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Case Reports
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
  • 9,645 View
  • 61 Download
  • 8 Crossref
AbstractAbstract 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

Citations to this article as recorded by  
  • Exploring the Enigma of a Urachal Mucinous Cystic Tumor of Low Malignant Potential (MCTLMP): A Case Report and Literature Review
    Klaas De Corte, Ali Ramadhan
    Cureus.2025;[Epub]     CrossRef
  • Mucinous Cystadenoma of the Urachus and Review of Current Classification of Urachal Mucinous Cystic Neoplasms
    Diping Wang, Norbert Sule
    Archives of Pathology & Laboratory Medicine.2019; 143(2): 258.     CrossRef
  • 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
Combined Xanthogranulomatous Urachitis and Bullous Cystitis: A Case Report.
Ji Eun Kwak, Han Seong Kim, Mee Joo, Sun Hee Chang, Sang Hwa Shim, Je G Chi, In Rae Cho
Korean J Pathol. 2008;42(1):41-44.
  • 1,982 View
  • 28 Download
AbstractAbstract PDF
Xanthogranulomatous inflammation of the urachus is a very rare benign chronic inflammatory disease of an unknown etiology. Herein we report a case of a 31-year-old woman who complained of lower abdominal pain and dysuria. Cystoscopy revealed a bullous change at the dome of the urinary bladder. MRI revealed a cystic mass above the bladder dome that extended to the umbilicus. A partial cystectomy with urachal resection was performed. Pathological examination revealed xanthogranulomatous urachitis combined with bullous cystitis.
Urachal Adenocarcinoma with a Concomitant Urachal Remnant: A Case Report.
Tae Hoon Kim, Mee Joo, Min Kyung Kim, Hanseong Kim, Je G Chi, Jae Y Ro
Korean J Pathol. 2004;38(4):280-283.
  • 1,886 View
  • 17 Download
AbstractAbstract PDF
Urachal adenocarcinoma is a rare tumor, and it has similarities with nonurachal adenocarcinoma; therefore, it is sometimes difficult to make a diagnosis. We present a typical case of urachal adenocarcinoma that had all the diagnostic criteria including the presence of an urachal remnant. A 65-year-old woman presented with complaints of a painless gross hematuria. Pelvic CT and cystoscopy showed an intraluminal protruding mass centered in the bladder wall. When diagnosed as adenocarcinoma with a signet ring cell component being noted by frozen biopsy, partial cystectomy with resection of the median umbilical ligament and peritoneum was carried out for a suspected urachal adenocarcinoma. The tumor morphology showed as typical mucinous adenocarcinoma. Characteristic tubular structures showing the typical histology of an urachal remnant was found in the perivesical fat. On immunohistochemical staining, the urachal adenocarcinoma showed a pattern similar to colonic adenocarcinoma, while the urachal remnant showed strong positivity for CK7 and Chromogranin A.

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