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Updated: Jul 15, 2026

Comparison of Predictive Performance of Three Lymph Node Staging Systems in Colorectal Signet Ring Cell Carcinoma Based on Machine Learning Model
Published on: April 18, 2025
Urachal signet ring cell carcinoma
Akihiro Morii1, Yuzo Furuya, Yasuyoshi Fujiuchi
1Department of Urology, Faculty of Medicine, University of Toyama, Toyama, Japan. amorii@med.u.toyama.ac.jp
This case study highlights a rare urachal signet ring cell carcinoma in a 65-year-old man. Despite advanced metastasis, the patient survived five years with chemotherapy and surgery.
Area of Science:
- Urologic Oncology
- Surgical Pathology
Background:
- Urachal adenocarcinoma is an uncommon malignancy with a generally poor prognosis.
- Signet ring cell carcinoma is a rare subtype, posing diagnostic and therapeutic challenges.
Observation:
- A 65-year-old male presented with microscopic hematuria.
- Initial investigations revealed an urachal tumor confirmed by cystoscopy and transurethral biopsy.
Findings:
- The patient underwent radical cystectomy and chemotherapy.
- Metastases to ureters causing bilateral hydronephrosis and para-aortic lymph nodes leading to bowel obstruction were observed.
- The patient survived for five years post-treatment, including chemotherapy and a bypass operation.
Implications:
- This case underscores the importance of considering rare urachal neoplasms.
- Aggressive multimodal treatment, including chemotherapy and surgical intervention, can lead to long-term survival even in advanced cases.
- Further research into urachal carcinoma subtypes and treatment strategies is warranted.
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