- Primary Follicular Lymphoma of the Duodenum: A Case Report
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Jin Roh, Jooryung Huh, Chan-Sik Park
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J Pathol Transl Med. 2016;50(6):479-481. Published online May 9, 2016
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DOI: https://doi.org/10.4132/jptm.2016.01.27
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- A Rare Case of Primary Duodenal Follicular Lymphoma
Hyun-Jung Kim, Jeongmin Choi Journal of Digestive Cancer Research.2022; 10(1): 39. CrossRef - The role of dual time point PET/CT for distinguishing malignant from benign focal 18F-FDG uptake duodenal lesions
Ri Sa, Hong-Guang Zhao, Yu-Yin Dai, Feng Guan Medicine.2018; 97(38): e12521. CrossRef
- Immunohistochemistry for Pathologists: Protocols, Pitfalls, and Tips
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So-Woon Kim, Jin Roh, Chan-Sik Park
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J Pathol Transl Med. 2016;50(6):411-418. Published online October 13, 2016
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DOI: https://doi.org/10.4132/jptm.2016.08.08
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Abstract
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- Immunohistochemistry (IHC) is an important auxiliary method for pathologists in routine diagnostic work as well as in basic and clinical research including exploration of biomarkers, as IHC allows confirmation of target molecule expressions in the context of microenvironment. Although there has been a considerable progress in automation and standardization of IHC, there are still many things to be considered in proper optimization and appropriate interpretation. In this review, we aim to provide possible pitfalls and useful tips for practicing pathologists and residents in pathology training. First, general procedure of IHC is summarized, followed by pitfalls and tips in each step and a summary of troubleshooting. Second, ways to an accurate interpretation of IHC are discussed, with introduction to general quantification and analysis methods. This review is not intended to provide complete information on IHC, but to be used as a basic reference for practice and publication.
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- Clear Cell Papulosis: A Case Report
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So-Woon Kim, Jin Roh, Chan-Sik Park
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J Pathol Transl Med. 2016;50(5):401-403. Published online May 29, 2016
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DOI: https://doi.org/10.4132/jptm.2016.02.16
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- CD99 Is Strongly Expressed in Basal Cells of the Normal Adult Epidermis and Some Subpopulations of Appendages: Comparison with Developing Fetal Skin
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Gawon Choi, Jin Roh, Chan-Sik Park
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J Pathol Transl Med. 2016;50(5):361-368. Published online August 7, 2016
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DOI: https://doi.org/10.4132/jptm.2016.06.19
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8,303
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Abstract
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- Background
CD99 is a cell surface transmembrane glycoprotein expressed in various tissues. CD99 is differentially expressed between subpopulations of each tissue and is highly expressed in certain hematopoietic and precursor cells. However, there has been no comprehensive study of CD99 expression in normal skin. We evaluated CD99 expression in normal human skin and developing fetal skin.
Methods Seventy-five adult skin samples containing normal skin and eight fetal skin samples of different gestational ages were collected. CD99 immunohistochemical staining was performed to evaluate expression pattern in adult and fetal skin samples. CD99 and CD34 expression were compared by double immunofluorescence.
Results In normal adult skin, CD99 was strongly expressed in the membrane of epidermal basal keratinocytes, hair follicle bulges and outer root sheaths, and inner secretory cells of eccrine sweat glands. In fetal skin, CD99 was not expressed on the periderm at 16 weeks of gestation but was expressed in basal cells of fetal skin at around 19 weeks of gestation. CD99 expression became comparable to that of the adult skin after 20 weeks of gestation. CD99 and CD34 were co-expressed in hair follicle outer root sheaths, as seen by double immunofluorescence study.
Conclusions This is the first study examining CD99 expression pattern in normal adult and fetal skin. CD99 tends to be expressed in the basal/precursor cells of epidermis and in hair follicles. These results provide a basis for future investigation on functions of CD99 in the skin and provide a novel potential target for the treatment of dermatologic lesions.
