Urological Cancers affect the organs of the urinary tract and the male reproductive system, including the kidneys, bladder, prostate, and testicles.
These cancers are among the most common, especially prostate cancer in men.
Early signs may include blood in the urine, pain during urination, or lower back pain.
Regular screening is vital for early detection and effective treatment.
Advanced diagnostic tools help in accurate assessment and staging of the disease.
Treatment options vary from surgery and radiation to chemotherapy and immunotherapy.
Consulting a urology specialist can significantly improve patient outcomes and recovery.
Kidney cancer, also known as renal cancer, is a type of cancer that starts in the kidneys β the two bean-shaped organs located behind your abdominal organs, with one kidney on each side of your spine.
The most common types include:
The most common form (~90% of adult kidney cancers).
Usually develops in the lining of the kidney's tubules.
Arises in the renal pelvis (where the kidney meets the ureter).
Similar to bladder cancer.
Most common in children, especially under age 5.
Rare type that begins in the connective tissue of the kidney.
Kidney cancer often doesnβt cause symptoms in early stages. As it progresses, common symptoms may include:
Blood in the urine (hematuria)
Persistent pain in the back or side
A mass or lump in the abdomen
Fatigue
Unexplained weight loss
Fever that isnβt caused by infection
Anemia (low red blood cell count)
Treatment depends on the type, stage, and overall health:
Partial nephrectomy: Removal of the tumor only.
Radical nephrectomy: Removal of the entire kidney.
Drugs that block specific pathways cancer cells use to grow.
Boosts the bodyβs immune response against cancer.
Less commonly used, typically for pain management or if surgery isn't an option.
In slow-growing tumors or for patients unable to undergo aggressive treatment.
The outlook depends on the stage at diagnosis and the overall health of the patient.
Early-stage kidney cancer often has a good prognosis if surgically removed.
Laparoscopic Radical Nephrectomy is a minimally invasive surgical procedure used to remove an entire kidney, typically due to kidney cancer or other serious kidney diseases.
Radical = complete removal
Nephrectomy = removal of the kidney
So, a radical nephrectomy involves removing:
The entire kidney
The adrenal gland (in some cases)
Surrounding fatty tissue
Sometimes nearby lymph nodes
It refers to a minimally invasive technique using small incisions and a camera (laparoscope).
The surgeon uses special instruments inserted through these incisions to perform the surgery.
Compared to open surgery, it usually results in:
Less pain
Smaller scars
Shorter hospital stay
Faster recovery
Renal cell carcinoma (kidney cancer)
Large or complex benign tumors
General anaesthesia is administered.
3β5 small incisions are made in the abdomen.
A laparoscope (camera) is inserted to guide the surgery.
The kidney and surrounding structures are detached and removed, usually through one slightly larger incision.
The incisions are closed.
Adrenocortical cancer (ACC) β also known as adrenal cortical carcinoma β is a rare and aggressive cancer that originates in the outer layer (cortex) of the adrenal glands. The adrenal glands sit atop the kidneys and are responsible for producing hormones such as cortisol, aldosterone, and androgens (sex hormones).
Rarity: ACC is very rare, affecting about 1β2 people per million each year.
Aggressiveness: Often diagnosed at an advanced stage and may spread (metastasize) to other organs.
Age groups: Can occur at any age but has two peak incidences β in children under 5 and adults in their 40sβ50s.
Symptoms depend on whether the tumor is functioning (hormone-producing) or non-functioning:
Produce excess hormones, causing symptoms like:
Cushingβs syndrome (excess cortisol):
Weight gain (especially in the face and abdomen)
Purple stretch marks
Muscle weakness
High blood pressure and blood sugar
Virilization or feminization (excess sex hormones):
In women: facial hair, deepening voice, irregular periods
In men: breast enlargement, decreased libido
Hyperaldosteronism (excess aldosterone):
High blood pressure
Low potassium
Flank or abdominal pain
Palpable abdominal mass
Unexplained weight loss
Fatigue
Imaging: CT or MRI scan of the abdomen to assess the adrenal mass.
Hormone testing: To detect overproduction of cortisol, aldosterone, or androgens.
Biopsy: Rarely done due to risk of spreading cancer cells β diagnosis usually confirmed after surgical removal.
