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Original Article
Eosinophils in Colorectal Neoplasms Associated with Expression of CCL11 and CCL24
Hyuck Cho, Sung-Jig Lim, Kyu Yeoun Won, Go Eun Bae, Gou Young Kim, Ji Won Min, Byeong-joo Noh
J Pathol Transl Med. 2016;50(1):45-51.   Published online December 14, 2015
DOI: https://doi.org/10.4132/jptm.2015.10.16
  • 9,096 View
  • 121 Download
  • 39 Web of Science
  • 39 Crossref
AbstractAbstract PDF
Background
A decrease in the number of tissue eosinophils is known to reflect the malignancy potential of neoplastic lesions and even prognosis. Increased levels of the chemokines CCL11 and CCL24 in serum and tissue are also known to have diagnostic value as serum tumor markers or prognostic factors. The aim of this study was to evaluate the correlation between the degree of tissue eosinophilia and the expression of these chemokines in the glandular and stromal cells of colorectal neoplastic lesions ranging from benign to malignant tumors. Methods: We counted the number of infiltrating eosinophils in neoplastic lesion tissue and we evaluated the expression of CCL11 and CCL24 in glandular cells and stromal cells by immunohistochemical staining. Results: The results showed that the number of eosinophils decreased significantly and the expression of CCL11 and CCL24 in glandular cells decreased with tumor progression, whereas the stromal expression of CCL11 and CCL24 appeared to increase. Conclusions: The discrepancy in CCL11 and CCL24 expression between glandular cells and stromal cells might shed light on how colorectal cancer evades the immune system, which would enable further development of immunotherapies that target these chemokines. Further research on eosinophil biology and the expression pattern of chemokines in tumor cells is needed.

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    International Journal of Molecular Sciences.2021; 22(7): 3801.     CrossRef
  • CCL24 Protects Renal Function by Controlling Inflammation in Podocytes
    Youdi Wang, Xue Wu, Mengya Geng, Jiamin Ding, Kangjia Lv, Hui Du, Jiahui Ding, Wenjun Pei, Xin Hu, Jing Gu, Lizhuo Wang, Yao Zhang, Jialin Gao, Roberta Rizzo
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  • Eotaxins and Their Receptor in Colorectal Cancer—A Literature Review
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    Cancers.2020; 12(6): 1383.     CrossRef
  • Eosinophilic peritonitis with colon cancer: a case report
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Brief Case Report
Ovarian Remnant Syndrome at the Trochar Site: A Report of a Rare Complication Following Laparoscopic Ovarian Surgery
Ki Yong Na, Ji-Youn Sung, Kyu Yeoun Won, Gou Young Kim, Sung-Jig Lim, Suk-Hwan Lee
Korean J Pathol. 2013;47(3):304-306.   Published online June 25, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.3.304
  • 7,640 View
  • 53 Download
  • 4 Crossref
PDF

Citations

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  • Síndrome de ovario remanente. Revisión bibliográfica. Evidencia actual
    M. Arnáez de la Cruz, J. Gallardo Martínez
    Clínica e Investigación en Ginecología y Obstetricia.2023; 50(4): 100902.     CrossRef
  • Clear cell carcinoma arising in an ovarian remnant 19 years after oophoerctomy: case report
    Ting-ting Yao, Shao-jie Zhao, Bing Zhang
    BMC Women's Health.2023;[Epub]     CrossRef
  • Clear-Cell Carcinoma Developing in Remnant Ovary After Hysterectomy and Bilateral Salpingo-Oophorectomy for Endometriosis
    Satoshi Ichigo, Hiroshi Takagi, Kazutoshi Matsunami, Takayuki Murase, Tsuneko Ikeda, Atsushi Imai
    Journal of Gynecologic Surgery.2014; 30(2): 114.     CrossRef
  • Malignant neoplasia arising from ovarian remnants following bilateral salpingo-oophorectomy (Review)
    ATSUSHI IMAI, KAZUTOSHI MATSUNAMI, HIROSHI TAKAGI, SATOSHI ICHIGO
    Oncology Letters.2014; 8(1): 3.     CrossRef
Case Study
Extrapelvic Uterus-like Masses Presenting as Colonic Submucosal Tumor: A Case Study and Review of Literature
Ki Yong Na, Gou Young Kim, Kyu Yeoun Won, Hyun-Soo Kim, Sang Won Kim, Chi Hoon Lee, Jae Myung Cha
Korean J Pathol. 2013;47(2):177-181.   Published online April 24, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.2.177
  • 7,800 View
  • 59 Download
  • 14 Crossref
AbstractAbstract PDF

A uterus-like mass (ULM) is a central cavity lined by endometrial glands and stroma and surrounded by thick-walled smooth muscles. To date, 31 cases of ULM have been reported in the English literature. ULM typically presents as a single mass and is located in the pelvic cavity. We report here a very rare case of multiple extrapelvic ULMs involving the cecum, descending colon, and mesocolon. After extensive literature research, our case appears to be the first case of multiple ULMs found in extrapelvic sites and the first case of ULM in the colon. The present case suggests that ULM should be included in the differential diagnosis of colonic submucosal tumors in female patients with chronic abdominal pain or menstruation-associated symptoms.

