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Journal articles on the topic 'Cytodiagnosis'

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1

Campbell, Terry W. "Cytodiagnosis." Journal of the Association of Avian Veterinarians 5, no. 2 (1991): 105. http://dx.doi.org/10.2307/30133287.

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2

Campbell, Terry W. "Cytodiagnosis." Journal of the Association of Avian Veterinarians 5, no. 1 (1991): 53. http://dx.doi.org/10.2307/27671015.

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3

Shana, Baby, Betsy Ambooken, and N. Asokan. "Cytodiagnosis in dermatology." Journal of Skin and Sexually Transmitted Diseases 1 (December 2, 2019): 112–16. http://dx.doi.org/10.25259/jsstd_40_2019.

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4

Dhawan, S. B., R. Aggarwal, H. Mohan, and S. Kumar. "Cytodiagnosis of enchondroma." Cytopathology 14, no. 3 (June 2003): 157–59. http://dx.doi.org/10.1046/j.1365-2303.2003.00050.x.

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5

Fernandes, Hilda, Clement R. S. D'Souza, Jayaprakash C. Shekar, Nisha J. Marla, Gumballi K. Swethadri, and Ramesh Naik. "Cytodiagnosis of actinomycetoma." Diagnostic Cytopathology 37, no. 7 (July 2009): 506–8. http://dx.doi.org/10.1002/dc.21040.

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6

Joob, Beuy, and Viroj Wiwanitkit. "Cysticercosis and cytodiagnosis." Diagnostic Cytopathology 46, no. 3 (November 28, 2017): 287. http://dx.doi.org/10.1002/dc.23864.

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7

Schnadig, Vicki J., Claudia P. Molina, and Judith F. Aronson. "Cytodiagnosis in the Autopsy Suite: A Tool for Improving Autopsy Quality and Resident Education." Archives of Pathology & Laboratory Medicine 131, no. 7 (July 1, 2007): 1056–62. http://dx.doi.org/10.5858/2007-131-1056-citasa.

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Abstract Context.—Despite several publications attesting to its accuracy and value, cytology is rarely used for preliminary autopsy diagnosis in the United States. Postmortem cytodiagnosis has the potential to increase the accuracy and specificity of the provisional and final autopsy diagnoses, increase resident interest in cytodiagnostic techniques, and direct pathologists to request pertinent special studies, such as microbial cultures and special stains. Objective.—To assess and illustrate the value of cytodiagnostic techniques for improving autopsy quality assurance and resident education. Design.—Eighty-five samples were evaluated from 49 nonconsecutive autopsies. Sixty-five focal lesions were sampled by direct scraping. Diffuse lung consolidation was sampled by fine-needle aspiration (20 samples). Smears and cytocentrifuge preparations of fine-needle aspirations were routinely stained by both Papanicolaou and Romanowski methods. Cytologic diagnoses were compared with final autopsy diagnoses, and both cytology and pertinent histology were reviewed. Results.—Clinical or radiographic antemortem site-specific diagnoses had been made in 28 (33%) of the 85 samples. A definite diagnosis was made by postmortem cytology in 68 (80%) of 85 samples, and these diagnoses could contribute to provisional autopsy diagnosis in 46 instances (68%). Resident and faculty enthusiasm for the use of cytology in the autopsy suite has increased during the 7 years following the study. Case examples illustrating the benefits of postmortem cytology are provided. Conclusions.—Postmortem cytology benefits both autopsy quality and resident education.
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8

Das, Subhashish, R. Kalyani, and ML Harendra Kumar. "Cytodiagnosis of tumoral calcinosis." Journal of Cytology 25, no. 4 (2008): 160. http://dx.doi.org/10.4103/0970-9371.50806.

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9

Walke, VaishaliA, SupritaP Nayak, MaitreyeeM Munshi, and SudhakarK Bobhate. "Cytodiagnosis of chondromyxoid fibroma." Journal of Cytology 27, no. 3 (2010): 96. http://dx.doi.org/10.4103/0970-9371.71873.