PET scan or bone scan: To check for metastasis.
Most ACCs occur sporadically, but some are linked to genetic syndromes, including:
Li-Fraumeni syndrome
Beckwith-Wiedemann syndrome
Multiple endocrine neoplasia type 1 (MEN1)
Familial adenomatous polyposis (FAP)
Treatment depends on stage and whether the tumor is producing hormones:
Complete surgical removal (adrenalectomy) is the goal, often with surrounding tissue.
Surgery may be curative in early stages.
An adrenal-specific drug used to destroy adrenal tissue.
Often used after surgery to reduce recurrence or for metastatic disease.
Regimens may include drugs like etoposide, doxorubicin, and cisplatin (EDP) plus mitotane.
Used for advanced or recurrent disease.
May be used after surgery or for symptom control in metastatic disease.
Being investigated in clinical trials, but not yet standard treatments.
Early-stage ACC (Stage I or II): Surgery may be curative.
Advanced-stage ACC (Stage III or IV): Prognosis is poorer, especially if metastases are present.
Stage I: ~80%
Stage IV: < 20%
Laparoscopic Adrenalectomy is a minimally invasive surgical procedure to remove one or both adrenal glands, which sit above the kidneys and produce important hormones like cortisol, aldosterone, and adrenaline.
This procedure is done using a laparoscope (a thin camera) and specialized instruments inserted through small incisions in the abdomen or flank.
Itβs typically used to treat:
Functioning (hormone-producing) tumors, such as:
Pheochromocytoma β produces excess adrenaline
Aldosteronoma (Connβs syndrome) β overproduces aldosterone
Cortisol-producing adenoma (Cushing's syndrome)
Non-functioning adrenal masses (usually >4β6 cm or growing)
Adrenocortical carcinoma (in selected cases)
Metastasis from other cancers
General anesthesia is administered.
The surgeon makes 3β5 small incisions in the abdomen or flank.
A laparoscope and surgical tools are inserted.
The adrenal gland is carefully separated from surrounding structures (e.g., kidney, major blood vessels).
The gland is placed in a retrieval bag and removed through one of the incisions.
Incisions are closed; a drain may be placed temporarily.
Transabdominal (most common): through the front or side of the abdomen
Posterior retroperitoneoscopic: through the back, avoiding abdominal organs (good for small tumors)
Smaller incisions, less scarring
Less pain after surgery
Shorter hospital stay (1β3 days)
Faster return to normal activities
Lower risk of infection and complications
Unilateral adrenalectomy: Most common (for tumors on one side)
Bilateral adrenalectomy: Rare; needed in some cases of Cushingβs disease, bilateral tumors, or genetic syndromes
Most patients go home in 1β3 days
Full recovery in 2β4 weeks
Hormonal monitoring continues post-op
If both glands are removed, lifelong hormone replacement is required
UTUC stands for Upper Tract Urothelial Carcinoma. It's a relatively rare type of urothelial cancer that occurs in the lining of the upper urinary tract, specifically in the:
Renal pelvis (part of the kidney that collects urine)
Ureters (tubes that carry urine from the kidneys to the bladder)
UTUC accounts for 5β10% of all urothelial cancers.
More common in older adults, typically in their 70s.
It shares many characteristics with bladder cancer, which also originates from the urothelium, but UTUC tends to be more aggressive and difficult to detect early.
Often nonspecific or silent in early stages:
Detect blood and abnormal cells in urine.
CT urogram (gold standard): Provides detailed images of the kidneys, ureters, and bladder.
MRI or ultrasound may also be used.
A scope is inserted into the urinary tract to visualize the tumor and obtain a biopsy.
