Urachal cancer: Difference between revisions

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'''Urachal cancer''' is a rare form of [[cancer]] that occurs in the [[urachus]], a primitive structure that connects the [[umbilical cord]] to the [[bladder]] in fetal development. This structure normally disappears before birth, but in some cases, it may persist and give rise to urachal cancer later in life.
== Urachal Cancer ==
 
'''Urachal cancer''' is a rare type of cancer that originates in the [[urachus]], a vestigial remnant of the [[allantois]] that connects the fetal bladder to the [[umbilicus]]. This type of cancer is most commonly found in the [[bladder]] dome and is often diagnosed at an advanced stage due to its asymptomatic nature in early development.
 
== Pathophysiology ==
The urachus is a fibrous cord that is usually obliterated after birth, forming the [[median umbilical ligament]]. However, in some cases, remnants of the urachus persist and can give rise to malignancies. Urachal cancer is predominantly [[adenocarcinoma]], accounting for about 90% of cases, with other histological types being much less common.


== Symptoms ==
== Symptoms ==
The symptoms of urachal cancer can be non-specific and may be mistaken for other conditions. They include [[hematuria]] (blood in the urine), pain or discomfort in the lower abdomen, and a palpable mass in the abdomen.
Symptoms of urachal cancer are often non-specific and may include [[hematuria]] (blood in urine), [[abdominal pain]], and a palpable mass. Due to the deep location of the urachus, these symptoms often appear only when the disease is advanced.


== Diagnosis ==
== Diagnosis ==
Diagnosis of urachal cancer can be challenging due to its rarity and non-specific symptoms. It often involves imaging studies such as [[ultrasound]], [[CT scan]], or [[MRI]], as well as [[biopsy]] of the suspected tumor. The definitive diagnosis is usually made by histopathological examination of the surgical specimen.
Diagnosis of urachal cancer typically involves imaging studies such as [[ultrasound]], [[CT scan]], or [[MRI]] to identify the presence of a mass. [[Cystoscopy]] may also be performed to visualize the bladder and obtain tissue samples for [[biopsy]].


== Treatment ==
== Treatment ==
Treatment of urachal cancer typically involves surgery to remove the tumor and any affected surrounding tissues. This may be followed by [[chemotherapy]] or [[radiation therapy]] depending on the stage of the disease and the patient's overall health status.
The primary treatment for urachal cancer is surgical resection, often involving a partial or radical [[cystectomy]] with en bloc resection of the urachus and umbilicus. [[Chemotherapy]] and [[radiation therapy]] may be considered in cases where the cancer is not completely resectable or has metastasized.


== Prognosis ==
== Prognosis ==
The prognosis of urachal cancer depends on various factors including the stage of the disease at diagnosis, the patient's overall health status, and the response to treatment. Early detection and treatment can significantly improve the prognosis.
The prognosis for urachal cancer depends on the stage at diagnosis and the completeness of surgical resection. Early-stage cancers that are completely resected have a better prognosis, while advanced-stage cancers have a poorer outcome.


== See also ==
== Related Pages ==
* [[Bladder cancer]]
* [[Bladder cancer]]
* [[Umbilical cord]]
* [[Adenocarcinoma]]
* [[Chemotherapy]]
* [[Cystectomy]]
* [[Radiation therapy]]
 
== References ==
* Herr, H. W., & Bochner, B. H. (2007). "Urachal carcinoma: the case for extended partial cystectomy." ''The Journal of Urology'', 178(4), 1122-1124.
* Ashley, R. A., Inman, B. A., Routh, J. C., & Rohlinger, A. L. (2006). "Urachal carcinoma: clinicopathologic features and long-term outcomes of an aggressive malignancy." ''Cancer'', 107(4), 712-720.


[[Category:Cancer]]
== Images ==
[[Category:Rare diseases]]
[[File:Urachal_carcinoma_-_high_mag.jpg|thumb|Urachal carcinoma under high magnification.]]
[[Category:Urological diseases]]
[[File:UrC_CDX2_200x.tif|thumb|CDX2 staining in urachal carcinoma.]]


{{stub}}
[[Category:Urological neoplasia]]
[[Category:Rare cancers]]

Revision as of 20:59, 9 February 2025

Urachal Cancer

Urachal cancer is a rare type of cancer that originates in the urachus, a vestigial remnant of the allantois that connects the fetal bladder to the umbilicus. This type of cancer is most commonly found in the bladder dome and is often diagnosed at an advanced stage due to its asymptomatic nature in early development.

Pathophysiology

The urachus is a fibrous cord that is usually obliterated after birth, forming the median umbilical ligament. However, in some cases, remnants of the urachus persist and can give rise to malignancies. Urachal cancer is predominantly adenocarcinoma, accounting for about 90% of cases, with other histological types being much less common.

Symptoms

Symptoms of urachal cancer are often non-specific and may include hematuria (blood in urine), abdominal pain, and a palpable mass. Due to the deep location of the urachus, these symptoms often appear only when the disease is advanced.

Diagnosis

Diagnosis of urachal cancer typically involves imaging studies such as ultrasound, CT scan, or MRI to identify the presence of a mass. Cystoscopy may also be performed to visualize the bladder and obtain tissue samples for biopsy.

Treatment

The primary treatment for urachal cancer is surgical resection, often involving a partial or radical cystectomy with en bloc resection of the urachus and umbilicus. Chemotherapy and radiation therapy may be considered in cases where the cancer is not completely resectable or has metastasized.

Prognosis

The prognosis for urachal cancer depends on the stage at diagnosis and the completeness of surgical resection. Early-stage cancers that are completely resected have a better prognosis, while advanced-stage cancers have a poorer outcome.

Related Pages

References

  • Herr, H. W., & Bochner, B. H. (2007). "Urachal carcinoma: the case for extended partial cystectomy." The Journal of Urology, 178(4), 1122-1124.
  • Ashley, R. A., Inman, B. A., Routh, J. C., & Rohlinger, A. L. (2006). "Urachal carcinoma: clinicopathologic features and long-term outcomes of an aggressive malignancy." Cancer, 107(4), 712-720.

Images

Urachal carcinoma under high magnification.
CDX2 staining in urachal carcinoma.