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10

Mukherjee, Sumana, Gautam Bandyopadhyay, Sandeep Saha, and Manoj Choudhuri. "Cytodiagnosis of glomus tumor." Journal of Cytology 27, no. 3 (2010): 104. http://dx.doi.org/10.4103/0970-9371.71876.

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11

Walke, Vaishali, Sushma Ramraje, and Vinod Jadhao. "Cytodiagnosis of gouty tophus." CytoJournal 10 (May 29, 2013): 11. http://dx.doi.org/10.4103/1742-6413.112649.

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12

Poflee, Sandhya, Anjali Bode, and Sonam Mahana. "Cytodiagnosis of scar endometriosis." CytoJournal 11 (January 31, 2014): 1. http://dx.doi.org/10.4103/1742-6413.126222.

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13

Hingway, S. R., and Poornima Kodate. "Cytodiagnosis of Scalp Lesions." Journal of Medical Sciences and Health 01, no. 01 (February 1, 2015): 1–9. http://dx.doi.org/10.46347/jmsh.2015.v01i01.001.

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14

Campbell, Terry W. "What Is Your Cytodiagnosis?" Journal of the Association of Avian Veterinarians 4, no. 3 (1990): 168. http://dx.doi.org/10.2307/30134955.

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15

Campbell, Terry W. "What Is Your Cytodiagnosis?" Journal of the Association of Avian Veterinarians 6, no. 2 (1992): 93. http://dx.doi.org/10.2307/30134991.

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16

Heeb, Laurie A., Craig A. Harms, and James W. Carpenter. "What Is Your Cytodiagnosis?" Journal of the Association of Avian Veterinarians 6, no. 4 (1992): 232. http://dx.doi.org/10.2307/30136973.

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17

Nayak, S. P., M. M. Munshi, and S. K. Bobhate. "Cytodiagnosis of fibromatosis colli." Cytopathology 18, no. 4 (August 2007): 266–67. http://dx.doi.org/10.1111/j.1365-2303.2006.00355.x.

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18

Suvarna, S. K., and R. D. Start. "Cytodiagnosis and the necropsy." Journal of Clinical Pathology 48, no. 5 (May 1, 1995): 443–46. http://dx.doi.org/10.1136/jcp.48.5.443.

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19

Goel, Garima, Sharada Rai, Ramadas Naik, Astha Gupta, Poornima Baliga, and Ruchi Sinha. "Cytodiagnosis of Extramedullary Plasmacytomas." Acta Cytologica 54, no. 3 (2010): 255–58. http://dx.doi.org/10.1159/000325031.

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20

Hudson, E. A. "Fine Needle Aspiration Cytodiagnosis." Journal of Clinical Pathology 38, no. 5 (May 1, 1985): 598. http://dx.doi.org/10.1136/jcp.38.5.598-e.

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21

Shukla, Saumya, Namrata Punit Awasthi, Nuzhat Husain, and Nidhi Anand. "Cytodiagnosis of Sacral Chordoma." Journal of Nepal Medical Association 52, no. 196 (December 31, 2014): 1014–16. http://dx.doi.org/10.31729/jnma.2804.

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We report the cytological findings of a sacro-coccygeal chordoma in a 53 year male diagnosed preoperatively by guided fine needle aspiration cytology. The smears shows characteristic Physalliphorous cells in a metachromatic background of myxoid material entrapping cords of cuboidal cells. Differential diagnosis in cytology include conventional and myxoid chondrosarcoma, myxoid liposarcoma, myxoid malignant fibrous histiocytoma, metastatic mucinous carcinoma and myxo-papillary ependymoma. The distinguishing features between these neoplasms are discussed. Preoperative diagnosis of chordoma permits optimum planned surgery. Keywords: chordoma; myxoid; sacral.
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22

Campbell, Terry W. "What Is Your Cytodiagnosis?" Journal of the Association of Avian Veterinarians 5, no. 3 (1991): 137. http://dx.doi.org/10.2307/27671038.