Smoking (most significant)
Occupational exposure to chemicals (e.g., aromatic amines, used in dye and chemical industries)
Chronic inflammation or urinary tract infections
Lynch syndrome (hereditary cancer syndrome)
History of bladder cancer
Non-muscle-invasive (low-grade, localized) β confined to the urothelium or lamina propria
Muscle-invasive (high-grade, invasive) β penetrates deeper layers, possibly into surrounding organs or lymph nodes
Treatment is based on tumor location, grade, and stage:
Endoscopic ablation or resection (using laser or electrocautery via ureteroscopy)
Surveillance with regular imaging and ureteroscopy
Nephroureterectomy (removal of the kidney, ureter, and part of the bladder)
Lymph node dissection
Adjuvant chemotherapy (typically cisplatin-based) may be given before or after surgery
Low-grade UTUC: Often curable with endoscopic or surgical treatment
High-grade/invasive UTUC: Has a higher risk of recurrence and metastasis
Localized: ~60β90%
Regional spread: ~30β50%
Distant metastasis: ~5β10%
Laparoscopic Radical Nephroureterectomy is a minimally invasive surgical procedure in which the entire kidney, ureter, and a portion of the bladder where the ureter inserts (called the bladder cuff) are removed. This surgery is primarily performed to treat upper urinary tract urothelial carcinoma (UTUC) β a type of cancer that affects the lining of the kidney and ureter.
The procedure is typically indicated for:
Urothelial carcinoma of the kidney or ureter
High-grade or invasive tumors
Tumors that are not suitable for kidney-sparing treatments
A cancer arising from the urothelium β the lining of the renal pelvis, ureter, and bladder
Similar to bladder cancer but located higher in the urinary tract
Often requires complete removal of the kidney and ureter to prevent recurrence
General anesthesia is administered.
Multiple small incisions are made in the abdomen or flank.
A laparoscope (camera) and instruments are inserted.
The surgeon removes:
The entire kidney
The entire ureter
The bladder cuff (the part of the bladder where the ureter connects)
Lymph nodes may be removed if cancer spread is suspected.
A specimen retrieval bag is used to remove the organs through a slightly larger incision.
Hospital stay: 2β4 days
Catheter: Often left in place for 1β2 weeks
Return to normal activities: 2β4 weeks
Full recovery: 4β6 weeks
Less blood loss
Smaller incisions and better cosmetic results
Shorter hospital stay and faster recovery
Comparable cancer control to open surgery
Procedure |
Scope |
Used For |
---|---|---|
Laparoscopic Radical Nephroureterectomy | Kidney + ureter + bladder cuff | UTUC (high-grade) |
Laparoscopic Nephrectomy | Kidney only | Kidney cancer (renal cell carcinoma) |
Segmental Ureterectomy | Part of ureter | Low-grade, localized ureteral tumors |
Endoscopic Resection | Tumor only | Select low-risk, small tumors |
Bladder cancer is a common type of cancer that begins in the cells lining the inside of the bladder, a hollow organ in the pelvis that stores urine.
Arises from the urothelial cells lining the bladder
Can also affect the ureters and renal pelvis (like in UTUC)
Squamous cell carcinoma
Adenocarcinoma
Small cell carcinoma
Hematuria (blood in the urine) β most common early sign
May be visible (gross hematuria) or microscopic
Frequent urination
Pain or burning during urination
Urgency to urinate
Pelvic or back pain (in advanced disease)
Smoking (major risk factor β causes >50% of cases)
Chemical exposures (e.g., dyes, rubber, leather industries)
Chronic bladder irritation (from infections, catheters)
Previous radiation or chemotherapy (e.g., cyclophosphamide)
Family history and genetic syndromes (e.g., Lynch syndrome)
Urinalysis and urine cytology: Detect blood and cancerous cells.
Cystoscopy: A scope is inserted into the bladder to directly view and biopsy suspicious areas.
Imaging:
CT urogram or MRI to evaluate the bladder and upper urinary tract.
TURBT (Transurethral Resection of Bladder Tumor):
Both diagnostic and therapeutic; used to determine depth of tumor invasion.