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  • Extrauterine adenomyoma: A case report and systematic review of the literature
    Matteo Giorgi, Luca Labanca, Gabriele Centini, Lucia Lazzeri, Francesco Giuseppe Martire, Ester Sorrentino, Virginia Mancini, Diego Raimondo, Antonio Raffone, Daniele Neola, Anna Chiara Aru, Nassir Habib, Paolo Casadio, Renato Seracchioli, Errico Zupi
    International Journal of Gynecology & Obstetrics.2024; 164(3): 869.     CrossRef
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    Neha Bakshi, Shashi Dhawan
    International Journal of Surgical Pathology.2023; 31(5): 791.     CrossRef
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    Yanlin Chen, Liangyong Deng, Jingbo Zhao, Tianwen Luo, Zhong Zuo
    Medicine.2022; 101(36): e30240.     CrossRef
  • Pelvic Pain and Adnexal Mass: Be Aware of Accessory and Cavitated Uterine Mass
    Pooya Iranpour, Sara Haseli, Pedram Keshavarz, Amirreza Dehghanian, Neda Khalili, Michael S. Firstenberg
    Case Reports in Medicine.2021; 2021: 1.     CrossRef
  • Endomyometriosis of the Rectum With Disseminated Peritoneal Leiomyomatosis 8 Years After Laparoscopic Myomectomy: A Case Report
    Giorgio La Greca, Cristina Colarossi, Paolo Di Mattia, Cecilia Gozzo, Marco De Zuanni, Eliana Piombino, Lorenzo Memeo
    Frontiers in Surgery.2021;[Epub]     CrossRef
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    Tharani Putta, Reetu John, Betty Simon, Kirthi Sathyakumar, Anuradha Chandramohan, Anu Eapen
    Indian Journal of Radiology and Imaging.2021; 31(03): 545.     CrossRef
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    Viola Liberale, Alessandra Surace, Lorenzo Daniele, Luca Liban Mariani
    Heliyon.2020; 6(7): e04406.     CrossRef
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    Winesh Ramphal, Chloé M L Peters, Luthy S M Alcalá, Dennis van Hamont, Paul D Gobardhan
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    Journal of Gynecologic Surgery.2020; 36(6): 350.     CrossRef
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    Lei Liu, Hui Yang, Shu-Peng Zhang
    Medicine.2019; 98(38): e17246.     CrossRef
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    P.G. Paul, Gunjan Gulati, Hemant Shintre, Sumina Mannur, George Paul, Santwan Mehta
    European Journal of Obstetrics & Gynecology and Reproductive Biology.2018; 228: 130.     CrossRef
  • Uterus-like mass
    Jian He, Jie Xu, Hong-Yan Zhou
    Medicine.2016; 95(39): e4961.     CrossRef
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    Michael A. Ulm, David B. Robins, Edwin M. Thorpe, Mark E. Reed
    Obstetrics & Gynecology.2014; 124(2): 445.     CrossRef
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    Raul S. González, Cindy L. Vnencak-Jones, Chanjuan Shi, Oluwole Fadare
    International Journal of Surgical Pathology.2014; 22(5): 421.     CrossRef
Case Report
Collision Tumor Composed of a Granulocytic Sarcoma and an Adenocarcinoma of the Stomach: A Case Report.
Kyu Yeoun Won, Juhie Lee, Yong Ho Kim, Youn Wha Kim
Korean J Pathol. 2011;45(2):201-204.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.2.201
  • 3,316 View
  • 13 Download
  • 2 Crossref
AbstractAbstract PDF
Granulocytic sarcoma, also called chloroma or myeloblastoma, is an extramedullary invasive tumor composed of neoplastic myeloid cells. In this report, we describe a 43-year-old male patient with a collision tumor composed of an adenocarcinoma and a granulocytic sarcoma in the stomach. The coexistence of a granulocytic sarcoma and adenocarcinoma in the stomach has, to the best of our knowledge, not been reported in the literature. The diagnosis of granulocytic sarcoma is very difficult; especially in the absence of concurrent hematologic disease or in the uncommon setting of coexistence with another tumor. Cautious observation is needed when a finding of unusual atypical cells admixed with an adenocarcinoma in the stomach is confronted.