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23

Campbell, Terry W. "What Is Your Cytodiagnosis?" Journal of the Association of Avian Veterinarians 5, no. 4 (1991): 201. http://dx.doi.org/10.2307/27671071.

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24

Keith, Julia, Lee-Cyn Ang, and Joseph Megyesi. "Cytodiagnosis of Supratentorial Hemangioblastoma." Acta Cytologica 52, no. 2 (2008): 260–63. http://dx.doi.org/10.1159/000325496.

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25

Gabhane, Sushma K., Nitin Gangane, and N. Anshu. "Cytodiagnosis of Eumycotic Mycetoma." Acta Cytologica 52, no. 3 (2008): 354–56. http://dx.doi.org/10.1159/000325522.

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26

Asotra, Sarita, Lekshmi Vijayamohanan, and Aditya Jamwal. "Cytodiagnosis of extramedullary plasmacytoma." Indian Journal of Pathology and Oncology 7, no. 3 (August 15, 2020): 508–10. http://dx.doi.org/10.18231/j.ijpo.2020.102.

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27

Giri, Ranjana, Anjali Agarwal, Prajna Dash, SubratK Sahu, and KabikantaK Samantray. "Cytodiagnosis of clival chordoma." Journal of Cytology 40, no. 3 (2023): 153. http://dx.doi.org/10.4103/joc.joc_145_22.

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28

Calton, Nalini, and Roma Isaacs. "Cytodiagnosis of Ewing's sarcoma." Journal of Cytology 18, no. 1 (2001): 31. http://dx.doi.org/10.4103/0970-9371.237794.

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29

Maheshwari, V., HA Ansari, P. Sood, and A. Jain. "Cytodiagnosis of lipomatous tumours." Journal of Cytology 23, no. 3 (2006): 119. http://dx.doi.org/10.4103/0970-9371.239478.

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30

Rocha, PremilaDesousa, NishaSunil Nadkarni, and RoqueGabriel Wiseman Pinto. "Cytodiagnosis of dermatofibrosarcoma protuberans." Journal of Cytology 16, no. 2 (1999): 121. http://dx.doi.org/10.4103/0970-9371.237665.

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31

Ammanagi, AnandS. "Cytodiagnosis of serous effusions:." Journal of Cytology 18, no. 3 (2001): 188. http://dx.doi.org/10.4103/0970-9371.237824.

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32

Mardi, Kavita, Lalita Negi, Sudarshan Sharma, and Liza Negi. "Cytodiagnosis of spermatic granuloma." Journal of Cytology 38, no. 1 (2021): 52. http://dx.doi.org/10.4103/joc.joc_133_20.

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33

Siddiqui, Dr Zahid. "AN EVALUATION OF THE EFFICACY OF PREDICTIVE SLIDES IN MITIGATING CROSS-CONTAMINATION RISK IN CYTOPATHOLOGY LABORATORY STAINING METHODS." Era's Journal of Medical Research 10, no. 2 (December 2023): 22–25. http://dx.doi.org/10.24041/ejmr2023.30.

