Journal of Pathology and Translational Medicine

Brief Case Report

Goblet Cell Carcinoid of the Rectum in a Patient with Neurofibromatosis Type 1: Youngjin Kang, Jung-Woo Choi, Younghye Kim, Hwa Eun Oh, Ju-Han Lee, Young-Sik Kim; J Pathol Transl Med. 2016;50(6):482-485. Published online May 29, 2016; DOI: https://doi.org/10.4132/jptm.2016.02.27

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Citations

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A rare goblet cell adenocarcinoma arising from Barrett’s esophagus: the first reported case in the esophagus
Chi Eun Oh, Sung Eun Kim, Sun-Ju Oh
Journal of Pathology and Translational Medicine.2024; 58(2): 81. CrossRef
Goblet cell adenocarcinoma of the anal canal with perianal Paget disease: A rare case report with literature review
Minhua Li, Xiaofei Yao
Medicine.2023; 102(16): e33598. CrossRef
A Case of Goblet Cell Carcinoid of the Transverse Colon
Yuko Kamata, Hiroshi Kuwabara, Masafumi Akasu, Morio Koike
Nippon Daicho Komonbyo Gakkai Zasshi.2022; 75(7): 366. CrossRef
Mixed Neuroendocrine Non-neuroendocrine Neoplasm of Anorectum with Goblet Cell Morphology
Sandhya Biswal, Anirban Kundu, Ankit Sahoo, Prakash Kumar Sasmal, Biswajit Sahoo, Suvradeep Mitra
Journal of Gastrointestinal Cancer.2021; 52(3): 1093. CrossRef
Goblet cell carcinoid of the rectum: a case report
Yoshiyuki Inoue, Hisanaga Horie, Yuko Homma, Ai Sadatomo, Makiko Tahara, Koji Koinuma, Hironori Yamaguchi, Toshiki Mimura, Atsushi Kihara, Alan Kawarai Lefor, Naohiro Sata
Surgical Case Reports.2020;[Epub] CrossRef

Case Study

Human Herpesvirus 8-Negative and Epstein-Barr Virus-Positive Effusion-Based Lymphoma in a Patient with Human Immunodeficiency Virus: Jung-Woo Choi, Younghye Kim, Ju-Han Lee, Young-Sik Kim; J Pathol Transl Med. 2015;49(5):409-412. Published online June 17, 2015; DOI: https://doi.org/10.4132/jptm.2015.06.03

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A 39-year-old man infected with human immunodeficiency virus (HIV) was admitted to our hospital because of sudden onset of chest pain. Chest radiography revealed pneumothorax of the right lung. Computed tomographic scans disclosed a 5.8-cm-sized emphysematous bulla in the right middle lobe of the lung. Histologically, the wedge-resected lung showed medium to large atypical cells within the bullous cavity of the Pneumocystis jirovecii pneumonia, without solid mass formation. These atypical cells were confirmed to be large B-cell lymphoma, Epstein-Barr virus–positive and human herpesvirus 8–negative. Therefore, this case was not diagnosed as primary effusion lymphoma, but effusion-based lymphoma arising in an emphysematous cavity of an HIV-infected patient. This type of effusion-based lymphoma has never been reported, and, although rare, it should be noted in order to clinically diagnose this lymphoma.

Citations

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Primary Effusion Lymphoma: A Timely Review on the Association with HIV, HHV8, and EBV
Chih-Yi Liu, Bo-Jung Chen, Shih-Sung Chuang
Diagnostics.2022; 12(3): 713. CrossRef
Human herpesvirus 8-negative effusion-based large B-cell lymphoma: a distinct entity with unique clinicopathologic characteristics
Savanah D. Gisriel, Ji Yuan, Ryan C. Braunberger, Danielle L.V. Maracaja, Xueyan Chen, Xiaojun Wu, Jenna McCracken, Mingyi Chen, Yi Xie, Laura E. Brown, Peng Li, Yi Zhou, Tarsheen Sethi, Austin McHenry, Ronald G. Hauser, Nathan Paulson, Haiming Tang, Eric
Modern Pathology.2022; 35(10): 1411. CrossRef
Age and CD20 Expression Are Significant Prognostic Factors in Human Herpes Virus-8-negative Effusion-based Lymphoma
Tomomi Kubota, Yosuke Sasaki, Eisuke Shiozawa, Masafumi Takimoto, Tsunekazu Hishima, Ja-Mun Chong
American Journal of Surgical Pathology.2018; 42(12): 1607. CrossRef

Case Report

Urachal Mucinous Tumor of Uncertain Malignant Potential: A Case Report: Jung-Woo Choi, Ju-Han Lee, Young-Sik Kim; Korean J Pathol. 2012;46(1):83-86. Published online February 23, 2012; DOI: https://doi.org/10.4132/KoreanJPathol.2012.46.1.83

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Abstract PDF

Urachal mucinous tumor of uncertain malignant potential is very rare and is characterized by a multilocular cyst showing the proliferation of atypical mucin-secreting cells without stromal invasion. As in ovarian and appendiceal borderline tumors, it represents a transitional stage of mucinous carcinogenesis in the urachus. In addition, this tumor may recur locally and develop into pseudomyxoma peritonei. Due to its scarcity and diagnostic challenges, we report a mucinous tumor of uncertain malignant potential arising in the urachus.

Citations

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Mucinous Cystadenoma of the Urachus and Review of Current Classification of Urachal Mucinous Cystic Neoplasms
Diping Wang, Norbert Sule
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Urachal Mucinous Cystic Tumor of Low Malignant Potential with Concurrent Sigmoid Colon Adenocarcinoma
Kelly Brennan, Paul Johnson, Heather Curtis, Thomas Arnason
Case Reports in Gastrointestinal Medicine.2019; 2019: 1. CrossRef
Pseudomyxoma Peritonei Arising from Mucinous Cystadenoma of the Urachus with Postoperative Disease-Free Survival over 15 Years
Tomoki Kobayashi, Shinichi Mizuno, Hideki Matsuba, Min Kanamori, Toshio Tamauchi, Makoto Urano
The Japanese Journal of Gastroenterological Surgery.2019; 52(6): 307. CrossRef
Urachal borderline mucinous cystadenoma
Jingjun Wu, Ailian Liu, Anliang Chen, Pengxin Zhang
Medicine.2017; 96(47): e8740. CrossRef
Incidental Finding of a Rare Urachal Pathology: Urachal Mucinous Cystic Tumour of Low Malignant Potential
Luke L. Wang, Heath Liddell, Sharman Tan Tanny, Briony Norris, Sree Appu, David Pan
Case Reports in Urology.2016; 2016: 1. CrossRef
A Case of Borderline Mucinous Cystadenoma Thought to be of Urachal Origin
Kiichiro YAGUCHI, Yoshihito GOMYO, Hiroyasu SAITO, Tatsuo IKENO, Hiromi SAKAGUCHI, Hideo MIYAMOTO
Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association).2014; 75(5): 1418. CrossRef
An unexpected mass of the urachus: a case report
Monica C. Pasternak, Jonathan D. Black, Natalia Buza, Masoud Azodi, Aileen Gariepy
American Journal of Obstetrics and Gynecology.2014; 211(4): e1. CrossRef

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