Includes Ta, T1, and carcinoma in situ (CIS)
Confined to the inner lining or lamina propria
Invades the detrusor muscle (T2 or higher)
More aggressive, higher risk of spread
Has spread to lymph nodes or distant organs (T4, N+, or M1)
Depends on stage and grade:
TURBT: Surgical removal via the urethra
Intravesical therapy:
BCG (Bacillus Calmette-GuΓ©rin) β most effective for high-risk NMIBC
Radical cystectomy: Removal of the bladder and nearby lymph nodes
Neoadjuvant chemotherapy (e.g., cisplatin-based) before surgery improves outcomes
Bladder-sparing approach (trimodality therapy):
TURBT + chemotherapy + radiation in select cases
Systemic chemotherapy
Immunotherapy:
Checkpoint inhibitors (e.g., atezolizumab, nivolumab)
Targeted therapy:
For tumors with specific mutations (e.g., FGFR)
NMIBC: High recurrence but good survival with treatment
MIBC: 5-year survival ~50% with cystectomy
Metastatic: 5-year survival < 10%
TURBT stands for Transurethral Resection of Bladder Tumor. It is a minimally invasive surgical procedure used to diagnose, stage, and treat bladder cancer.
Removing bladder tumors
Diagnosing bladder cancer (determining if it's superficial or invasive)
Staging the disease (evaluating how deep the tumor has grown into the bladder wall)
It is used primarily for non-muscle invasive bladder cancer (NMIBC), and sometimes for initial diagnosis in muscle-invasive cases.
Spinal or general anesthesia is given.
A resectoscope (a special instrument with a camera and electric loop) is inserted through the urethra (no incision needed).
The surgeon:
Visualizes the tumor inside the bladder
Resects (cuts and removes) the tumor in pieces
Sends tissue samples for pathology
In some cases, intravesical chemotherapy (e.g., mitomycin C) is given immediately after the procedure to reduce recurrence risk.
The visible tumor
A sample of the bladder wall beneath the tumor to assess invasion depth
No external incisions (performed entirely through the urethra)
Short hospital stay (same day or 1β2 nights)
Minimal recovery time
Essential for accurate diagnosis and treatment planning
Mild burning or blood in urine for a few days
Avoid heavy lifting or strenuous activity for ~2 weeks
Repeat TURBT may be needed for large, high-grade, or recurrent tumors
Regular cystoscopic follow-ups are required to monitor for recurrence
Low-grade NMIBC: Often followed with intravesical therapy and surveillance
High-grade or invasive cancer: May require BCG therapy, radical cystectomy, or other interventions
Laparoscopic Radical Cystectomy is a minimally invasive surgery to remove the entire urinary bladder (and nearby tissues/organs) through small abdominal incisions using a laparoscope (a thin camera). It is primarily used to treat muscle-invasive bladder cancer or high-risk non-muscle invasive bladder cancer that has not responded to other treatments.
Primarily for:
Muscle-invasive bladder cancer (MIBC)
High-grade non-muscle invasive bladder cancer (NMIBC) unresponsive to BCG therapy
Certain aggressive bladder tumors or large, multifocal tumors
Urinary bladder
Surrounding lymph nodes
Nearby organs, depending on gender:
Prostate
Seminal vesicles
Uterus
Ovaries
Part of the vagina
General anesthesia is given.
4β6 small incisions are made.
A laparoscope and specialized instruments are inserted.
The bladder, surrounding structures, and lymph nodes are carefully removed.
A urinary diversion is created to allow urine to exit the body:
Ileal conduit (most common)
Continent urinary reservoir (e.g., Indiana pouch)
Neobladder (a bladder substitute using intestine)
Smaller incisions
Less blood loss
Faster recovery
Less postoperative pain
Shorter hospital stay
Hospital stay: 5β10 days
Full recovery: 6β8 weeks
May require a urinary stoma or learning to self-catheterize, depending on the diversion type
Good long-term cancer control for muscle-invasive bladder cancer
5-year survival varies with cancer stage
Prostate cancer is a common cancer that forms in the prostate gland, a small walnut-shaped gland in men that produces seminal fluid. It is one of the most frequently diagnosed cancers in men, especially in older age groups.
Most prostate cancers are adenocarcinomas, arising from glandular cells.
Typically slow-growing, but some forms are aggressive.
Commonly affects men over age 50.
Often detected early through screening.
Early-stage prostate cancer may cause no symptoms. When symptoms do occur, they might include:
Difficulty starting or stopping urination
Weak or interrupted urine stream
Frequent urination, especially at night
Painful urination or ejaculation
Blood in urine or semen
Bone pain (in advanced stages)
Many of these symptoms can also result from benign prostatic hyperplasia (BPH), not just cancer.