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The utilization of Diff-Quik stain has emerged as a potent assessment tool for triaging potentially malignant specimens. This evaluation procedure not only streamlines the diagnostic process but has also proven to be an effective means of identifying cases that warrant further scrutiny. In particular, the sensitivity of cytodiagnosis in effusions is significantly enhanced through the meticulous preparation of Diff-Quik stained slides. To check efficacy of predictive slides in mitigating cross-contamination risk in cytopathology laboratory staining methods. To evaluate the cytological disparencies in cytology reporting. The Methodology involves the subjection of the collected effusion samples to the Diff-Quik staining process for prompt identification of any cellular abnormalities enabling the early detection of potential malignancies. Due to the high importance of cytodiagnostic procedures with high sensitivity for distinguishing between benign and malignant samples, the application of the Diff-Quik staining process deems to be a pertinent tool in detecting subtle cellular alterations indicative of malignancy. It is imperative to note that the evaluation process using Diff-Quik staining method primarily focuses on minimizing the false negatives, this is to reduce the risk of contamination of subsequent slides. Due to this reduction, the probability of cross-contamination as also been reduced enhancing the validity of the subsequent diagnostic procedures. The preparation of Diff-Quik stained slides not only improves the accuracy of diagnosis but also contributes to the expedition of reporting, which enhances efficient workflow dynamic. In doing so, health care professionals can receive their results in a timely manner enabling them to make prompt decisions. In conclusion, the Diff-Quik staining method has proven to be an effective triage method for the identification of potentially malignant specimens due to its elevated sensitivity for cytodiagnosis and its enhanced efficiency for timely patient care.
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34

Usuda, Daisuke, Masahisa Arahata, Kento Takeshima, Ryusho Sangen, Akiteru Takamura, Yasuhiro Kawai, Yuji Kasamaki, Yoshitsugu Iinuma, and Tsugiyasu Kanda. "A Case of Diffuse Large B-Cell Lymphoma Mimicking Primary Effusion Lymphoma-Like Lymphoma." Case Reports in Oncology 10, no. 3 (November 16, 2017): 1013–22. http://dx.doi.org/10.1159/000484042.

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A 93-year-old female was transferred to the emergency ward of our hospital due to disturbance of consciousness and hypotension. Computed tomography showed bilateral pleural and pericardial effusion without evidence of tumor masses or lymphadenopathy. Cytodiagnosis of pleural effusion revealed proliferation of atypical lymphoid-like cells with pan-B surface markers. We suspected primary effusion lymphoma-like lymphoma; however, the monoclonality of these cells was not confirmed. Cytodiagnosis of bone marrow revealed lymphoma cells with monoclonal B-cell markers. These findings prompted a diagnosis of diffuse large B-cell lymphoma with bone marrow invasion. In the case of pericardial or pleural effusion, clinicians should consider carefully both hematological malignancy and its classification.
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35

Kar, Asaranti, Debasis Mukhopadhyay, SidharathaSankar Das, NarendraNath Swain, BhubanMohan Das, Manjushree Nayak, Jayashree Rath, and Surama Satpathy. "Cytodiagnosis of angiosarcoma of breast." Indian Journal of Pathology and Microbiology 51, no. 3 (2008): 427. http://dx.doi.org/10.4103/0377-4929.42551.

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36

Oland, J., A. Rosen, R. Reif, J. Sayfan, and R. Orda. "Cytodiagnosis of Soft Tissue Tumors." Journal of Urology 140, no. 5 Part 1 (November 1988): 1078. http://dx.doi.org/10.1016/s0022-5347(17)41951-3.

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37

Afroz, Nishat, Nazoora Khan, and R. S. Chana. "Cytodiagnosis of yolk sac tumor." Indian Journal of Pediatrics 71, no. 10 (October 2004): 939–42. http://dx.doi.org/10.1007/bf02830842.

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38

Anshu, A., Nitin Gangane, Sunita Vagha, and N. Samal. "Cytodiagnosis of Erythema Nodosum Leprosum." Acta Cytologica 46, no. 2 (2002): 386–88. http://dx.doi.org/10.1159/000326738.

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39

Oland, Jan, Ada Rosen, Renata Reif, Joel Sayfan, and Ruben Orda. "Cytodiagnosis of soft tissue tumors." Journal of Surgical Oncology 37, no. 3 (March 1988): 168–70. http://dx.doi.org/10.1002/jso.2930370307.

