Medicine:Urethral cancer
Urethral cancer | |
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Micrograph of a urethral cancer, urothelial cell carcinoma, found on a prostate core biopsy. H&E stain. | |
Specialty | Oncology Urology |
Symptoms | Blood in the urine, lump at end of penis,[1] Bloody urethral discharge.[2] |
Urethral cancer is a rare cancer originating from the urethra.[1] The disease has been classified by the TNM staging system and the World Health Organization.[1][3][4]
Symptoms include blood in the urine, lump at end of penis,[1] or bloody penile discharge.[2]
Diagnosis is established by transurethral biopsy.[1]
The most common type is papillary urothelial carcinoma.[1][5] Risk factors suggested include prolonged irritations of the urethra due to urinary catheterization, chronic inflammation due to infection, radiation, diverticula of the urethra, and urethral strictures.[1]
Signs and symptoms
Symptoms that may be caused by urethral cancer include:
- Blood visible in urine.[1]
- Bloody urethral discharge.[2]
- Weak or interrupted flow of urine.
- Urination occurs often, painful urination, inability to pass urine.
- A lump or thickness in the perineum or penis.[1]
- Enlarged lymph nodes or pain in the groin or vaginal area.
Diagnosis
Diagnosis is established by transurethral biopsy and histological findings.[1] Bladder cystoscopy is performed to detect if there is simultaneous bladder cancer.[1]
Histology
Types of urethral cancer include the most common type urothelial carcinoma, and others including squamous cell carcinoma, and adenocarcinoma. Melanoma and sarcoma are rare.[1]
Staging
The World Health Organization classification of tumours of the urinary system and male genital organs (4th edn) was published in January 2016.[3] Urethral cancer has also been classified by the TNM staging system.[4]
T-category | Description |
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TX | Primary tumor cannot be assessed |
T0 | No evidence of primary tumor |
Urethra (male and female) | |
Ta | Noninvasive papillary, polypoid, or verrucous carcinoma |
Tis | Carcinoma in situ |
T1 | Tumor invades subepithelial connective tissue |
T2 | Tumor invades any of the following: corpus spongiosum, prostate, periurethral muscle |
T3 | Tumor invades any of the following: corpus cavernosum, beyond prostatic capsule, anterior vagina, bladder neck (extraprostatic extension) |
T4 | Tumor invades other adjacent organs (invasion of the bladder) |
Urothelial (transitional cell) carcinoma of the prostate | |
Tis pu | Carcinoma in situ, involvement of prostatic urethra |
Tis pd | Carcinoma in situ, involvement of prostatic ducts |
T1 | Tumor invades subepithelial connective tissue (for tumors involving prostatic urethra only) |
T2 | Tumor invades any of the following: prostatic stroma, corpus spongiosum, periurethral muscle |
Ta | Noninvasive papillary, polypoid, or verrucous carcinoma |
T3 | Tumor invades any of the following: corpus cavernosum, beyond prostatic capsule, bladder neck (extraprostatic extension) |
T4 | Tumor invades other adjacent organs (invasion of the bladder or rectum) |
N—regional lymph nodes | |
NX | Regional lymph nodes cannot be assessed |
N0 | No regional lymph node metastasis |
N1 | Metastasis in a single lymph node |
N2 | Metastasis in multiple lymph nodes |
M—Distant Metastasis | |
M0 | No distant metastasis |
M1 | Distant metastasis |
Treatment
Surgery is the most common treatment for cancer of the urethra.[6] One of the following types of surgery may be done: Open excision, Electro-resection with flash, Laser surgery, Cystourethrectomy, Cystoprostatectomy, Anterior body cavity, or Incomplete or basic penectomy surgery.