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Michela Pasello, Maria Cristina Manara, Katia Scotlandi Journal of Cell Communication and Signaling.2018; 12(1): 55. CrossRef - CD99: A Cell Surface Protein with an Oncojanus Role in Tumors
Maria Manara, Michela Pasello, Katia Scotlandi Genes.2018; 9(3): 159. CrossRef
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Jin Roh, So-Woon Kim, Chan-Sik Park
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J Pathol Transl Med. 2016;50(1):78-81. Published online August 4, 2015
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DOI: https://doi.org/10.4132/jptm.2015.07.03
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Jin Roh, Min Jeong Song, Mi Woo Lee, Chan-Sik Park
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Korean J Pathol. 2014;48(5):394-397. Published online October 27, 2014
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DOI: https://doi.org/10.4132/KoreanJPathol.2014.48.5.394
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- Current Concepts in Primary Effusion Lymphoma and Other Effusion-Based Lymphomas
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Yoonjung Kim, Chan Jeong Park, Jin Roh, Jooryung Huh
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Korean J Pathol. 2014;48(2):81-90. Published online April 28, 2014
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DOI: https://doi.org/10.4132/KoreanJPathol.2014.48.2.81
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Primary effusion lymphoma (PEL) is a human herpes virus 8 (HHV8)-positive large B-cell neoplasm that presents as an effusion with no detectable tumor in individuals with human immunodeficiency virus infection or other immune deficiencies. PEL is an aggressive neoplasm with a poor prognosis. PEL cells show diverse morphologies, ranging from immunoblastic or plasmablastic to anaplastic. The immunophenotype of PEL is distinct, but its lineage can be misdiagnosed if not assessed thoroughly. PEL cells usually express CD45, lack B- and T-cell-associated antigens, and characteristically express lymphocyte activation antigens and plasma cell-associated antigens. Diagnosis of PEL often requires the demonstration of a B-cell genotype. HHV8 must be detected in cells to diagnose PEL. In most cases, PEL cells also harbor the Epstein-Barr virus (EBV) genome. Similar conditions associated with HHV8 but not effusion-based are called "extracavitary PELs." PELs should be differentiated from HHV8-negative, EBV-positive, body cavity-based lymphomas in patients with long-standing chronic inflammation; the latter can occur in tuberculous pleuritis, artificial pneumothorax, chronic liver disease and various other conditions. Despite their morphological similarity, these various lymphomas require different therapeutic strategies and have different prognostic implications. Correct diagnosis is essential to manage and predict the outcome of patients with PEL and related disorders.
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- Prognostic Significance of Absolute Lymphocyte Count/Absolute Monocyte Count Ratio at Diagnosis in Patients with Multiple Myeloma
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Su-Jin Shin, Jin Roh, Misung Kim, Min Jung Jung, Young Wha Koh, Chan-Sik Park, Dok Hyun Yoon, Cheolwon Suh, Chan-Jeong Park, Hyun Sook Chi, Jooryung Huh
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Korean J Pathol. 2013;47(6):526-533. Published online December 24, 2013
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DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.6.526
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Abstract
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- Background
Absolute lymphocyte count (ALC) in peripheral blood has recently been reported to be an independent prognostic factor in multiple myeloma (MM). Previous studies indicated that the absolute monocyte count (AMC) in peripheral blood reflects the state of the tumor microenvironment in lymphomas. Neither the utility of the AMC nor its relationship with ALC has been studied in MM. MethodsThe prognostic value of ALC, AMC, and the ALC/AMC ratio at the time of diagnosis was retrospectively examined in 189 patients with MM. ResultsOn univariate analysis, low ALC (<1,400 cells/µL), high AMC (≥490 cells/µL), and low ALC/AMC ratio (<2.9) were correlated with worse overall survival (OS) (p=.002, p=.038, and p=.001, respectively). On multivariate analysis, the ALC/AMC ratio was an independent prognostic factor (p=.047), whereas ALC and AMC were no longer statistical significant. Low ALC, high AMC, and low ALC/AMC ratio were associated with poor prognostic factors such as high International Staging System stage, plasmablastic morphology, hypoalbuminemia, and high β2-microglobulin. ConclusionsUnivariate analysis demonstrated that changes in ALC, AMC, and the ALC/AMC ratio are associated with patient survival in MM. Multivariate analysis showed that, of these factors, the ALC/AMC ratio was an independent prognostic factor for OS.
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