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40

Renshaw, Andrew A., Edward Wang, Dina R. Mody, David C. Wilbur, Diane D. Davey, and Terence J. Colgan. "Measuring the Significance of Field Validation in the College of American Pathologists Interlaboratory Comparison Program in Cervicovaginal Cytology: How Good Are the Experts?" Archives of Pathology & Laboratory Medicine 129, no. 5 (May 1, 2005): 609–13. http://dx.doi.org/10.5858/2005-129-0609-mtsofv.

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Abstract Context.—Expert opinion is often used as a gold standard for gynecologic cytology in the evaluation of new technologies, in the legal setting, and in the validation of cases for use in educational programs and proficiency testing. However, the reliability of expert opinion alone in selecting slides of a specific cytodiagnosis that can be reproducibly and reliably identified by subsequent reviewers has not been determined. Objective.—To assess the ability of expert opinion to select slides that are validated in subsequent reviews. Design.—In the College of American Pathologists Interlaboratory Comparison Program in Cervicovaginal Cytology, each case in every cytodiagnostic category is accepted for circulation only after review by 3 expert cytopathologists. The percentage of these cases that could not be reliably and reproducibly identified by program participants for each cytodiagnostic category (“failed field validation”) was determined during the duration of the program from 1989 to 2004. Results.—More than 10 000 conventional smears and ThinPrep cases were selected by the expert panel for circulation. Of these selected slides, 19% of conventional smears and 15% of ThinPrep specimens failed field validation. Compared with the overall slide performance, significantly higher percentages (P < .001) of conventional smears with reference diagnoses of unsatisfactory (51.7%), repair (58%), or low-grade intraepithelial lesion (31.8%) and of ThinPrep specimens with reference diagnoses of unsatisfactory (54.5%) and repair (76.9%) failed field validation. In contrast, significantly lower percentages of conventional smears with reference diagnoses of squamous cell carcinoma (4.5%), high-grade squamous intraepithelial lesion (9%), Trichomonas vaginalis infection (11.7%), or herpes (9.9%) and of ThinPrep specimens with reference diagnoses of adenocarcinoma (5.1%), herpes (2.1%), and fungal organism consistent with Candida (8.4%) failed field validation (P < .001 for all). Conclusions.—Between 15% and 19% of gynecologic cytologic cases that have been selected by expert cytopathologists as good examples of cytodiagnostic abnormalities fail field validation. The proportion of cases failing field validation varies with cytodiagnostic category, but it occurs in all cytodiagnostic entities.
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41

Tsuneki, Masayuki, Makoto Abe, and Fahdi Kanavati. "Deep Learning-Based Screening of Urothelial Carcinoma in Whole Slide Images of Liquid-Based Cytology Urine Specimens." Cancers 15, no. 1 (December 30, 2022): 226. http://dx.doi.org/10.3390/cancers15010226.

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Urinary cytology is a useful, essential diagnostic method in routine urological clinical practice. Liquid-based cytology (LBC) for urothelial carcinoma screening is commonly used in the routine clinical cytodiagnosis because of its high cellular yields. Since conventional screening processes by cytoscreeners and cytopathologists using microscopes is limited in terms of human resources, it is important to integrate new deep learning methods that can automatically and rapidly diagnose a large amount of specimens without delay. The goal of this study was to investigate the use of deep learning models for the classification of urine LBC whole-slide images (WSIs) into neoplastic and non-neoplastic (negative). We trained deep learning models using 786 WSIs by transfer learning, fully supervised, and weakly supervised learning approaches. We evaluated the trained models on two test sets, one of which was representative of the clinical distribution of neoplastic cases, with a combined total of 750 WSIs, achieving an area under the curve for diagnosis in the range of 0.984–0.990 by the best model, demonstrating the promising potential use of our model for aiding urine cytodiagnostic processes.
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42

Dwivedi, Gunja, Dharmendra Kumar Garg, and Ajay Gupta. "Cytodiagnosis of cutaneous leishmaniasis- a case report." Asian Pacific Journal of Health Sciences, Supplimentary 2014 (2014): 20–22. http://dx.doi.org/10.21276/apjhs.2014.1.1s.4.