Age: Risk increases significantly after age 50
Family history: Especially if father or brother had it
Race: African American men have a higher risk and more aggressive disease
Genetics: BRCA1/BRCA2 mutations, Lynch syndrome
Diet and lifestyle: High-fat diets and obesity may contribute
Blood test to measure PSA levels β elevated levels may suggest cancer, BPH, or prostatitis.
A doctor checks for abnormal shape or texture of the prostate.
MRI can help guide a targeted prostate biopsy if cancer is suspected.
Grading system from biopsy (ranges 6β10) based on how aggressive the cancer looks under a microscope.
Localized: Confined to the prostate
Locally advanced: Spread to nearby tissues (e.g., seminal vesicles)
Advanced/metastatic: Spread to distant organs, commonly bones or lymph nodes
Staging uses TNM classification, PSA level, and Gleason score.
Treatment is based on cancer risk category, age, overall health, and preferences:
For low-risk, slow-growing cancers
Regular PSA, DRE, and biopsy
Radical prostatectomy: Removes the prostate gland and surrounding tissues
Risk of side effects like incontinence and erectile dysfunction
External beam radiation or brachytherapy (radioactive seeds)
Often combined with hormone therapy for higher-risk cancer
Lowers testosterone to slow cancer growth
Used for advanced or recurrent cancer
Side effects: fatigue, hot flashes, bone thinning
For metastatic or hormone-resistant prostate cancer
Immunotherapy (e.g., sipuleucel-T)
Targeted therapy for cancers with specific mutations (e.g., PARP inhibitors for BRCA mutations)
Radiopharmaceuticals (e.g., lutetium-177-PSMA therapy)
Localized prostate cancer has an excellent prognosis: 5-year survival >99%
Advanced disease: Prognosis depends on response to therapy, but many patients live for years with treatment
Monitoring is essential, as recurrence can occur even years later
Laparoscopic Radical Prostatectomy is a minimally invasive surgical procedure to remove the entire prostate gland along with some surrounding tissue (and sometimes lymph nodes) to treat prostate cancer.
Localized prostate cancer (confined to the prostate)
Some cases of locally advanced prostate cancer
Remove the cancer completely
Preserve urinary control and sexual function if possible
General anesthesia is used.
5β6 small incisions are made in the lower abdomen.
A laparoscope (camera) and long instruments are inserted.
The surgeon:
Removes the entire prostate gland
Removes the seminal vesicles
May also remove nearby lymph nodes
Reconnects the urethra to the bladder (vesicourethral anastomosis)
A urinary catheter is placed temporarily (usually for 7β14 days).
Smaller incisions and less scarring
Less blood loss
Shorter hospital stay (1β2 days)
Faster recovery and return to normal activity
Similar cancer control in early-stage cases
Entire prostate gland
Seminal vesicles
Sometimes surrounding lymph nodes
Nerve-sparing techniques may be used depending on cancer location and patient priorities
1β2 days Hospital stay
1β2 weeks Catheter removal
2β4 weeks Light activity, fatigue common
6+ weeks Return to normal activities
Months Gradual return of urinary control and erectile function
Urinary incontinence (improves over months)
Erectile dysfunction (may improve with time or treatment)
Infection, bleeding, or blood clots
Scar tissue at bladder-urethra junction (rare)
Very effective for localized prostate cancer
PSA levels monitored post-op to detect recurrence
Testicular cancer is a rare but highly treatable and often curable cancer that occurs in the testicles (testes) β the male reproductive glands located in the scrotum. It most commonly affects young and middle-aged men, especially those aged 15 to 35.
Most common cancer in young men (15β35 years old)
Usually highly responsive to treatment, even in advanced stages
Two main categories:
Seminomas
Non-seminomas
Leydig cell tumors
Sertoli cell tumors
Painless lump or swelling in a testicle
Heaviness or aching in the scrotum or lower abdomen
Sudden collection of fluid in the scrotum
Breast tenderness or growth (from hormone-secreting tumors)
Back or abdominal pain (if cancer has spread)
A lump in the testicle is the most common early sign.