Radiation therapy has also been used in some cases.[1]
Chemotherapy is sometimes used to destroy urethral cancer cells. It is a systemic urethral cancer treatment (i.e., destroys urethral cancer cells throughout the body) that is administered orally or intravenously. Medications are often used in combination to destroy urethral cancer that has metastasized. Commonly used drugs include cisplatin, vincristine, and methotrexate.[clarification needed]
Side effects include anemia (causing fatigue, weakness), nausea and vomiting, loss of appetite, hair loss, mouth sores, increased risk for infection, shortness of breath, or excessive bleeding and bruising.[7]
Epidemiology
Primary urethral cancer is rare and contributes to less than 1% of all cancers. It is three times more common in men than women and its incidence rises after the age of 75.[1]
Around half of affected people have locally advanced disease when they first present.[1] 54–65% of cases are of the urothelial carcinoma type.[1]
Prolonged irritations of the urethra due to urinary catheterization, chronic inflammation due to infection, radiation, diverticula of the urethra, and urethral strictures, may increase the risk of primary urethral cancer.[1] Other risk factors include squamous cell carcinoma (SCC) and genital lichen sclerosus.[1]
Prognosis
A study of the National Cancer Database in the United States assessed cases of primary urethral cancer from 2004 to 2013, finding that median survival was 49 months with 5- and 10-year survival rates estimated at 46% and 31% respectively.[8] A study of the RARECARE project, aimed at investigating rare cancers in Europe, estimated a 5-year relative survival rate of 54% in patients with cancer of the urethra.[9]
See also
- Anterior urethral cancer
- Penile cancer
References
- ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 1.14 1.15 1.16 1.17 1.18 Janisch, Florian; Abufaraj, Mohammad; Fajkovic, Harun; Kimura, Shoji; Iwata, Takehiro; Nyirady, Peter; Rink, Michael; Shariat, Shahrokh F. (1 September 2019). "Current Disease Management of Primary Urethral Carcinoma" (in en). European Urology Focus 5 (5): 722–734. doi:10.1016/j.euf.2019.07.001. ISSN 2405-4569. PMID 31307949. https://www.eu-focus.europeanurology.com/article/S2405-4569(19)30172-5/fulltext.
- ↑ 2.0 2.1 2.2 Kahan, Scott; Miller, Redonda; Smith, Ellen G. (2008). "126. Penile Discharge" (in en). Signs and Symptoms. Lippincott Williams & Wilkins. ISBN 978-0-7817-7043-9. https://books.google.com/books?id=iDCuxfnbBgIC&pg=PA252.
- ↑ 3.0 3.1 3.2 Compérat, Eva; Varinot, Justine (2016). "Immunochemical and molecular assessment of urothelial neoplasms and aspects of the 2016 World Health Organization classification" (in en). Histopathology 69 (5): 717–726. doi:10.1111/his.13025. ISSN 1365-2559. PMID 27353436. https://onlinelibrary.wiley.com/doi/abs/10.1111/his.13025.
- ↑ 4.0 4.1 4.2 Brierley, James D.; Gospodarowicz, Mary K.; Wittekind, Christian (2017). "Urological Tumours" (in en). TNM Classification of Malignant Tumours (8th ed.). John Wiley & Sons. p. 208. ISBN 978-1-119-26354-8. https://books.google.com/books?id=642GDQAAQBAJ&pg=PP208.
- ↑ Ries, LAG; Young, JL; Keel, GE et al., eds (2007). "Chapter 30: Cancers of Rare Sites". SEER Survival Monograph: Cancer Survival Among Adults: US SEER Program, 1988–2001, Patient and Tumor Characteristics. SEER Program. NIH Pub. No. 07-6215. Bethesda, MD: National Cancer Institute. pp. 251–262. http://seer.cancer.gov/publications/survival. Retrieved 18 October 2013.
- ↑ Pagliaro, Lance (28 June 2016) (in en). Rare Genitourinary Tumors. Springer. p. 157. ISBN 978-3-319-30046-7. https://books.google.com/books?id=cgGPDAAAQBAJ&pg=PA157.
- ↑ Urethral Cancer Treatment
- ↑ Sui W, RoyChoudhury A, Wenske S, Decastro GJ, McKiernan JM, Anderson CB (2017). "Outcomes and Prognostic Factors of Primary Urethral Cancer.". Urology 100: 180–186. doi:10.1016/j.urology.2016.09.042. PMID 27720774.
- ↑ Visser O, Adolfsson J, Rossi S, Verne J, Gatta G, Maffezzini M (2012). "Incidence and survival of rare urogenital cancers in Europe.". Eur J Cancer 48 (4): 456–64. doi:10.1016/j.ejca.2011.10.031. PMID 22119351.
Classification | |
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External resources |
de:Urothelkarzinom
Original source: https://en.wikipedia.org/wiki/Urethral cancer.
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