo; Yun Gong; Jianping Wang; Marilyn Dawlett; Shobha Patel; Ping Liu; Therese B. Bevers; Nour Sneige

The authors compared the predictive value of type 16 and/or 18 human papillomavirus (HPV) versus non‐16/18 HPV types for high‐grade (grade ≥2) cervical neoplasm/vaginal intraepithelial neoplasm and carcinoma (CIN/VAIN2+) in women with mildly abnormal Papanicolaou (Pap) results (ie, atypical squamous cells of undetermined significance [ASCUS] or low‐grade squamous epithelial lesion [LSIL]).


Cancer Cytopathology | 2012

Endosalpingiosis in peritoneal washings in women with benign gynecologic conditions: Thirty-eight cases confirmed with paired box-8 immunohistochemical staining and correlation with surgical biopsy findings

Nour Sneige; Marilyn Dawlett; Teresa Kologinczak; Ming Guo

To better define the cytomorphologic spectrum of endosalpingiosis in peritoneal washings (PWs) and thereby facilitate their distinction from well differentiated serous carcinoma, the authors examined PWs from women who underwent surgery and pathologic staging of lesions other than Mullerian malignancies and correlated the findings with surgical specimens.


Cancer Cytopathology | 2017

Three-year risk of high-grade CIN for women aged 30 years or older who undergo baseline Pap cytology and HPV co-screening

Ming Guo; Abha Khanna; Jianping Wang; Marilyn Dawlett; Teresa Kologinczak; Genevieve Lyons; Roland L. Bassett; Nour Sneige; Yun Gong; Therese B. Bevers

Papanicolaou (Pap) cytology and high‐risk human papillomavirus (HPV) DNA cotesting for women aged ≥30 years are recommended for the prevention of cervical cancer. The objective of the current study was to evaluate the efficacy of this cotesting for predicting the risk of high‐grade cervical intraepithelial neoplasia 3 (CIN3) during a 3‐year follow‐up period.


Cancer Cytopathology | 2014

Reliability of immunostaining using pan‐melanoma cocktail, SOX10, and microphthalmia transcription factor in confirming a diagnosis of melanoma on fine‐needle aspiration smears

Jessica Clevenger; Cicily Joseph; Marilyn Dawlett; Ming Guo; Yun Gong


Cancer Cytopathology | 2014

The role of SOX11 immunostaining in confirming the diagnosis of mantle cell lymphoma on fine-needle aspiration samples

Y. Helen Zhang; Joe Liu; Marilyn Dawlett; Ming Guo; Xiaoping Sun; Yun Gong


Archives of Pathology & Laboratory Medicine | 2015

Clinical Performance of Hybrid Capture 2 Human Papillomavirus Testing for Recurrent High-Grade Cervical/Vaginal Intraepithelial Neoplasm in Patients With an ASC-US Papanicolaou Test Result During Long-Term Posttherapy Follow-up Monitoring

Andrea Diaz De Vivar; Marilyn Dawlett; Jianping Wang; Annie Jack; Yun Gong; Gregg Staerkel; Ming Guo


Journal of the American Society of Cytopathology | 2016

Efficacy of reflex HPV16/18 genotyping in predicting CIN3/VAIN3 in women with HPV+/Pap– results

Ming Guo; Abha Khanna; Marilyn Dawlett; Shobha Patel; Yun Gong; Gregg Staerkel

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Ming Guo

University of Texas MD Anderson Cancer Center

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Yun Gong

University of Texas MD Anderson Cancer Center

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Jianping Wang

University of Texas MD Anderson Cancer Center

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Nour Sneige

University of Texas MD Anderson Cancer Center

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Abha Khanna

University of Texas MD Anderson Cancer Center

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Gregg Staerkel

University of Texas MD Anderson Cancer Center

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Teresa Kologinczak

University of Texas MD Anderson Cancer Center

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Therese B. Bevers

University of Texas MD Anderson Cancer Center

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Nancy P. Caraway

University of Texas MD Anderson Cancer Center

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Shobha Patel

University of Texas MD Anderson Cancer Center

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