Cryptorchidism (undescended testicle)
Family history of testicular cancer
Personal history (higher risk in the other testicle)
Klinefelter syndrome (for certain types)
Infertility or abnormal testicular development
Physical exam
Scrotal ultrasound: First-line imaging test to evaluate a mass
Tumor markers in blood:
AFP (alpha-fetoprotein) β elevated in non-seminomas
Ξ²-hCG (beta-human chorionic gonadotropin) β elevated in both
LDH (lactate dehydrogenase) β less specific, correlates with tumor burden
High inguinal orchiectomy:
Removal of the affected testicle
Confirms the diagnosis (biopsy not done before surgery to avoid spread)
Stage I: Confined to the testicle
Stage II: Spread to retroperitoneal lymph nodes
Stage III: Spread to distant organs (lungs, liver, brain)
Staging includes CT scan of abdomen/pelvis and chest, plus tumor marker levels.
Depends on type, stage, and risk category:
High inguinal orchiectomy (standard for all cases)
May be followed by further treatment based on pathology and staging
For early-stage, low-risk tumors (especially seminoma or stage I non-seminoma)
Close follow-up with imaging and tumor markers
Mainly for seminomas (stage I or II)
Seminomas are very radiosensitive
Common in higher-stage disease or non-seminomas
Regimens: BEP (Bleomycin, Etoposide, Cisplatin) is most standard
Often curative even in advanced disease
Surgical removal of lymph nodes in select non-seminoma cases
One of the most curable cancers, especially when detected early
Localized (Stage I): ~99%
Regional (Stage II): ~96%
Distant (Stage III): ~73β80%+
Painless testicular lumps should always be evaluated promptly.
Early detection = very high cure rates.
Lifelong follow-up is important due to risk of late recurrence or secondary cancers from treatment.
High Inguinal Orchidectomy is a surgical procedure in which the entire testicle and spermatic cord are removed through an incision in the groin (inguinal) area. It is primarily performed to diagnose and treat testicular cancer.
High inguinal orchidectomy is usually indicated for:
Suspected or confirmed testicular cancer
Occasionally for severely damaged, atrophic, or infected testicles
As part of treatment for hormone-related conditions (less common)
The incision is made in the groin, not the scrotum.
This approach allows removal of the entire spermatic cord up to the internal inguinal ring, reducing the risk of cancer cell spread.
Scrotal incision is avoided to prevent tumor seeding in cancer cases.
General or regional anesthesia is administered.
A 4β6 cm incision is made in the groin area.
The testicle and spermatic cord are carefully isolated and removed together.
The area is closed with sutures.
The removed tissue is sent for histopathological examination to confirm the diagnosis and cancer type (e.g., seminoma, non-seminoma).
Aspect |
Details |
---|---|
Purpose | Treatment and diagnosis of testicular cancer |
Incision site | Groin (not scrotum) |
Preserves function? | No β testicle and spermatic cord are removed |
Recovery | 1β2 weeks; light activity only initially |
Risks | Bleeding, infection, damage to nearby structures, psychological impact |
Fertility and hormone levels usually unaffected if the other testicle is normal
Testicular prosthesis can be inserted for cosmetic reasons, either during the same surgery or later
Penile cancer is a rare type of cancer that occurs on the skin or in the tissues of the penis. It most often begins in the squamous cells of the penis, so it's usually referred to as squamous cell carcinoma of the penis.
Most penile cancers are squamous cell carcinomas
Typically occurs in men over age 50
Rare in developed countries but more common in parts of Africa, Asia, and South America
Early symptoms can resemble non-cancerous conditions, which may delay diagnosis. Signs to watch for:
Growth or sore on the penis, usually on the glans (head) or foreskin
Redness, irritation, or rash
Thickening or color change of the skin
Foul-smelling discharge
Lump in the groin (from spread to lymph nodes)
Bleeding or pain in advanced stages
Human papillomavirus (HPV) infection (especially HPV-16 and HPV-18)
Lack of circumcision (linked to poor hygiene and chronic inflammation)
Phimosis (inability to retract foreskin)
Smoking
Chronic inflammation or infections
UV light treatment (for psoriasis)
AIDS/HIV (weakened immune system)
Physical exam
Biopsy of the lesion (essential for definitive diagnosis)
Imaging tests (if cancer is invasive):
Ultrasound, MRI, or CT scan of the penis and pelvis
Sentinel lymph node biopsy or groin lymph node assessment
Stage 0 (CIS): Carcinoma in situ β confined to top skin layer
Stage IβII: Localized to the penis
Stage IIIβIV: Spread to nearby lymph nodes or distant organs
Treatment depends on stage, tumor location, and overall health:
Topical therapy (e.g., imiquimod or 5-FU cream)
Laser therapy or cryotherapy
Wide local excision or Mohs micrographic surgery
Partial penectomy (removal of part of the penis)
Total penectomy (in advanced cases)
Reconstruction may be possible
Inguinal lymph node dissection: If cancer has spread to lymph nodes
Radiation therapy
Chemotherapy (e.g., cisplatin-based regimens)
Immunotherapy (in clinical trials or for recurrent cases)
High survival rates if caught early
Localized: ~85β90%
Regional (lymph node spread): ~50β65%
Distant metastasis: < 20%
Early detection is key β delays in seeking care often worsen outcomes.