Citations

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    Isabel Cunningham, Daniel Worthley
    American Journal of Hematology.2018; 93(11): 1327.     CrossRef
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    D Tucker, P Sarsfield, I Chandler, P Kerr
    Journal of Clinical Pathology.2014; 67(1): 70.     CrossRef
Original Article
Uncoupling Protein 2 (UCP2) and p53 Expression in Invasive Ductal Carcinoma of Breast.
Kyu Yeoun Won, Gou Young Kim, Youn Wha Kim, Sung Jig Lim, Jeong Yoon Song
Korean J Pathol. 2010;44(6):565-570.
DOI: https://doi.org/10.4132/KoreanJPathol.2010.44.6.565
  • 3,912 View
  • 26 Download
  • 2 Crossref
AbstractAbstract PDF
BACKGROUND
Uncoupling protein 2 (UCP2) is a recently identified mitochondrial inner membrane anion carrier and a negative regulator of reactive oxygen species production. In this study, we evaluated the characteristics and relationships of UCP2 and p53 expression in breast cancer tissues.
METHODS
Tissue microarray slides from 107 cases of invasive ductal carcinoma of the breast were constructed, UCP2 and p53 immunohistochemical staining was conducted, and clinicopathological correlations were investigated.
RESULTS
UCP2 expression in invasive ductal carcinoma was high in 53 cases (49.5%), while p53 expression in invasive ductal carcinoma was high in 37 cases (34.6%). UCP2 expression was correlated significantly with histological grade (p = 0.038) and mitotic count (p = 0.050). UCP2 expression was correlated significantly with p53 expression in invasive ductal carcinoma of the breast (p = 0.045). UCP2 expression (p = 0.8308) and p53 expression (p = 0.3292) showed no significant difference for the overall survival rate in patients with invasive ductal carcinoma.
CONCLUSIONS
UCP2 expression in invasive ductal carcinoma increased proportionally with histological grade and mitotic count. High UCP2 expression in invasive ductal carcinoma was observed in conjunction with high p53 expression.

Citations

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  • Forkhead box protein A1 inhibits the expression of uncoupling protein 2 in hydrogen peroxide-induced A549 cell line
    Lan Song, Zhaojun Xu, Ling Li, Mei Hu, Lijuan Cheng, Lingli Chen, Bo Zhang
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    Delira Robbins, Yunfeng Zhao
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Case Report
Chondromyxoid Fibroma of the Ethmoid Sinus Complicated by a Brain Abscess: A Case Report and Literature Review.
Kyu Yeoun Won, Juhie Lee, Youn Wha Kim, Eui Jong Kim, Sung Wan Kim, Yong Koo Park
Korean J Pathol. 2010;44(5):547-550.
DOI: https://doi.org/10.4132/KoreanJPathol.2010.44.5.547
  • 3,012 View
  • 20 Download
  • 2 Crossref
AbstractAbstract PDF
Chondromyxoid fibroma (CMF) is a relatively rare bone tumor that was first described by Jaffe and Lichtenstein in 1948. CMF of the sinonasal tract is very rare. A 28-year-old male presented with long-standing, intermittent, pulsatile pain in the right temporal area. A computed tomography scan showed a 20 x 19 mm round, bony density in the right ethmoid sinus with fluid collection in the ethmoid and frontal sinuses. Additionally, a cystic lesion with surrounding edema was found in the right frontal lobe. The patient underwent a partial ethmoidectomy and frontostomy. A histological examination showed polygonal and stellate cells in a myxoid and chondroid background with a pattern of lobulation and plaque-like calcification. The bone lesion was revealed as a CMF of the ethmoidal sinus, and the frontal lobe cystic lesion was a brain abscess associated with the CMF. We present the case of a CMF of the ethmoid sinus complicated by a brain abscess.

Citations

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  • Juxtacortical chondromyxoid fibroma in the small bones: two cases with unusual location and a literature review
    Sun-Ju Oh, So Hak Chung
    Journal of Pathology and Translational Medicine.2022; 56(3): 157.     CrossRef
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    Zhi-Chao Zhu, Yi-Fei Yang, Xu Yang, Yan Liu, Yi-nan Cheng, Zhao-Yao Sun, Tian-Shu Xu, Wen-Jun Yang
    Medicine.2018; 97(31): e11707.     CrossRef

J Pathol Transl Med : Journal of Pathology and Translational Medicine