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43

Pol, Jaydeep N., Neha M. Bhosale, Girish A. Kadkol, Madhura D. Phadke, and Swpana S. Magdum. "FNAC Diagnosis of eosinophilic variant of chromophobe renal cell carcinoma – A challenge for cytopathologists." IP Archives of Cytology and Histopathology Research 6, no. 4 (December 15, 2021): 283–87. http://dx.doi.org/10.18231/j.achr.2021.061.

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Chromophobe Renal Cell Carcinoma (ChRCC) is a rare distinct subtype of Renal cell carcinoma. It arises from intercalated cells of the renal cortex. The cytomorphological features of ChRCC show significant overlap with Clear cell Renal Cell Carcinoma (CCRCC) and Oncocytoma. The prognosis of ChRCC is intermediate between benign Renal Oncocytoma and the relatively aggressive CCRCC. Hence, a correct pre or intra-operative cytodiagnosis helps in deciding the extent of surgery. We report a case of eosinophilic variant of ChRCC in a 70 years female, diagnosed on Fine Needle Aspiration Cytology (FNAC).The Immunocytochemistry (ICC), histology and Immunohistochemistry confirmed the diagnosis of ChRCC. Diagnosing ChRCC; especially its eosinophilic variant on FNAC is very challenging. Prominent cellular heterogeneity, pleomorphism, perinuclear halos and binucleation are important diagnostic clues for cytodiagnosis of ChRCC. In difficult cases, ICC helps in confirming the diagnosis.
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44

Singh, Swati, and Mayurika S Tyagi. "Cytodiagnosis of multiarticular chronic tophaceous gout." Santosh University Journal of Health Sciences 5, no. 1 (July 15, 2019): 46–47. http://dx.doi.org/10.18231/j.sujhs.2019.011.

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45

Baisakh, ManasR, Radhika Narayanan, Minakshi Minakshi, and Rajesh Mohanty. "Cytodiagnosis of sternocleidomastoid tumor of infancy." Journal of Cytology 29, no. 2 (2012): 149. http://dx.doi.org/10.4103/0970-9371.97164.

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46

Walke, Vaishali A., Shubhangi V. Aagle, Vikas C. Maindad, Wasif Ali Khan, and Grace F. D’Costa. "Cytodiagnosis of Sebaceous Carcinoma of Eyelid." Journal of Case Reports 3, no. 1 (April 10, 2013): 110–13. http://dx.doi.org/10.17659/01.2013.0027.

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47

ANDO, Ichiro, Fuyuki ENIMOTO, Eiko NAKAZAWA, and Masato FUJIMORI. "Aspiration Cytodiagnosis in Salivary Gland Tumor." Practica Oto-Rhino-Laryngologica 95, no. 12 (2002): 1247–54. http://dx.doi.org/10.5631/jibirin.95.1247.

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48

NAKAGUCHI, Takenori, Isao ONO, Akio TASHIRO, Masayuki SOMA, Chieko ISHIWATA, Isamu ISHIWATA, and Makio MUKAI. "Cytodiagnosis of uterine mixed mesodermal tumor." Journal of the Japanese Society of Clinical Cytology 24, no. 4 (1985): 725–31. http://dx.doi.org/10.5795/jjscc.24.725.

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49

HIROKAWA, Mitsuyoshi. "A quality assurance program for cytodiagnosis." Journal of the Japanese Society of Clinical Cytology 33, no. 3 (1994): 407–13. http://dx.doi.org/10.5795/jjscc.33.407.

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50

AKOSA, A. B., L. A. DESA, I. PHILLIPS, I. S. BENJAMIN, J. M. POLAK, and T. KRAUSZ. "Aspiration cytodiagnosis of pancreatic endocrine tumours." Cytopathology 5, no. 6 (December 1994): 369–79. http://dx.doi.org/10.1111/j.1365-2303.1994.tb00442.x.

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