HPV vaccination (prevents high-risk HPV types)
Good genital hygiene
Avoid smoking
Manage phimosis or chronic inflammation
Penectomy is a surgical procedure involving the removal of part or all of the penis, usually performed to treat penile cancer or, rarely, severe trauma or infection.
There are two main types:
πΉ Partial Penectomy
Removal of part of the penis, usually the glans (head) and some surrounding tissue.
Aims to preserve urinary and sexual function as much as possible.
Localized penile cancer that has not invaded deeply into the base or shaft
Tumor-free surgical margins can be achieved while preserving a penile stump
Urination is usually possible while standing
Sexual function may be preserved, depending on how much tissue remains
May involve reconstructing the urethral opening at the end of the remaining shaft
πΉ Total Penectomy
Removal of the entire penis, including the root at the base.
Required for extensive or deeply invasive tumors where partial removal wouldnβt be sufficient.
Advanced penile cancer
Tumors involving the shaft, base, or deeply invading tissues
Failure of previous treatments (e.g., radiation or partial penectomy)
Urethrostomy is created: a new urinary opening in the perineum (area between scrotum and anus)
Patient urinates while sitting
Sexual function is lost
Testicles are typically preserved, unless also involved
Feature |
Partial Penectomy |
Total Penectomy |
---|---|---|
Extent of removal | Part of penis (typically distal) | Entire penis including base |
Urination | Through remaining shaft | Through perineal urethrostomy |
Sexual function | May be retained (erection possible) | Lost |
Cosmetic impact | Less severe | More significant |
Cancer cases treated | Localized, distal tumors | Extensive or invasive tumors |
Hospital stay: Typically 2β5 days
Return to light activity: 2β4 weeks
Long-term follow-up to monitor for recurrence or metastasis
Psychological support and counseling are often recommended
VEIL is a minimally invasive surgical technique used to remove lymph nodes from the groin (inguinal region) using endoscopic (keyhole) instruments. Itβs primarily performed in patients with penile cancer to manage or prevent the spread of cancer to the inguinal lymph nodes.
Lymph nodes in the groin are often the first site of spread in penile cancer. VEIL is done to:
Stage the cancer (find out how far it has spread)
Treat cancer that may have reached the lymph nodes
Prevent recurrence in high-risk cases
General anesthesia is given.
Small incisions (usually 3) are made in the upper thigh or groin.
A camera (endoscope) and long instruments are inserted under the skin.
The surgeon:
Dissects and removes inguinal lymphatic tissue
Avoids cutting large skin flaps, unlike open surgery
A drain is often left in place temporarily to prevent fluid buildup.
Feature |
VEIL |
Open Lymphadenectomy |
---|---|---|
Incisions | Small | Large skin incisions |
Recovery | Faster | Longer |
Infection risk | Lower | Higher |
Wound complications | Fewer | Common (e.g. skin necrosis) |
Hospital stay | Shorter | Longer |
Hospital stay: Usually 1β3 days
Drain: Removed in 1β2 weeks
Resume light activity in 2β3 weeks
Regular follow-up for cancer surveillance
VEIL is a modern, less invasive option for inguinal lymph node dissection, especially in patients with penile cancer, offering similar cancer control to open surgery with fewer complications.